Feingold J - Search Results

1

Penetrance of familial hypertrophic cardiomyopathy.

Charron P, Carrier L, Dubourg O, Tesson F, Desnos M, Richard P, Bonne G, Guicheney P, Hainque B, Bouhour JB, Mallet A, Feingold J, Schwartz K, Komajda M. Charron P, et al. Among authors: feingold j. Genet Couns. 1997;8(2):107-14. Genet Couns. 1997. PMID: 9219008

2

Prenatal molecular diagnosis in hypertrophic cardiomyopathy: report of the first case.

Charron P, Héron D, Gargiulo M, Feingold J, Oury JF, Richard P, Komajda M. Charron P, et al. Among authors: feingold j. Prenat Diagn. 2004 Sep;24(9):701-3. doi: 10.1002/pd.969. Prenat Diagn. 2004. PMID: 15386449

3

Genetic testing and genetic counselling in hypertrophic cardiomyopathy: the French experience.

Charron P, Héron D, Gargiulo M, Richard P, Dubourg O, Desnos M, Bouhour JB, Feingold J, Carrier L, Hainque B, Schwartz K, Komajda M. Charron P, et al. Among authors: feingold j. J Med Genet. 2002 Oct;39(10):741-6. doi: 10.1136/jmg.39.10.741. J Med Genet. 2002. PMID: 12362031 Free PMC article.

4

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. Among authors: feingold j. J Mol Cell Cardiol. 1997 Feb;29(2):831-8. doi: 10.1006/jmcc.1996.0332. J Mol Cell Cardiol. 1997. PMID: 9140839

5

Genotype-phenotype correlations in familial hypertrophic cardiomyopathy. A comparison between mutations in the cardiac protein-C and the beta-myosin heavy chain genes.

Charron P, Dubourg O, Desnos M, Isnard R, Hagege A, Bonne G, Carrier L, Tesson F, Bouhour JB, Buzzi JC, Feingold J, Schwartz K, Komajda M. Charron P, et al. Among authors: feingold j. Eur Heart J. 1998 Jan;19(1):139-45. doi: 10.1053/euhj.1997.0575. Eur Heart J. 1998. PMID: 9503187

6

A new locus for autosomal dominant dilated cardiomyopathy identified on chromosome 6q12-q16.

Sylvius N, Tesson F, Gayet C, Charron P, Bénaïche A, Peuchmaurd M, Duboscq-Bidot L, Feingold J, Beckmann JS, Bouchier C, Komajda M. Sylvius N, et al. Among authors: feingold j. Am J Hum Genet. 2001 Jan;68(1):241-6. doi: 10.1086/316929. Epub 2000 Nov 20. Am J Hum Genet. 2001. PMID: 11085912 Free PMC article.

7

Female predominance and transmission distortion in the long-QT syndrome.

Imboden M, Swan H, Denjoy I, Van Langen IM, Latinen-Forsblom PJ, Napolitano C, Fressart V, Breithardt G, Berthet M, Priori S, Hainque B, Wilde AA, Schulze-Bahr E, Feingold J, Guicheney P. Imboden M, et al. Among authors: feingold j. N Engl J Med. 2006 Dec 28;355(26):2744-51. doi: 10.1056/NEJMoa042786. N Engl J Med. 2006. PMID: 17192539 Free article.

8

Segregation analysis of IgE levels in 335 French families (EGEA) using different strategies to correct for the ascertainment through a correlated trait (asthma).

Sampogna F, Demenais F, Hochez J, Oryszczyn MP, Maccario J, Kauffmann F, Feingold J, Dizier MH. Sampogna F, et al. Among authors: feingold j. Genet Epidemiol. 2000 Feb;18(2):128-42. doi: 10.1002/(SICI)1098-2272(200002)18:2<128::AID-GEPI3>3.0.CO;2-9. Genet Epidemiol. 2000. PMID: 10642426

9

Implications of prenatal diagnosis of sickle cell disease.

de Montalembert M, Guilloud-Bataille M, Ducros A, Galacteros F, Girot R, Herve C, Maier-Redelsperger M, Feingold J. de Montalembert M, et al. Among authors: feingold j. Genet Couns. 1996;7(1):9-15. Genet Couns. 1996. PMID: 8652095

10

Phenotypic variability in autosomal dominant cerebellar ataxia type I is unrelated to genetic heterogeneity.

Dürr A, Chneiweiss H, Khati C, Stevanin G, Cancel G, Feingold J, Agid Y, Brice A. Dürr A, et al. Among authors: feingold j. Brain. 1993 Dec;116 ( Pt 6):1497-508. doi: 10.1093/brain/116.6.1497. Brain. 1993. PMID: 8293283

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