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Journal of Neurovirology
|
August 1, 1997
Human immunodeficiency virus type 1 DNA and RNA load in brains of demented and nondemented patients with acquired immunodeficiency syndrome
F Lazarini, D Seilhean, O Rosenblum, et al.
Neuromuscular Disorders : NMD
|
March 11, 2000
Autosomal recessive hereditary neuropathy with focally folded myelin sheaths and linked to chromosome 11q23: a distinct and homogeneous entity
M A Salih, T Maisonobe, M Kabiraj, et al.
Neurology
|
June 11, 2003
Histopathological differences of myotonic dystrophy type 1 (DM1) and PROMM/DM2
A Vihola, G Bassez, G Meola, et al.
Acta Oncologica (Stockholm, Sweden)
|
December 16, 2017
Antineoplastic agents exacerbating Charcot Marie Tooth disease: red flags to avoid permanent disability
M J Ibañez-Juliá, G Berzero, G Reyes-Botero, et al.
Brain : a Journal of Neurology
|
May 4, 2001
Central nervous system disease in patients with macrophagic myofasciitis
F J Authier, P Cherin, A Creange, et al.
Neuromuscular Disorders : NMD
|
July 26, 2008
Electron microscopy in myofibrillar myopathies reveals clues to the mutated gene
K G Claeys, M Fardeau, R Schröder, et al.
Neuropathology and Applied Neurobiology
|
September 30, 2018
Diagnostic potential of sarcoplasmic myxovirus resistance protein A expression in subsets of dermatomyositis
A Uruha, Y Allenbach, J-L Charuel, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
June 7, 2006
Parkinson's disease with camptocormia
F Bloch, J L Houeto, S Tezenas du Montcel, et al.
Revue Neurologique
|
December 21, 2005
[Chronic inflammatory demyelinating polyradiculoneuropathy: diagnostic strategy. Guidelines of the French CIDP study group]
J C Antoine, J P Azulay, P Bouche, et al.
Revue Neurologique
|
September 7, 2015
Myofibrillar myopathies: State of the art, present and future challenges
A Béhin, E Salort-Campana, K Wahbi, et al.
Page
of 13
Search research articles
Search
Showing results (111-120 of 122) with videos related to
Sort By:
Page
of 13
Journal of Neurovirology
|
August 1, 1997
Human immunodeficiency virus type 1 DNA and RNA load in brains of demented and nondemented patients with acquired immunodeficiency syndrome
F Lazarini, D Seilhean, O Rosenblum, et al.
Neuromuscular Disorders : NMD
|
March 11, 2000
Autosomal recessive hereditary neuropathy with focally folded myelin sheaths and linked to chromosome 11q23: a distinct and homogeneous entity
M A Salih, T Maisonobe, M Kabiraj, et al.
Neurology
|
June 11, 2003
Histopathological differences of myotonic dystrophy type 1 (DM1) and PROMM/DM2
A Vihola, G Bassez, G Meola, et al.
Acta Oncologica (Stockholm, Sweden)
|
December 16, 2017
Antineoplastic agents exacerbating Charcot Marie Tooth disease: red flags to avoid permanent disability
M J Ibañez-Juliá, G Berzero, G Reyes-Botero, et al.
Brain : a Journal of Neurology
|
May 4, 2001
Central nervous system disease in patients with macrophagic myofasciitis
F J Authier, P Cherin, A Creange, et al.
Neuromuscular Disorders : NMD
|
July 26, 2008
Electron microscopy in myofibrillar myopathies reveals clues to the mutated gene
K G Claeys, M Fardeau, R Schröder, et al.
Neuropathology and Applied Neurobiology
|
September 30, 2018
Diagnostic potential of sarcoplasmic myxovirus resistance protein A expression in subsets of dermatomyositis
A Uruha, Y Allenbach, J-L Charuel, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
June 7, 2006
Parkinson's disease with camptocormia
F Bloch, J L Houeto, S Tezenas du Montcel, et al.
Revue Neurologique
|
December 21, 2005
[Chronic inflammatory demyelinating polyradiculoneuropathy: diagnostic strategy. Guidelines of the French CIDP study group]
J C Antoine, J P Azulay, P Bouche, et al.
Revue Neurologique
|
September 7, 2015
Myofibrillar myopathies: State of the art, present and future challenges
A Béhin, E Salort-Campana, K Wahbi, et al.
Page
of 13