nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A developmental component to Huntington's disease
|
Ratié, L. |
|
|
180 |
5 |
p. 357-362 |
artikel |
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 |
artikel |
3 |
Contents
|
|
|
|
180 |
5 |
p. iii-iv |
artikel |
4 |
C9ORF72 hexanucleotide repeat expansion: From ALS and FTD to a broader pathogenic role?
|
Sellier, C. |
|
|
180 |
5 |
p. 417-428 |
artikel |
5 |
Directional deep brain stimulation is useful to correct the misplacement of intracerebral electrode after reimplantation
|
Costentin, G. |
|
|
180 |
5 |
p. 463-465 |
artikel |
6 |
Editorial Board
|
|
|
|
180 |
5 |
p. i |
artikel |
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 |
artikel |
8 |
Epileptic encephalopathies and progressive neurodegeneration
|
Guerrini, R. |
|
|
180 |
5 |
p. 363-367 |
artikel |
9 |
Gene editing as a therapeutic strategy for spinocerebellar ataxia type-3
|
Déglon, N. |
|
|
180 |
5 |
p. 378-382 |
artikel |
10 |
Guillain-Barré syndrome following subthalamic nucleus – Deep Brain Stimulation in Parkinson's disease: A case report
|
Theuriet, J. |
|
|
180 |
5 |
p. 459-461 |
artikel |
11 |
Identification and characterization of repeat expansions in neurological disorders: Methodologies, tools, and strategies
|
Leitão, E. |
|
|
180 |
5 |
p. 383-392 |
artikel |
12 |
Lessons from genetic studies in Alzheimer disease
|
Nicolas, G. |
|
|
180 |
5 |
p. 368-377 |
artikel |
13 |
Neurological disorders related to recreational nitrous oxide abuse: Two sides of the same coin
|
Delsanti, R. |
|
|
180 |
5 |
p. 467-469 |
artikel |
14 |
Prevalence of multiple sclerosis in France in 2021: Data from the French health insurance database
|
Pierret, C. |
|
|
180 |
5 |
p. 429-437 |
artikel |
15 |
Prevalence of multiple system atrophy: A literature review
|
Kaplan, S. |
|
|
180 |
5 |
p. 438-450 |
artikel |
16 |
RFC1: Motifs and phenotypes
|
Delforge, V. |
|
|
180 |
5 |
p. 393-409 |
artikel |
17 |
Sensorimotor deficit: To worm information out of white blood cell count!
|
Camard, M. |
|
|
180 |
5 |
p. 469-470 |
artikel |
18 |
Spinocerebellar ataxia 27B (SCA27B), a frequent late-onset cerebellar ataxia
|
Clément, G. |
|
|
180 |
5 |
p. 410-416 |
artikel |
19 |
Stroke-like manifestations of angioedema: A case report and the identification of a novel mutation
|
Karam, J.-D. |
|
|
180 |
5 |
p. 465-467 |
artikel |
20 |
Updates in neurogenetics
|
Durr, A. |
|
|
180 |
5 |
p. 355-356 |
artikel |
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 |
artikel |