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Vincent Timmerman

Showing results (111-120 of 152) with videos related to

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Brain : a Journal of Neurology|February 11, 2022
NCAM1 and GDF15 are biomarkers of Charcot-Marie-Tooth disease in patients and miceMatthew J Jennings, Alexia Kagiava, Leen Vendredy, et al.
Experimental & Molecular Medicine|June 2, 2024
Advances and challenges in modeling inherited peripheral neuropathies using iPSCsJonas Van Lent, Robert Prior, Gonzalo Pérez Siles, et al.
Molecular and Cellular Neurosciences|September 6, 2005
Synaptopodin and 4 novel genes identified in primary sensory neuronsNathalie Verpoorten, Kristien Verhoeven, Stefan Weckx, et al.
Human Mutation|February 2, 2017
Axonal Neuropathies due to Mutations in Small Heat Shock Proteins: Clinical, Genetic, and Functional Insights into Novel MutationsAndoni Echaniz-Laguna, Thomas Geuens, Philippe Petiot, et al.
Brain : a Journal of Neurology|June 9, 2009
Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathyKristl G Claeys, Stephan Züchner, Marina Kennerson, et al.
Annals of Neurology|January 27, 2006
Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2Stephan Züchner, Peter De Jonghe, Albena Jordanova, et al.
Nature Genetics|February 26, 2004
Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndromeChristian Windpassinger, Michaela Auer-Grumbach, Joy Irobi, et al.
Brain Pathology (Zurich, Switzerland)|August 15, 2023
Myelin protein zero mutation-related hereditary neuropathies: Neuropathological insight from a new nerve biopsy cohortJuliane Bremer, Axel Meinhardt, Istvan Katona, et al.
American Journal of Human Genetics|May 25, 2010
Mechanisms for nonrecurrent genomic rearrangements associated with CMT1A or HNPP: rare CNVs as a cause for missing heritabilityFeng Zhang, Pavel Seeman, Pengfei Liu, et al.
Cell Stress & Chaperones|February 14, 2019
Small heat shock proteins: multifaceted proteins with important implications for lifeSerena Carra, Simon Alberti, Justin L P Benesch, et al.
Pageof 16

Showing results (111-120 of 152) with videos related to

Sort By:
Pageof 16
Brain : a Journal of Neurology|February 11, 2022
NCAM1 and GDF15 are biomarkers of Charcot-Marie-Tooth disease in patients and miceMatthew J Jennings, Alexia Kagiava, Leen Vendredy, et al.
Experimental & Molecular Medicine|June 2, 2024
Advances and challenges in modeling inherited peripheral neuropathies using iPSCsJonas Van Lent, Robert Prior, Gonzalo Pérez Siles, et al.
Molecular and Cellular Neurosciences|September 6, 2005
Synaptopodin and 4 novel genes identified in primary sensory neuronsNathalie Verpoorten, Kristien Verhoeven, Stefan Weckx, et al.
Human Mutation|February 2, 2017
Axonal Neuropathies due to Mutations in Small Heat Shock Proteins: Clinical, Genetic, and Functional Insights into Novel MutationsAndoni Echaniz-Laguna, Thomas Geuens, Philippe Petiot, et al.
Brain : a Journal of Neurology|June 9, 2009
Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathyKristl G Claeys, Stephan Züchner, Marina Kennerson, et al.
Annals of Neurology|January 27, 2006
Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2Stephan Züchner, Peter De Jonghe, Albena Jordanova, et al.
Nature Genetics|February 26, 2004
Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndromeChristian Windpassinger, Michaela Auer-Grumbach, Joy Irobi, et al.
Brain Pathology (Zurich, Switzerland)|August 15, 2023
Myelin protein zero mutation-related hereditary neuropathies: Neuropathological insight from a new nerve biopsy cohortJuliane Bremer, Axel Meinhardt, Istvan Katona, et al.
American Journal of Human Genetics|May 25, 2010
Mechanisms for nonrecurrent genomic rearrangements associated with CMT1A or HNPP: rare CNVs as a cause for missing heritabilityFeng Zhang, Pavel Seeman, Pengfei Liu, et al.
Cell Stress & Chaperones|February 14, 2019
Small heat shock proteins: multifaceted proteins with important implications for lifeSerena Carra, Simon Alberti, Justin L P Benesch, et al.
Pageof 16