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V Timmerman

Showing results (71-80 of 105) with videos related to

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Neuroscience Letters|March 6, 1998
Absence of mutations in peripheral myelin protein-22, myelin protein zero, and connexin 32 in autosomal recessive Dejerine-Sottas syndromeF Stögbauer, P Young, H Wiebusch, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 17, 1999
Autosomal dominant burning feet syndromeF Stögbauer, P Young, G Kuhlenbäumer, et al.
Neuromuscular Disorders : NMD|September 5, 2002
Hereditary neuropathy with liability to pressure palsies with a small deletion interrupting the PMP22 geneR A C van de Wetering, A A W M Gabreëls-Festen, V Timmerman, et al.
Neurology|March 24, 2004
SPTLC1 mutation in twin sisters with hereditary sensory neuropathy type IK Verhoeven, K Coen, E De Vriendt, et al.
Neurology|October 15, 2003
Charcot-Marie-Tooth disease with giant axons: a clinicopathological and genetic entityG Lus, E Nelis, A Jordanova, et al.
Human Genetics|June 21, 2001
Mutation analysis of 4 candidate genes for hereditary neuralgic amyotrophy (HNA)J Meuleman, G Kuhlenbäumer, D Audenaert, et al.
Clinical Genetics|November 15, 2006
Spastin gene mutations in Bulgarian patients with hereditary spastic paraplegiaN Ivanova, A Löfgren, I Tournev, et al.
Human Mutation|February 17, 2001
A novel connexin 32 missense mutation (E208G) causing Charcot-Marie-Tooth diseaseA Kochanski, A Lofgren, H Jedrzejowska, et al.
Nature Genetics|June 1, 1992
The peripheral myelin protein gene PMP-22 is contained within the Charcot-Marie-Tooth disease type 1A duplicationV Timmerman, E Nelis, W Van Hul, et al.
European Journal of Human Genetics : EJHG|August 31, 2001
A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2F) maps to chromosome 7q11-q21S M Ismailov, V P Fedotov, E L Dadali, et al.
Pageof 11

Showing results (71-80 of 105) with videos related to

Sort By:
Pageof 11
Neuroscience Letters|March 6, 1998
Absence of mutations in peripheral myelin protein-22, myelin protein zero, and connexin 32 in autosomal recessive Dejerine-Sottas syndromeF Stögbauer, P Young, H Wiebusch, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 17, 1999
Autosomal dominant burning feet syndromeF Stögbauer, P Young, G Kuhlenbäumer, et al.
Neuromuscular Disorders : NMD|September 5, 2002
Hereditary neuropathy with liability to pressure palsies with a small deletion interrupting the PMP22 geneR A C van de Wetering, A A W M Gabreëls-Festen, V Timmerman, et al.
Neurology|March 24, 2004
SPTLC1 mutation in twin sisters with hereditary sensory neuropathy type IK Verhoeven, K Coen, E De Vriendt, et al.
Neurology|October 15, 2003
Charcot-Marie-Tooth disease with giant axons: a clinicopathological and genetic entityG Lus, E Nelis, A Jordanova, et al.
Human Genetics|June 21, 2001
Mutation analysis of 4 candidate genes for hereditary neuralgic amyotrophy (HNA)J Meuleman, G Kuhlenbäumer, D Audenaert, et al.
Clinical Genetics|November 15, 2006
Spastin gene mutations in Bulgarian patients with hereditary spastic paraplegiaN Ivanova, A Löfgren, I Tournev, et al.
Human Mutation|February 17, 2001
A novel connexin 32 missense mutation (E208G) causing Charcot-Marie-Tooth diseaseA Kochanski, A Lofgren, H Jedrzejowska, et al.
Nature Genetics|June 1, 1992
The peripheral myelin protein gene PMP-22 is contained within the Charcot-Marie-Tooth disease type 1A duplicationV Timmerman, E Nelis, W Van Hul, et al.
European Journal of Human Genetics : EJHG|August 31, 2001
A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2F) maps to chromosome 7q11-q21S M Ismailov, V P Fedotov, E L Dadali, et al.
Pageof 11