French J - Search Results

1

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. Among authors: french j. 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.

2

An additional marker for familial hypertrophic cardiomyopathy?

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

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. Among authors: french ja. 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

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. Among authors: french j. 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.

5

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. Among authors: french ja. 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.

6

DNA testing in familial hypertrophic cardiomyopathy: clinical and laboratory implications.

Smart RV, Yu B, Le H, French JA, Richmond DR, Jeremy RW, Semsarian C, Cheung L, Ross DA, Trent RJ. Smart RV, et al. Among authors: french ja. Clin Genet. 1996 Oct;50(4):169-75. doi: 10.1111/j.1399-0004.1996.tb02621.x. Clin Genet. 1996. PMID: 9001794

7

Counselling issues in familial hypertrophic cardiomyopathy.

Yu B, French JA, Jeremy RW, French P, McTaggart DR, Nicholson MR, Semsarian C, Richmond DR, Trent RJ. Yu B, et al. Among authors: french ja, french p. J Med Genet. 1998 Mar;35(3):183-8. doi: 10.1136/jmg.35.3.183. J Med Genet. 1998. PMID: 9541100 Free PMC article.

8

Molecular pathology of familial hypertrophic cardiomyopathy caused by mutations in the cardiac myosin binding protein C gene.

Yu B, French JA, Carrier L, Jeremy RW, McTaggart DR, Nicholson MR, Hambly B, Semsarian C, Richmond DR, Schwartz K, Trent RJ. Yu B, et al. Among authors: french ja. J Med Genet. 1998 Mar;35(3):205-10. doi: 10.1136/jmg.35.3.205. J Med Genet. 1998. PMID: 9541104 Free PMC article.

9

The natural history of left ventricular wall thickening in hypertrophic cardiomyopathy.

Semsarian C, French J, Trent RJ, Richmond DR, Jeremy RW. Semsarian C, et al. Among authors: french j. Aust N Z J Med. 1997 Feb;27(1):51-8. doi: 10.1111/j.1445-5994.1997.tb00914.x. Aust N Z J Med. 1997. PMID: 9079254

10

RsaI and MaeI intragenic RFLPs in the human HERG gene.

Fung D, Zhang L, French J, Bailey B, Trent RJ. Fung D, et al. Among authors: french j. Clin Genet. 1998 Jun;53(6):504. doi: 10.1111/j.1399-0004.1998.tb02605.x. Clin Genet. 1998. PMID: 9712545 No abstract available.

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