al-Mahdawi S - Search Results

1

The influence of the angiotensin I converting enzyme genotype in familial hypertrophic cardiomyopathy varies with the disease gene mutation.

Tesson F, Dufour C, Moolman JC, Carrier L, al-Mahdawi S, Chojnowska L, Dubourg O, Soubrier E, Brink P, Komajda M, Guicheney P, Schwartz K, Feingold J. Tesson F, et al. J Mol Cell Cardiol. 1997 Feb;29(2):831-8. doi: 10.1006/jmcc.1996.0332. J Mol Cell Cardiol. 1997. PMID: 9140839

2

Familial hypertrophic cardiomyopathy. Microsatellite haplotyping and identification of a hot spot for mutations in the beta-myosin heavy chain gene.

Dausse E, Komajda M, Fetler L, Dubourg O, Dufour C, Carrier L, Wisnewsky C, Bercovici J, Hengstenberg C, al-Mahdawi S, et al. Dausse E, et al. J Clin Invest. 1993 Dec;92(6):2807-13. doi: 10.1172/JCI116900. J Clin Invest. 1993. PMID: 8254035 Free PMC article.

3

The standard electrocardiogram as a screening test for hypertrophic cardiomyopathy.

Ryan MP, Cleland JG, French JA, Joshi J, Choudhury L, Chojnowska L, Michalak E, al-Mahdawi S, Nihoyannopoulos P, Oakley CM. Ryan MP, et al. Am J Cardiol. 1995 Oct 1;76(10):689-94. doi: 10.1016/s0002-9149(99)80198-2. Am J Cardiol. 1995. PMID: 7572626 Clinical Trial.

4

The electrocardiogram is a more sensitive indicator than echocardiography of hypertrophic cardiomyopathy in families with a mutation in the MYH7 gene.

al-Mahdawi S, Chamberlain S, Chojnowska L, Michalak E, Nihoyannopoulos P, Ryan M, Kusnierczyk B, French JA, Gilligan DM, Cleland J, et al. al-Mahdawi S, et al. Br Heart J. 1994 Aug;72(2):105-11. doi: 10.1136/hrt.72.2.105. Br Heart J. 1994. PMID: 7848420 Free PMC article.

5

An additional marker for familial hypertrophic cardiomyopathy?

Choudhury L, al-Mahdawi S, French J, Oakley CM, Camici PG. Choudhury L, et al. Coron Artery Dis. 1993 Jun;4(6):565-7. doi: 10.1097/00019501-199306000-00011. Coron Artery Dis. 1993. PMID: 8261235

6

Identification of a mutation in the beta cardiac myosin heavy chain gene in a family with hypertrophic cardiomyopathy.

al-Mahdawi S, Chamberlain S, Cleland J, Nihoyannopoulos P, Gilligan D, French J, Choudhury L, Williamson R, Oakley C. al-Mahdawi S, et al. Br Heart J. 1993 Feb;69(2):136-41. doi: 10.1136/hrt.69.2.136. Br Heart J. 1993. PMID: 8435239 Free PMC article.

7

Genetic testing for familial hypertrophic cardiomyopathy in newborn infants.

Ryan MP, French J, al-Mahdawi S, Nihoyannopoulos P, Cleland JG, Oakley CM, Harper PS, Clarke A, Davis J, Grigg L. Ryan MP, et al. BMJ. 1995 Apr 1;310(6983):856-9. doi: 10.1136/bmj.310.6983.856. BMJ. 1995. PMID: 7677835 Free PMC article. No abstract available.

8

A novel missense mutation (L198R) in the Friedreich's ataxia gene.

Al-Mahdawi S, Pook M, Chamberlain S. Al-Mahdawi S, et al. Hum Mutat. 2000 Jul;16(1):95. doi: 10.1002/1098-1004(200007)16:1<95::AID-HUMU29>3.0.CO;2-E. Hum Mutat. 2000. PMID: 10874325 No abstract available.

9

Friedreich's ataxia: a defect in signal transduction?

Carvajal JJ, Pook MA, Doudney K, Hillermann R, Wilkes D, al-Mahdawi S, Williamson R, Chamberlain S. Carvajal JJ, et al. Hum Mol Genet. 1995 Aug;4(8):1411-9. doi: 10.1093/hmg/4.8.1411. Hum Mol Genet. 1995. PMID: 7581382

10

YAC transgenic mice carrying pathological alleles of the MJD1 locus exhibit a mild and slowly progressive cerebellar deficit.

Cemal CK, Carroll CJ, Lawrence L, Lowrie MB, Ruddle P, Al-Mahdawi S, King RH, Pook MA, Huxley C, Chamberlain S. Cemal CK, et al. Hum Mol Genet. 2002 May 1;11(9):1075-94. doi: 10.1093/hmg/11.9.1075. Hum Mol Genet. 2002. PMID: 11978767

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