Peter Tebben, MD
Endocrinology, Pediatric Endocrinology & Diabetes
Telehealth is available
Patient type treated
Child, Adult
Accepting new patients
Yes
Referral required
Not Applicable
Board Certified in
Endocrinology Diabetes & Metabolism and Pediatric Endocrinology
Education & Training
- FellowMayo Clinic (2006)
- FellowMayo Clinic (2004)
- ResidentUniversity of Minnesota (2002)
- MDUniversity of Kansas (1998)
- BSUniversity of Kansas (1994)
- BSKansas State University (1991)
Additional Information
Honors & Recognitions
- Top Doctor 2020: Minnesota Monthly Magazine (2020)
- Top Performer (99th%) Mayo Clinic Patient Experience: Mayo Clinic College of Medicine and Science (2019), (2020), (2021), (2022), (2023)
- Faculty Education Recognition Award: Mayo Clinic College of Medicine and Science (2014)
- Department of Medicine Career Development Time Award: Mayo Clinic College of Medicine and Science (2008)
- Randall G. Sprague Award in Endocrinology and Metabolism: Mayo Clinic College of Medicine and Science (2005)
Board Certifications
- AB of Pediatrics, Pediatric Endocrinology (2007)
- AB of Internal Medicine, Endocrinology Diabetes & Metabolism (2005)
Professional Service
- Pediatric and Adolescent Research Committee, Mayo Clinic (2023 - 2024): Chair
- Rochester and Midwest Outpatient Practice Sub-Committee (2023 - 2024): Member
- American Society for Bone and Mineral Research (2022 - Present): Member
- Adult Endocrine Fellows Career Development Mentoring Committee (CDMC) (2020 - 2023): Member
- Pediatric Nephrology Faculty Search Committee, Mayo Clinic (2019): Member
- American Society for Bone and Mineral Research (2019 - Present): Program Committee for Annual Meeting
- International Society for Clinical Densitometry (2018 - Present): Clinical Practice Guidelines Task Force for Pediatric Bone Density
- Pediatric Endocrine Faculty Search Committee, Mayo Clinic (2018): Member
- Mayo Clinic (2016 - 2024): Review Editorial Board
- American Society for Bone and Mineral Research (2016 - 2023): Pediatric Bone and Mineral Working Group Committee
Publications
- Ing S, Harmatz P, Mora S, Imel E, Tebben P, Warren M, Ma N, Khan A, Palermo A, Decallonne B, Lemoine S, Mantovani G, Linglart A, Wasserman H, Barbosa A, Cardot-Bauters C, Roberts M, Mathew A, Adler S, Zillikens M, Clifton-Bligh R, Rejnmark L. 9295 Characteristics Of Adults with Autosomal Dominant Hypocalcemia Type 1 (ADH1) Enrolled In The CLARIFY Disease Monitoring Study. Journal Of The Endocrine Society 2024, 8: bvae163.383. PMCID: PMC11454366, DOI: 10.1210/jendso/bvae163.383.
- Ing S, Harmatz P, Mora S, Imel E, Tebben P, Warren M, Ma N, Khan A, Palermo A, Decallonne B, Lemoine S, Mantovani G, Linglart A, Wasserman H, Barbosa A, Cardot-Bauters C, Roberts M, Mathew A, Adler S, Zillikens M, Clifton-Bligh R, Rejnmark L. 8669 Characteristics Of Adults with Autosomal Dominant Hypocalcemia Type 1 (ADH1) Enrolled In The CLARIFY Disease Monitoring Study. Journal Of The Endocrine Society 2024, 8: bvae163.384. PMCID: PMC11454712, DOI: 10.1210/jendso/bvae163.384.
- Zhu Z, Bo-Ran Ho B, Chen A, Amrhein J, Apetrei A, Carpenter T, Lazaretti-Castro M, Colazo J, McCrystal Dahir K, Geßner M, Gurevich E, Heier C, Simmons J, Hunley T, Hoppe B, Jacobsen C, Kouri A, Ma N, Majumdar S, Molin A, Nokoff N, Ott S, Peña H, Santos F, Tebben P, Topor L, Deng Y, Bergwitz C. Erratum to “An update on clinical presentation and responses to therapy of patients with hereditary hypophosphatemic rickets with hypercalciuria (HHRH).” Kidney International 2023;105:1058–1076. Kidney International 2024, 106: 159. PMID: 38906648, DOI: 10.1016/j.kint.2024.05.005.
- Pinto e Vairo F, Kemppainen J, Vitek C, Whalen D, Kolbert K, Sikkink K, Kroc S, Kruisselbrink T, Shupe G, Knudson A, Burke E, Loftus E, Bandel L, Prochnow C, Mulvihill L, Thomas B, Gable D, Graddy C, Garzon G, Ekpoh I, Porquera E, Fervenza F, Hogan M, El Ters M, Warrington K, Davis J, Koster M, Orandi A, Basiaga M, Vella A, Kumar S, Creo A, Lteif A, Pittock S, Tebben P, Abate E, Joshi A, Ristagno E, Patnaik M, Schimmenti L, Dhamija R, Sabrowsky S, Wierenga K, Keddis M, Samadder N, Presutti R, Robinson S, Stephens M, Roberts L, Faubion W, Driscoll S, Wong-Kisiel L, Selcen D, Flanagan E, Ramanan V, Jackson L, Mauermann M, Ortega V, Anderson S, Aoudia S, Klee E, McAllister T, Lazaridis K. Correction: Implementation of genomic medicine for rare disease in a tertiary healthcare system: Mayo Clinic Program for Rare and Undiagnosed Diseases (PRaUD). Journal Of Translational Medicine 2024, 22: 400. PMID: 38689323, PMCID: PMC11061992, DOI: 10.1186/s12967-024-05185-9.
- Salama M, Tebben P, Nofal A. An infant developing hypercalcemia and hypophosphatemia due to the use of exclusively almond milk. Journal Of Pediatric Endocrinology And Metabolism 2024, 37: 375-379. PMID: 38414167, DOI: 10.1515/jpem-2023-0494.
- Mohan S, Sheehan M, Tebben P, Wermers R. Efficacy of Oral Cinacalcet in Non-PTH Nonmalignant Hypercalcemia from Excess 1,25-Dihydroxyvitamin D. JCEM Case Reports 2024, 2: luae022. PMID: 38476635, PMCID: PMC10928506, DOI: 10.1210/jcemcr/luae022.
- Zhu Z, Bo-Ran Ho B, Chen A, Amrhein J, Apetrei A, Carpenter T, Lazaretti-Castro M, Colazo J, McCrystal Dahir K, Geßner M, Gurevich E, Heier C, Simmons J, Hunley T, Hoppe B, Jacobsen C, Kouri A, Ma N, Majumdar S, Molin A, Nokoff N, Ott S, Peña H, Santos F, Tebben P, Topor L, Deng Y, Bergwitz C. An update on clinical presentation and responses to therapy of patients with hereditary hypophosphatemic rickets with hypercalciuria (HHRH). Kidney International 2024, 105: 1058-1076. PMID: 38364990, PMCID: PMC11106756, DOI: 10.1016/j.kint.2024.01.031.
- Vitamin D and the kidneyKritmetapak K, Tebben PJ, Kumar R. Vitamin d and the kidney. In: Hewison M; Et al editors., Feldman and Pike's vitamin d: biochemistry, physiology and diagnostics. Fifth Edition. London: Academic Press/Elsevier; 2024. vol. One. p. 301-30
- Shariq O, Abrantes V, Lu L, Tebben P, Foster T, Dy B, Lyden M, Young W, McKenzie T. Primary hyperparathyroidism in patients with multiple endocrine neoplasia type 1: Impact of genotype and surgical approach on long-term postoperative outcomes. Surgery 2023, 175: 8-16. PMID: 37891063, DOI: 10.1016/j.surg.2023.05.044.
- Mohan S, Sheehan M, Tebben P, Wermers R. SAT257 Efficacy Of Oral Cinacalcet In Non-PTH Non-Malignant Hypercalcemia From Excess 1,25 Dihydroxyvitamin D. Journal Of The Endocrine Society 2023, 7: bvad114.553. PMCID: PMC10554413, DOI: 10.1210/jendso/bvad114.553.
- Salama M, Tebben P. THU461 Severe Hypercalcemia Associated With Perinatal Hypophosphatasia While Receiving Enzyme Replacement Therapy. Journal Of The Endocrine Society 2023, 7: bvad114.422. PMCID: PMC10555444, DOI: 10.1210/jendso/bvad114.422.
- Pinto e Vairo F, Kemppainen J, Vitek C, Whalen D, Kolbert K, Sikkink K, Kroc S, Kruisselbrink T, Shupe G, Knudson A, Burke E, Loftus E, Bandel L, Prochnow C, Mulvihill L, Thomas B, Gable D, Graddy C, Garzon G, Ekpoh I, Porquera E, Fervenza F, Hogan M, El Ters M, Warrington K, Davis J, Koster M, Orandi A, Basiaga M, Vella A, Kumar S, Creo A, Lteif A, Pittock S, Tebben P, Abate E, Joshi A, Ristagno E, Patnaik M, Schimmenti L, Dhamija R, Sabrowsky S, Wierenga K, Keddis M, Samadder N, Presutti R, Robinson S, Stephens M, Roberts L, Faubion W, Driscoll S, Wong-Kisiel L, Selcen D, Flanagan E, Ramanan V, Jackson L, Mauermann M, Ortega V, Anderson S, Aoudia S, Klee E, McAllister T, Lazaridis K. Implementation of genomic medicine for rare disease in a tertiary healthcare system: Mayo Clinic Program for Rare and Undiagnosed Diseases (PRaUD). Journal Of Translational Medicine 2023, 21: 410. PMID: 37353797, PMCID: PMC10288779, DOI: 10.1186/s12967-023-04183-7.
