Taha D - Search Results

1

Wolcott-Rallison Syndrome: clinical, genetic, and functional study of EIF2AK3 mutations and suggestion of genetic heterogeneity.

Senée V, Vattem KM, Delépine M, Rainbow LA, Haton C, Lecoq A, Shaw NJ, Robert JJ, Rooman R, Diatloff-Zito C, Michaud JL, Bin-Abbas B, Taha D, Zabel B, Franceschini P, Topaloglu AK, Lathrop GM, Barrett TG, Nicolino M, Wek RC, Julier C. Senée V, et al. Among authors: taha d. Diabetes. 2004 Jul;53(7):1876-83. doi: 10.2337/diabetes.53.7.1876. Diabetes. 2004. PMID: 15220213

2

Mutations in GLIS3 are responsible for a rare syndrome with neonatal diabetes mellitus and congenital hypothyroidism.

Senée V, Chelala C, Duchatelet S, Feng D, Blanc H, Cossec JC, Charon C, Nicolino M, Boileau P, Cavener DR, Bougnères P, Taha D, Julier C. Senée V, et al. Among authors: taha d. Nat Genet. 2006 Jun;38(6):682-7. doi: 10.1038/ng1802. Epub 2006 May 21. Nat Genet. 2006. PMID: 16715098

3

Re: EIF2AK3 mutations in patients with Wolcott-Rallison syndrome.

Taha D. Taha D. Ann Saudi Med. 2005 Jul-Aug;25(4):350; author reply 350. doi: 10.5144/0256-4947.2005.350a. Ann Saudi Med. 2005. PMID: 16212134 Free PMC article. No abstract available.

4

Neonatal diabetes mellitus because of pancreatic agenesis with dysmorphic features and recurrent bacterial infections.

Taha D, Bardise J, Hegab A, Bonnefond A, Marchand M, Drunat S, Vaxillaire M, Polak M. Taha D, et al. Pediatr Diabetes. 2008 Jun;9(3 Pt 1):240-4. doi: 10.1111/j.1399-5448.2007.00365.x. Pediatr Diabetes. 2008. PMID: 18547237

5

An emerging, recognizable facial phenotype in association with mutations in GLI-similar 3 (GLIS3).

Dimitri P, De Franco E, Habeb AM, Gurbuz F, Moussa K, Taha D, Wales JK, Hogue J, Slavotinek A, Shetty A, Balasubramanian M. Dimitri P, et al. Among authors: taha d. Am J Med Genet A. 2016 Jul;170(7):1918-23. doi: 10.1002/ajmg.a.37680. Epub 2016 May 5. Am J Med Genet A. 2016. PMID: 27148679 Free article.

6

Expanding the Clinical Spectrum Associated With GLIS3 Mutations.

Dimitri P, Habeb AM, Gurbuz F, Millward A, Wallis S, Moussa K, Akcay T, Taha D, Hogue J, Slavotinek A, Wales JK, Shetty A, Hawkes D, Hattersley AT, Ellard S, De Franco E. Dimitri P, et al. Among authors: taha d. J Clin Endocrinol Metab. 2015 Oct;100(10):E1362-9. doi: 10.1210/jc.2015-1827. Epub 2015 Aug 10. J Clin Endocrinol Metab. 2015. PMID: 26259131 Free PMC article.

7

Neonatal diabetes mellitus, congenital hypothyroidism, hepatic fibrosis, polycystic kidneys, and congenital glaucoma: a new autosomal recessive syndrome?

Taha D, Barbar M, Kanaan H, Williamson Balfe J. Taha D, et al. Am J Med Genet A. 2003 Oct 15;122A(3):269-73. doi: 10.1002/ajmg.a.20267. Am J Med Genet A. 2003. PMID: 12966531

8

Type 2 diabetes mellitus in African-American adolescents: impaired beta-cell function in the face of severe insulin resistance.

Taha D, Umpaichitra V, Banerji MA, Castells S. Taha D, et al. J Pediatr Endocrinol Metab. 2006 Feb;19(2):135-42. doi: 10.1515/jpem.2006.19.2.135. J Pediatr Endocrinol Metab. 2006. PMID: 16562586 Clinical Trial.

9

Hyperglycemia and hypoinsulinemia in patients with Fanconi-Bickel syndrome.

Taha D, Al-Harbi N, Al-Sabban E. Taha D, et al. J Pediatr Endocrinol Metab. 2008 Jun;21(6):581-6. J Pediatr Endocrinol Metab. 2008. PMID: 18717244

10

Arthrogryposis, renal tubular acidosis and cholestasis (ARC) syndrome: two new cases and review.

Abu-Sa'da O, Barbar M, Al-Harbi N, Taha D. Abu-Sa'da O, et al. Among authors: taha d. Clin Dysmorphol. 2005 Oct;14(4):191-196. Clin Dysmorphol. 2005. PMID: 16155421 Review.

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