nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Adult-onset spinal muscular atrophy: An update
|
Juntas Morales, R. |
|
2017 |
173 |
5 |
p. 308-319 12 p. |
artikel |
2 |
ALS and frontotemporal dementia belong to a common disease spectrum
|
Couratier, P. |
|
2017 |
173 |
5 |
p. 273-279 7 p. |
artikel |
3 |
Amyotrophic lateral sclerosis or not: Keys for the diagnosis
|
Lenglet, T. |
|
2017 |
173 |
5 |
p. 280-287 8 p. |
artikel |
4 |
Benign focal amyotrophy
|
Cintas, P. |
|
2017 |
173 |
5 |
p. 338-344 7 p. |
artikel |
5 |
Care management in amyotrophic lateral sclerosis
|
Soriani, M.-H. |
|
2017 |
173 |
5 |
p. 288-299 12 p. |
artikel |
6 |
Clinical features of amyotrophic lateral sclerosis and their prognostic value
|
Tard, C. |
|
2017 |
173 |
5 |
p. 263-272 10 p. |
artikel |
7 |
Current issues in ALS epidemiology: Variation of ALS occurrence between populations and physical activity as a risk factor
|
Luna, J. |
|
2017 |
173 |
5 |
p. 244-253 10 p. |
artikel |
8 |
Disorders of motor neurons manifested by hyperactivity
|
Grapperon, A.M. |
|
2017 |
173 |
5 |
p. 345-351 7 p. |
artikel |
9 |
Editorial Board
|
|
|
2017 |
173 |
5 |
p. i- 1 p. |
artikel |
10 |
Ethical considerations and palliative care in patients with amyotrophic lateral sclerosis: A review
|
Danel-Brunaud, V. |
|
2017 |
173 |
5 |
p. 300-307 8 p. |
artikel |
11 |
Genetics of amyotrophic lateral sclerosis
|
Corcia, P. |
|
2017 |
173 |
5 |
p. 254-262 9 p. |
artikel |
12 |
Hereditary spastic paraplegia: More than an upper motor neuron disease
|
Parodi, L. |
|
2017 |
173 |
5 |
p. 352-360 9 p. |
artikel |
13 |
Kennedy disease (X-linked recessive bulbospinal neuronopathy): A comprehensive review from pathophysiology to therapy
|
Querin, G. |
|
2017 |
173 |
5 |
p. 326-337 12 p. |
artikel |
14 |
Motor neuropathies and lower motor neuron syndromes
|
Verschueren, A. |
|
2017 |
173 |
5 |
p. 320-325 6 p. |
artikel |
15 |
New advances in the field of motor neuron diseases
|
Couratier, P. |
|
2017 |
173 |
5 |
p. 243- 1 p. |
artikel |