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Vincent Timmerman

Showing results (31-40 of 152) with videos related to

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Acta Neuropathologica|June 4, 2013
Charcot-Marie-Tooth causing HSPB1 mutations increase Cdk5-mediated phosphorylation of neurofilamentsAnne Holmgren, Delphine Bouhy, Vicky De Winter, et al.
Journal of Child Neurology|March 29, 2003
Andermann syndrome in a Turkish patientErcan Demir, Joy Irobi, Sevim Erdem, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|April 24, 2010
Cell death-mediated cleavage of the attraction signal p43 in human atherosclerosis: implications for plaque destabilizationWim Martinet, Inge De Meyer, Nathalie Cools, et al.
Scientific Reports|May 31, 2020
BAG3 Pro209 mutants associated with myopathy and neuropathy relocate chaperones of the CASA-complex to aggresomesElias Adriaenssens, Barbara Tedesco, Laura Mediani, et al.
Archives of Neurology|March 14, 2003
Autosomal dominant inherited neuropathies with prominent sensory loss and mutilations: a reviewMichaela Auer-Grumbach, Peter De Jonghe, Kristien Verhoeven, et al.
Clinical Chemistry|January 4, 2007
Mutation scanning the GJB1 gene with high-resolution melting analysis: implications for mutation scanning of genes for Charcot-Marie-Tooth diseaseMarina L Kennerson, Trent Warburton, Eva Nelis, et al.
Archives of Neurology|July 11, 2007
Clinical and electrophysiological features in Charcot-Marie-Tooth disease with mutations in the NEFL geneGabriel Miltenberger-Miltenyi, Andreas R Janecke, Julia V Wanschitz, et al.
Amino Acids|March 9, 2011
Drosophila as a platform to predict the pathogenicity of novel aminoacyl-tRNA synthetase mutations in CMTRicardo Leitão-Gonçalves, Biljana Ermanoska, An Jacobs, et al.
Autophagy|January 24, 2019
Neuropathy-causing mutations in HSPB1 impair autophagy by disturbing the formation of SQSTM1/p62 bodiesMansour Haidar, Bob Asselbergh, Elias Adriaenssens, et al.
Journal of the Peripheral Nervous System : JPNS|July 2, 2002
Mutation analysis of 12 candidate genes for distal hereditary motor neuropathy type II (distal HMN II) linked to 12q24.3Joy Irobi, Eva Nelis, Kristien Verhoeven, et al.
Pageof 16

Showing results (31-40 of 152) with videos related to

Sort By:
Pageof 16
Acta Neuropathologica|June 4, 2013
Charcot-Marie-Tooth causing HSPB1 mutations increase Cdk5-mediated phosphorylation of neurofilamentsAnne Holmgren, Delphine Bouhy, Vicky De Winter, et al.
Journal of Child Neurology|March 29, 2003
Andermann syndrome in a Turkish patientErcan Demir, Joy Irobi, Sevim Erdem, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|April 24, 2010
Cell death-mediated cleavage of the attraction signal p43 in human atherosclerosis: implications for plaque destabilizationWim Martinet, Inge De Meyer, Nathalie Cools, et al.
Scientific Reports|May 31, 2020
BAG3 Pro209 mutants associated with myopathy and neuropathy relocate chaperones of the CASA-complex to aggresomesElias Adriaenssens, Barbara Tedesco, Laura Mediani, et al.
Archives of Neurology|March 14, 2003
Autosomal dominant inherited neuropathies with prominent sensory loss and mutilations: a reviewMichaela Auer-Grumbach, Peter De Jonghe, Kristien Verhoeven, et al.
Clinical Chemistry|January 4, 2007
Mutation scanning the GJB1 gene with high-resolution melting analysis: implications for mutation scanning of genes for Charcot-Marie-Tooth diseaseMarina L Kennerson, Trent Warburton, Eva Nelis, et al.
Archives of Neurology|July 11, 2007
Clinical and electrophysiological features in Charcot-Marie-Tooth disease with mutations in the NEFL geneGabriel Miltenberger-Miltenyi, Andreas R Janecke, Julia V Wanschitz, et al.
Amino Acids|March 9, 2011
Drosophila as a platform to predict the pathogenicity of novel aminoacyl-tRNA synthetase mutations in CMTRicardo Leitão-Gonçalves, Biljana Ermanoska, An Jacobs, et al.
Autophagy|January 24, 2019
Neuropathy-causing mutations in HSPB1 impair autophagy by disturbing the formation of SQSTM1/p62 bodiesMansour Haidar, Bob Asselbergh, Elias Adriaenssens, et al.
Journal of the Peripheral Nervous System : JPNS|July 2, 2002
Mutation analysis of 12 candidate genes for distal hereditary motor neuropathy type II (distal HMN II) linked to 12q24.3Joy Irobi, Eva Nelis, Kristien Verhoeven, et al.
Pageof 16