- Pediatric primary hyperparathyroidism: Surgical pathology and long-term outcomes in sporadic and familial cases54. Szabo Yamashita T, Gudmundsdottir H, Foster TR, Lyden ML, Dy BM, Tebben PJ, McKenzie T. Pediatric primary hyperparathyroidism: Surgical pathology and long-term outcomes in sporadic and familial cases. Am J Surg. 2023 Apr;225(4):699-702. doi: 10.1016/j.amjsurg.2022.10.018. Epub 2022 Oct 17. PMID: 36270819
- Fanconi syndrome and renal tubular acidosis. In: Favus MJ. Primer on the metabolic bone diseases and disorders of mineral metabolismTebben PJ, Kumar R. Fanconi syndrome and renal tubular acidosis. In: Favus MJ. Primer on the metabolic bone diseases and disorders of mineral metabolism. 5th ed. Washington, DC: American Society for Bone and Mineral Research; 2003. p. 426-30
- Szabo Yamashita T, Gudmundsdottir H, Foster T, Lyden M, Dy B, Tebben P, McKenzie T. Pediatric primary hyperparathyroidism: Surgical pathology and long-term outcomes in sporadic and familial cases. The American Journal Of Surgery 2022, 225: 699-702. PMID: 36270819, DOI: 10.1016/j.amjsurg.2022.10.018.
- Tebben P. Hypophosphatemia: A Practical Guide to Evaluation and Management. Endocrine Practice 2022, 28: 1091-1099. PMID: 35940468, DOI: 10.1016/j.eprac.2022.07.005.
- Kemppainen J, Thomas B, Pinto e Vairo F, Lazaridis K, Tebben P, Lteif A, Pittock S, Kumar S, Creo A. eP155: Genetic investigation of idiopathic short stature in the endocrinology practice: The Mayo Clinic experience. Genetics In Medicine 2022, 24: s94-s95. DOI: 10.1016/j.gim.2022.01.191.
- Hanna C, Potretzke T, Chedid M, Rangel L, Arroyo J, Zubidat D, Tebben P, Cogal A, Torres V, Harris P, Sas D, Lieske J, Milliner D, Chebib F. Kidney Cysts in Hypophosphatemic Rickets With Hypercalciuria: A Case Series. Kidney Medicine 2022, 4: 100419. PMID: 35386604, PMCID: PMC8978140, DOI: 10.1016/j.xkme.2022.100419.
- Milioto A, Reyes M, Hanna P, Kiuchi Z, Turan S, Zeve D, Agarwal C, Grigelioniene G, Chen A, Mericq V, Frangos M, Ten S, Mantovani G, Salusky I, Tebben P, Jüppner H. Lack of GNAS Remethylation During Oogenesis May Be a Cause of Sporadic Pseudohypoparathyroidism Type Ib. The Journal Of Clinical Endocrinology & Metabolism 2021, 107: e1610-e1619. PMID: 34791361, PMCID: PMC8947795, DOI: 10.1210/clinem/dgab830.
- Christensen S, Tebben P, Sas D, Creo A. Variable Clinical Presentation of Children with Hereditary Hypophosphatemic Rickets with Hypercalciuria: A Case Series and Review of the Literature. Hormone Research In Paediatrics 2021, 94: 374-389. PMID: 34666334, DOI: 10.1159/000520299.
- Kiuchi Z, Reyes M, Hanna P, Sharma A, DeClue T, Olney R, Tebben P, Jüppner H. Progression of PTH Resistance in Autosomal Dominant Pseudohypoparathyroidism Type Ib Due to Maternal STX16 Deletions. The Journal Of Clinical Endocrinology & Metabolism 2021, 107: e681-e687. PMID: 34477200, PMCID: PMC8899049, DOI: 10.1210/clinem/dgab660.
- Hanna C, Arroyo J, Tebben P, Torres V, Harris P, Goldfarb D, Sas D, Milliner D, Lieske J, Chebib F, Potretzke T. High Prevalence of Kidney Cysts in Hereditary Hypophosphatemic Rickets with Hypercalciuria. Journal Of The American Society Of Nephrology 2021, 32: 392-392. DOI: 10.1681/asn.20213210s1392b.
- Dahl A, Armellino A, Tran C, Tebben P. Skimmed breast milk for treatment of hypertriglyceridemia in an infant with congenital nephrotic syndrome. Nutrition In Clinical Practice 2021, 37: 383-387. PMID: 34486165, DOI: 10.1002/ncp.10759.
- Wang Z, Joshi A, Leopold K, Jackson S, Christensen S, Nayfeh T, Mohammed K, Creo A, Tebben P, Kumar S. Association of vitamin D deficiency with COVID‐19 infection severity: Systematic review and meta‐analysis. Clinical Endocrinology 2021, 96: 281-287. PMID: 34160843, PMCID: PMC8444883, DOI: 10.1111/cen.14540.
- Azer S, Vaughan L, Tebben P, Sas D. 24-Hydroxylase Deficiency Due to CYP24A1 Sequence Variants: Comparison With Other Vitamin D−mediated Hypercalcemia Disorders. Journal Of The Endocrine Society 2021, 5: bvab119. PMID: 34337279, PMCID: PMC8317629, DOI: 10.1210/jendso/bvab119.
- Gupta N, Gregory S, Deyle D, Tebben P. Three Patient Kindred with a Novel Phenotype of Osteogenesis Imperfecta due to a COL1A1 Variant. Journal Of Clinical Research In Pediatric Endocrinology 2021, 0: 0-0. PMID: 32519829, PMCID: PMC8186326, DOI: 10.4274/jcrpe.galenos.2020.2020.0012.
- Hanna C, Potretzke T, Cogal A, Mkhaimer Y, Tebben P, Torres V, Lieske J, Harris P, Sas D, Milliner D, Chebib F. High Prevalence of Kidney Cysts in Patients With CYP24A1 Deficiency. Kidney International Reports 2021, 6: 1895-1903. PMID: 34307984, PMCID: PMC8258502, DOI: 10.1016/j.ekir.2021.04.030.
- Christensen S, Tebben P, Sas D, Creo A. Variable Clinical Presentation of Children With Hereditary Hypophosphatemic Rickets With Hypercalciuria: A Case Series. Journal Of The Endocrine Society 2021, 5: a708-a708. PMCID: PMC8090272, DOI: 10.1210/jendso/bvab048.1442.
- Zavatta G, Tebben P, Clarke B. Basal Ganglia Calcification in Hypoparathyroidism Is Associated With Low Serum Calcium/Phosphate Ratio. Journal Of The Endocrine Society 2021, 5: a255-a256. PMCID: PMC8091468, DOI: 10.1210/jendso/bvab048.519.
- Zavatta G, Tebben P, McCollough C, Yu L, Vrieze T, Clarke B. Basal Ganglia Calcification Is Associated With Local and Systemic Metabolic Mechanisms in Adult Hypoparathyroidism. The Journal Of Clinical Endocrinology & Metabolism 2021, 106: 1900-1917. PMID: 33788935, DOI: 10.1210/clinem/dgab162.
- Tebben P, Kumar R. Chapter 10 Phosphatonins. 2021, 215-233. DOI: 10.1016/b978-0-12-813073-5.00010-1.
- Hawkes C, Roy S, Dekelbab B, Frazier B, Grover M, Haidet J, Listman J, Madsen S, Roan M, Rodd C, Sopher A, Tebben P, Levine M. Hypercalcemia in Children Using the Ketogenic Diet: A Multicenter Study. The Journal Of Clinical Endocrinology & Metabolism 2020, 106: e485-e495. PMID: 33124662, PMCID: PMC7823241, DOI: 10.1210/clinem/dgaa759.
- Muthusamy K, Hanna C, Johnson D, Cramer C, Tebben P, Libi S, Poling G, Lanpher B, Morava E, Schimmenti L. Growth hormone deficiency in a child with branchio‐oto‐renal spectrum disorder: Clinical evidence of EYA1 in pituitary development and a recommendation for pituitary function surveillance. American Journal Of Medical Genetics Part A 2020, 185: 261-266. PMID: 33098377, DOI: 10.1002/ajmg.a.61942.
- Hanna C, Potretzke T, Tebben P, Torres V, Harris P, Lieske J, Sas D, Milliner D, Chebib F. CYP24A1 Mutations Are Associated with Renal Cystic Disease. Journal Of The American Society Of Nephrology 2020, 31: 488-488. DOI: 10.1681/asn.20203110s1488c.
- Qureshi M, Patterson M, Clark V, Johnson J, Moutvic M, Driscoll S, Kemppainen J, Huston J, Anderson J, Badley A, Tebben P, Wackel P, Oglesbee D, Glockner J, Schreiner G, Dugar S, Touchette J, Gavrilova R. Safety and efficacy of (+)‐epicatechin in subjects with Friedreich's ataxia: A phase II, open‐label, prospective study. Journal Of Inherited Metabolic Disease 2020, 44: 502-514. PMID: 32677106, DOI: 10.1002/jimd.12285.
- Muthusamy K, Macke E, Klee E, Tebben P, Hand J, Hasadsri L, Marcou C, Schimmenti L. Congenital ichthyosis in Prader–Willi syndrome associated with maternal chromosome 15 uniparental disomy: Case report and review of autosomal recessive conditions unmasked by UPD. American Journal Of Medical Genetics Part A 2020, 182: 2442-2449. PMID: 32815268, DOI: 10.1002/ajmg.a.61792.
