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Vincent Timmerman

Showing results (41-50 of 152) with videos related to

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Neurogenetics|January 10, 2009
A systematic comparison of all mutations in hereditary sensory neuropathy type I (HSAN I) reveals that the G387A mutation is not disease associatedThorsten Hornemann, Anke Penno, Stephane Richard, et al.
Neurobiology of Disease|February 14, 2014
Human Rab7 mutation mimics features of Charcot-Marie-Tooth neuropathy type 2B in DrosophilaKatrien Janssens, Sofie Goethals, Derek Atkinson, et al.
Neurogenetics|May 28, 2002
Search for mutations in the EGR2 corepressor proteins, NAB1 and NAB2, in human peripheral neuropathiesKoen Venken, Emilio Di Maria, Emilia Bellone, et al.
Journal of Neurology|June 19, 2008
Magnetic resonance imaging findings of leg musculature in Charcot-Marie-Tooth disease type 2 due to dynamin 2 mutationElena Gallardo, Kristl G Claeys, Eva Nelis, et al.
Nature Reviews. Disease Primers|January 22, 2026
Charcot-Marie-Tooth disease and related neuropathiesJoshua Burns, Vincent Timmerman, Matilde Laurá, et al.
Neuromuscular Disorders : NMD|October 26, 2002
A novel homozygous missense mutation in the myotubularin-related protein 2 gene associated with recessive Charcot-Marie-Tooth disease with irregularly folded myelin sheathsEva Nelis, Sevim Erdem, Ersin Tan, et al.
Iscience|May 4, 2026
Unperturbed dye-based imaging of spontaneous synchronized calcium activity in iPSC-derived neuronal culturesNina Dirkx, Bob Asselbergh, Peter Verstraelen, et al.
Cell Communication and Signaling : CCS|May 5, 2022
Oligodendroglia-derived extracellular vesicles activate autophagy via LC3B/BAG3 to protect against oxidative stress with an enhanced effect for HSPB8 enriched vesiclesBram Van den Broek, Charlotte Wuyts, Angela Sisto, et al.
Neuromuscular Disorders : NMD|October 17, 2003
Identification of novel GDAP1 mutations causing autosomal recessive Charcot-Marie-Tooth diseaseNadia Ammar, Eva Nelis, Luciano Merlini, et al.
Human Molecular Genetics|October 20, 2018
Sensory neuropathy-causing mutations in ATL3 affect ER-mitochondria contact sites and impair axonal mitochondrial distributionMichiel Krols, Bob Asselbergh, Riet De Rycke, et al.
Pageof 16

Showing results (41-50 of 152) with videos related to

Sort By:
Pageof 16
Neurogenetics|January 10, 2009
A systematic comparison of all mutations in hereditary sensory neuropathy type I (HSAN I) reveals that the G387A mutation is not disease associatedThorsten Hornemann, Anke Penno, Stephane Richard, et al.
Neurobiology of Disease|February 14, 2014
Human Rab7 mutation mimics features of Charcot-Marie-Tooth neuropathy type 2B in DrosophilaKatrien Janssens, Sofie Goethals, Derek Atkinson, et al.
Neurogenetics|May 28, 2002
Search for mutations in the EGR2 corepressor proteins, NAB1 and NAB2, in human peripheral neuropathiesKoen Venken, Emilio Di Maria, Emilia Bellone, et al.
Journal of Neurology|June 19, 2008
Magnetic resonance imaging findings of leg musculature in Charcot-Marie-Tooth disease type 2 due to dynamin 2 mutationElena Gallardo, Kristl G Claeys, Eva Nelis, et al.
Nature Reviews. Disease Primers|January 22, 2026
Charcot-Marie-Tooth disease and related neuropathiesJoshua Burns, Vincent Timmerman, Matilde Laurá, et al.
Neuromuscular Disorders : NMD|October 26, 2002
A novel homozygous missense mutation in the myotubularin-related protein 2 gene associated with recessive Charcot-Marie-Tooth disease with irregularly folded myelin sheathsEva Nelis, Sevim Erdem, Ersin Tan, et al.
Iscience|May 4, 2026
Unperturbed dye-based imaging of spontaneous synchronized calcium activity in iPSC-derived neuronal culturesNina Dirkx, Bob Asselbergh, Peter Verstraelen, et al.
Cell Communication and Signaling : CCS|May 5, 2022
Oligodendroglia-derived extracellular vesicles activate autophagy via LC3B/BAG3 to protect against oxidative stress with an enhanced effect for HSPB8 enriched vesiclesBram Van den Broek, Charlotte Wuyts, Angela Sisto, et al.
Neuromuscular Disorders : NMD|October 17, 2003
Identification of novel GDAP1 mutations causing autosomal recessive Charcot-Marie-Tooth diseaseNadia Ammar, Eva Nelis, Luciano Merlini, et al.
Human Molecular Genetics|October 20, 2018
Sensory neuropathy-causing mutations in ATL3 affect ER-mitochondria contact sites and impair axonal mitochondrial distributionMichiel Krols, Bob Asselbergh, Riet De Rycke, et al.
Pageof 16