E-LIB Suche - Ergebnisse für: Azzedine, H.

1

KIF1A missense mutations in SPG30: Distinct phenotypes acco..:

Klebe, S. ; Lossos, A. ; Azzedine, H....
Basal Ganglia. 3 (2013) 1 - p. 66 , 2013

Link: https://doi.org/10.1016/..

2

PO19-WE-05 Linkage analysis and mutation screening in PANK2..:

Azzedine, H. ; Salih, M.A.M. ; Khan, A....
Journal of the Neurological Sciences. 285 (2009) - p. S266 , 2009

Link: https://doi.org/10.1016/..

3

FP54-FR-05 Genotype and phenotype study in Sudanese and Yem..:

Salih, M.A.M. ; Mikesova, E. ; Elmalik, S.A....
Journal of the Neurological Sciences. 285 (2009) - p. S144 , 2009

Link: https://doi.org/10.1016/..

4

M - 3 Identification d'une nouvelle forme d'Ataxie Spastiqu..:

Bouslam, N. ; Bouhouche, A. ; Benomar, A....
Revue Neurologique. 163 (2007) 4 - p. 111 , 2007

Link: https://doi.org/10.1016/..

5

Phenotypical features of 11 Moroccan families with autosoma..:

Birouk, N. ; Bouhouche, A. ; Azzedine, H....
Revue Neurologique. 163 (2007) 4 - p. 489-490 , 2007

Link: https://doi.org/10.1016/..

6

G.P.11.12 Phenotypical features of 11 Moroccan families wit..:

Bouhouche, A. ; Azzedine, H. ; Dubourg, O....
Neuromuscular Disorders. 17 (2007) 9-10 - p. 826 , 2007

Link: https://doi.org/10.1016/..

7

Autosomal-recessive forms of demyelinating Charcot-Marie-To..:

Dubourg, O. ; Azzedine, H. ; Verny, C....
NeuroMolecular Medicine. 8 (2006) 1-2 - p. 75-85 , 2006

Link: https://doi.org/10.1385/..

8

Autosomal recessive axonal Charcot-Marie-Tooth disease (ARC..:

Bouhouche, A. ; Birouk, N. ; Azzedine, H....
Brain. 130 (2006) 4 - p. 1062-1075 , 2006

Link: https://doi.org/10.1093/..

9

Spine deformities in Charcot-Marie-Tooth 4C caused bySH3TC2..:

Azzedine, H. ; Ravisé, N. ; Verny, C....
Neurology. 67 (2006) 4 - p. 602-606 , 2006

Link: https://doi.org/10.1212/..

10

The G526R glycyl-tRNA synthetase gene mutation in distal he..:

Dubourg, O. ; Azzedine, H. ; Yaou, R. Ben...
Neurology. 66 (2006) 11 - p. 1721-1726 , 2006

Link: https://doi.org/10.1212/..

11

Forme axonale de la maladie de Charcot-Marie-Tooth autosomi..:

Bouhouche, A. ; Birouk, N. ; Azzedine, H....
Revue Neurologique. 160 (2004) 10 - p. 971 , 2004

Link: https://doi.org/10.1016/..

12

Variability of disease progression in a family with autosom..:

Azzedine, H ; Ruberg, M ; Ente, D...
Neuromuscular Disorders. 13 (2003) 4 - p. 341-346 , 2003

Link: https://doi.org/10.1016/..

13

Charcot–Marie–Tooth 2-like presentation of an Algerian fami..:

Zemmouri, R. ; Azzedine, H. ; Assami, S....
Neuromuscular Disorders. 10 (2000) 8 - p. 592-598 , 2000

Link: https://doi.org/10.1016/..

14

Impact of rare-earth elements on the corrosion performance ..:

Azzedine, H ; Hanna, A ; Dakhouche, A...
https://dx.doi.org/10.1016/j.jallcom.2020.154569. , 2020

Link: https://publications.her..

15

Loss-of-Function Mutations in FRRS1L Lead to an Epileptic-D..:

Madeo, M ; Stewart, M ; Sun, Y...
https://discovery.ucl.ac.uk/id/eprint/1498362/1/Madeo_Loss-of-Function_Mutations_AAM.pdf. , 2016

Link: https://discovery.ucl.ac..