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Karima Ghorab

Showing results (11-20 of 26) with videos related to

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Biomedicines|June 28, 2023
The First Large Deletion of <i>ATL3</i> Identified in a Patient Presenting with a Sensory PolyneuropathyIoanna Pyromali, Laurence Richard, Paco Derouault, et al.
Journal of the Neurological Sciences|August 29, 2021
CIDP and hemopathies, an underestimated associationNathalie Deschamps, Stéphane Mathis, Mathilde Duchesne, et al.
Expert Review of Neurotherapeutics|June 21, 2018
Value of nerve biopsy in the management of peripheral neuropathiesStéphane Mathis, Laurent Magy, Gwendal Le Masson, et al.
Journal of the Neurological Sciences|August 15, 2018
Some new proposals for the classification of inherited myopathiesStéphane Mathis, Meriem Tazir, Guilhem Solé, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 4, 2022
GM2 gangliosidosis AB variant: first case of late onset and review of the literatureBenjamin Ganne, Benjamin Dauriat, Laurence Richard, et al.
Journal of the Neurological Sciences|December 19, 2017
History and current difficulties in classifying inherited myopathies and muscular dystrophiesStéphane Mathis, Meriem Tazir, Laurent Magy, et al.
Archives of Neurology|December 17, 2009
Genotype-phenotype correlations in Charcot-Marie-Tooth disease type 2 caused by mitofusin 2 mutationsJudith Calvo, Benoît Funalot, Robert A Ouvrier, et al.
European Journal of Medical Genetics|September 18, 2020
A novel pathogenic variant in DYNC1H1 causes various upper and lower motor neuron anomaliesLouis M Viollet, Kathryn J Swoboda, Rong Mao, et al.
American Journal of Human Genetics|January 22, 2013
Constitutive activation of the calcium sensor STIM1 causes tubular-aggregate myopathyJohann Böhm, Frédéric Chevessier, André Maues De Paula, et al.
Neuromuscular Disorders : NMD|June 29, 2026
Severe dilated cardiomyopathy in females with dystrophinopathy : a case series of nine patientsSolène Conrad, Claire Toquet, Mélanie Fradin, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
Biomedicines|June 28, 2023
The First Large Deletion of <i>ATL3</i> Identified in a Patient Presenting with a Sensory PolyneuropathyIoanna Pyromali, Laurence Richard, Paco Derouault, et al.
Journal of the Neurological Sciences|August 29, 2021
CIDP and hemopathies, an underestimated associationNathalie Deschamps, Stéphane Mathis, Mathilde Duchesne, et al.
Expert Review of Neurotherapeutics|June 21, 2018
Value of nerve biopsy in the management of peripheral neuropathiesStéphane Mathis, Laurent Magy, Gwendal Le Masson, et al.
Journal of the Neurological Sciences|August 15, 2018
Some new proposals for the classification of inherited myopathiesStéphane Mathis, Meriem Tazir, Guilhem Solé, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 4, 2022
GM2 gangliosidosis AB variant: first case of late onset and review of the literatureBenjamin Ganne, Benjamin Dauriat, Laurence Richard, et al.
Journal of the Neurological Sciences|December 19, 2017
History and current difficulties in classifying inherited myopathies and muscular dystrophiesStéphane Mathis, Meriem Tazir, Laurent Magy, et al.
Archives of Neurology|December 17, 2009
Genotype-phenotype correlations in Charcot-Marie-Tooth disease type 2 caused by mitofusin 2 mutationsJudith Calvo, Benoît Funalot, Robert A Ouvrier, et al.
European Journal of Medical Genetics|September 18, 2020
A novel pathogenic variant in DYNC1H1 causes various upper and lower motor neuron anomaliesLouis M Viollet, Kathryn J Swoboda, Rong Mao, et al.
American Journal of Human Genetics|January 22, 2013
Constitutive activation of the calcium sensor STIM1 causes tubular-aggregate myopathyJohann Böhm, Frédéric Chevessier, André Maues De Paula, et al.
Neuromuscular Disorders : NMD|June 29, 2026
Severe dilated cardiomyopathy in females with dystrophinopathy : a case series of nine patientsSolène Conrad, Claire Toquet, Mélanie Fradin, et al.
Pageof 3