Abdulrazzaq Y - Search Results

1

Abnormal folate metabolism and genetic polymorphism of the folate pathway in a child with Down syndrome and neural tube defect.

Al-Gazali LI, Padmanabhan R, Melnyk S, Yi P, Pogribny IP, Pogribna M, Bakir M, Hamid ZA, Abdulrazzaq Y, Dawodu A, James SJ. Al-Gazali LI, et al. Among authors: abdulrazzaq y. Am J Med Genet. 2001 Oct 1;103(2):128-32. doi: 10.1002/ajmg.1509. Am J Med Genet. 2001. PMID: 11568918

2

Folic acid awareness and intake survey in the United Arab Emirates.

Abdulrazzaq YM, Al-Gazali LI, Bener A, Hossein M, Verghese M, Dawodu A, Padmanabhan R. Abdulrazzaq YM, et al. Reprod Toxicol. 2003 Mar-Apr;17(2):171-6. doi: 10.1016/s0890-6238(02)00120-x. Reprod Toxicol. 2003. PMID: 12642149

3

A study of possible deleterious effects of consanguinity.

Abdulrazzaq YM, Bener A, al-Gazali LI, al-Khayat AI, Micallef R, Gaber T. Abdulrazzaq YM, et al. Clin Genet. 1997 Mar;51(3):167-73. doi: 10.1111/j.1399-0004.1997.tb02447.x. Clin Genet. 1997. PMID: 9137881

4

Pattern of central nervous system anomalies in a population with a high rate of consanguineous marriages.

Al-Gazali LI, Sztriha L, Dawodu A, Bakir M, Varghese M, Varady E, Scorer J, Abdulrazzaq YM, Bener A, Padmanabhan R. Al-Gazali LI, et al. Among authors: abdulrazzaq ym. Clin Genet. 1999 Feb;55(2):95-102. doi: 10.1034/j.1399-0004.1999.550205.x. Clin Genet. 1999. PMID: 10189086

5

A syndrome of immune complex glomerulonephritis and ophthalmic abnormalities.

Amirlak I, Sabnis SG, Al-Gazali L, Abdulrazzaq YM. Amirlak I, et al. Among authors: abdulrazzaq ym. J Med Genet. 1999 Aug;36(8):641-4. J Med Genet. 1999. PMID: 10465118 Free PMC article.

6

United Arab Emirates: communities and community genetics.

Al-Gazali LI, Alwash R, Abdulrazzaq YM. Al-Gazali LI, et al. Among authors: abdulrazzaq ym. Community Genet. 2005;8(3):186-96. doi: 10.1159/000086764. Community Genet. 2005. PMID: 16113536

7

Sociodemographic risk factors associated with low birthweight in United Arab Emirates.

Bener A, Abdulrazzaq YM, Dawodu A. Bener A, et al. Among authors: abdulrazzaq ym. J Biosoc Sci. 1996 Jul;28(3):339-46. doi: 10.1017/s0021932000022409. J Biosoc Sci. 1996. PMID: 8698713

8

Diversity in expression of glucose-6-phosphate dehydrogenase deficiency in females.

Abdulrazzaq YM, Micallef R, Qureshi M, Dawodu A, Ahmed I, Khidr A, Bastaki SM, Al-Khayat A, Bayoumi RA. Abdulrazzaq YM, et al. Clin Genet. 1999 Jan;55(1):13-9. doi: 10.1034/j.1399-0004.1999.550103.x. Clin Genet. 1999. PMID: 10066026

9

Teratogenic effects of vigabatrin in TO mouse fetuses.

Abdulrazzaq YM, Bastaki SM, Padmanabhan R. Abdulrazzaq YM, et al. Teratology. 1997 Mar;55(3):165-76. doi: 10.1002/(SICI)1096-9926(199703)55:3<165::AID-TERA1>3.0.CO;2-1. Teratology. 1997. PMID: 9181670

10

Abnormal myelination in peroxisomal isolated dihydroxyacetonephosphate acyltransferase deficiency.

Sztriha LS, Nork MP, Abdulrazzaq YM, al-Gazali LI, Bakalinova DB. Sztriha LS, et al. Among authors: abdulrazzaq ym. Pediatr Neurol. 1997 Apr;16(3):232-6. doi: 10.1016/s0887-8994(97)00014-3. Pediatr Neurol. 1997. PMID: 9165515

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