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JAMA Neurology
|
August 18, 2015
Clinical Spectrum of Encephalitis Associated With Antibodies Against the α-Amino-3-Hydroxy-5-Methyl-4-Isoxazolepropionic Acid Receptor: Case Series and Review of the Literature
Bastien Joubert, Philippe Kerschen, Anastasia Zekeridou, et al.
Neurology(R) Neuroimmunology & Neuroinflammation
|
November 17, 2015
CSF IgA NMDAR antibodies are potential biomarkers for teratomas in anti-NMDAR encephalitis
Virginie Desestret, Aude Chefdeville, Aurélien Viaccoz, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)
|
February 17, 2026
Pathogenic Role of FGFR3 Autoantibodies in Small Fiber Neuropathy
Lyuba Y Salih, Nicolas L A Dumaire, Clémence Gieré, 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.
Journal of Neurology
|
August 15, 2024
Specific clinical and radiological characteristics of anti-NMDA receptor autoimmune encephalitis following herpes encephalitis
Pauline Dumez, Macarena Villagrán-García, Alexandre Bani-Sadr, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
November 1, 2017
Early intravenous immunoglobulin treatment in paraneoplastic neurological syndromes with onconeural antibodies
Giulia Berzero, Evgenia Karantoni, Caroline Dehais, et al.
Journal of the Neurological Sciences
|
January 27, 2016
Identifying a therapeutic window in acute and subacute inflammatory sensory neuronopathies
Jean-Christophe Antoine, Florence Robert-Varvat, Thierry Maisonobe, et al.
Neurology. Genetics
|
February 12, 2020
Spastic paraplegia due to recessive or dominant mutations in <i>ERLIN2</i> can convert to ALS
Maria-Del-Mar Amador, François Muratet, Elisa Teyssou, et al.
Journal of Neurology
|
March 24, 2016
Clinical features and prognostic factors of spinal cord sarcoidosis: a multicenter observational study of 20 BIOPSY-PROVEN patients
Cécile-Audrey Durel, Romain Marignier, Delphine Maucort-Boulch, et al.
Muscle & Nerve
|
April 14, 2017
Hereditary neuropathy with liability to pressure palsy in patients under 30 years old: Neurophysiological data and proposed electrodiagnostic criteria
Florence Robert-Varvat, Guillemette Jousserand, Françoise Bouhour, et al.
Page
of 10
Search research articles
Search
Showing results (71-80 of 96) with videos related to
Sort By:
Page
of 10
JAMA Neurology
|
August 18, 2015
Clinical Spectrum of Encephalitis Associated With Antibodies Against the α-Amino-3-Hydroxy-5-Methyl-4-Isoxazolepropionic Acid Receptor: Case Series and Review of the Literature
Bastien Joubert, Philippe Kerschen, Anastasia Zekeridou, et al.
Neurology(R) Neuroimmunology & Neuroinflammation
|
November 17, 2015
CSF IgA NMDAR antibodies are potential biomarkers for teratomas in anti-NMDAR encephalitis
Virginie Desestret, Aude Chefdeville, Aurélien Viaccoz, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)
|
February 17, 2026
Pathogenic Role of FGFR3 Autoantibodies in Small Fiber Neuropathy
Lyuba Y Salih, Nicolas L A Dumaire, Clémence Gieré, 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.
Journal of Neurology
|
August 15, 2024
Specific clinical and radiological characteristics of anti-NMDA receptor autoimmune encephalitis following herpes encephalitis
Pauline Dumez, Macarena Villagrán-García, Alexandre Bani-Sadr, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
November 1, 2017
Early intravenous immunoglobulin treatment in paraneoplastic neurological syndromes with onconeural antibodies
Giulia Berzero, Evgenia Karantoni, Caroline Dehais, et al.
Journal of the Neurological Sciences
|
January 27, 2016
Identifying a therapeutic window in acute and subacute inflammatory sensory neuronopathies
Jean-Christophe Antoine, Florence Robert-Varvat, Thierry Maisonobe, et al.
Neurology. Genetics
|
February 12, 2020
Spastic paraplegia due to recessive or dominant mutations in <i>ERLIN2</i> can convert to ALS
Maria-Del-Mar Amador, François Muratet, Elisa Teyssou, et al.
Journal of Neurology
|
March 24, 2016
Clinical features and prognostic factors of spinal cord sarcoidosis: a multicenter observational study of 20 BIOPSY-PROVEN patients
Cécile-Audrey Durel, Romain Marignier, Delphine Maucort-Boulch, et al.
Muscle & Nerve
|
April 14, 2017
Hereditary neuropathy with liability to pressure palsy in patients under 30 years old: Neurophysiological data and proposed electrodiagnostic criteria
Florence Robert-Varvat, Guillemette Jousserand, Françoise Bouhour, et al.
Page
of 10