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V Timmerman

Showing results (21-30 of 105) with videos related to

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Journal of Medical Genetics|October 1, 1994
Linkage and mutation analysis in an extended family with Charcot-Marie-Tooth disease type 1BE Nelis, V Timmerman, P De Jonghe, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 1997
Mutilating neuropathic ulcerations in a chromosome 3q13-q22 linked Charcot-Marie-Tooth disease type 2B familyP De Jonghe, V Timmerman, D FitzPatrick, et al.
Pflugers Archiv : European Journal of Physiology|February 1, 2000
Hereditary motor and sensory neuropathy associated with auditory neuropathy in a Gypsy familyL Leonardis, J Zidar, M Popovic, et al.
Neuroreport|August 10, 2001
Caspr1/Paranodin/Neurexin IV is most likely not a common disease-causing gene for inherited peripheral neuropathiesK Venken, J Meuleman, J Irobi, et al.
Pflugers Archiv : European Journal of Physiology|February 9, 2017
Hereditary motor and sensory neuropathy associated with auditory neuropathy in a Gypsy familyL Leonardis, J Zidar, M Popovič, et al.
Prenatal Diagnosis|July 1, 1995
Prenatal diagnosis of Charcot-Marie-Tooth disease type 1A (CMT1A) using molecular genetic techniquesR Navon, V Timmerman, A Löfgren, et al.
Annals of the New York Academy of Sciences|November 1, 2017
Molecular Diagnostic Testing in Charcot-Marie-Tooth Disease and Related Disorders: Approaches and ResultsP De Jonghe, E Nelis, V Timmerman, et al.
Human Mutation|January 1, 1996
A de novo duplication in 17p11.2 and a novel mutation in the Po gene in two Déjérine-Sottas syndrome patientsK Silander, P Meretoja, E Nelis, et al.
Human Genetics|May 1, 1997
Refinement of the hereditary neuralgic amyotrophy (HNA) locus to chromosome 17q24-q25F Stögbauer, P Young, V Timmerman, et al.
Annals of Human Genetics|February 20, 2002
Exclusion of 5 functional candidate genes for distal hereditary motor neuropathy type II (distal HMN II) linked to 12q24.3J Irobi, E Nelis, J Meuleman, et al.
Pageof 11

Showing results (21-30 of 105) with videos related to

Sort By:
Pageof 11
Journal of Medical Genetics|October 1, 1994
Linkage and mutation analysis in an extended family with Charcot-Marie-Tooth disease type 1BE Nelis, V Timmerman, P De Jonghe, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 1997
Mutilating neuropathic ulcerations in a chromosome 3q13-q22 linked Charcot-Marie-Tooth disease type 2B familyP De Jonghe, V Timmerman, D FitzPatrick, et al.
Pflugers Archiv : European Journal of Physiology|February 1, 2000
Hereditary motor and sensory neuropathy associated with auditory neuropathy in a Gypsy familyL Leonardis, J Zidar, M Popovic, et al.
Neuroreport|August 10, 2001
Caspr1/Paranodin/Neurexin IV is most likely not a common disease-causing gene for inherited peripheral neuropathiesK Venken, J Meuleman, J Irobi, et al.
Pflugers Archiv : European Journal of Physiology|February 9, 2017
Hereditary motor and sensory neuropathy associated with auditory neuropathy in a Gypsy familyL Leonardis, J Zidar, M Popovič, et al.
Prenatal Diagnosis|July 1, 1995
Prenatal diagnosis of Charcot-Marie-Tooth disease type 1A (CMT1A) using molecular genetic techniquesR Navon, V Timmerman, A Löfgren, et al.
Annals of the New York Academy of Sciences|November 1, 2017
Molecular Diagnostic Testing in Charcot-Marie-Tooth Disease and Related Disorders: Approaches and ResultsP De Jonghe, E Nelis, V Timmerman, et al.
Human Mutation|January 1, 1996
A de novo duplication in 17p11.2 and a novel mutation in the Po gene in two Déjérine-Sottas syndrome patientsK Silander, P Meretoja, E Nelis, et al.
Human Genetics|May 1, 1997
Refinement of the hereditary neuralgic amyotrophy (HNA) locus to chromosome 17q24-q25F Stögbauer, P Young, V Timmerman, et al.
Annals of Human Genetics|February 20, 2002
Exclusion of 5 functional candidate genes for distal hereditary motor neuropathy type II (distal HMN II) linked to 12q24.3J Irobi, E Nelis, J Meuleman, et al.
Pageof 11