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Amrit Pal Singh Bhangoo

Title(s)Associate Health Sciences Professor, Pediatrics
Address1001 Health Sciences Road
Irvine CA 92697-3950
Phone(714) 509-8634
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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    1. 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.
      View in: PubMed   Mentions:
    2. 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.
      View in: PubMed   Mentions:
    3. 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.
      View in: PubMed   Mentions:
    4. 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: 3     Fields:    Translation:Humans
    5. 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.
      View in: PubMed   Mentions:
    6. 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.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    7. 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: 14     Fields:    Translation:HumansAnimals
    8. 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:    Fields:    Translation:Humans
    9. 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: 10     Fields:    Translation:HumansCells
    10. 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: 3     Fields:    Translation:Humans
    11. 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
    12. HIV and thyroid dysfunction. Rev Endocr Metab Disord. 2013 Jun; 14(2):127-31. Parsa AA, Bhangoo A. PMID: 23743889.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    13. Role of 11ßHSD 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: 6     Fields:    Translation:Humans
    14. 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.
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    15. 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.
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    16. 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.
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    17. 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.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    18. 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: 3     Fields:    Translation:HumansCells
    19. Isolated mild clitoral hypertrophy may reveal 46,XY disorders of sex development in infancy due to 17ßHSD-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: 1     Fields:    Translation:Humans
    20. 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
    21. 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: 14     Fields:    Translation:Humans
    22. 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: 7     Fields:    Translation:HumansAnimals
    23. The clinical and molecular heterogeneity of 17ßHSD-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: 13     Fields:    Translation:Humans
    24. 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.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    25. 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: 7     Fields:    Translation:Humans
    26. 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: 1     Fields:    Translation:Humans
    27. 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
    28. 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: 6     Fields:    Translation:Humans
    29. 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
    30. 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
    31. 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: 3     Fields:    Translation:HumansCells
    32. 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.
      View in: PubMed   Mentions: 18     Fields:    Translation:HumansAnimals
    33. 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: 6     Fields:    Translation:HumansCells
    34. 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: 6     Fields:    Translation:Humans
    35. 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: 8     Fields:    Translation:HumansAnimals
    36. 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: 27     Fields:    Translation:HumansCells
    37. 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: 7     Fields:    Translation:Humans