Meyer BF - Search Results

1

A new susceptibility locus for myocardial infarction, hypertension, type 2 diabetes mellitus, and dyslipidemia on chromosome 12q24.

Wakil SM, Muiya NP, Tahir AI, Al-Najai M, Baz B, Andres E, Mazhar N, Al Tassan N, Alshahid M, Meyer BF, Dzimiri N. Wakil SM, et al. Among authors: meyer bf. Dis Markers. 2014;2014:291419. doi: 10.1155/2014/291419. Epub 2014 Jun 26. Dis Markers. 2014. PMID: 25057215 Free PMC article.

2

Relevance of apolipoprotein E polymorphism for coronary artery disease in the Saudi population.

Dzimiri N, Meyer BF, Hussain SS, Basco C, Afrane B, Halees Z. Dzimiri N, et al. Among authors: meyer bf. Arch Pathol Lab Med. 1999 Dec;123(12):1241-5. doi: 10.5858/1999-123-1241-ROAEPF. Arch Pathol Lab Med. 1999. PMID: 10583930 Free article.

3

Angiotensin-converting enzyme polymorphism and the risk of coronary heart disease in the Saudi male population.

Dzimiri N, Basco C, Moorji A, Meyer BF. Dzimiri N, et al. Among authors: meyer bf. Arch Pathol Lab Med. 2000 Apr;124(4):531-4. doi: 10.5858/2000-124-0531-ACEPAT. Arch Pathol Lab Med. 2000. PMID: 10747309 Free article.

4

Mutation of the slow myosin heavy chain rod domain underlies hyaline body myopathy.

Bohlega S, Abu-Amero SN, Wakil SM, Carroll P, Al-Amr R, Lach B, Al-Sayed Y, Cupler EJ, Meyer BF. Bohlega S, et al. Among authors: meyer bf. Neurology. 2004 May 11;62(9):1518-21. doi: 10.1212/01.wnl.0000123255.92062.37. Neurology. 2004. PMID: 15136674

5

The peroxisome proliferator-activated receptor-gamma2 P12A polymorphism and type 2 diabetes in an Arab population.

Wakil SM, Al-Rubeaan K, Alsmadi O, Imtiaz F, Carroll P, Rajab M, Al-Katari S, Al-Katari M, Meyer BF. Wakil SM, et al. Among authors: meyer bf. Diabetes Care. 2006 Jan;29(1):171-2. doi: 10.2337/diacare.29.1.171. Diabetes Care. 2006. PMID: 16373923 No abstract available.

6

Phenotypic variation and allelic heterogeneity in young patients with Papillon-Lefèvre syndrome.

Ullbro C, El-Samadi S, Boumah C, Al-Yousef N, Wakil S, Twetman S, Alfadley A, Thestrup-Pedersen K, Meyer B. Ullbro C, et al. Acta Derm Venereol. 2006;86(1):3-7. doi: 10.1080/00015550510011619. Acta Derm Venereol. 2006. PMID: 16585980 Free article.

7

Genetic study of Saudi diabetes (GSSD): significant association of the KCNJ11 E23K polymorphism with type 2 diabetes.

Alsmadi O, Al-Rubeaan K, Wakil SM, Imtiaz F, Mohamed G, Al-Saud H, Al-Saud NA, Aldaghri N, Mohammad S, Meyer BF. Alsmadi O, et al. Among authors: meyer bf. Diabetes Metab Res Rev. 2008 Feb;24(2):137-40. doi: 10.1002/dmrr.777. Diabetes Metab Res Rev. 2008. PMID: 17922473

8

Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 (FGF3).

Alsmadi O, Meyer BF, Alkuraya F, Wakil S, Alkayal F, Al-Saud H, Ramzan K, Al-Sayed M. Alsmadi O, et al. Among authors: meyer bf. Eur J Hum Genet. 2009 Jan;17(1):14-21. doi: 10.1038/ejhg.2008.141. Epub 2008 Aug 13. Eur J Hum Genet. 2009. PMID: 18701883 Free PMC article.

9

Haplotypes encompassing the KIAA0391 and PSMA6 gene cluster confer a genetic link for myocardial infarction and coronary artery disease.

Alsmadi O, Muiya P, Khalak H, Al-Saud H, Meyer BF, Al-Mohanna F, Alshahid M, Dzimiri N. Alsmadi O, et al. Among authors: meyer bf. Ann Hum Genet. 2009 Sep;73(Pt 5):475-83. doi: 10.1111/j.1469-1809.2009.00534.x. Epub 2009 Jun 16. Ann Hum Genet. 2009. PMID: 19624571

10

A study of the role of the Myocyte-specific Enhancer Factor-2A gene in coronary artery disease.

Elhawari S, Al-Boudari O, Muiya P, Khalak H, Andres E, Al-Shahid M, Al-Dosari M, Meyer BF, Al-Mohanna F, Dzimiri N. Elhawari S, et al. Among authors: meyer bf. Atherosclerosis. 2010 Mar;209(1):152-4. doi: 10.1016/j.atherosclerosis.2009.09.005. Epub 2009 Sep 9. Atherosclerosis. 2010. PMID: 19782985

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