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Page 1
Diagnosis of "sporadic" Huntington's disease.
Dürr A, Dodé C, Hahn V, Pêcheux C, Pillon B, Feingold J, Kaplan JC, Agid Y, Brice A. Dürr A, et al. Among authors: pecheux c. J Neurol Sci. 1995 Mar;129(1):51-5. doi: 10.1016/0022-510x(94)00250-r. J Neurol Sci. 1995. PMID: 7751845
Homozygosity in Huntington's disease.
Dürr A, Hahn-Barma V, Brice A, Pêcheux C, Dodé C, Feingold J. Dürr A, et al. Among authors: pecheux c. J Med Genet. 1999 Feb;36(2):172-3. J Med Genet. 1999. PMID: 10051023 Free PMC article. No abstract available.
A novel missense mutation (C30S) in the gene encoding tumor necrosis factor receptor 1 linked to autosomal-dominant recurrent fever with localized myositis in a French family.
Dodé C, Papo T, Fieschi C, Pêcheux C, Dion E, Picard F, Godeau P, Bienvenu J, Piette JC, Delpech M, Grateau G. Dodé C, et al. Among authors: pecheux c. Arthritis Rheum. 2000 Jul;43(7):1535-42. doi: 10.1002/1529-0131(200007)43:7<1535::AID-ANR18>3.0.CO;2-C. Arthritis Rheum. 2000. PMID: 10902757 Free article.
MEFV-Gene analysis in armenian patients with Familial Mediterranean fever: diagnostic value and unfavorable renal prognosis of the M694V homozygous genotype-genetic and therapeutic implications.
Cazeneuve C, Sarkisian T, Pêcheux C, Dervichian M, Nédelec B, Reinert P, Ayvazyan A, Kouyoumdjian JC, Ajrapetyan H, Delpech M, Goossens M, Dodé C, Grateau G, Amselem S. Cazeneuve C, et al. Among authors: pecheux c. Am J Hum Genet. 1999 Jul;65(1):88-97. doi: 10.1086/302459. Am J Hum Genet. 1999. PMID: 10364520 Free PMC article.
Kallmann syndrome: 14 novel mutations in KAL1 and FGFR1 (KAL2).
Albuisson J, Pêcheux C, Carel JC, Lacombe D, Leheup B, Lapuzina P, Bouchard P, Legius E, Matthijs G, Wasniewska M, Delpech M, Young J, Hardelin JP, Dodé C. Albuisson J, et al. Among authors: pecheux c. Hum Mutat. 2005 Jan;25(1):98-9. doi: 10.1002/humu.9298. Hum Mutat. 2005. PMID: 15605412
34 results