Amrit Pal Singh Bhangoo

Title(s)Associate Health Sciences Professor, Pediatrics
SchoolSchool of Medicine
Address1001 Health Sciences Road
Irvine CA 92697-3950
Phone(714) 509-8634
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    1. Genetic conditions of short stature: A review of three classic examples. Front Endocrinol (Lausanne). 2022; 13:1011960. Butler MG, Miller BS, Romano A, Ross J, Abuzzahab MJ, Backeljauw P, Bamba V, Bhangoo A, Mauras N, Geffner M. PMID: 36339399; PMCID: PMC9634554.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    2. Multicenter, Randomized Trial of a Bionic Pancreas in Type 1 Diabetes. N Engl J Med. 2022 09 29; 387(13):1161-1172. Bionic Pancreas Research Group, Russell SJ, Beck RW, Damiano ER, El-Khatib FH, Ruedy KJ, Balliro CA, Li Z, Calhoun P, Wadwa RP, Buckingham B, Zhou K, Daniels M, Raskin P, White PC, Lynch J, Pettus J, Hirsch IB, Goland R, Buse JB, Kruger D, Mauras N, Muir A, McGill JB, Cogen F, Weissberg-Benchell J, Sherwood JS, Castellanos LE, Hillard MA, Tuffaha M, Putman MS, Sands MY, Forlenza G, Slover R, Messer LH, Cobry E, Shah VN, Polsky S, Lal R, Ekhlaspour L, Hughes MS, Basina M, Hatipoglu B, Olansky L, Bhangoo A, Forghani N, Kashmiri H, Sutton F, Choudhary A, Penn J, Jafri R, Rayas M, Escaname E, Kerr C, Favela-Prezas R, Boeder S, Trikudanathan S, Williams KM, Leibel N, Kirkman MS, Bergamo K, Klein KR, Dostou JM, Machineni S, Young LA, Diner JC, Bhan A, Jones JK, Benson M, Bird K, Englert K, Permuy J, Cossen K, Felner E, Salam M, Silverstein JM, Adamson S, Cedeno A, Meighan S, Dauber A. PMID: 36170500; PMCID: PMC10028490.
      View in: PubMed   Mentions: 27     Fields:    Translation:Humans
    3. Fasting Serum IGFBP-1 as a Marker of Insulin Resistance in Diverse School Age Groups. Front Endocrinol (Lausanne). 2022; 13:840361. Bhangoo A, Gupta R, Shelov SP, Carey DE, Accacha S, Fennoy I, Altshuler L, Lowell B, Rapaport R, Rosenfeld W, Speiser PW, Ten S, Rosenbaum M. PMID: 35586622; PMCID: PMC9108162.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    4. Response to Letter to the Editor: "Glucocorticoid Resistance in Premature Adrenarche and PCOS: From Childhood to Adulthood". J Endocr Soc. 2021 Feb 01; 5(2):bvaa166. Panayiotopoulos A, Bhangoo A, Khurana D, Ten S, Michl J, Ghanny S. PMID: 33381669; PMCID: PMC7750923.
      View in: PubMed   Mentions:
    5. Glucocorticoid Resistance in Premature Adrenarche and PCOS: From Childhood to Adulthood. J Endocr Soc. 2020 Sep 01; 4(9):bvaa111. Panayiotopoulos A, Bhangoo A, Khurana D, Ten S, Michl J, Ghanny S. PMID: 32904537; PMCID: PMC7456159.
      View in: PubMed   Mentions: 4  
    6. LHX3 deficiency presenting in the United States with severe developmental delay in a child of Syrian refugee parents. Endocrinol Diabetes Metab Case Rep. 2018; 2018. Ahern S, Daniels M, Bhangoo A. PMID: 30481152; PMCID: PMC6280131.
      View in: PubMed   Mentions: 1  
    7. Baseline IGFBP - 3 as the Key Element to Predict Growth Response to Growth Hormone and IGF - 1 Therapy in Subjects with Non - GH Deficient Short Stature and IGF - 1 Deficiency. Int J Endocrinol Metab. 2018 Jul; 16(3):e58928. Perez-Colon S, Lazareva O, Purushothaman R, Malik S, Ten S, Bhangoo A. PMID: 30197657; PMCID: PMC6113715.
