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20篇 您的检索式：作者名="Allamand"

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	题名	作者	年代	出处	被引量
1	Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A显示文摘	Richard I Broux O Allamand V	1995	Cell1995，81，1：	1
2	Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A显示文摘	Richard I Broux O Allamand V	1995	Cell1995，81，：	1
3	Mutations in the protelytic enzyme calpain 3 cause limbgirdle muscular dystrophy type-A显示文摘	RICHARD I BROUX O ALLAMAND V	1995	Cell1995，81，1：	1
4	A novel mechanism leading to muscular dystrophy: mutations in calpain 3 cause limb-girdle muscular dystrophy type 2A显示文摘	Richard I Broux O Allamand V	1995	Cell1995，81，：	1
5	Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A 显示文摘	RICHARD I BROUX O ALLAMAND V	1995	Cell1995，81，1：	1
6	Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A显示文摘	Richard I Broux O Allamand V	1995	Cell1995，81，：	1
7	Molecular markers in thyroid fine - needle aspiration biopsy : a prospective study 显示文摘	Franco C Martinez V Allamand JP	2009	Appl Immunohistochem Mol Morphol2009，17，3：	1
8	Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A显示文摘	Richard I Broux O Allamand V	1995	Cell1995，81，1：	1
9	Drug - induced readthrough of premature stop codons leads to the stabilization of laminin a2 chain mRNA in CMD myotubes 显示文摘	Allamand V Bidou L Arakawa M	2008	J Gene Med2008，10，2：	1
10	Mild congenital muscular dystrophy in two patients with an internally deleted laminin alpha2-chain显示文摘	Allamand V Sunada Y Salih MA	1997	Hum Mol Genet1997，6，：	1
11	Bethlem myopathy: long-term follow-up identifies COL6 mutations pre- dicting severe clinical evolution显示文摘	DECONINCK N RICHARD P ALLAMAND V	2015	J Neurol Neurosurg Psychia- try2015，86，12：	1
12	Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A显示文摘	Isabelle Richard Odile Broux Valéerie Allamand Fran?oise Fougerousse Nuchanard Chiannilkulchai Nathalie Bourg Lydie Brenguier Catherine Devaud Patricia Pasturaud Carinne Roudaut Dominique Hillaire Maria-Rita Passos-Bueno Mayana Zatz Jay A Tischfield Miche	1995	Cell1995，，1：	1
13	Mutations in the protoelytic enzrime calpain 3 cause limb-girdle muscular dystrophy type 2A显示文摘	Richard I Broux O Allamand V	1995	Cell1995，81，1：	1
14	Mutations in the proteolytic enzyme calpain3 cause limb-girdle muscular dystrophy type 2A显示文摘	Richard l Broux O Allamand V	1995	Cell1995，81，：	1
15	Sense from nonsense: therapies for premature stop codon diseases显示文摘	Bidou L Allamand V Rousset JP	2012	Trends in Molec- ular Medicine2012，18，11：	1
16	A single ho-mozygous point mutation in a 3 'untranslated region motif of seleno-protein N mRNA causes SEPN1-related myopathy 显示文摘	ALLAMAND V RICHARD P LESCURE A	2006	EMBO Rep2006，7，4：	1
17	Sense from nonsense: therapies for premature stop codon diseases 显示文摘	Bidou L Allamand V Rousset JP	2012	Trends Mol Med2012，18，11：	1
18	Molecular markers in thyroid fine-needle aspiration biopsy:a prospective study显示文摘	Franco C Mart?′nez V Allamand JP	2009	Appl Immunohistochem Mol Morphol2009，17，3：	1
19	Mutations in COL6A3 cause severe and mild phenotypes of ullrich congenital muscular dystrophy显示文摘	Demir E Sabatelli P Allamand V	2002	AmJ HumGenet2002，70，：	1
20	Molecular markers in thyroidfineneedle aspiration biopsy: aprospective study 显示文摘	Franco C Mart nez V Allamand JP etal	2009	ApplImmunohistochem Mol Morphol2009，17，3：	1

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