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Philippe Latour

Showing results (1-10 of 74) with videos related to

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Methods in Cell Biology|February 11, 2015
Laboratory diagnosis of Niemann-Pick disease type C: the filipin staining testMarie T Vanier, Philippe Latour
Neurology|January 7, 2015
Author responseAndoni Echaniz-Laguna, Philippe Latour
Journal of the Peripheral Nervous System : JPNS|January 26, 2019
A cryptic splicing mutation in the INF2 gene causing Charcot-Marie-Tooth disease with minimal glomerular dysfunctionAndoni Echaniz-Laguna, Philippe Latour
Neuromuscular Disorders : NMD|December 24, 2005
Clinical, electrophysiological and molecular genetic studies in a family with X-linked dominant Charcot-Marie-Tooth neuropathy presenting a novel mutation in GJB1 Promoter and a rare polymorphism in LITAF/SIMPLEKatell Beauvais, Alain Furby, Philippe Latour
Journal of Neurology, Neurosurgery, and Psychiatry|March 25, 2016
Hereditary and inflammatory neuropathies: a review of reported associations, mimics and misdiagnosesYusuf A Rajabally, David Adams, Philippe Latour, et al.
Parkinsonism & Related Disorders|January 9, 2017
Abnormal dopamine transporter imaging in adult-onset Niemann-Pick disease type CJoanne Terbeek, Philippe Latour, Koen Van Laere, et al.
Muscle & Nerve|July 30, 2008
A new MPZ mutation associated with a mild CMT1 phenotype presenting with recurrent nerve compressionArmelle Magot, Philippe Latour, Jean-Marie Mussini, et al.
Journal of the Peripheral Nervous System : JPNS|November 14, 2009
Ultrastructural mitochondrial modifications characteristic of mitofusin 2 mutations (CMT2A)Guilhem Sole, Xavier Ferrer, Claude Vital, et al.
Neurogenetics|February 4, 2018
WES homozygosity mapping in a recessive form of Charcot-Marie-Tooth neuropathy reveals intronic GDAP1 variant leading to a premature stop codonMarion Masingue, Jimmy Perrot, Robert-Yves Carlier, et al.
Neuromuscular Disorders : NMD|December 3, 2014
Clinical and electrophysiological features in a French family presenting with seipinopathyYolaine Ollivier, Armelle Magot, Philippe Latour, et al.
Pageof 8

Showing results (1-10 of 74) with videos related to

Sort By:
Pageof 8
Methods in Cell Biology|February 11, 2015
Laboratory diagnosis of Niemann-Pick disease type C: the filipin staining testMarie T Vanier, Philippe Latour
Neurology|January 7, 2015
Author responseAndoni Echaniz-Laguna, Philippe Latour
Journal of the Peripheral Nervous System : JPNS|January 26, 2019
A cryptic splicing mutation in the INF2 gene causing Charcot-Marie-Tooth disease with minimal glomerular dysfunctionAndoni Echaniz-Laguna, Philippe Latour
Neuromuscular Disorders : NMD|December 24, 2005
Clinical, electrophysiological and molecular genetic studies in a family with X-linked dominant Charcot-Marie-Tooth neuropathy presenting a novel mutation in GJB1 Promoter and a rare polymorphism in LITAF/SIMPLEKatell Beauvais, Alain Furby, Philippe Latour
Journal of Neurology, Neurosurgery, and Psychiatry|March 25, 2016
Hereditary and inflammatory neuropathies: a review of reported associations, mimics and misdiagnosesYusuf A Rajabally, David Adams, Philippe Latour, et al.
Parkinsonism & Related Disorders|January 9, 2017
Abnormal dopamine transporter imaging in adult-onset Niemann-Pick disease type CJoanne Terbeek, Philippe Latour, Koen Van Laere, et al.
Muscle & Nerve|July 30, 2008
A new MPZ mutation associated with a mild CMT1 phenotype presenting with recurrent nerve compressionArmelle Magot, Philippe Latour, Jean-Marie Mussini, et al.
Journal of the Peripheral Nervous System : JPNS|November 14, 2009
Ultrastructural mitochondrial modifications characteristic of mitofusin 2 mutations (CMT2A)Guilhem Sole, Xavier Ferrer, Claude Vital, et al.
Neurogenetics|February 4, 2018
WES homozygosity mapping in a recessive form of Charcot-Marie-Tooth neuropathy reveals intronic GDAP1 variant leading to a premature stop codonMarion Masingue, Jimmy Perrot, Robert-Yves Carlier, et al.
Neuromuscular Disorders : NMD|December 3, 2014
Clinical and electrophysiological features in a French family presenting with seipinopathyYolaine Ollivier, Armelle Magot, Philippe Latour, et al.
Pageof 8