      View in: PubMed   Mentions: 3  
    8. Phenotypic spectrum and responses to recombinant human IGF1 (rhIGF1) therapy in patients with homozygous intronic pseudoexon growth hormone receptor mutation. Eur J Endocrinol. 2018 May; 178(5):481-489. Chatterjee S, Shapiro L, Rose SJ, Mushtaq T, Clayton PE, Ten SB, Bhangoo A, Kumbattae U, Dias R, Savage MO, Metherell LA, Storr HL. PMID: 29500309.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    9. Pseudohypoaldosteronism in a neonate presenting as life-threatening arrhythmia. Endocrinol Diabetes Metab Case Rep. 2014; 2014:130077. Rajpoot SK, Maggi C, Bhangoo A. PMID: 24688761; PMCID: PMC3969520.
      View in: PubMed   Mentions: 12  
    10. Racial/ethnic differences in clinical and biochemical type 2 diabetes mellitus risk factors in children. Obesity (Silver Spring). 2013 Oct; 21(10):2081-90. Rosenbaum M, Fennoy I, Accacha S, Altshuler L, Carey DE, Holleran S, Rapaport R, Shelov SP, Speiser PW, Ten S, Bhangoo A, Boucher-Berry C, Espinal Y, Gupta R, Hassoun AA, Iazetti L, Jean-Jacques F, Jean AM, Klein ML, Levine R, Lowell B, Michel L, Rosenfeld W. PMID: 23596082; PMCID: PMC3766484.
      View in: PubMed   Mentions: 15     Fields:    Translation:Humans
    11. Insulin resistance, lipodystrophy and cardiometabolic syndrome in HIV/AIDS. Rev Endocr Metab Disord. 2013 Jun; 14(2):133-40. Galescu O, Bhangoo A, Ten S. PMID: 23700046.
      View in: PubMed   Mentions: 20     Fields:    Translation:HumansAnimals
    12. Endocrinopathies in HIV, AIDS and HAART. Rev Endocr Metab Disord. 2013 Jun; 14(2):101-3. Bhangoo A, Desai N. PMID: 23712383.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    13. Human immune deficiency virus (HIV) infection and the hypothalamic pituitary adrenal axis. Rev Endocr Metab Disord. 2013 Jun; 14(2):105-12. George MM, Bhangoo A. PMID: 23728720.
      View in: PubMed   Mentions: 16     Fields:    Translation:HumansCells
    14. Pathophysiology of GHRH-growth hormone-IGF1 axis in HIV/AIDS. Rev Endocr Metab Disord. 2013 Jun; 14(2):113-8. Jain S, Desai N, Bhangoo A. PMID: 23657561.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    15. Bone and vitamin D metabolism in HIV. Rev Endocr Metab Disord. 2013 Jun; 14(2):119-25. Panayiotopoulos A, Bhat N, Bhangoo A. PMID: 23657562.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansAnimals
    16. HIV and thyroid dysfunction. Rev Endocr Metab Disord. 2013 Jun; 14(2):127-31. Parsa AA, Bhangoo A. PMID: 23743889.
      View in: PubMed   Mentions: 18     Fields:    Translation:Humans
    17. Role of 11βHSD type 2 enzyme activity in essential hypertension and children with chronic kidney disease (CKD). J Clin Endocrinol Metab. 2012 Oct; 97(10):3622-9. Mongia A, Vecker R, George M, Pandey A, Tawadrous H, Schoeneman M, Muneyyirci-Delale O, Nacharaju V, Ten S, Bhangoo A. PMID: 22872687.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    18. Altered glucose disposition and insulin sensitivity in peri-pubertal first-degree relatives of women with polycystic ovary syndrome. Int J Pediatr Endocrinol. 2012 May 29; 2012(1):14. Raissouni N, Kolesnikov A, Purushothaman R, Sinha S, Bhandari S, Bhangoo A, Malik S, Mathew R, Baillargeon JP, Hernandez MI, Rosenbaum M, Ten S, Geller D. PMID: 22643321; PMCID: PMC3477027.