- Eswarakumar AS, S. N, Ward LM, Backeljauw P, Wasserman H, Weber DR, DiMeglio LA, Imel EA, Gagne J, Cody D, Zimakas P, Topor LS, Agrawal S, Calabria A, Tebben P, Faircloth RS, Gordon R, Casey L, Carpenter TO. Long-Term Follow-up of Hypophosphatemic Bone Disease Associated With Elemental Formula Use: Sustained Correction of Bone Disease After Formula Change or Phosphate Supplementation. Clinical Pediatrics 2020, 59: 1080-1085. PMID: 32666808, DOI: 10.1177/0009922820941097.
- Wadams H, Gupta N, Novotny P, Tebben P. Onset of pituitary hormone deficiencies in optic nerve hypoplasia: a temporal trend analysis of 32 children at Mayo Clinic. Journal Of Pediatric Endocrinology And Metabolism 2019, 33: 139-145. PMID: 31811804, DOI: 10.1515/jpem-2019-0269.
- Weber D, Boyce A, Gordon C, Högler W, Kecskemethy H, Misra M, Swolin-Eide D, Tebben P, Ward L, Wasserman H, Shuhart C, Zemel B. The Utility of DXA Assessment at the Forearm, Proximal Femur, and Lateral Distal Femur, and Vertebral Fracture Assessment in the Pediatric Population: 2019 ISCD Official Position. Journal Of Clinical Densitometry 2019, 22: 567-589. PMID: 31421951, PMCID: PMC7010480, DOI: 10.1016/j.jocd.2019.07.002.
- Creo A, Anderson H, Cannon B, Lteif A, Kumar S, Tebben P, Iqbal A, Ramakrishna A, Pittock S. Patterns of amiodarone-induced thyroid dysfunction in infants and children. Heart Rhythm 2019, 16: 1436-1442. PMID: 30904484, DOI: 10.1016/j.hrthm.2019.03.015.
- Thacher TD, Pettifor JM, Tebben PJ, Creo AL, Skrinar A, Mao M, Chen CY, Chang T, San Martin J, Carpenter TO. Rickets severity predicts clinical outcomes in children with X-linked hypophosphatemia: Utility of the radiographic Rickets Severity Score. Bone 2019, 122: 76-81. PMID: 30772600, DOI: 10.1016/j.bone.2019.02.010.
- Creo A, Epp L, Buchholtz J, Tebben P. Prevalence of Metabolic Bone Disease in Tube-Fed Children Receiving Elemental Formula. Hormone Research In Paediatrics 2018, 90: 291-298. PMID: 30497080, DOI: 10.1159/000494726.
- Gupta N, Lteif A, Creo A, Iqbal A, Pittock S, Tebben P, Hansen J, Heyrman M, Spee R, Scanlan‐Hanson L, Kumar S. Improved utilization of waist‐to‐height ratio in cardiometabolic risk counselling in children: Application of DMAIC strategy. Journal Of Evaluation In Clinical Practice 2018, 25: 300-305. PMID: 30378218, DOI: 10.1111/jep.13055.
- Lo H, Muskardin T, Tebben P. Blau Syndrome: An Unusual Cause of Hypercalcemia in a Child. AACE Clinical Case Reports 2018, 4: e278-e281. DOI: 10.4158/accr-2017-0041.
- Dahl A, Iqbal A, Lteif A, Pittock S, Tebben P, Kumar S. Mild subclinical hypothyroidism is associated with paediatric dyslipidaemia. Clinical Endocrinology 2018, 89: 330-335. PMID: 29846957, DOI: 10.1111/cen.13752.
- Boland J, Tebben P, Folpe A. Phosphaturic mesenchymal tumors: what an endocrinologist should know. Journal Of Endocrinological Investigation 2018, 41: 1173-1184. PMID: 29446010, DOI: 10.1007/s40618-018-0849-5.
- Tebben P, Kumar R. Chapter 26 Vitamin D and the Kidney. 2018, 437-459. DOI: 10.1016/b978-0-12-809965-0.00026-4.
- Creo A, Tebben P, Fischer P, Thacher T, Pittock S. Cardiac Arrest in a Vitamin D–Deficient Infant. Global Pediatric Health 2018, 5: 2333794x18765064. PMID: 29581997, PMCID: PMC5863858, DOI: 10.1177/2333794x18765064.
- Sakka S, Gafni R, Davies J, Clarke B, Tebben P, Samuels M, Saraff V, Klaushofer K, Fratzl-Zelman N, Roschger P, Rauch F, Högler W. Bone Structural Characteristics and Response to Bisphosphonate Treatment in Children With Hajdu-Cheney Syndrome. The Journal Of Clinical Endocrinology & Metabolism 2017, 102: 4163-4172. PMID: 28938420, PMCID: PMC5673271, DOI: 10.1210/jc.2017-01102.
- Ballesteros L, S. N, Gordon RJ, Ward L, Backeljauw P, Wasserman H, Weber DR, DiMeglio LA, Gagne J, Stein R, Cody D, Simmons K, Zimakas P, Topor LS, Agrawal S, Calabria A, Tebben P, Faircloth R, Imel EA, Casey L, Carpenter TO. Unexpected widespread hypophosphatemia and bone disease associated with elemental formula use in infants and children. Bone 2017, 97: 287-292. PMID: 28167344, PMCID: PMC5884631, DOI: 10.1016/j.bone.2017.02.003.
- Diabetes mellitusJaved A, Schwenk WF, Tebben P. Diabetes mellitus. In: McInerny TK; et al editors., American Academy of Pediatrics textbook of pediatric care. 2nd Edition. Elk Grove Village: American Academy Of Pediatrics; 2017. p. 1952-62
- Diabetic ketoacidosisAl Nofal A, Schwenk WF, Tebben P. Diabetic ketoacidosis. In: McInerny TK; et al editors., American Academy of Pediatrics textbook of pediatric care. 2nd Edition. Elk Grove Village: American Academy Of Pediatrics; 2017. p. 2813-9
- Kumar A, Wermers R, Tebben P. Iron Replacement as A Therapeutic Approach For Renal Phosphate Wasting With Associated Iron Deficiency. AACE Clinical Case Reports 2017, 3: e260-e263. DOI: 10.4158/ep161330.cr.
- Tebben P, Singh R, Kumar R. Vitamin D-Mediated Hypercalcemia: Mechanisms, Diagnosis, and Treatment. Endocrine Reviews 2016, 37: 521-547. PMID: 27588937, PMCID: PMC5045493, DOI: 10.1210/er.2016-1070.
- O’Keeffe D, Tebben P, Kumar R, Singh R, Wu Y, Wermers R. Clinical and biochemical phenotypes of adults with monoallelic and biallelic CYP24A1 mutations: evidence of gene dose effect. Osteoporosis International 2016, 27: 3121-3125. PMID: 27129455, DOI: 10.1007/s00198-016-3615-6.
- Bone Pain in a 4-year-old Boy with Chronic Granulomatous Disease and History of Aspergillus pneumonia19. Uzodi AS, Tebben PJ, Boyce TG. Bone Pain in a 4-year-old Boy with Chronic Granulomatous Disease and History of Aspergillus pneumonia. Pediatr Infect Dis J. 2016 Apr; 35: (4)464-5, 469. PMID: 26967683 DOI: 10.1097/INF.0000000000001042
- Uzodi A, Tebben P, Boyce T. Bone Pain in a 4-year-old Boy with Chronic Granulomatous Disease and History of Aspergillus pneumonia. The Pediatric Infectious Disease Journal 2016, 35: 464-465. PMID: 26967683, DOI: 10.1097/inf.0000000000001042.
- Trivedi S, Al-Nofal A, Kumar S, Tripathi S, Kahoud R, Tebben P. Severe non-infective systemic inflammatory response syndrome, shock, and end-organ dysfunction after zoledronic acid administration in a child. Osteoporosis International 2016, 27: 2379-2382. PMID: 26892041, DOI: 10.1007/s00198-016-3528-4.
- Lo H, Tebben P. Primary Hyperparathyroidism in Children and Adolescents. 2016, 117-128. DOI: 10.1007/978-3-319-25880-5_14.
- Trivedi S, Al-Nofal A, Kumar S, Tripathi S, Kahoud R, Tebben P. 1281. Critical Care Medicine 2015, 43: 322. DOI: 10.1097/01.ccm.0000475112.99592.ef.
- Al Nofal A, Altayar O, BenKhadra K, Qasim Agha O, Asi N, Nabhan M, Prokop L, Tebben P, Murad M. Bone turnover markers in Paget’s disease of the bone: A Systematic review and meta-analysis. Osteoporosis International 2015, 26: 1875-1891. PMID: 26037791, DOI: 10.1007/s00198-015-3095-0.
- James H, Griebeler M, Tebben P. 70-Year-Old Woman With Buttock Pain and Hypercalcemia. Mayo Clinic Proceedings 2014, 89: 1313-1317. PMID: 25192617, DOI: 10.1016/j.mayocp.2013.10.033.
- Kundel A, Thompson G, Richards M, Qiu L, Cai Y, Schwenk F, Lteif A, Pittock S, Kumar S, Tebben P, Hay I, Grant C. Pediatric Endocrine Surgery: A 20-Year Experience at the Mayo Clinic. The Journal Of Clinical Endocrinology & Metabolism 2013, 99: 399-406. PMID: 24423286, DOI: 10.1210/jc.2013-2617.
- Javed A, Tebben P, Fischer P, Lteif A. Female Athlete Triad and Its Components: Toward Improved Screening and Management. Mayo Clinic Proceedings 2013, 88: 996-1009. PMID: 24001492, DOI: 10.1016/j.mayocp.2013.07.001.
