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V Timmerman

Showing results (31-40 of 105) with videos related to

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Neuromuscular Disorders : NMD|June 27, 2008
Autosomal dominant congenital spinal muscular atrophy--a possible developmental deficiency of motor neurones?S Reddel, R A Ouvrier, G Nicholson, et al.
Neuroscience Letters|February 14, 1997
Mutation analysis of the human pancreatic phospholipase A2 gene in a family with distal hereditary motor neuropathy type II linked to 12q24J Beuten, E De Vriendt, P De Jonghe, et al.
Annals of Human Genetics|January 25, 2008
Charcot-Marie-Tooth disease: a clinico-genetic confrontationN Barisic, K G Claeys, M Sirotković-Skerlev, et al.
Genomics|April 25, 2000
A clone contig of 12q24.3 encompassing the distal hereditary motor neuropathy type II geneJ Irobi, F Tissir, P De Jonghe, et al.
Neuromuscular Disorders : NMD|August 26, 1998
Charcot-Marie-Tooth disease: an intermediate formM Villanova, V Timmerman, P De Jonghe, et al.
Fortschritte Der Neurologie-Psychiatrie|April 8, 1998
[Hereditary neural amyotrophy (HNA): clinical and molecular genetic basis]F Stögbauer, P Young, G Kuhlenbäumer, et al.
Journal of Medical Genetics|January 1, 1992
Estimation of the size of the chromosome 17p11.2 duplication in Charcot-Marie-Tooth neuropathy type 1a (CMT1a). HMSN Collaborative Research GroupP Raeymaekers, V Timmerman, E Nelis, et al.
Journal of the Neurological Sciences|July 6, 2010
N88S mutation in the BSCL2 gene in a Serbian family with distal hereditary motor neuropathy type V or Silver syndromeV Rakocević-Stojanović, V Milić-Rasić, S Perić, et al.
Human Mutation|January 1, 1997
Mutation analysis of the connexin 32 (Cx32) gene in Charcot-Marie-Tooth neuropathy type 1: identification of five new mutationsE Nelis, S Simokovic, V Timmerman, et al.
Journal of the Neurological Sciences|May 1, 1992
Linkage analysis of distal hereditary motor neuropathy type II (distal HMN II) in a single pedigreeV Timmerman, P Raeymaekers, E Nelis, et al.
Pageof 11

Showing results (31-40 of 105) with videos related to

Sort By:
Pageof 11
Neuromuscular Disorders : NMD|June 27, 2008
Autosomal dominant congenital spinal muscular atrophy--a possible developmental deficiency of motor neurones?S Reddel, R A Ouvrier, G Nicholson, et al.
Neuroscience Letters|February 14, 1997
Mutation analysis of the human pancreatic phospholipase A2 gene in a family with distal hereditary motor neuropathy type II linked to 12q24J Beuten, E De Vriendt, P De Jonghe, et al.
Annals of Human Genetics|January 25, 2008
Charcot-Marie-Tooth disease: a clinico-genetic confrontationN Barisic, K G Claeys, M Sirotković-Skerlev, et al.
Genomics|April 25, 2000
A clone contig of 12q24.3 encompassing the distal hereditary motor neuropathy type II geneJ Irobi, F Tissir, P De Jonghe, et al.
Neuromuscular Disorders : NMD|August 26, 1998
Charcot-Marie-Tooth disease: an intermediate formM Villanova, V Timmerman, P De Jonghe, et al.
Fortschritte Der Neurologie-Psychiatrie|April 8, 1998
[Hereditary neural amyotrophy (HNA): clinical and molecular genetic basis]F Stögbauer, P Young, G Kuhlenbäumer, et al.
Journal of Medical Genetics|January 1, 1992
Estimation of the size of the chromosome 17p11.2 duplication in Charcot-Marie-Tooth neuropathy type 1a (CMT1a). HMSN Collaborative Research GroupP Raeymaekers, V Timmerman, E Nelis, et al.
Journal of the Neurological Sciences|July 6, 2010
N88S mutation in the BSCL2 gene in a Serbian family with distal hereditary motor neuropathy type V or Silver syndromeV Rakocević-Stojanović, V Milić-Rasić, S Perić, et al.
Human Mutation|January 1, 1997
Mutation analysis of the connexin 32 (Cx32) gene in Charcot-Marie-Tooth neuropathy type 1: identification of five new mutationsE Nelis, S Simokovic, V Timmerman, et al.
Journal of the Neurological Sciences|May 1, 1992
Linkage analysis of distal hereditary motor neuropathy type II (distal HMN II) in a single pedigreeV Timmerman, P Raeymaekers, E Nelis, et al.
Pageof 11