      View in: PubMed   Mentions: 7  
    19. Blood Pressure over Height Ratios: Simple and Accurate Method of Detecting Elevated Blood Pressure in Children. Int J Pediatr. 2012; 2012:253497. Galescu O, George M, Basetty S, Predescu I, Mongia A, Ten S, Bhangoo A. PMID: 22577400; PMCID: PMC3332207.
      View in: PubMed   Mentions: 16  
    20. Hyperandrogenism Does Not Influence Metabolic Parameters in Adolescent Girls with PCOS. Int J Endocrinol. 2012; 2012:434830. Forrester-Dumont K, Galescu O, Kolesnikov A, Raissouni N, Bhangoo A, Ten S, Suss A. PMID: 22536232; PMCID: PMC3320022.
      View in: PubMed   Mentions: 8  
    21. Endothelial function as measured by peripheral arterial tonometry increases during pubertal advancement. Horm Res Paediatr. 2011; 76(4):226-33. Bhangoo A, Sinha S, Rosenbaum M, Shelov S, Ten S. PMID: 21778688; PMCID: PMC3224510.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    22. Isolated 'idiopathic' micropenis: hidden genetic defects? Int J Androl. 2011 Dec; 34(6 Pt 2):e518-25. Paris F, De Ferran K, Bhangoo A, Ten S, Lahlou N, Audran F, Servant N, Poulat F, Philibert P, Sultan C. PMID: 21535007.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansCells
    23. Isolated mild clitoral hypertrophy may reveal 46,XY disorders of sex development in infancy due to 17βHSD-3 defect confirmed by molecular analysis. Gynecol Endocrinol. 2011 Nov; 27(11):890-4. George MM, Sinha S, Mamkin I, Philibert P, New MI, Wilson RC, Sultan C, Ten S, Bhangoo A. PMID: 21214500.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    24. Leydig cell hypoplasia due to inactivating luteinizing hormone/chorionic gonadotropin receptor gene mutation presenting as a 46,XY DSD. Adv Exp Med Biol. 2011; 707:147-8. Sinha SK, Bhangoo A, Ten S, Gromoll J. PMID: 21691974.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    25. The prevalence of non-alcoholic fatty liver disease and metabolic syndrome in obese children. J Pediatr Endocrinol Metab. 2011; 24(11-12):907-11. Gupta R, Bhangoo A, Matthews NA, Anhalt H, Matta Y, Lamichhane B, Malik S, Narwal S, Wetzler G, Ten S. PMID: 22308841.
      View in: PubMed   Mentions: 18     Fields:    Translation:Humans
    26. Functional and physiological consequences of StAR deficiency: role in lipoid congenital adrenal hyperplasia. Endocr Dev. 2011; 20:47-53. King SR, Bhangoo A, Stocco DM. PMID: 21164258.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansAnimals
    27. The clinical and molecular heterogeneity of 17βHSD-3 enzyme deficiency. Horm Res Paediatr. 2010; 74(4):229-40. George MM, New MI, Ten S, Sultan C, Bhangoo A. PMID: 20689261.
