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Journal of the Neurological Sciences
|
August 15, 2018
Some new proposals for the classification of inherited myopathies
Stéphane Mathis, Meriem Tazir, Guilhem Solé, et al.
Journal of Neuropathology and Experimental Neurology
|
November 8, 2016
Contactin-Associated Protein 1 (CNTNAP1) Mutations Induce Characteristic Lesions of the Paranodal Region
Jean-Michel Vallat, Mathilde Nizon, Alex Magee, et al.
Neuromuscular Disorders : NMD
|
May 6, 2014
Peripheral myelin protein 22 gene duplication with atypical presentations: a new example of the wide spectrum of Charcot-Marie-Tooth 1A disease
Stéphane Mathis, Philippe Corcia, Meriem Tazir, et al.
Journal of Neurology
|
May 23, 2019
Myopathy and scleromyxedema
Antoine Soulages, Hoang Marie-Ange Tang, Anne Pham-Ledard, et al.
Journal of the Neurological Sciences
|
December 19, 2017
History and current difficulties in classifying inherited myopathies and muscular dystrophies
Stéphane Mathis, Meriem Tazir, Laurent Magy, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
May 16, 2014
Autosomal dominant eccentric core disease caused by a heterozygous mutation in the MYH7 gene
Norma B Romero, Ting Xie, Edoardo Malfatti, et al.
The Neurologist
|
November 6, 2019
Papilledema and Peripheral Neuropathies
Stéphane Mathis, Gwendal Le Masson, Antoine Soulages, et al.
Journal of Neurology
|
February 6, 2022
Neurologic manifestations of giant cell arteritis
Antoine Soulages, Igor Sibon, Jean-Michel Vallat, et al.
Clinical Neurology and Neurosurgery
|
January 22, 2018
An in-frame deletion in BICD2 associated with a non-progressive form of SMALED
Aurélien Trimouille, Émilie Obre, Guillaume Banneau, et al.
Journal of Neurology
|
August 11, 2014
Testing the validity of a set of diagnostic criteria for sensory neuronopathies: a francophone collaborative study
Jean-Christophe Antoine, Florence Robert-Varvat, Thierry Maisonobe, et al.
Page
of 12
Search research articles
Search
Showing results (101-110 of 117) with videos related to
Sort By:
Page
of 12
Journal of the Neurological Sciences
|
August 15, 2018
Some new proposals for the classification of inherited myopathies
Stéphane Mathis, Meriem Tazir, Guilhem Solé, et al.
Journal of Neuropathology and Experimental Neurology
|
November 8, 2016
Contactin-Associated Protein 1 (CNTNAP1) Mutations Induce Characteristic Lesions of the Paranodal Region
Jean-Michel Vallat, Mathilde Nizon, Alex Magee, et al.
Neuromuscular Disorders : NMD
|
May 6, 2014
Peripheral myelin protein 22 gene duplication with atypical presentations: a new example of the wide spectrum of Charcot-Marie-Tooth 1A disease
Stéphane Mathis, Philippe Corcia, Meriem Tazir, et al.
Journal of Neurology
|
May 23, 2019
Myopathy and scleromyxedema
Antoine Soulages, Hoang Marie-Ange Tang, Anne Pham-Ledard, et al.
Journal of the Neurological Sciences
|
December 19, 2017
History and current difficulties in classifying inherited myopathies and muscular dystrophies
Stéphane Mathis, Meriem Tazir, Laurent Magy, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
May 16, 2014
Autosomal dominant eccentric core disease caused by a heterozygous mutation in the MYH7 gene
Norma B Romero, Ting Xie, Edoardo Malfatti, et al.
The Neurologist
|
November 6, 2019
Papilledema and Peripheral Neuropathies
Stéphane Mathis, Gwendal Le Masson, Antoine Soulages, et al.
Journal of Neurology
|
February 6, 2022
Neurologic manifestations of giant cell arteritis
Antoine Soulages, Igor Sibon, Jean-Michel Vallat, et al.
Clinical Neurology and Neurosurgery
|
January 22, 2018
An in-frame deletion in BICD2 associated with a non-progressive form of SMALED
Aurélien Trimouille, Émilie Obre, Guillaume Banneau, et al.
Journal of Neurology
|
August 11, 2014
Testing the validity of a set of diagnostic criteria for sensory neuronopathies: a francophone collaborative study
Jean-Christophe Antoine, Florence Robert-Varvat, Thierry Maisonobe, et al.
Page
of 12