- Gardner K, Shon W, Folpe A, Wieland C, Tebben P, Baum C. Cover Quizlet. Journal Of Cutaneous Pathology 2013, 40: 779-779. DOI: 10.1111/cup.12208.
- Gardner K, Shon W, Folpe A, Wieland C, Tebben P, Baum C. Tumor‐Induced Osteomalacia Resulting from Primary Cutaneous Phosphaturic Mesenchymal Tumor: A Case and Review of the Medical Literature. Journal Of Cutaneous Pathology 2013, 40: 780-784. PMID: 23962115, DOI: 10.1111/cup.12209.
- Thacher T, Fischer P, Tebben P, Singh R, S. S, Maxson J, Yawn B. Increasing Incidence of Nutritional Rickets: A Population-Based Study in Olmsted County, Minnesota. Mayo Clinic Proceedings 2013, 88: 176-183. PMID: 23374621, PMCID: PMC3612965, DOI: 10.1016/j.mayocp.2012.10.018.
- Berkseth K, Tebben P, Drake M, Hefferan T, Jewison D, Wermers R. Clinical spectrum of hypophosphatasia diagnosed in adults. Bone 2013, 54: 21-27. PMID: 23352924, DOI: 10.1016/j.bone.2013.01.024.
- HypocalcemiaTebben P. Hypocalcemia. In: Endocrine Self-Assessment Program 2013
- Tebben P, Berndt T, Kumar R. Chapter 16 Phosphatonins. 2013, 373-390. DOI: 10.1016/b978-0-12-415853-5.00016-9.
- Tebben P, Kumar R. Chapter 65 The Hormonal Regulation of Calcium Metabolism. 2013, 2249-2272. DOI: 10.1016/b978-0-12-381462-3.00065-3.
- Kumar R, Tebben P, Thompson J. Vitamin D and the kidney. Archives Of Biochemistry And Biophysics 2012, 523: 77-86. PMID: 22426203, PMCID: PMC3361542, DOI: 10.1016/j.abb.2012.03.003.
- Tebben P, Milliner D, Horst R, Harris P, Singh R, Wu Y, Foreman J, Chelminski P, Kumar R. Hypercalcemia, Hypercalciuria, and Elevated Calcitriol Concentrations with Autosomal Dominant Transmission Due to CYP24A1 Mutations: Effects of Ketoconazole Therapy. The Journal Of Clinical Endocrinology & Metabolism 2012, 97: e423-e427. PMID: 22337913, PMCID: PMC3319216, DOI: 10.1210/jc.2011-1935.
- Hormonal Regulation of Calcium MetabolismTebben PJ, Kumar R. Hormonal Regulation of Calcium Metabolism. In: Alpern RJ and Hebert SC. The Kidney: Physiology and Pathophysiology: Clinical and Physiologic Phosphate Disturbances 5th Edition ed. Elsevier Academic Press; 2011
- Tebben P, Kumar R. Chapter 26 Vitamin D and the Kidney. 2011, 471-491. DOI: 10.1016/b978-0-12-381978-9.10026-5.
- Dy BM, Vazquez B, Tebben PJ, Kumar S, Thompson GB. Severe hypercalcemia due to primary hyperparathyroidism with MEN 2A. World J Endocr Surg.2010;2:(3):131-3.
- Thompson G, Dy B, Vazquez B, Tebben P, Kumar S. Severe Hypercalcemia due to Primary Hyperparathyroidism with MEN 2A. World Journal Of Endocrine Surgery 2010, 2: 131-133. DOI: 10.5005/jp-journals-10002-1037.
- Kirmani S, Tebben P, Lteif A, Gordon D, Clarke B, Hefferan T, Yaszemski M, McGrann P, Lindor N, Ellison J. Germline TGF‐β receptor mutations and skeletal fragility: A report on two patients with Loeys–Dietz syndrome. American Journal Of Medical Genetics Part A 2010, 152A: 1016-1019. PMID: 20358619, DOI: 10.1002/ajmg.a.33356.
- EndocrinologyMcIver B, Tebben PJ, Shah P. Endocrinology. In: Ghosh AK; et al, editor. Mayo Clinic internal medicine board review. 9th Edition. Rochester: Mayo Clinic Scientific Press; 2010. p. 185-231
- PhosphatoninsTebben PJ, Berndt TJ, Kumar R. Phosphatonins. In: Marcus R; et al, editor. Fundamentals of osteoporosis. Burlington; London: Academic Press; 2010. p. 413-28
- Tebben P, Berndt T, Kumar R. Chapter 14 Phosphatonins. 2010, 413-428. DOI: 10.1016/b978-0-12-375098-3.50017-2.
- Novel human pathological mutations. Gene symbol: PHEX. Disease: rickets, hypophosphataemicEllison J, Tebben P. Novel human pathological mutations. Gene symbol: PHEX. Disease: rickets, hypophosphataemic. Hum Genet. 2009 Apr; 125(3):339. PMID: 19309785
- Diabetes mellitusTebben PJ, Schwenk WF. Diabetes mellitus. In: McInerny TK, Adam HM, Campbell D, Kamat DK, Keller KJ. Pediatric primary care. 5th ed. Elk Grove Village, IL: American Academy of Pediatrics; 2008
- Diabetic KetoacidosisTebben PJ, Schwenk WF. Diabetic Ketoacidosis. In: McInerny TK, Adam HM, Campbell D, Kamat DK, Keller KJ. Pediatric Primary Care 5th ed. Elk Grove Village, IL: American Academy of Pediatrics; 2008
- The hormonal regulation of calcium metabolismTebben PJ, Kumar R. The hormonal regulation of calcium metabolism. In: Seldin and Giebisch's the kidney. 2008. p. 1891-909
- Tebben P, Kumar R. CHAPTER 66 The Hormonal Regulation of Calcium Metabolism. 2008, 1891-1909. DOI: 10.1016/b978-012088488-9.50069-3.
- TEBBEN P, BERNDT T, KUMAR R. CHAPTER 16 Phosphatonins. 2008, 451-466. DOI: 10.1016/b978-012370544-0.50018-5.
- Tebben P, Atkinson J, Scheithauer B, Erickson D. Granulomatous Adenohypophysitis after Interferon and Ribavirin Therapy. Endocrine Practice 2007, 13: 169-175. PMID: 17490932, DOI: 10.4158/ep.13.2.169.
- Fanconi syndrome and renal tubular acidosis. In: Favus MJ, editor. Primer on the metabolic bone diseases and disorders of mineral metabolism.Tebben PJ, Thomas LF, Kumar R. Fanconi syndrome and renal tubular acidosis. In: Favus MJ, editor. Primer on the metabolic bone diseases and disorders of mineral metabolism. 6th ed. Washington, DC: 2006. p. 354-8.
- Kudva Y, Khoo T, Tebben P. The Patient With Type 1 Diabetes and Hypoglycemia. Contemporary Endocrinology 2006, 259-273. DOI: 10.1007/978-1-59745-008-9_17.
- Hodgson S, Clarke B, Tebben P, Mullan B, Cooney W, Shives T. Oncogenic Osteomalacia: Localization of Underlying Peripheral Mesenchymal Tumors with Use of Tc 99m Sestamibi Scintigraphy. Endocrine Practice 2006, 12: 35-42. PMID: 16524861, DOI: 10.4158/ep.12.1.35.
- Berndt T, Bielesz B, Craig T, Tebben P, Bacic D, Wagner C, O’Brien S, Schiavi S, Biber J, Murer H, Kumar R. Secreted frizzled-related protein-4 reduces sodium–phosphate co-transporter abundance and activity in proximal tubule cells. Pflügers Archiv - European Journal Of Physiology 2005, 451: 579-587. PMID: 16151791, DOI: 10.1007/s00424-005-1495-2.
- Tebben P, Kalli K, Cliby W, Hartmann L, Grande J, Singh R, Kumar R. Elevated Fibroblast Growth Factor 23 in Women With Malignant Ovarian Tumors. Mayo Clinic Proceedings 2005, 80: 745-751. DOI: 10.4065/80.6.745.
- Tebben P, Kalli K, Cliby W, Hartmann L, Grande J, Singh R, Kumar R. Elevated fibroblast growth factor 23 in women with malignant ovarian tumors. Mayo Clinic Proceedings 2005, 80: 745-51. PMID: 15948297, DOI: 10.1016/s0025-6196(11)61528-0.
- TEBBEN P, KUMAR R. CHAPTER 29 Vitamin D and the Kidney. 2005, 515-536. DOI: 10.1016/b978-012252687-9/50032-2.
- Tebben P, Singh R, Clarke B, Kumar R. Fibroblast Growth Factor 23, Parathyroid Hormone, and 1α,25-Dihydroxyvitamin D in Surgically Treated Primary Hyperparathyroidism. Mayo Clinic Proceedings 2004, 79: 1508-1513. PMID: 15595334, DOI: 10.4065/79.12.1508.
- Three-dimensional computerized reconstruction. Illustration of incremental articular cartilage thinningTebben PJ, Pope TW, Hinson G, Batnitzky S, Wetzel LH, DePaolis DC, Munns S, Wilkinson SB, Gordon MA. Three-dimensional computerized reconstruction. Illustration of incremental articular cartilage thinning. Invest Radiol. 1997 Aug; 32(8):475-84. PMID: 9258736
- TEBBEN P, POPE T, HINSON G, BATNITZKY S, WETZEL L, DEPAOLIS D, MUNNS S, WILKINSON S, GORDON M. Three-Dimensional Computerized Reconstruction Illustration of Incremental Articular Cartilage Thinning. Investigative Radiology 1997, 32: 475-484. PMID: 9258736, DOI: 10.1097/00004424-199708000-00007.
