Feingold J - Search Results

1

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

2

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.

3

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

4

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

5

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

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

A locus for simple pure febrile seizures maps to chromosome 6q22-q24.

Nabbout R, Prud'homme JF, Herman A, Feingold J, Brice A, Dulac O, LeGuern E. Nabbout R, et al. Among authors: feingold j. Brain. 2002 Dec;125(Pt 12):2668-80. doi: 10.1093/brain/awf281. Brain. 2002. PMID: 12429594

8

Acute clinical events in 299 homozygous sickle cell patients living in France. French Study Group on Sickle Cell Disease.

Neonato MG, Guilloud-Bataille M, Beauvais P, Bégué P, Belloy M, Benkerrou M, Ducrocq R, Maier-Redelsperger M, de Montalembert M, Quinet B, Elion J, Feingold J, Girot R. Neonato MG, et al. Among authors: feingold j. Eur J Haematol. 2000 Sep;65(3):155-64. doi: 10.1034/j.1600-0609.2000.90210.x. Eur J Haematol. 2000. PMID: 11007050

9

Phenotypic variability at the TGF-beta1 locus in Camurati-Engelmann disease.

Campos-Xavier B, Saraiva JM, Savarirayan R, Verloes A, Feingold J, Faivre L, Munnich A, Le Merrer M, Cormier-Daire V. Campos-Xavier B, et al. Among authors: feingold j. Hum Genet. 2001 Dec;109(6):653-8. doi: 10.1007/s00439-001-0644-8. Epub 2001 Nov 9. Hum Genet. 2001. PMID: 11810278

10

Genetic polymorphism of the mannose-binding protein gene in children with sickle cell disease: identification of three new variant alleles and relationship to infections.

Neonato MG, Lu CY, Guilloud-Bataille M, Lapouméroulie C, Nabeel-Jassim H, Dabit D, Girot R, Krishnamoorthy R, Feingold J, Besmond C, Elion J. Neonato MG, et al. Among authors: feingold j. Eur J Hum Genet. 1999 Sep;7(6):679-86. doi: 10.1038/sj.ejhg.5200360. Eur J Hum Genet. 1999. PMID: 10482957

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