Bhangoo A - Search Results

1

Role of 11βHSD type 2 enzyme activity in essential hypertension and children with chronic kidney disease (CKD).

Mongia A, Vecker R, George M, Pandey A, Tawadrous H, Schoeneman M, Muneyyirci-Delale O, Nacharaju V, Ten S, Bhangoo A. Mongia A, et al. Among authors: bhangoo a. J Clin Endocrinol Metab. 2012 Oct;97(10):3622-9. doi: 10.1210/jc.2012-1411. Epub 2012 Aug 7. J Clin Endocrinol Metab. 2012. PMID: 22872687

2

Phenotypic features associated with mutations in steroidogenic acute regulatory protein.

Bhangoo A, Gu WX, Pavlakis S, Anhalt H, Heier L, Ten S, Jameson JL. Bhangoo A, et al. J Clin Endocrinol Metab. 2005 Nov;90(11):6303-9. doi: 10.1210/jc.2005-0434. Epub 2005 Aug 23. J Clin Endocrinol Metab. 2005. PMID: 16118340

3

Clinical case seminar: a novel LHX3 mutation presenting as combined pituitary hormonal deficiency.

Bhangoo AP, Hunter CS, Savage JJ, Anhalt H, Pavlakis S, Walvoord EC, Ten S, Rhodes SJ. Bhangoo AP, et al. J Clin Endocrinol Metab. 2006 Mar;91(3):747-53. doi: 10.1210/jc.2005-2360. Epub 2006 Jan 4. J Clin Endocrinol Metab. 2006. PMID: 16394081

4

Phenotypic variations in lipoid congenital adrenal hyperplasia.

Bhangoo A, Anhalt H, Ten S, King SR. Bhangoo A, et al. Pediatr Endocrinol Rev. 2006 Mar;3(3):258-71. Pediatr Endocrinol Rev. 2006. PMID: 16639391

5

An intronic growth hormone receptor mutation causing activation of a pseudoexon is associated with a broad spectrum of growth hormone insensitivity phenotypes.

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. David A, et al. Among authors: bhangoo a. J Clin Endocrinol Metab. 2007 Feb;92(2):655-9. doi: 10.1210/jc.2006-1527. Epub 2006 Dec 5. J Clin Endocrinol Metab. 2007. PMID: 17148568

6

Donor splice mutation in the 11beta-hydroxylase (CypllB1) gene resulting in sex reversal: a case report and review of the literature.

Bhangoo A, Wilson R, New MI, Ten S. Bhangoo A, et al. J Pediatr Endocrinol Metab. 2006 Oct;19(10):1267-82. doi: 10.1515/jpem.2006.19.10.1267. J Pediatr Endocrinol Metab. 2006. PMID: 17172090

7

Role of a founder c.201_202delCT mutation and new phenotypic features of congenital lipoid adrenal hyperplasia in Palestinians.

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. Abdulhadi-Atwan M, et al. Among authors: bhangoo a. J Clin Endocrinol Metab. 2007 Oct;92(10):4000-8. doi: 10.1210/jc.2007-1306. Epub 2007 Jul 31. J Clin Endocrinol Metab. 2007. PMID: 17666473

8

Characterization of insulin resistance syndrome in children and young adults. When to screen for prediabetes?

Ten S, Bhangoo A, Ramchandani N, Mueller C, Vogiatzi M, New M, Lesser M, Maclaren N. Ten S, et al. Among authors: bhangoo a. J Pediatr Endocrinol Metab. 2007 Sep;20(9):989-99. doi: 10.1515/jpem.2007.20.9.989. J Pediatr Endocrinol Metab. 2007. PMID: 18038708

9

Effect of metformin and rosiglitazone in a prepubertal boy with Alström syndrome.

Sinha SK, Bhangoo A, Anhalt H, Maclaren N, Marshall JD, Collin GB, Naggert JK, Ten S. Sinha SK, et al. Among authors: bhangoo a. J Pediatr Endocrinol Metab. 2007 Sep;20(9):1045-52. doi: 10.1515/jpem.2007.20.9.1045. J Pediatr Endocrinol Metab. 2007. PMID: 18038714

10

Phenotypic features of 46, XX females with StAR protein mutations.

Bhangoo A, Buyuk E, Oktay K, Ten S. Bhangoo A, et al. Pediatr Endocrinol Rev. 2007 Dec;5(2):633-41. Pediatr Endocrinol Rev. 2007. PMID: 18084157 Review.

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