Meyer B - Search Results

1

Clinical profile and mutation spectrum of long QT syndrome in Saudi Arabia: The impact of consanguinity.

Al-Hassnan ZN, Al-Fayyadh M, Al-Ghamdi B, Shafquat A, Mallawi Y, Al-Hadeq F, Tulbah S, Shinwari ZMA, Almesned A, Alakhfash A, Al Fadly F, Hersi AS, Alhayani A, Al-Hashem A, Arafah D, Dzimiri N, Meyer B, Rababh M, Al-Manea W. Al-Hassnan ZN, et al. Among authors: meyer b. Heart Rhythm. 2017 Aug;14(8):1191-1199. doi: 10.1016/j.hrthm.2017.04.028. Epub 2017 Apr 22. Heart Rhythm. 2017. PMID: 28438721

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

Recessive cornea plana in the Kingdom of Saudi Arabia.

Khan AO, Aldahmesh M, Meyer B. Khan AO, et al. Among authors: meyer b. Ophthalmology. 2006 Oct;113(10):1773-8. doi: 10.1016/j.ophtha.2006.04.026. Ophthalmology. 2006. PMID: 17011957

5

Array comparative genomic hybridization (aCGH) reveals the largest novel deletion in PCCA found in a Saudi family with propionic acidemia.

Kaya N, Al-Owain M, Albakheet A, Colak D, Al-Odaib A, Imtiaz F, Coskun S, Al-Sayed M, Al-Hassnan Z, Al-Zaidan H, Meyer B, Ozand P. Kaya N, et al. Among authors: meyer b. Eur J Med Genet. 2008 Nov-Dec;51(6):558-65. doi: 10.1016/j.ejmg.2008.08.001. Epub 2008 Aug 26. Eur J Med Genet. 2008. PMID: 18790721

6

Genome-wide gene expression profiling and mutation analysis of Saudi patients with Canavan disease.

Kaya N, Imtiaz F, Colak D, Al-Sayed M, Al-Odaib A, Al-Zahrani F, Al-Mubarak BR, Al-Owain M, Al-Dhalaan H, Chedrawi A, Al-Hassnan Z, Coskun S, Sakati N, Ozand P, Meyer BF. Kaya N, et al. Genet Med. 2008 Sep;10(9):675-84. doi: 10.1097/gim.0b013e31818337a8. Genet Med. 2008. PMID: 18978679 Free article.

7

Allelic heterogeneity in inbred populations: the Saudi experience with Alström syndrome as an illustrative example.

Aldahmesh MA, Abu-Safieh L, Khan AO, Al-Hassnan ZN, Shaheen R, Rajab M, Monies D, Meyer BF, Alkuraya FS. Aldahmesh MA, et al. Am J Med Genet A. 2009 Feb 15;149A(4):662-5. doi: 10.1002/ajmg.a.32753. Am J Med Genet A. 2009. PMID: 19283855

8

Mutational spectrum of SLC4A11 in autosomal recessive CHED in Saudi Arabia.

Aldahmesh MA, Khan AO, Meyer BF, Alkuraya FS. Aldahmesh MA, et al. Invest Ophthalmol Vis Sci. 2009 Sep;50(9):4142-5. doi: 10.1167/iovs.08-3006. Epub 2009 Apr 15. Invest Ophthalmol Vis Sci. 2009. PMID: 19369245

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. 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. Atherosclerosis. 2010 Mar;209(1):152-4. doi: 10.1016/j.atherosclerosis.2009.09.005. Epub 2009 Sep 9. Atherosclerosis. 2010. PMID: 19782985

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

3,353 results

Search Page