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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.
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5 Fields:
Translation:
Humans
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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.
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39 Fields:
Translation:
Humans
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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.
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2 Fields:
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Humans
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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.
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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.
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5
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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.
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2
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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.
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PubMed Mentions:
3
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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.
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PubMed Mentions:
11 Fields:
Translation:
Humans
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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.
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PubMed Mentions:
12
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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.
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PubMed Mentions:
15 Fields:
Translation:
Humans
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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.
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PubMed Mentions:
21 Fields:
Translation:
HumansAnimals
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Endocrinopathies in HIV, AIDS and HAART. Rev Endocr Metab Disord. 2013 Jun; 14(2):101-3.
Bhangoo A, Desai N. PMID: 23712383.
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PubMed Mentions:
2 Fields:
Translation:
Humans
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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.
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PubMed Mentions:
16 Fields:
Translation:
HumansCells
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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.
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PubMed Mentions:
5 Fields:
Translation:
Humans
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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.
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PubMed Mentions:
11 Fields:
Translation:
HumansAnimals
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HIV and thyroid dysfunction. Rev Endocr Metab Disord. 2013 Jun; 14(2):127-31.
Parsa AA, Bhangoo A. PMID: 23743889.
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20 Fields:
Translation:
Humans
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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.
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PubMed Mentions:
8 Fields:
Translation:
Humans
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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.
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7
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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.
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16
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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.
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8
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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.
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18 Fields:
Translation:
Humans
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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.
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7 Fields:
Translation:
HumansCells
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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.
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2 Fields:
Translation:
Humans
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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.
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HumansCells
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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.
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19 Fields:
Translation:
Humans
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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.
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PubMed Mentions:
8 Fields:
Translation:
HumansAnimals
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The clinical and molecular heterogeneity of 17βHSD-3 enzyme deficiency. Horm Res Paediatr. 2010; 74(4):229-240.
George MM, New MI, Ten S, Sultan C, Bhangoo A. PMID: 20689261.
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PubMed Mentions:
30 Fields:
Translation:
Humans
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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.
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PubMed Mentions:
9 Fields:
Translation:
Humans
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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.
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9 Fields:
Translation:
Humans
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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.
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PubMed Mentions:
3 Fields:
Translation:
Humans
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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.
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4 Fields:
Translation:
Humans
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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.
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7 Fields:
Translation:
Humans
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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.
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PubMed Mentions:
5 Fields:
Translation:
Humans
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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.
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Humans
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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.
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6 Fields:
Translation:
HumansCells
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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.
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31 Fields:
Translation:
HumansAnimals
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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.
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PubMed Mentions:
15 Fields:
Translation:
HumansCells
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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.
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PubMed Mentions:
7 Fields:
Translation:
Humans
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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.
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PubMed Mentions:
11 Fields:
Translation:
HumansAnimals
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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.
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PubMed Mentions:
32 Fields:
Translation:
HumansCells
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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.
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PubMed Mentions:
10 Fields:
Translation:
Humans