Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

V Timmerman

Showing results (91-100 of 105) with videos related to

Pageof 11
Sort By:
Neurology|June 24, 2004
Autosomal dominant striatal degeneration (ADSD): clinical description and mapping to 5q13-5q14G Kuhlenbäumer, P Lüdemann, A Schirmacher, et al.
Neurology|March 15, 2006
Novel mutations in the HSN2 gene causing hereditary sensory and autonomic neuropathy type IIK Coen, D Pareyson, M Auer-Grumbach, et al.
Journal of Medical Genetics|January 1, 1997
Detection of the CMT1A/HNPP recombination hotspot in unrelated patients of European descentV Timmerman, B Rautenstrauss, L T Reiter, et al.
European Journal of Human Genetics : EJHG|December 22, 1999
Genetic refinement of the hereditary neuralgic amyotrophy (HNA) locus at chromosome 17q25J Meulemann, G Kuhlenbäumer, A Schirmacher, et al.
Molecular Psychiatry|June 4, 2014
MIR137 variants identified in psychiatric patients affect synaptogenesis and neuronal transmission gene setsM Strazisar, S Cammaerts, K van der Ven, et al.
Neuropediatrics|May 28, 2008
Two novel mutations in the GDAP1 and PRX genes in early onset Charcot-Marie-Tooth syndromeM Auer-Grumbach, C Fischer, L Papić, et al.
Neurology|January 10, 2001
Clinical and genetic study of a large Charcot-Marie-Tooth type 2A family from southern ItalyM Muglia, M Zappia, V Timmerman, et al.
Human Genetics|June 1, 2000
Fine mapping of the neurally expressed gene SOX14 to human 3q23, relative to three congenital diseasesM Hargrave, K James, K Nield, et al.
Neurology|May 16, 2007
Phenotype of Charcot-Marie-Tooth disease Type 2H M E Bienfait, F Baas, J H T M Koelman, et al.
Neurology|December 25, 2002
Mutations in GDAP1: autosomal recessive CMT with demyelination and axonopathyE Nelis, S Erdem, P Y K Van Den Bergh, et al.
Pageof 11

Showing results (91-100 of 105) with videos related to

Sort By:
Pageof 11
Neurology|June 24, 2004
Autosomal dominant striatal degeneration (ADSD): clinical description and mapping to 5q13-5q14G Kuhlenbäumer, P Lüdemann, A Schirmacher, et al.
Neurology|March 15, 2006
Novel mutations in the HSN2 gene causing hereditary sensory and autonomic neuropathy type IIK Coen, D Pareyson, M Auer-Grumbach, et al.
Journal of Medical Genetics|January 1, 1997
Detection of the CMT1A/HNPP recombination hotspot in unrelated patients of European descentV Timmerman, B Rautenstrauss, L T Reiter, et al.
European Journal of Human Genetics : EJHG|December 22, 1999
Genetic refinement of the hereditary neuralgic amyotrophy (HNA) locus at chromosome 17q25J Meulemann, G Kuhlenbäumer, A Schirmacher, et al.
Molecular Psychiatry|June 4, 2014
MIR137 variants identified in psychiatric patients affect synaptogenesis and neuronal transmission gene setsM Strazisar, S Cammaerts, K van der Ven, et al.
Neuropediatrics|May 28, 2008
Two novel mutations in the GDAP1 and PRX genes in early onset Charcot-Marie-Tooth syndromeM Auer-Grumbach, C Fischer, L Papić, et al.
Neurology|January 10, 2001
Clinical and genetic study of a large Charcot-Marie-Tooth type 2A family from southern ItalyM Muglia, M Zappia, V Timmerman, et al.
Human Genetics|June 1, 2000
Fine mapping of the neurally expressed gene SOX14 to human 3q23, relative to three congenital diseasesM Hargrave, K James, K Nield, et al.
Neurology|May 16, 2007
Phenotype of Charcot-Marie-Tooth disease Type 2H M E Bienfait, F Baas, J H T M Koelman, et al.
Neurology|December 25, 2002
Mutations in GDAP1: autosomal recessive CMT with demyelination and axonopathyE Nelis, S Erdem, P Y K Van Den Bergh, et al.
Pageof 11