Feingold J - Search Results

1

Glucocorticoid receptor gene polymorphisms associated with progression of lung disease in young patients with cystic fibrosis.

Corvol H, Nathan N, Charlier C, Chadelat K, Le Rouzic P, Tabary O, Fauroux B, Henrion-Caude A, Feingold J, Boelle PY, Clement A. Corvol H, et al. Among authors: feingold j. Respir Res. 2007 Nov 29;8(1):88. doi: 10.1186/1465-9921-8-88. Respir Res. 2007. PMID: 18047640 Free PMC article.

2

Genetic variations in inflammatory mediators influence lung disease progression in cystic fibrosis.

Corvol H, Boelle PY, Brouard J, Knauer N, Chadelat K, Henrion-Caude A, Flamant C, Muselet-Charlier C, Boule M, Fauroux B, Vallet C, Feingold J, Ratjen F, Grasemann H, Clement A. Corvol H, et al. Among authors: feingold j. Pediatr Pulmonol. 2008 Dec;43(12):1224-32. doi: 10.1002/ppul.20935. Pediatr Pulmonol. 2008. PMID: 19009622

3

Origin of the prevalent SFTPB indel g.1549C > GAA (121ins2) mutation causing surfactant protein B (SP-B) deficiency.

Tredano M, Cooper DN, Stuhrmann M, Christodoulou J, Chuzhanova NA, Roudot-Thoraval F, Boëlle PY, Elion J, Jeanpierre M, Feingold J, Couderc R, Bahuau M. Tredano M, et al. Among authors: feingold j. Am J Med Genet A. 2006 Jan 1;140(1):62-9. doi: 10.1002/ajmg.a.31050. Am J Med Genet A. 2006. PMID: 16333843

4

The mannose binding lectin gene influences the severity of chronic liver disease in cystic fibrosis.

Gabolde M, Hubert D, Guilloud-Bataille M, Lenaerts C, Feingold J, Besmond C. Gabolde M, et al. Among authors: feingold j. J Med Genet. 2001 May;38(5):310-1. doi: 10.1136/jmg.38.5.310. J Med Genet. 2001. PMID: 11333866 Free PMC article.

5

Mutation in a primate-conserved retrotransposon reveals a noncoding RNA as a mediator of infantile encephalopathy.

Cartault F, Munier P, Benko E, Desguerre I, Hanein S, Boddaert N, Bandiera S, Vellayoudom J, Krejbich-Trotot P, Bintner M, Hoarau JJ, Girard M, Génin E, de Lonlay P, Fourmaintraux A, Naville M, Rodriguez D, Feingold J, Renouil M, Munnich A, Westhof E, Fähling M, Lyonnet S, Henrion-Caude A. Cartault F, et al. Among authors: feingold j. Proc Natl Acad Sci U S A. 2012 Mar 27;109(13):4980-5. doi: 10.1073/pnas.1111596109. Epub 2012 Mar 12. Proc Natl Acad Sci U S A. 2012. PMID: 22411793 Free PMC article.

6

An abnormal distribution of delta F508 genotypes in cystic fibrosis patient registries.

Feingold J, Guilloud-Bataille M, De Crozes D. Feingold J, et al. Ann Genet. 1998;41(1):31-3. Ann Genet. 1998. PMID: 9599649

7

Genetic comparisons of patients with cystic fibrosis with or without meconium ileus. Clinical Centers of the French CF Registry.

Feingold J, Guilloud-Bataille M. Feingold J, et al. Ann Genet. 1999;42(3):147-50. Ann Genet. 1999. PMID: 10526657

8

Association of variant alleles of mannose binding lectin with severity of pulmonary disease in cystic fibrosis: cohort study.

Gabolde M, Guilloud-Bataille M, Feingold J, Besmond C. Gabolde M, et al. Among authors: feingold j. BMJ. 1999 Oct 30;319(7218):1166-7. doi: 10.1136/bmj.319.7218.1166. BMJ. 1999. PMID: 10541506 Free PMC article. No abstract available.

9

Cystic fibrosis mutations: report from the French Registry. The Clinical Centers of the CF.

Guilloud-Bataille M, De Crozes D, Rault G, Degioanni A, Feingold J. Guilloud-Bataille M, et al. Among authors: feingold j. Hum Hered. 2000 Mar-Apr;50(2):142-5. doi: 10.1159/000022903. Hum Hered. 2000. PMID: 10799974

10

Genome screen for asthma and related phenotypes in the French EGEA study.

Dizier MH, Besse-Schmittler C, Guilloud-Bataille M, Annesi-Maesano I, Boussaha M, Bousquet J, Charpin D, Degioanni A, Gormand F, Grimfeld A, Hochez J, Hyne G, Lockhart A, Luillier-Lacombe M, Matran R, Meunier F, Neukirch F, Pacheco Y, Parent V, Paty E, Pin I, Pison C, Scheinmann P, Thobie N, Vervloet D, Kauffmann F, Feingold J, Lathrop M, Demenais F. Dizier MH, et al. Among authors: feingold j. Am J Respir Crit Care Med. 2000 Nov;162(5):1812-8. doi: 10.1164/ajrccm.162.5.2002113. Am J Respir Crit Care Med. 2000. PMID: 11069818

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