Mathew RP - Search Results

1

Exome sequencing for the diagnosis of 46,XY disorders of sex development.

Baxter RM, Arboleda VA, Lee H, Barseghyan H, Adam MP, Fechner PY, Bargman R, Keegan C, Travers S, Schelley S, Hudgins L, Mathew RP, Stalker HJ, Zori R, Gordon OK, Ramos-Platt L, Pawlikowska-Haddal A, Eskin A, Nelson SF, Délot E, Vilain E. Baxter RM, et al. Among authors: mathew rp. J Clin Endocrinol Metab. 2015 Feb;100(2):E333-44. doi: 10.1210/jc.2014-2605. Epub 2014 Nov 10. J Clin Endocrinol Metab. 2015. PMID: 25383892 Free PMC article.

2

Profile of Daughters and Sisters of Women With Polycystic Ovary Syndrome: The Role of Proband's Glucose Tolerance.

Harnois-Leblanc S, Hernandez MI, Codner E, Cassorla F, Oberfield SE, Leibel NI, Mathew RP, Ten S, Magoffin DA, Lane CJ, Goran MI, Azziz R, Baillargeon JP, Geller DH. Harnois-Leblanc S, et al. Among authors: mathew rp. J Clin Endocrinol Metab. 2022 Feb 17;107(3):e912-e923. doi: 10.1210/clinem/dgab812. J Clin Endocrinol Metab. 2022. PMID: 34752621 Free PMC article.

3

Changes in carotid artery sonogram in premature adrenarche.

Mathew RP, Hernanz-Schulman M, Wang W, Saville B, Bremer A. Mathew RP, et al. J Pediatr Endocrinol Metab. 2012;25(1-2):139-45. doi: 10.1515/jpem.2011.411. J Pediatr Endocrinol Metab. 2012. PMID: 22570963

4

Short stature in a patient with familial glucocorticoid deficiency.

Mathew RP, Kovacs WJ. Mathew RP, et al. J Pediatr Endocrinol Metab. 2011;24(7-8):569-71. doi: 10.1515/jpem.2011.203. J Pediatr Endocrinol Metab. 2011. PMID: 21932602

5

Evidence of metabolic syndrome in lean children with premature pubarche at diagnosis.

Mathew RP, Byrne DW, Linton MF, Vaughan DE, Fazio S, Russell WE. Mathew RP, et al. Metabolism. 2008 Jun;57(6):733-40. doi: 10.1016/j.metabol.2008.01.010. Metabolism. 2008. PMID: 18502254

6

Premature pubarche in girls is associated with functional adrenal but not ovarian hyperandrogenism.

Mathew RP, Najjar JL, Lorenz RA, Mayes DE, Russell WE. Mathew RP, et al. J Pediatr. 2002 Jul;141(1):91-8. doi: 10.1067/mpd.2002.125492. J Pediatr. 2002. PMID: 12091857

7

Altered glucose disposition and insulin sensitivity in peri-pubertal first-degree relatives of women with polycystic ovary syndrome.

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. Raissouni N, et al. Int J Pediatr Endocrinol. 2012 May 29;2012(1):14. doi: 10.1186/1687-9856-2012-14. Int J Pediatr Endocrinol. 2012. PMID: 22643321 Free PMC article.

8

Autoimmune alternating hypo- and hyperthyroidism in children.

Mathew RP, Moore DJ. Mathew RP, et al. Clin Pediatr (Phila). 2011 Nov;50(11):1040-4. doi: 10.1177/0009922811412583. Epub 2011 Jun 23. Clin Pediatr (Phila). 2011. PMID: 21700620 Free PMC article.

9

A unique case of hyperammonemia due to CA5A deficiency: Impact of coexisting gene mutations, pseudogene, and microdeletion.

Mathew RP, Ranya Raghavendra P, Disha B, Dalal A, Govindaraj P. Mathew RP, et al. Am J Med Genet A. 2024 Nov;194(11):e63809. doi: 10.1002/ajmg.a.63809. Epub 2024 Jul 1. Am J Med Genet A. 2024. PMID: 38949089

10

Vascular compression syndromes in the abdomen and pelvis: a concise pictorial review.

M Koshy R, Chee RKW, Wilson MP, Singh R, Mathew RP, Tu W, Low G. M Koshy R, et al. Among authors: mathew rp. Abdom Radiol (NY). 2024 May;49(5):1747-1761. doi: 10.1007/s00261-024-04315-7. Epub 2024 Apr 29. Abdom Radiol (NY). 2024. PMID: 38683215 Review.

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