Departments and Programs
Education & Training
- FellowMayo Clinic (2006)
- FellowMayo Clinic (2004)
- ResidentUniversity of Minnesota (2002)
- MDUniversity of Kansas (1998)
- BSUniversity of Kansas (1994)
- BSKansas State University (1991)
Additional Information
Honors & Recognitions
- Top Doctor 2020: Minnesota Monthly Magazine (2020)
- Top Performer (99th%) Mayo Clinic Patient Experience: Mayo Clinic College of Medicine and Science (2019), (2020), (2021), (2022), (2023)
- Faculty Education Recognition Award: Mayo Clinic College of Medicine and Science (2014)
- Department of Medicine Career Development Time Award: Mayo Clinic College of Medicine and Science (2008)
- Randall G. Sprague Award in Endocrinology and Metabolism: Mayo Clinic College of Medicine and Science (2005)
Board Certifications
- AB of Pediatrics, Pediatric Endocrinology (2007)
- AB of Internal Medicine, Endocrinology Diabetes & Metabolism (2005)
Professional Service
- Pediatric and Adolescent Research Committee, Mayo Clinic (2023 - 2024): Chair
- Rochester and Midwest Outpatient Practice Sub-Committee (2023 - 2024): Member
- American Society for Bone and Mineral Research (2022 - Present): Member
- Adult Endocrine Fellows Career Development Mentoring Committee (CDMC) (2020 - 2023): Member
- Pediatric Nephrology Faculty Search Committee, Mayo Clinic (2019): Member
- American Society for Bone and Mineral Research (2019 - Present): Program Committee for Annual Meeting
- International Society for Clinical Densitometry (2018 - Present): Clinical Practice Guidelines Task Force for Pediatric Bone Density
- Pediatric Endocrine Faculty Search Committee, Mayo Clinic (2018): Member
- Mayo Clinic (2016 - 2024): Review Editorial Board
- American Society for Bone and Mineral Research (2016 - 2023): Pediatric Bone and Mineral Working Group Committee
Publications
- Ing S, Harmatz P, Mora S, Imel E, Tebben P, Warren M, Ma N, Khan A, Palermo A, Decallonne B, Lemoine S, Mantovani G, Linglart A, Wasserman H, Barbosa A, Cardot-Bauters C, Roberts M, Mathew A, Adler S, Zillikens M, Clifton-Bligh R, Rejnmark L. 9295 Characteristics Of Adults with Autosomal Dominant Hypocalcemia Type 1 (ADH1) Enrolled In The CLARIFY Disease Monitoring Study. Journal Of The Endocrine Society 2024, 8: bvae163.383. PMCID: PMC11454366, DOI: 10.1210/jendso/bvae163.383.
- Ing S, Harmatz P, Mora S, Imel E, Tebben P, Warren M, Ma N, Khan A, Palermo A, Decallonne B, Lemoine S, Mantovani G, Linglart A, Wasserman H, Barbosa A, Cardot-Bauters C, Roberts M, Mathew A, Adler S, Zillikens M, Clifton-Bligh R, Rejnmark L. 8669 Characteristics Of Adults with Autosomal Dominant Hypocalcemia Type 1 (ADH1) Enrolled In The CLARIFY Disease Monitoring Study. Journal Of The Endocrine Society 2024, 8: bvae163.384. PMCID: PMC11454712, DOI: 10.1210/jendso/bvae163.384.
- Zhu Z, Bo-Ran Ho B, Chen A, Amrhein J, Apetrei A, Carpenter T, Lazaretti-Castro M, Colazo J, McCrystal Dahir K, Geßner M, Gurevich E, Heier C, Simmons J, Hunley T, Hoppe B, Jacobsen C, Kouri A, Ma N, Majumdar S, Molin A, Nokoff N, Ott S, Peña H, Santos F, Tebben P, Topor L, Deng Y, Bergwitz C. Erratum to “An update on clinical presentation and responses to therapy of patients with hereditary hypophosphatemic rickets with hypercalciuria (HHRH).” Kidney International 2023;105:1058–1076. Kidney International 2024, 106: 159. PMID: 38906648, DOI: 10.1016/j.kint.2024.05.005.
- Pinto e Vairo F, Kemppainen J, Vitek C, Whalen D, Kolbert K, Sikkink K, Kroc S, Kruisselbrink T, Shupe G, Knudson A, Burke E, Loftus E, Bandel L, Prochnow C, Mulvihill L, Thomas B, Gable D, Graddy C, Garzon G, Ekpoh I, Porquera E, Fervenza F, Hogan M, El Ters M, Warrington K, Davis J, Koster M, Orandi A, Basiaga M, Vella A, Kumar S, Creo A, Lteif A, Pittock S, Tebben P, Abate E, Joshi A, Ristagno E, Patnaik M, Schimmenti L, Dhamija R, Sabrowsky S, Wierenga K, Keddis M, Samadder N, Presutti R, Robinson S, Stephens M, Roberts L, Faubion W, Driscoll S, Wong-Kisiel L, Selcen D, Flanagan E, Ramanan V, Jackson L, Mauermann M, Ortega V, Anderson S, Aoudia S, Klee E, McAllister T, Lazaridis K. Correction: Implementation of genomic medicine for rare disease in a tertiary healthcare system: Mayo Clinic Program for Rare and Undiagnosed Diseases (PRaUD). Journal Of Translational Medicine 2024, 22: 400. PMID: 38689323, PMCID: PMC11061992, DOI: 10.1186/s12967-024-05185-9.
- Salama M, Tebben P, Nofal A. An infant developing hypercalcemia and hypophosphatemia due to the use of exclusively almond milk. Journal Of Pediatric Endocrinology And Metabolism 2024, 37: 375-379. PMID: 38414167, DOI: 10.1515/jpem-2023-0494.
- Mohan S, Sheehan M, Tebben P, Wermers R. Efficacy of Oral Cinacalcet in Non-PTH Nonmalignant Hypercalcemia from Excess 1,25-Dihydroxyvitamin D. JCEM Case Reports 2024, 2: luae022. PMID: 38476635, PMCID: PMC10928506, DOI: 10.1210/jcemcr/luae022.
- Zhu Z, Bo-Ran Ho B, Chen A, Amrhein J, Apetrei A, Carpenter T, Lazaretti-Castro M, Colazo J, McCrystal Dahir K, Geßner M, Gurevich E, Heier C, Simmons J, Hunley T, Hoppe B, Jacobsen C, Kouri A, Ma N, Majumdar S, Molin A, Nokoff N, Ott S, Peña H, Santos F, Tebben P, Topor L, Deng Y, Bergwitz C. An update on clinical presentation and responses to therapy of patients with hereditary hypophosphatemic rickets with hypercalciuria (HHRH). Kidney International 2024, 105: 1058-1076. PMID: 38364990, PMCID: PMC11106756, DOI: 10.1016/j.kint.2024.01.031.
- Vitamin D and the kidneyKritmetapak K, Tebben PJ, Kumar R. Vitamin d and the kidney. In: Hewison M; Et al editors., Feldman and Pike's vitamin d: biochemistry, physiology and diagnostics. Fifth Edition. London: Academic Press/Elsevier; 2024. vol. One. p. 301-30
- Shariq O, Abrantes V, Lu L, Tebben P, Foster T, Dy B, Lyden M, Young W, McKenzie T. Primary hyperparathyroidism in patients with multiple endocrine neoplasia type 1: Impact of genotype and surgical approach on long-term postoperative outcomes. Surgery 2023, 175: 8-16. PMID: 37891063, DOI: 10.1016/j.surg.2023.05.044.
- Mohan S, Sheehan M, Tebben P, Wermers R. SAT257 Efficacy Of Oral Cinacalcet In Non-PTH Non-Malignant Hypercalcemia From Excess 1,25 Dihydroxyvitamin D. Journal Of The Endocrine Society 2023, 7: bvad114.553. PMCID: PMC10554413, DOI: 10.1210/jendso/bvad114.553.
- Salama M, Tebben P. THU461 Severe Hypercalcemia Associated With Perinatal Hypophosphatasia While Receiving Enzyme Replacement Therapy. Journal Of The Endocrine Society 2023, 7: bvad114.422. PMCID: PMC10555444, DOI: 10.1210/jendso/bvad114.422.
- Pinto e Vairo F, Kemppainen J, Vitek C, Whalen D, Kolbert K, Sikkink K, Kroc S, Kruisselbrink T, Shupe G, Knudson A, Burke E, Loftus E, Bandel L, Prochnow C, Mulvihill L, Thomas B, Gable D, Graddy C, Garzon G, Ekpoh I, Porquera E, Fervenza F, Hogan M, El Ters M, Warrington K, Davis J, Koster M, Orandi A, Basiaga M, Vella A, Kumar S, Creo A, Lteif A, Pittock S, Tebben P, Abate E, Joshi A, Ristagno E, Patnaik M, Schimmenti L, Dhamija R, Sabrowsky S, Wierenga K, Keddis M, Samadder N, Presutti R, Robinson S, Stephens M, Roberts L, Faubion W, Driscoll S, Wong-Kisiel L, Selcen D, Flanagan E, Ramanan V, Jackson L, Mauermann M, Ortega V, Anderson S, Aoudia S, Klee E, McAllister T, Lazaridis K. Implementation of genomic medicine for rare disease in a tertiary healthcare system: Mayo Clinic Program for Rare and Undiagnosed Diseases (PRaUD). Journal Of Translational Medicine 2023, 21: 410. PMID: 37353797, PMCID: PMC10288779, DOI: 10.1186/s12967-023-04183-7.