      View in: PubMed   Mentions: 30     Fields:    Translation:Humans
    28. Isolated micropenis reveals partial androgen insensitivity syndrome confirmed by molecular analysis. Asian J Androl. 2010 Jul; 12(4):561-6. Bhangoo A, Paris F, Philibert P, Audran F, Ten S, Sultan C. PMID: 20305676; PMCID: PMC3739378.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    29. The genetics of idiopathic hypogonadotropic hypogonadism:unraveling the biology of human sexual development. Pediatr Endocrinol Rev. 2009 Mar; 6(3):395-404. Bhangoo A, Jacobson-Dickman E. PMID: 19396025.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    30. Resting energy expenditure in insulin resistance falls with decompensation of insulin secretion in obese children. J Pediatr Endocrinol Metab. 2008 04; 21(4):359-67. Ten S, Bhangoo A, Ramchandani N, Mueller C, Vogiatzi M, New M, Lesser M, Maclaren N. PMID: 18556967.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    31. Novel mutation in cytochrome P450c17 causes complete combined 17alpha-hydroxylase/17,20-lyase deficiency. J Pediatr Endocrinol Metab. 2008 Feb; 21(2):185-90. Bhangoo A, Aisenberg J, Chartoffe A, Ten S, Wallerstein RJ, Wolf R, Auchus RJ. PMID: 18422032.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    32. Phenotypic features of 46, XX females with StAR protein mutations. Pediatr Endocrinol Rev. 2007 Dec; 5(2):633-41. Bhangoo A, Buyuk E, Oktay K, Ten S. PMID: 18084157.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    33. Effect of metformin and rosiglitazone in a prepubertal boy with Alström syndrome. J Pediatr Endocrinol Metab. 2007 Sep; 20(9):1045-52. Sinha SK, Bhangoo A, Anhalt H, Maclaren N, Marshall JD, Collin GB, Naggert JK, Ten S. PMID: 18038714.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    34. Characterization of insulin resistance syndrome in children and young adults. When to screen for prediabetes? J Pediatr Endocrinol Metab. 2007 Sep; 20(9):989-99. Ten S, Bhangoo A, Ramchandani N, Mueller C, Vogiatzi M, New M, Lesser M, Maclaren N. PMID: 18038708.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    35. Role of a founder c.201_202delCT mutation and new phenotypic features of congenital lipoid adrenal hyperplasia in Palestinians. J Clin Endocrinol Metab. 2007 Oct; 92(10):4000-8. Abdulhadi-Atwan M, Jean A, Chung WK, Meir K, Ben Neriah Z, Stratigopoulos G, Oberfield SE, Fennoy I, Hirsch HJ, Bhangoo A, Ten S, Lerer I, Zangen DH. PMID: 17666473.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansCells
    36. Roles of the LHX3 and LHX4 LIM-homeodomain factors in pituitary development. Mol Cell Endocrinol. 2007 Feb; 265-266:190-5. Mullen RD, Colvin SC, Hunter CS, Savage JJ, Walvoord EC, Bhangoo AP, Ten S, Weigel J, Pfäffle RW, Rhodes SJ. PMID: 17210222; PMCID: PMC1853274.
      View in: PubMed   Mentions: 27     Fields:    Translation:HumansAnimals
    37. An intronic growth hormone receptor mutation causing activation of a pseudoexon is associated with a broad spectrum of growth hormone insensitivity phenotypes. J Clin Endocrinol Metab. 2007 Feb; 92(2):655-9. David A, Camacho-Hübner C, Bhangoo A, Rose SJ, Miraki-Moud F, Akker SA, Butler GE, Ten S, Clayton PE, Clark AJ, Savage MO, Metherell LA. PMID: 17148568.
      View in: PubMed   Mentions: 15     Fields:    Translation:HumansCells
    38. Donor splice mutation in the 11beta-hydroxylase (CypllB1) gene resulting in sex reversal: a case report and review of the literature. J Pediatr Endocrinol Metab. 2006 Oct; 19(10):1267-82. Bhangoo A, Wilson R, New MI, Ten S. PMID: 17172090.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    39. Phenotypic variations in lipoid congenital adrenal hyperplasia. Pediatr Endocrinol Rev. 2006 Mar; 3(3):258-71. Bhangoo A, Anhalt H, Ten S, King SR. PMID: 16639391.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansAnimals
    40. Clinical case seminar: a novel LHX3 mutation presenting as combined pituitary hormonal deficiency. J Clin Endocrinol Metab. 2006 Mar; 91(3):747-53. Bhangoo AP, Hunter CS, Savage JJ, Anhalt H, Pavlakis S, Walvoord EC, Ten S, Rhodes SJ. PMID: 16394081.
      View in: PubMed   Mentions: 30     Fields:    Translation:HumansCells
    41. Phenotypic features associated with mutations in steroidogenic acute regulatory protein. J Clin Endocrinol Metab. 2005 Nov; 90(11):6303-9. Bhangoo A, Gu WX, Pavlakis S, Anhalt H, Heier L, Ten S, Jameson JL. PMID: 16118340.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
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