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Hamid Azzedine

Showing results (1-10 of 21) with videos related to

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Brain : a Journal of Neurology|February 14, 2015
Dysfunction in endoplasmic reticulum-mitochondria crosstalk underlies SIGMAR1 loss of function mediated motor neuron degenerationNathalie Bernard-Marissal, Jean-Jacques Médard, Hamid Azzedine, et al.
Acta Neuropathologica|November 30, 2016
Towards a functional pathology of hereditary neuropathiesJoachim Weis, Kristl G Claeys, Andreas Roos, et al.
Annals of Neurology|January 6, 2004
Spinocerebellar ataxia with sensory neuropathy (SCA25) maps to chromosome 2pGiovanni Stevanin, Naima Bouslam, Stéphane Thobois, et al.
The British Journal of Ophthalmology|February 14, 2014
Ophthalmic features of PLA2G6-related paediatric neurodegeneration with brain iron accumulationArif O Khan, Abdulmajeed AlDrees, Salah A Elmalik, et al.
Annals of Neurology|March 24, 2005
Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28)Naima Bouslam, Ali Benomar, Hamid Azzedine, et al.
Brain : a Journal of Neurology|January 26, 2006
Autosomal recessive spastic paraplegia (SPG30) with mild ataxia and sensory neuropathy maps to chromosome 2q37.3Stephan Klebe, Hamid Azzedine, Alexandra Durr, et al.
Brain and Behavior|April 19, 2016
Underestimated associated features in CMT neuropathies: clinical indicators for the causative gene?Friederike Werheid, Hamid Azzedine, Eva Zwerenz, et al.
Archives of Neurology|April 23, 2003
Phenotypical features of a Moroccan family with autosomal recessive Charcot-Marie-Tooth disease associated with the S194X mutation in the GDAP1 geneNazha Birouk, Hamid Azzedine, Odile Dubourg, et al.
Neuromuscular Disorders : NMD|July 10, 2021
Leukoencephalopathy and conduction blocks in PLEKHG5-associated intermediate CMT diseaseRocio-Nur Villar-Quiles, Van Thuy Le, Sarah Leonard-Louis, et al.
Brain : a Journal of Neurology|March 10, 2007
Autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2): phenotype-genotype correlations in 13 Moroccan familiesAhmed Bouhouche, Nazha Birouk, Hamid Azzedine, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Brain : a Journal of Neurology|February 14, 2015
Dysfunction in endoplasmic reticulum-mitochondria crosstalk underlies SIGMAR1 loss of function mediated motor neuron degenerationNathalie Bernard-Marissal, Jean-Jacques Médard, Hamid Azzedine, et al.
Acta Neuropathologica|November 30, 2016
Towards a functional pathology of hereditary neuropathiesJoachim Weis, Kristl G Claeys, Andreas Roos, et al.
Annals of Neurology|January 6, 2004
Spinocerebellar ataxia with sensory neuropathy (SCA25) maps to chromosome 2pGiovanni Stevanin, Naima Bouslam, Stéphane Thobois, et al.
The British Journal of Ophthalmology|February 14, 2014
Ophthalmic features of PLA2G6-related paediatric neurodegeneration with brain iron accumulationArif O Khan, Abdulmajeed AlDrees, Salah A Elmalik, et al.
Annals of Neurology|March 24, 2005
Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28)Naima Bouslam, Ali Benomar, Hamid Azzedine, et al.
Brain : a Journal of Neurology|January 26, 2006
Autosomal recessive spastic paraplegia (SPG30) with mild ataxia and sensory neuropathy maps to chromosome 2q37.3Stephan Klebe, Hamid Azzedine, Alexandra Durr, et al.
Brain and Behavior|April 19, 2016
Underestimated associated features in CMT neuropathies: clinical indicators for the causative gene?Friederike Werheid, Hamid Azzedine, Eva Zwerenz, et al.
Archives of Neurology|April 23, 2003
Phenotypical features of a Moroccan family with autosomal recessive Charcot-Marie-Tooth disease associated with the S194X mutation in the GDAP1 geneNazha Birouk, Hamid Azzedine, Odile Dubourg, et al.
Neuromuscular Disorders : NMD|July 10, 2021
Leukoencephalopathy and conduction blocks in PLEKHG5-associated intermediate CMT diseaseRocio-Nur Villar-Quiles, Van Thuy Le, Sarah Leonard-Louis, et al.
Brain : a Journal of Neurology|March 10, 2007
Autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2): phenotype-genotype correlations in 13 Moroccan familiesAhmed Bouhouche, Nazha Birouk, Hamid Azzedine, et al.
Pageof 3