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                             21 results found
no title author magazine year volume issue page(s) type
1 A developmental component to Huntington's disease Ratié, L.

180 5 p. 357-362
article
2 Antibody responses to SARS-CoV-2 vaccines in neuromuscular disorders may depend on their etiology and current drug treatment Finsterer, J.

180 5 p. 470-471
article
3 Contents
180 5 p. iii-iv
article
4 C9ORF72 hexanucleotide repeat expansion: From ALS and FTD to a broader pathogenic role? Sellier, C.

180 5 p. 417-428
article
5 Directional deep brain stimulation is useful to correct the misplacement of intracerebral electrode after reimplantation Costentin, G.

180 5 p. 463-465
article
6 Editorial Board
180 5 p. i
article
7 Epidemiology of myasthenia gravis in France: Incidence, prevalence, and comorbidities based on national healthcare insurance claims data Keovilayhong, S.

180 5 p. 451-458
article
8 Epileptic encephalopathies and progressive neurodegeneration Guerrini, R.

180 5 p. 363-367
article
9 Gene editing as a therapeutic strategy for spinocerebellar ataxia type-3 Déglon, N.

180 5 p. 378-382
article
10 Guillain-Barré syndrome following subthalamic nucleus – Deep Brain Stimulation in Parkinson's disease: A case report Theuriet, J.

180 5 p. 459-461
article
11 Identification and characterization of repeat expansions in neurological disorders: Methodologies, tools, and strategies Leitão, E.

180 5 p. 383-392
article
12 Lessons from genetic studies in Alzheimer disease Nicolas, G.

180 5 p. 368-377
article
13 Neurological disorders related to recreational nitrous oxide abuse: Two sides of the same coin Delsanti, R.

180 5 p. 467-469
article
14 Prevalence of multiple sclerosis in France in 2021: Data from the French health insurance database Pierret, C.

180 5 p. 429-437
article
15 Prevalence of multiple system atrophy: A literature review Kaplan, S.

180 5 p. 438-450
article
16 RFC1: Motifs and phenotypes Delforge, V.

180 5 p. 393-409
article
17 Sensorimotor deficit: To worm information out of white blood cell count! Camard, M.

180 5 p. 469-470
article
18 Spinocerebellar ataxia 27B (SCA27B), a frequent late-onset cerebellar ataxia Clément, G.

180 5 p. 410-416
article
19 Stroke-like manifestations of angioedema: A case report and the identification of a novel mutation Karam, J.-D.

180 5 p. 465-467
article
20 Updates in neurogenetics Durr, A.

180 5 p. 355-356
article
21 Vanishing white matter in multiple mitochondrial dysfunction syndrome-2 due to compound heterozygosity for novel BOLA3 variants Finsterer, J.

180 5 p. 461-463
article
                             21 results found
 
 Koninklijke Bibliotheek - National Library of the Netherlands