Feingold J - Search Results

1

[Contribution of genetics to knowledge and management of hereditary kidney diseases progressing to renal failure].

Levy M, Gubler MC, Feingold J. Levy M, et al. Among authors: feingold j. Arch Pediatr. 2001 Oct;8(10):1086-98. doi: 10.1016/s0929-693x(01)00593-0. Arch Pediatr. 2001. PMID: 11683102 French.

2

Genetic heterogeneity of Alport syndrome.

Feingold J, Bois E, Chompret A, Broyer M, Gubler MC, Grünfeld JP. Feingold J, et al. Kidney Int. 1985 Apr;27(4):672-7. doi: 10.1038/ki.1985.63. Kidney Int. 1985. PMID: 4010153 Free article.

3

Genetics of Alport's syndrome.

Feingold J, Bois E. Feingold J, et al. Pediatr Nephrol. 1987 Jul;1(3):436-8. doi: 10.1007/BF00849250. Pediatr Nephrol. 1987. PMID: 3153314 Review.

4

[Genetics of epilepsy in children].

Dulac O, Bulteau C, Malafosse A, Aubourg P, Feingold J. Dulac O, et al. Among authors: feingold j. Arch Pediatr. 1995 Apr;2(4):306-9. doi: 10.1016/0929-693x(96)81150-x. Arch Pediatr. 1995. PMID: 7780536 French. No abstract available.

5

Identifying modifier genes of monogenic disease: strategies and difficulties.

Génin E, Feingold J, Clerget-Darpoux F. Génin E, et al. Among authors: feingold j. Hum Genet. 2008 Nov;124(4):357-68. doi: 10.1007/s00439-008-0560-2. Epub 2008 Sep 11. Hum Genet. 2008. PMID: 18784943 Free PMC article. Review.

6

[Identification and management of HNPCC syndrome (hereditary non polyposis colon cancer), hereditary predisposition to colorectal and endometrial adenocarcinomas].

Olschwang S, Bonaïti C, Feingold J, Frébourg T, Grandjouan S, Lasset C, Laurent-Puig P, Lecuru F, Millat B, Sobol H, Thomas G, Eisinger F. Olschwang S, et al. Among authors: feingold j. Bull Cancer. 2004 Apr;91(4):303-15. Bull Cancer. 2004. PMID: 15242312 Free article. Review. French.

7

[Genetic counseling for adults: the risk of late-onset inherited diseases].

Dürr A, Feingold J. Dürr A, et al. Among authors: feingold j. Rev Prat. 2011 Apr;61(4):535-8. Rev Prat. 2011. PMID: 21548239 French.

8

[HNPCC syndrome (hereditary non polyposis colon cancer): identification and management].

Olschwang S, Bonaïti C, Feingold J, Frébourg T, Grandjouan S, Lasset C, Laurent-Puig P, Lecuru F, Millat B, Sobol H, Thomas G, Eisinger F. Olschwang S, et al. Among authors: feingold j. Rev Med Interne. 2005 Feb;26(2):109-18. doi: 10.1016/j.revmed.2004.06.004. Rev Med Interne. 2005. PMID: 15710257 Review. French.

9

[Multifactorial diseases: a nightmare for the geneticist].

Feingold J. Feingold J. Med Sci (Paris). 2005 Nov;21(11):927-33. doi: 10.1051/medsci/20052111927. Med Sci (Paris). 2005. PMID: 16274643 Free article. Review. French.

10

[Hereditary nephropathies].

Royer P, Frezal J, Bois E, Feingold J. Royer P, et al. Among authors: feingold j. Arch Fr Pediatr. 1970 Mar;27(3):293-317. Arch Fr Pediatr. 1970. PMID: 4916279 Review. French. No abstract available.

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