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Straub Volker
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http://hub.abes.fr/bmj/periodical/jmedgenet/2004/volume_41/issue_5/B3598D6B61717CBEE053120B220A90C5/authorship/5
http://hub.abes.fr/bmj/periodical/jnnp/2009/volume_80/issue_5/B35A82167D6A4C40E053120B220AF6DD/authorship/8
http://hub.abes.fr/oup/periodical/cardiovascres/2008/volume_79/issue_4/101093cvrcvn131/authorship/5
http://hub.abes.fr/oup/periodical/hmg/2003/volume_12/issue_5/101093hmgddg043/authorship/16
http://hub.abes.fr/oup/periodical/hmg/1997/volume_6/issue_5/101093hmg65747/authorship/4
http://hub.abes.fr/oup/periodical/brainj/2007/volume_130/issue_8/101093brainawm096/authorship/7
http://hub.abes.fr/oup/periodical/brainj/2009/volume_132/issue_11/101093brainawp236/authorship/6
http://hub.abes.fr/oup/periodical/brainj/2008/volume_131/issue_6/101093brainawn078/authorship/5
http://hub.abes.fr/oup/periodical/hmg/1998/volume_7/issue_5/101093hmg75823/authorship/2
http://hub.abes.fr/oup/periodical/hmg/2000/volume_9/issue_15/101093oxfordjournalshmga018926/authorship/2
http://hub.abes.fr/oup/periodical/hmg/2001/volume_10/issue_25/101093hmg10252851/authorship/14
http://hub.abes.fr/oup/periodical/hmg/2009/volume_18/issue_11/101093hmgddp121/authorship/8
http://hub.abes.fr/oup/periodical/brainj/2009/volume_132/issue_1/101093brainawn289/authorship/10
http://hub.abes.fr/oup/periodical/hmg/2010/volume_19/issue_9/101093hmgddq049/authorship/5
http://hub.abes.fr/oup/periodical/brainj/2007/volume_130/issue_10/101093brainawm212/authorship/7
http://hub.abes.fr/bmj/periodical/jnnp/2013/volume_84/issue_6/B35A17CA23C05B19E053120B220AE1F6/authorship/17
http://hub.abes.fr/bmj/periodical/jnnp/2009/volume_81/issue_9/B35A17CA1C465B19E053120B220AE1F6/authorship/9
http://hub.abes.fr/springer/periodical/431/1996/volume_155/issue_11/B90485A698AD52DAE053120B220AAC7B/authorship/2
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Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies
Refining genotype-phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan
Dissociation of the dystroglycan complex in caveolin-3-deficient limb girdle muscular dystrophy
Mild Congenital Muscular Dystrophy in Two Patients with an Internally Deleted Laminin α2-Chain
Steroid treatment causes deterioration of myocardial function in the δ-sarcoglycan-deficient mouse model for dilated cardiomyopathy
Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C
Worldwide distribution and broader clinical spectrum of muscle-eye-brain disease
Prevalence of genetic muscle disease in Northern England: in-depth analysis of a muscle clinic population
Cyclosporine A treatment for Ullrich congenital muscular dystrophy: a cellular study of mitochondrial dysfunction and its rescue
Developmental defects in a zebrafish model for muscular dystrophies associated with the loss of fukutin-related protein (FKRP)
mdx Muscle Pathology is Independent of nNOS Perturbation
Attenuated muscle regeneration is a key factor in dysferlin-deficient muscular dystrophy
Dok-7 promotes slow muscle integrity as well as neuromuscular junction formation in a zebrafish model of congenital myasthenic syndromes
Congenital muscular dystrophy with laminin α2 chain deficiency: Identification of a new intermediate phenotype and correlation of clinical findings to muscle immunohistochemistry
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