E-LIB Suche - Ergebnisse für: Amouri, R

1

Profils génétiques et cliniques des ataxies cérébelleuses a..:

Hentati, E. ; Nahdi, H. ; El Euch, G....
Revue Neurologique. 170 (2014) - p. A151 , 2014

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

2

Études des troubles dysautonomiques chez les malades parkin..:

Lakhdar, I. ; Nahdi, H. ; Ben Sassi, S...
Revue Neurologique. 170 (2014) - p. A130-A131 , 2014

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

3

Les dystrophies musculaires des ceintures autosomiques réce..:

Farhata, E. ; Kéfi, M. ; Hentati, F..
Revue Neurologique. 169 (2013) - p. A16 , 2013

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

4

Autonomic dysfunction in Tunisian patients with Parkinson's..:

Lakhdar, I. ; Ben Sassi, S. ; Nabli, F....
Journal of the Neurological Sciences. 333 (2013) - p. e93-e94 , 2013

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

5

Primary mitochondrial DNA mutations and probable variants i..:

Bekri, I. ; Nahdi, H. ; Hentati, F..
Journal of the Neurological Sciences. 333 (2013) - p. e637 , 2013

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

6

Exome sequencing: an efficient diagnostic tool for complex ..:

Hammer, M. B. ; Eleuch‐Fayache, G. ; Gibbs, J. R....
European Journal of Neurology. 20 (2012) 3 - p. 486-492 , 2012

Link: https://doi.org/10.1111/..

7

Molecular diagnosis of known recessive ataxias by homozygos..:

H'mida-Ben Brahim, D. ; M'zahem, A. ; Assoum, M....
Journal of Neurology. 258 (2010) 1 - p. 56-67 , 2010

Link: https://doi.org/10.1007/..

8

Neuropathie axonale révélant un lymphome pleural primitif s..:

Fajraoui, N. ; Ben Hamida, K. ; Hadj Kacem, A....
La Revue de Médecine Interne. 31 (2010) 8 - p. e3-e6 , 2010

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

9

FP42-TH-03 Muscular dystrophies in Tunisia – 10 years exper..:

Farhat, E. ; Kefi, M. ; Hentati, F..
Journal of the Neurological Sciences. 285 (2009) - p. S124 , 2009

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

10

FP54-FR-04 Giant axonal neuropathy: clinical and genetic st..:

Kacem, A. ; Kefi, M. ; Amouri, R..
Journal of the Neurological Sciences. 285 (2009) - p. S143 , 2009

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

11

FP31-WE-03 Hereditary spastic paraplegia with thin corpus c..:

Zouari, M. ; Nehdi, H. ; Ben Hamed, M...
Journal of the Neurological Sciences. 285 (2009) - p. S106 , 2009

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

12

FP31-WE-02 Three Tunisian families with abetalipoproteinemi..:

Ben Hamed, M. ; El Euch Fayache, G. ; Feki, M...
Journal of the Neurological Sciences. 285 (2009) - p. S106 , 2009

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

13

PINK1mutations and parkinsonism:

Ishihara-Paul, L. ; Hulihan, M. M. ; Kachergus, J....
Neurology. 71 (2008) 12 - p. 896-902 , 2008

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

14

l‐2‐Hydroxyglutaric aciduria: Clinical and molecular study ..:

Larnaout, A. ; Amouri, R. ; Kefi, M..
Journal of Inherited Metabolic Disease. 31 (2008) S2 - p. 375-379 , 2008

Link: https://doi.org/10.1007/..

15

2.116 Genetic characterization of ATP13A2 in Parkinson's di..:

Vilarino-Guell, C. ; Soto, A.I. ; Hulihan, M.M....
Parkinsonism & Related Disorders. 13 (2007) - p. S96 , 2007

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