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Predominant dystonia with marked cerebellar atrophy: a rare phenotype in familial dystonia.
Neurology. 2006 Nov 28;67(10):1769-73. doi: 10.1212/01.wnl.0000244484.60489.50.
Neurology. 2006.
PMID: 17130408
Large pathogenic expansions in the SCA2 and SCA7 genes can be detected by fluorescent repeat-primed polymerase chain reaction assay.
Cagnoli C, Stevanin G, Michielotto C, Gerbino Promis G, Brussino A, Pappi P, Durr A, Dragone E, Viemont M, Gellera C, Brice A, Migone N, Brusco A.
Cagnoli C, et al. Among authors: viemont m.
J Mol Diagn. 2006 Feb;8(1):128-32. doi: 10.2353/jmoldx.2006.050043.
J Mol Diagn. 2006.
PMID: 16436644
Free PMC article.
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A novel variant of transthyretin (Glu42Asp) associated with sporadic late-onset cardiac amyloidosis.
Dupuy O, Blétry O, Blanc AS, Droz D, Viémont M, Delpech M, Grateau G.
Dupuy O, et al. Among authors: viemont m.
Amyloid. 1998 Dec;5(4):285-7. doi: 10.3109/13506129809007302.
Amyloid. 1998.
PMID: 10036587
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Prevalence, male germ-line origin and new patterns of inversions in haemophilia A.
Valleix S, Nafa K, Stieltjes N, Viemont M, Sultan Y, Kaplan JC, Delpech M.
Valleix S, et al. Among authors: viemont m.
Ann Genet. 1997;40(1):35-40.
Ann Genet. 1997.
PMID: 9150848
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Unbalanced X-chromosome inactivation with a novel FVIII gene mutation resulting in severe hemophilia A in a female.
Favier R, Lavergne JM, Costa JM, Caron C, Mazurier C, Viémont M, Delpech M, Valleix S.
Favier R, et al. Among authors: viemont m.
Blood. 2000 Dec 15;96(13):4373-5.
Blood. 2000.
PMID: 11110718
Free article.
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Screening for mutations in factor VIII gene using the single-strand conformation polymorphism.
Nafa K, Meriane F, Chellali T, Benabadji M, Reghis A, Viemont M, Kaplan JC, Delpech M.
Nafa K, et al. Among authors: viemont m.
Hum Mutat. 1995;5(4):357-9. doi: 10.1002/humu.1380050418.
Hum Mutat. 1995.
PMID: 7627196
No abstract available.
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Late-onset familial amyloid polyneuropathy with the TTR Met 30 mutation in France.
Grateau G, Adams D, Malapert D, Viemont M, Delpech M, Said G.
Grateau G, et al. Among authors: viemont m.
Clin Genet. 1993 Mar;43(3):143-5. doi: 10.1111/j.1399-0004.1993.tb04439.x.
Clin Genet. 1993.
PMID: 8500260
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