- Pediatric primary hyperparathyroidism: Surgical pathology and long-term outcomes in sporadic and familial cases54. Szabo Yamashita T, Gudmundsdottir H, Foster TR, Lyden ML, Dy BM, Tebben PJ, McKenzie T. Pediatric primary hyperparathyroidism: Surgical pathology and long-term outcomes in sporadic and familial cases. Am J Surg. 2023 Apr;225(4):699-702. doi: 10.1016/j.amjsurg.2022.10.018. Epub 2022 Oct 17. PMID: 36270819
- Fanconi syndrome and renal tubular acidosis. In: Favus MJ. Primer on the metabolic bone diseases and disorders of mineral metabolismTebben PJ, Kumar R. Fanconi syndrome and renal tubular acidosis. In: Favus MJ. Primer on the metabolic bone diseases and disorders of mineral metabolism. 5th ed. Washington, DC: American Society for Bone and Mineral Research; 2003. p. 426-30
- Szabo Yamashita T, Gudmundsdottir H, Foster T, Lyden M, Dy B, Tebben P, McKenzie T. Pediatric primary hyperparathyroidism: Surgical pathology and long-term outcomes in sporadic and familial cases. The American Journal Of Surgery 2022, 225: 699-702. PMID: 36270819, DOI: 10.1016/j.amjsurg.2022.10.018.
- Tebben P. Hypophosphatemia: A Practical Guide to Evaluation and Management. Endocrine Practice 2022, 28: 1091-1099. PMID: 35940468, DOI: 10.1016/j.eprac.2022.07.005.
- Kemppainen J, Thomas B, Pinto e Vairo F, Lazaridis K, Tebben P, Lteif A, Pittock S, Kumar S, Creo A. eP155: Genetic investigation of idiopathic short stature in the endocrinology practice: The Mayo Clinic experience. Genetics In Medicine 2022, 24: s94-s95. DOI: 10.1016/j.gim.2022.01.191.
- Hanna C, Potretzke T, Chedid M, Rangel L, Arroyo J, Zubidat D, Tebben P, Cogal A, Torres V, Harris P, Sas D, Lieske J, Milliner D, Chebib F. Kidney Cysts in Hypophosphatemic Rickets With Hypercalciuria: A Case Series. Kidney Medicine 2022, 4: 100419. PMID: 35386604, PMCID: PMC8978140, DOI: 10.1016/j.xkme.2022.100419.
- Milioto A, Reyes M, Hanna P, Kiuchi Z, Turan S, Zeve D, Agarwal C, Grigelioniene G, Chen A, Mericq V, Frangos M, Ten S, Mantovani G, Salusky I, Tebben P, Jüppner H. Lack of GNAS Remethylation During Oogenesis May Be a Cause of Sporadic Pseudohypoparathyroidism Type Ib. The Journal Of Clinical Endocrinology & Metabolism 2021, 107: e1610-e1619. PMID: 34791361, PMCID: PMC8947795, DOI: 10.1210/clinem/dgab830.
- Christensen S, Tebben P, Sas D, Creo A. Variable Clinical Presentation of Children with Hereditary Hypophosphatemic Rickets with Hypercalciuria: A Case Series and Review of the Literature. Hormone Research In Paediatrics 2021, 94: 374-389. PMID: 34666334, DOI: 10.1159/000520299.
- Kiuchi Z, Reyes M, Hanna P, Sharma A, DeClue T, Olney R, Tebben P, Jüppner H. Progression of PTH Resistance in Autosomal Dominant Pseudohypoparathyroidism Type Ib Due to Maternal STX16 Deletions. The Journal Of Clinical Endocrinology & Metabolism 2021, 107: e681-e687. PMID: 34477200, PMCID: PMC8899049, DOI: 10.1210/clinem/dgab660.
- Hanna C, Arroyo J, Tebben P, Torres V, Harris P, Goldfarb D, Sas D, Milliner D, Lieske J, Chebib F, Potretzke T. High Prevalence of Kidney Cysts in Hereditary Hypophosphatemic Rickets with Hypercalciuria. Journal Of The American Society Of Nephrology 2021, 32: 392-392. DOI: 10.1681/asn.20213210s1392b.
- Dahl A, Armellino A, Tran C, Tebben P. Skimmed breast milk for treatment of hypertriglyceridemia in an infant with congenital nephrotic syndrome. Nutrition In Clinical Practice 2021, 37: 383-387. PMID: 34486165, DOI: 10.1002/ncp.10759.
- Wang Z, Joshi A, Leopold K, Jackson S, Christensen S, Nayfeh T, Mohammed K, Creo A, Tebben P, Kumar S. Association of vitamin D deficiency with COVID‐19 infection severity: Systematic review and meta‐analysis. Clinical Endocrinology 2021, 96: 281-287. PMID: 34160843, PMCID: PMC8444883, DOI: 10.1111/cen.14540.
- Azer S, Vaughan L, Tebben P, Sas D. 24-Hydroxylase Deficiency Due to CYP24A1 Sequence Variants: Comparison With Other Vitamin D−mediated Hypercalcemia Disorders. Journal Of The Endocrine Society 2021, 5: bvab119. PMID: 34337279, PMCID: PMC8317629, DOI: 10.1210/jendso/bvab119.
- Gupta N, Gregory S, Deyle D, Tebben P. Three Patient Kindred with a Novel Phenotype of Osteogenesis Imperfecta due to a COL1A1 Variant. Journal Of Clinical Research In Pediatric Endocrinology 2021, 0: 0-0. PMID: 32519829, PMCID: PMC8186326, DOI: 10.4274/jcrpe.galenos.2020.2020.0012.
- Hanna C, Potretzke T, Cogal A, Mkhaimer Y, Tebben P, Torres V, Lieske J, Harris P, Sas D, Milliner D, Chebib F. High Prevalence of Kidney Cysts in Patients With CYP24A1 Deficiency. Kidney International Reports 2021, 6: 1895-1903. PMID: 34307984, PMCID: PMC8258502, DOI: 10.1016/j.ekir.2021.04.030.
- Christensen S, Tebben P, Sas D, Creo A. Variable Clinical Presentation of Children With Hereditary Hypophosphatemic Rickets With Hypercalciuria: A Case Series. Journal Of The Endocrine Society 2021, 5: a708-a708. PMCID: PMC8090272, DOI: 10.1210/jendso/bvab048.1442.
- Zavatta G, Tebben P, Clarke B. Basal Ganglia Calcification in Hypoparathyroidism Is Associated With Low Serum Calcium/Phosphate Ratio. Journal Of The Endocrine Society 2021, 5: a255-a256. PMCID: PMC8091468, DOI: 10.1210/jendso/bvab048.519.
- Zavatta G, Tebben P, McCollough C, Yu L, Vrieze T, Clarke B. Basal Ganglia Calcification Is Associated With Local and Systemic Metabolic Mechanisms in Adult Hypoparathyroidism. The Journal Of Clinical Endocrinology & Metabolism 2021, 106: 1900-1917. PMID: 33788935, DOI: 10.1210/clinem/dgab162.
- Tebben P, Kumar R. Chapter 10 Phosphatonins. 2021, 215-233. DOI: 10.1016/b978-0-12-813073-5.00010-1.
- Hawkes C, Roy S, Dekelbab B, Frazier B, Grover M, Haidet J, Listman J, Madsen S, Roan M, Rodd C, Sopher A, Tebben P, Levine M. Hypercalcemia in Children Using the Ketogenic Diet: A Multicenter Study. The Journal Of Clinical Endocrinology & Metabolism 2020, 106: e485-e495. PMID: 33124662, PMCID: PMC7823241, DOI: 10.1210/clinem/dgaa759.
- Muthusamy K, Hanna C, Johnson D, Cramer C, Tebben P, Libi S, Poling G, Lanpher B, Morava E, Schimmenti L. Growth hormone deficiency in a child with branchio‐oto‐renal spectrum disorder: Clinical evidence of EYA1 in pituitary development and a recommendation for pituitary function surveillance. American Journal Of Medical Genetics Part A 2020, 185: 261-266. PMID: 33098377, DOI: 10.1002/ajmg.a.61942.
- Hanna C, Potretzke T, Tebben P, Torres V, Harris P, Lieske J, Sas D, Milliner D, Chebib F. CYP24A1 Mutations Are Associated with Renal Cystic Disease. Journal Of The American Society Of Nephrology 2020, 31: 488-488. DOI: 10.1681/asn.20203110s1488c.
- Qureshi M, Patterson M, Clark V, Johnson J, Moutvic M, Driscoll S, Kemppainen J, Huston J, Anderson J, Badley A, Tebben P, Wackel P, Oglesbee D, Glockner J, Schreiner G, Dugar S, Touchette J, Gavrilova R. Safety and efficacy of (+)‐epicatechin in subjects with Friedreich's ataxia: A phase II, open‐label, prospective study. Journal Of Inherited Metabolic Disease 2020, 44: 502-514. PMID: 32677106, DOI: 10.1002/jimd.12285.
- Muthusamy K, Macke E, Klee E, Tebben P, Hand J, Hasadsri L, Marcou C, Schimmenti L. Congenital ichthyosis in Prader–Willi syndrome associated with maternal chromosome 15 uniparental disomy: Case report and review of autosomal recessive conditions unmasked by UPD. American Journal Of Medical Genetics Part A 2020, 182: 2442-2449. PMID: 32815268, DOI: 10.1002/ajmg.a.61792.
