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V Timmerman

Showing results (41-50 of 105) with videos related to

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The International Journal of Tuberculosis and Lung Disease : the Official Journal of the International Union Against Tuberculosis and Lung Disease|February 6, 2010
Effect on tuberculosis outcomes of educational outreach to South African clinics during two randomised trialsM O Bachmann, L R Fairall, C Lombard, et al.
Brain Pathology (Zurich, Switzerland)|April 14, 2000
Charcot-Marie-Tooth neuropathy type 2 and P0 point mutations: two novel amino acid substitutions (Asp61Gly; Tyr119Cys) and a possible "hotspot" on Thr124MetJ Senderek, B Hermanns, U Lehmann, et al.
Neuromuscular Disorders : NMD|May 23, 2001
A novel 3'-splice site mutation in peripheral myelin protein 22 causing hereditary neuropathy with liability to pressure palsiesJ Meuleman, A Pou-Serradell, A Löfgren, et al.
Annals of Neurology|February 28, 2001
Further evidence that neurofilament light chain gene mutations can cause Charcot-Marie-Tooth disease type 2EP De Jonghe, I Mersivanova, E Nelis, et al.
Neurology|April 1, 1998
PCR-based strategy for the diagnosis of hereditary neuropathy with liability to pressure palsies and Charcot-Marie-Tooth disease type 1AP Young, F Stögbauer, H Wiebusch, et al.
Archives of Neurology|October 16, 1999
A novel type of hereditary motor and sensory neuropathy characterized by a mild phenotypeP De Jonghe, V Timmerman, E Nelis, et al.
Journal of Neurology|November 8, 2001
Hereditary Neuralgic Amyotrophy (HNA) is genetically heterogeneousG Kuhlenbäumer, J Meuleman, P De Jonghe, et al.
Annals of the New York Academy of Sciences|November 1, 2017
Hereditary Neuralgic Amyotrophy: Mutation Analysis of Candidate GenesJ Meuleman, G Kuhlenbäumer, A Schirmacher, et al.
Journal of Medical Genetics|February 27, 2004
Autosomal dominant axonal Charcot-Marie-Tooth disease type 2 (CMT2G) maps to chromosome 12q12-q13.3E Nelis, J Berciano, N Verpoorten, et al.
Annals of the New York Academy of Sciences|December 10, 1999
Hereditary neuralgic amyotrophy: mutation analysis of candidate genesJ Meuleman, G Kuhlenbäumer, A Schirmacher, et al.
Pageof 11

Showing results (41-50 of 105) with videos related to

Sort By:
Pageof 11
The International Journal of Tuberculosis and Lung Disease : the Official Journal of the International Union Against Tuberculosis and Lung Disease|February 6, 2010
Effect on tuberculosis outcomes of educational outreach to South African clinics during two randomised trialsM O Bachmann, L R Fairall, C Lombard, et al.
Brain Pathology (Zurich, Switzerland)|April 14, 2000
Charcot-Marie-Tooth neuropathy type 2 and P0 point mutations: two novel amino acid substitutions (Asp61Gly; Tyr119Cys) and a possible "hotspot" on Thr124MetJ Senderek, B Hermanns, U Lehmann, et al.
Neuromuscular Disorders : NMD|May 23, 2001
A novel 3'-splice site mutation in peripheral myelin protein 22 causing hereditary neuropathy with liability to pressure palsiesJ Meuleman, A Pou-Serradell, A Löfgren, et al.
Annals of Neurology|February 28, 2001
Further evidence that neurofilament light chain gene mutations can cause Charcot-Marie-Tooth disease type 2EP De Jonghe, I Mersivanova, E Nelis, et al.
Neurology|April 1, 1998
PCR-based strategy for the diagnosis of hereditary neuropathy with liability to pressure palsies and Charcot-Marie-Tooth disease type 1AP Young, F Stögbauer, H Wiebusch, et al.
Archives of Neurology|October 16, 1999
A novel type of hereditary motor and sensory neuropathy characterized by a mild phenotypeP De Jonghe, V Timmerman, E Nelis, et al.
Journal of Neurology|November 8, 2001
Hereditary Neuralgic Amyotrophy (HNA) is genetically heterogeneousG Kuhlenbäumer, J Meuleman, P De Jonghe, et al.
Annals of the New York Academy of Sciences|November 1, 2017
Hereditary Neuralgic Amyotrophy: Mutation Analysis of Candidate GenesJ Meuleman, G Kuhlenbäumer, A Schirmacher, et al.
Journal of Medical Genetics|February 27, 2004
Autosomal dominant axonal Charcot-Marie-Tooth disease type 2 (CMT2G) maps to chromosome 12q12-q13.3E Nelis, J Berciano, N Verpoorten, et al.
Annals of the New York Academy of Sciences|December 10, 1999
Hereditary neuralgic amyotrophy: mutation analysis of candidate genesJ Meuleman, G Kuhlenbäumer, A Schirmacher, et al.
Pageof 11