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V Timmerman

Showing results (1-10 of 105) with videos related to

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Revue Neurologique|November 19, 2013
[Animal models of Charcot-Marie-Tooth disease and their relevance for understanding the disease in humans]D Bouhy, V Timmerman
Neuromuscular Disorders : NMD|September 21, 2000
71st ENMC International Workshop, 6th workshop of the European Charcot-Marie-Tooth disease consortium: hereditary recurrent focal neuropathies, 24-25 September 1999, Soestduinen, the NetherlandsF Stögbauer, V Timmerman, C Van Broeckhoven
Journal of the Peripheral Nervous System : JPNS|January 21, 2000
Report of the 8th annual symposium of the European Charcot-Marie-Tooth Consortium, Antwerpen, Belgium, July 2-4, 1999V Timmerman, P De Jonghe, C Van Broeckhoven
Nature Genetics|November 4, 2000
Of giant axons and curly hairV Timmerman, P De Jonghe, C Van Broeckhoven
Acta Neurologica Belgica|December 1, 2000
Molecular genetics of inherited peripheral neuropathies: who are the actors?J Meuleman, V Timmerman, E Nelis, et al.
Neuromuscular Disorders : NMD|September 21, 2000
Diagnostic guidelines for hereditary neuralgic amyotrophy or heredofamilial neuritis with brachial plexus predilection. On behalf of the European CMT ConsortiumG Kuhlenbäumer, F Stögbauer, V Timmerman, et al.
Neurogenetics|August 29, 2001
Hereditary neuralgic amyotrophyJ Meuleman, V Timmerman, C Van Broeckhoven, et al.
Human Molecular Genetics|March 1, 1994
Identification of a 5' splice site mutation in the PMP-22 gene in autosomal dominant Charcot-Marie-Tooth disease type 1E Nelis, V Timmerman, P De Jonghe, et al.
Neurology|February 19, 2000
Hereditary recurrent focal neuropathies: clinical and molecular featuresF Stögbauer, P Young, G Kuhlenbäumer, et al.
Neurogenetics|December 14, 1999
Molecular genetics and biology of inherited peripheral neuropathies: a fast-moving fieldE Nelis, V Timmerman, P De Jonghe, et al.
Pageof 11

Showing results (1-10 of 105) with videos related to

Sort By:
Pageof 11
Revue Neurologique|November 19, 2013
[Animal models of Charcot-Marie-Tooth disease and their relevance for understanding the disease in humans]D Bouhy, V Timmerman
Neuromuscular Disorders : NMD|September 21, 2000
71st ENMC International Workshop, 6th workshop of the European Charcot-Marie-Tooth disease consortium: hereditary recurrent focal neuropathies, 24-25 September 1999, Soestduinen, the NetherlandsF Stögbauer, V Timmerman, C Van Broeckhoven
Journal of the Peripheral Nervous System : JPNS|January 21, 2000
Report of the 8th annual symposium of the European Charcot-Marie-Tooth Consortium, Antwerpen, Belgium, July 2-4, 1999V Timmerman, P De Jonghe, C Van Broeckhoven
Nature Genetics|November 4, 2000
Of giant axons and curly hairV Timmerman, P De Jonghe, C Van Broeckhoven
Acta Neurologica Belgica|December 1, 2000
Molecular genetics of inherited peripheral neuropathies: who are the actors?J Meuleman, V Timmerman, E Nelis, et al.
Neuromuscular Disorders : NMD|September 21, 2000
Diagnostic guidelines for hereditary neuralgic amyotrophy or heredofamilial neuritis with brachial plexus predilection. On behalf of the European CMT ConsortiumG Kuhlenbäumer, F Stögbauer, V Timmerman, et al.
Neurogenetics|August 29, 2001
Hereditary neuralgic amyotrophyJ Meuleman, V Timmerman, C Van Broeckhoven, et al.
Human Molecular Genetics|March 1, 1994
Identification of a 5' splice site mutation in the PMP-22 gene in autosomal dominant Charcot-Marie-Tooth disease type 1E Nelis, V Timmerman, P De Jonghe, et al.
Neurology|February 19, 2000
Hereditary recurrent focal neuropathies: clinical and molecular featuresF Stögbauer, P Young, G Kuhlenbäumer, et al.
Neurogenetics|December 14, 1999
Molecular genetics and biology of inherited peripheral neuropathies: a fast-moving fieldE Nelis, V Timmerman, P De Jonghe, et al.
Pageof 11