- Eswarakumar AS, S. N, Ward LM, Backeljauw P, Wasserman H, Weber DR, DiMeglio LA, Imel EA, Gagne J, Cody D, Zimakas P, Topor LS, Agrawal S, Calabria A, Tebben P, Faircloth RS, Gordon R, Casey L, Carpenter TO. Long-Term Follow-up of Hypophosphatemic Bone Disease Associated With Elemental Formula Use: Sustained Correction of Bone Disease After Formula Change or Phosphate Supplementation. Clinical Pediatrics 2020, 59: 1080-1085. PMID: 32666808, DOI: 10.1177/0009922820941097.
- Wadams H, Gupta N, Novotny P, Tebben P. Onset of pituitary hormone deficiencies in optic nerve hypoplasia: a temporal trend analysis of 32 children at Mayo Clinic. Journal Of Pediatric Endocrinology And Metabolism 2019, 33: 139-145. PMID: 31811804, DOI: 10.1515/jpem-2019-0269.
- Weber D, Boyce A, Gordon C, Högler W, Kecskemethy H, Misra M, Swolin-Eide D, Tebben P, Ward L, Wasserman H, Shuhart C, Zemel B. The Utility of DXA Assessment at the Forearm, Proximal Femur, and Lateral Distal Femur, and Vertebral Fracture Assessment in the Pediatric Population: 2019 ISCD Official Position. Journal Of Clinical Densitometry 2019, 22: 567-589. PMID: 31421951, PMCID: PMC7010480, DOI: 10.1016/j.jocd.2019.07.002.
- Creo A, Anderson H, Cannon B, Lteif A, Kumar S, Tebben P, Iqbal A, Ramakrishna A, Pittock S. Patterns of amiodarone-induced thyroid dysfunction in infants and children. Heart Rhythm 2019, 16: 1436-1442. PMID: 30904484, DOI: 10.1016/j.hrthm.2019.03.015.
- Thacher TD, Pettifor JM, Tebben PJ, Creo AL, Skrinar A, Mao M, Chen CY, Chang T, San Martin J, Carpenter TO. Rickets severity predicts clinical outcomes in children with X-linked hypophosphatemia: Utility of the radiographic Rickets Severity Score. Bone 2019, 122: 76-81. PMID: 30772600, DOI: 10.1016/j.bone.2019.02.010.
- Creo A, Epp L, Buchholtz J, Tebben P. Prevalence of Metabolic Bone Disease in Tube-Fed Children Receiving Elemental Formula. Hormone Research In Paediatrics 2018, 90: 291-298. PMID: 30497080, DOI: 10.1159/000494726.
- Gupta N, Lteif A, Creo A, Iqbal A, Pittock S, Tebben P, Hansen J, Heyrman M, Spee R, Scanlan‐Hanson L, Kumar S. Improved utilization of waist‐to‐height ratio in cardiometabolic risk counselling in children: Application of DMAIC strategy. Journal Of Evaluation In Clinical Practice 2018, 25: 300-305. PMID: 30378218, DOI: 10.1111/jep.13055.
- Lo H, Muskardin T, Tebben P. Blau Syndrome: An Unusual Cause of Hypercalcemia in a Child. AACE Clinical Case Reports 2018, 4: e278-e281. DOI: 10.4158/accr-2017-0041.
- Dahl A, Iqbal A, Lteif A, Pittock S, Tebben P, Kumar S. Mild subclinical hypothyroidism is associated with paediatric dyslipidaemia. Clinical Endocrinology 2018, 89: 330-335. PMID: 29846957, DOI: 10.1111/cen.13752.
- Boland J, Tebben P, Folpe A. Phosphaturic mesenchymal tumors: what an endocrinologist should know. Journal Of Endocrinological Investigation 2018, 41: 1173-1184. PMID: 29446010, DOI: 10.1007/s40618-018-0849-5.
- Tebben P, Kumar R. Chapter 26 Vitamin D and the Kidney. 2018, 437-459. DOI: 10.1016/b978-0-12-809965-0.00026-4.
- Creo A, Tebben P, Fischer P, Thacher T, Pittock S. Cardiac Arrest in a Vitamin D–Deficient Infant. Global Pediatric Health 2018, 5: 2333794x18765064. PMID: 29581997, PMCID: PMC5863858, DOI: 10.1177/2333794x18765064.
- Sakka S, Gafni R, Davies J, Clarke B, Tebben P, Samuels M, Saraff V, Klaushofer K, Fratzl-Zelman N, Roschger P, Rauch F, Högler W. Bone Structural Characteristics and Response to Bisphosphonate Treatment in Children With Hajdu-Cheney Syndrome. The Journal Of Clinical Endocrinology & Metabolism 2017, 102: 4163-4172. PMID: 28938420, PMCID: PMC5673271, DOI: 10.1210/jc.2017-01102.
- Ballesteros L, S. N, Gordon RJ, Ward L, Backeljauw P, Wasserman H, Weber DR, DiMeglio LA, Gagne J, Stein R, Cody D, Simmons K, Zimakas P, Topor LS, Agrawal S, Calabria A, Tebben P, Faircloth R, Imel EA, Casey L, Carpenter TO. Unexpected widespread hypophosphatemia and bone disease associated with elemental formula use in infants and children. Bone 2017, 97: 287-292. PMID: 28167344, PMCID: PMC5884631, DOI: 10.1016/j.bone.2017.02.003.
- Diabetes mellitusJaved A, Schwenk WF, Tebben P. Diabetes mellitus. In: McInerny TK; et al editors., American Academy of Pediatrics textbook of pediatric care. 2nd Edition. Elk Grove Village: American Academy Of Pediatrics; 2017. p. 1952-62
- Diabetic ketoacidosisAl Nofal A, Schwenk WF, Tebben P. Diabetic ketoacidosis. In: McInerny TK; et al editors., American Academy of Pediatrics textbook of pediatric care. 2nd Edition. Elk Grove Village: American Academy Of Pediatrics; 2017. p. 2813-9
- Kumar A, Wermers R, Tebben P. Iron Replacement as A Therapeutic Approach For Renal Phosphate Wasting With Associated Iron Deficiency. AACE Clinical Case Reports 2017, 3: e260-e263. DOI: 10.4158/ep161330.cr.
- Tebben P, Singh R, Kumar R. Vitamin D-Mediated Hypercalcemia: Mechanisms, Diagnosis, and Treatment. Endocrine Reviews 2016, 37: 521-547. PMID: 27588937, PMCID: PMC5045493, DOI: 10.1210/er.2016-1070.
- O’Keeffe D, Tebben P, Kumar R, Singh R, Wu Y, Wermers R. Clinical and biochemical phenotypes of adults with monoallelic and biallelic CYP24A1 mutations: evidence of gene dose effect. Osteoporosis International 2016, 27: 3121-3125. PMID: 27129455, DOI: 10.1007/s00198-016-3615-6.
- Bone Pain in a 4-year-old Boy with Chronic Granulomatous Disease and History of Aspergillus pneumonia19. Uzodi AS, Tebben PJ, Boyce TG. Bone Pain in a 4-year-old Boy with Chronic Granulomatous Disease and History of Aspergillus pneumonia. Pediatr Infect Dis J. 2016 Apr; 35: (4)464-5, 469. PMID: 26967683 DOI: 10.1097/INF.0000000000001042
- Uzodi A, Tebben P, Boyce T. Bone Pain in a 4-year-old Boy with Chronic Granulomatous Disease and History of Aspergillus pneumonia. The Pediatric Infectious Disease Journal 2016, 35: 464-465. PMID: 26967683, DOI: 10.1097/inf.0000000000001042.
- Trivedi S, Al-Nofal A, Kumar S, Tripathi S, Kahoud R, Tebben P. Severe non-infective systemic inflammatory response syndrome, shock, and end-organ dysfunction after zoledronic acid administration in a child. Osteoporosis International 2016, 27: 2379-2382. PMID: 26892041, DOI: 10.1007/s00198-016-3528-4.
- Lo H, Tebben P. Primary Hyperparathyroidism in Children and Adolescents. 2016, 117-128. DOI: 10.1007/978-3-319-25880-5_14.
- Trivedi S, Al-Nofal A, Kumar S, Tripathi S, Kahoud R, Tebben P. 1281. Critical Care Medicine 2015, 43: 322. DOI: 10.1097/01.ccm.0000475112.99592.ef.
- Al Nofal A, Altayar O, BenKhadra K, Qasim Agha O, Asi N, Nabhan M, Prokop L, Tebben P, Murad M. Bone turnover markers in Paget’s disease of the bone: A Systematic review and meta-analysis. Osteoporosis International 2015, 26: 1875-1891. PMID: 26037791, DOI: 10.1007/s00198-015-3095-0.
- James H, Griebeler M, Tebben P. 70-Year-Old Woman With Buttock Pain and Hypercalcemia. Mayo Clinic Proceedings 2014, 89: 1313-1317. PMID: 25192617, DOI: 10.1016/j.mayocp.2013.10.033.
- Kundel A, Thompson G, Richards M, Qiu L, Cai Y, Schwenk F, Lteif A, Pittock S, Kumar S, Tebben P, Hay I, Grant C. Pediatric Endocrine Surgery: A 20-Year Experience at the Mayo Clinic. The Journal Of Clinical Endocrinology & Metabolism 2013, 99: 399-406. PMID: 24423286, DOI: 10.1210/jc.2013-2617.
- Javed A, Tebben P, Fischer P, Lteif A. Female Athlete Triad and Its Components: Toward Improved Screening and Management. Mayo Clinic Proceedings 2013, 88: 996-1009. PMID: 24001492, DOI: 10.1016/j.mayocp.2013.07.001.
- Gardner K, Shon W, Folpe A, Wieland C, Tebben P, Baum C. Cover Quizlet. Journal Of Cutaneous Pathology 2013, 40: 779-779. DOI: 10.1111/cup.12208.
- Gardner K, Shon W, Folpe A, Wieland C, Tebben P, Baum C. Tumor‐Induced Osteomalacia Resulting from Primary Cutaneous Phosphaturic Mesenchymal Tumor: A Case and Review of the Medical Literature. Journal Of Cutaneous Pathology 2013, 40: 780-784. PMID: 23962115, DOI: 10.1111/cup.12209.
- Thacher T, Fischer P, Tebben P, Singh R, S. S, Maxson J, Yawn B. Increasing Incidence of Nutritional Rickets: A Population-Based Study in Olmsted County, Minnesota. Mayo Clinic Proceedings 2013, 88: 176-183. PMID: 23374621, PMCID: PMC3612965, DOI: 10.1016/j.mayocp.2012.10.018.
- Berkseth K, Tebben P, Drake M, Hefferan T, Jewison D, Wermers R. Clinical spectrum of hypophosphatasia diagnosed in adults. Bone 2013, 54: 21-27. PMID: 23352924, DOI: 10.1016/j.bone.2013.01.024.
- HypocalcemiaTebben P. Hypocalcemia. In: Endocrine Self-Assessment Program 2013
- Tebben P, Berndt T, Kumar R. Chapter 16 Phosphatonins. 2013, 373-390. DOI: 10.1016/b978-0-12-415853-5.00016-9.
- Tebben P, Kumar R. Chapter 65 The Hormonal Regulation of Calcium Metabolism. 2013, 2249-2272. DOI: 10.1016/b978-0-12-381462-3.00065-3.
- Kumar R, Tebben P, Thompson J. Vitamin D and the kidney. Archives Of Biochemistry And Biophysics 2012, 523: 77-86. PMID: 22426203, PMCID: PMC3361542, DOI: 10.1016/j.abb.2012.03.003.
- Tebben P, Milliner D, Horst R, Harris P, Singh R, Wu Y, Foreman J, Chelminski P, Kumar R. Hypercalcemia, Hypercalciuria, and Elevated Calcitriol Concentrations with Autosomal Dominant Transmission Due to CYP24A1 Mutations: Effects of Ketoconazole Therapy. The Journal Of Clinical Endocrinology & Metabolism 2012, 97: e423-e427. PMID: 22337913, PMCID: PMC3319216, DOI: 10.1210/jc.2011-1935.
- Hormonal Regulation of Calcium MetabolismTebben PJ, Kumar R. Hormonal Regulation of Calcium Metabolism. In: Alpern RJ and Hebert SC. The Kidney: Physiology and Pathophysiology: Clinical and Physiologic Phosphate Disturbances 5th Edition ed. Elsevier Academic Press; 2011
- Tebben P, Kumar R. Chapter 26 Vitamin D and the Kidney. 2011, 471-491. DOI: 10.1016/b978-0-12-381978-9.10026-5.
- Dy BM, Vazquez B, Tebben PJ, Kumar S, Thompson GB. Severe hypercalcemia due to primary hyperparathyroidism with MEN 2A. World J Endocr Surg.2010;2:(3):131-3.
- Thompson G, Dy B, Vazquez B, Tebben P, Kumar S. Severe Hypercalcemia due to Primary Hyperparathyroidism with MEN 2A. World Journal Of Endocrine Surgery 2010, 2: 131-133. DOI: 10.5005/jp-journals-10002-1037.
- Kirmani S, Tebben P, Lteif A, Gordon D, Clarke B, Hefferan T, Yaszemski M, McGrann P, Lindor N, Ellison J. Germline TGF‐β receptor mutations and skeletal fragility: A report on two patients with Loeys–Dietz syndrome. American Journal Of Medical Genetics Part A 2010, 152A: 1016-1019. PMID: 20358619, DOI: 10.1002/ajmg.a.33356.
- EndocrinologyMcIver B, Tebben PJ, Shah P. Endocrinology. In: Ghosh AK; et al, editor. Mayo Clinic internal medicine board review. 9th Edition. Rochester: Mayo Clinic Scientific Press; 2010. p. 185-231
- PhosphatoninsTebben PJ, Berndt TJ, Kumar R. Phosphatonins. In: Marcus R; et al, editor. Fundamentals of osteoporosis. Burlington; London: Academic Press; 2010. p. 413-28
- Tebben P, Berndt T, Kumar R. Chapter 14 Phosphatonins. 2010, 413-428. DOI: 10.1016/b978-0-12-375098-3.50017-2.
- Novel human pathological mutations. Gene symbol: PHEX. Disease: rickets, hypophosphataemicEllison J, Tebben P. Novel human pathological mutations. Gene symbol: PHEX. Disease: rickets, hypophosphataemic. Hum Genet. 2009 Apr; 125(3):339. PMID: 19309785
- Diabetes mellitusTebben PJ, Schwenk WF. Diabetes mellitus. In: McInerny TK, Adam HM, Campbell D, Kamat DK, Keller KJ. Pediatric primary care. 5th ed. Elk Grove Village, IL: American Academy of Pediatrics; 2008
- Diabetic KetoacidosisTebben PJ, Schwenk WF. Diabetic Ketoacidosis. In: McInerny TK, Adam HM, Campbell D, Kamat DK, Keller KJ. Pediatric Primary Care 5th ed. Elk Grove Village, IL: American Academy of Pediatrics; 2008
- The hormonal regulation of calcium metabolismTebben PJ, Kumar R. The hormonal regulation of calcium metabolism. In: Seldin and Giebisch's the kidney. 2008. p. 1891-909
- Tebben P, Kumar R. CHAPTER 66 The Hormonal Regulation of Calcium Metabolism. 2008, 1891-1909. DOI: 10.1016/b978-012088488-9.50069-3.
- TEBBEN P, BERNDT T, KUMAR R. CHAPTER 16 Phosphatonins. 2008, 451-466. DOI: 10.1016/b978-012370544-0.50018-5.
- Tebben P, Atkinson J, Scheithauer B, Erickson D. Granulomatous Adenohypophysitis after Interferon and Ribavirin Therapy. Endocrine Practice 2007, 13: 169-175. PMID: 17490932, DOI: 10.4158/ep.13.2.169.
- Fanconi syndrome and renal tubular acidosis. In: Favus MJ, editor. Primer on the metabolic bone diseases and disorders of mineral metabolism.Tebben PJ, Thomas LF, Kumar R. Fanconi syndrome and renal tubular acidosis. In: Favus MJ, editor. Primer on the metabolic bone diseases and disorders of mineral metabolism. 6th ed. Washington, DC: 2006. p. 354-8.
- Kudva Y, Khoo T, Tebben P. The Patient With Type 1 Diabetes and Hypoglycemia. Contemporary Endocrinology 2006, 259-273. DOI: 10.1007/978-1-59745-008-9_17.
- Hodgson S, Clarke B, Tebben P, Mullan B, Cooney W, Shives T. Oncogenic Osteomalacia: Localization of Underlying Peripheral Mesenchymal Tumors with Use of Tc 99m Sestamibi Scintigraphy. Endocrine Practice 2006, 12: 35-42. PMID: 16524861, DOI: 10.4158/ep.12.1.35.
- Berndt T, Bielesz B, Craig T, Tebben P, Bacic D, Wagner C, O’Brien S, Schiavi S, Biber J, Murer H, Kumar R. Secreted frizzled-related protein-4 reduces sodium–phosphate co-transporter abundance and activity in proximal tubule cells. Pflügers Archiv - European Journal Of Physiology 2005, 451: 579-587. PMID: 16151791, DOI: 10.1007/s00424-005-1495-2.
- Tebben P, Kalli K, Cliby W, Hartmann L, Grande J, Singh R, Kumar R. Elevated Fibroblast Growth Factor 23 in Women With Malignant Ovarian Tumors. Mayo Clinic Proceedings 2005, 80: 745-751. DOI: 10.4065/80.6.745.
- Tebben P, Kalli K, Cliby W, Hartmann L, Grande J, Singh R, Kumar R. Elevated fibroblast growth factor 23 in women with malignant ovarian tumors. Mayo Clinic Proceedings 2005, 80: 745-51. PMID: 15948297, DOI: 10.1016/s0025-6196(11)61528-0.
- TEBBEN P, KUMAR R. CHAPTER 29 Vitamin D and the Kidney. 2005, 515-536. DOI: 10.1016/b978-012252687-9/50032-2.
- Tebben P, Singh R, Clarke B, Kumar R. Fibroblast Growth Factor 23, Parathyroid Hormone, and 1α,25-Dihydroxyvitamin D in Surgically Treated Primary Hyperparathyroidism. Mayo Clinic Proceedings 2004, 79: 1508-1513. PMID: 15595334, DOI: 10.4065/79.12.1508.
- Three-dimensional computerized reconstruction. Illustration of incremental articular cartilage thinningTebben PJ, Pope TW, Hinson G, Batnitzky S, Wetzel LH, DePaolis DC, Munns S, Wilkinson SB, Gordon MA. Three-dimensional computerized reconstruction. Illustration of incremental articular cartilage thinning. Invest Radiol. 1997 Aug; 32(8):475-84. PMID: 9258736
- TEBBEN P, POPE T, HINSON G, BATNITZKY S, WETZEL L, DEPAOLIS D, MUNNS S, WILKINSON S, GORDON M. Three-Dimensional Computerized Reconstruction Illustration of Incremental Articular Cartilage Thinning. Investigative Radiology 1997, 32: 475-484. PMID: 9258736, DOI: 10.1097/00004424-199708000-00007.
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