E-LIB Suche - Ergebnisse für: Salem, Ikhlass Haj

1

Autosomal Recessive Ataxias:

, In: Essentials of Cerebellum and Cerebellar Disorders,

Beaudin, Marie ; Salem, Ikhlass Haj ; Dupré, Nicolas - p. 547-554 , 2023

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

2

Genetic and epidemiological study of hereditary ataxia and ..:

SALEM, ikhlass HAJ ; Brunet, Francis ; Stumpf, Monica..
Neurology. 94 (2020) 15_supplement - p. , 2020

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

3

A shift in the IL-6/STAT3 signalling pathway imbalance towa..:

Salem, Ikhlass Haj ; Plante, Sophie ; Gounni, Abdelilah S...
Cellular Signalling. 43 (2018) - p. 47-54 , 2018

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

4

The mitochondrial ND1 m.3337G>A mutation associated to mult..:

Mezghani, Najla ; Mnif, Mouna ; Mkaouar-Rebai, Emna...
Biochemical and Biophysical Research Communications. 411 (2011) 2 - p. 247-252 , 2011

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

5

Evidence for Non‐Mendelian Inheritance in Spastic Paraplegi..:

Estiar, Mehrdad A. ; Yu, Eric ; Haj Salem, Ikhlass...
Movement Disorders. 36 (2021) 7 - p. 1664-1675 , 2021

Link: https://doi.org/10.1002/..

6

Genetic and Epidemiological Study of Adult Ataxia and Spast..:

Haj Salem, Ikhlass ; Beaudin, Marie ; Stumpf, Monica...
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 48 (2021) 5 - p. 655-665 , 2021

Link: https://doi.org/10.1017/..

7

Exposure to Pesticides and Welding Hastens the Age-at-Onset..:

Gamache, Pierre-Luc ; Haj Salem, Ikhlass ; Roux-Dubois, Noémie...
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 46 (2019) 6 - p. 711-716 , 2019

Link: https://doi.org/10.1017/..

8

Dysregulated invertebrate tropomyosin–dectin-1 interaction ..:

Gour, Naina ; Lajoie, Stephane ; Smole, Ursula...
qt8cr52118. , 2018

Link: https://escholarship.org..

9

CAPN3 mRNA processing alteration caused by splicing mutatio..:

Salem, Ikhlass Hadj ; Hsairi, Ines ; Mezghani, Najla...
Journal of Human Genetics. 57 (2011) 2 - p. 92-100 , 2011

Link: https://doi.org/10.1038/..

10

The First Genome-Wide Scan in a Tunisian Family With Genera..:

Fendri-Kriaa, Nourhene ; Louhichi, Nacim ; Mkaouar-Rebai, Emna...
Journal of Child Neurology. 25 (2010) 11 - p. 1362-1368 , 2010

Link: https://doi.org/10.1177/..

11

Enhancement of magnetoresistance by strontium deficiency in..:

Ben Salem, Ikhlass ; Krichene, Akram ; Boujelben, Wahiba
Applied Physics A. 129 (2023) 5 - p. , 2023

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

12

Splicing defects in ABCD1 gene leading to both exon skippin..:

Kallabi, Fakhri ; Hadj Salem, Ikhlass ; Ben Chehida, Amel...
Neuroscience Research. 97 (2015) - p. 7-12 , 2015

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

13

Founder effect confirmation of c.241A>G mutation in the L2H..:

Tunisian Network on Mental Retardation study ; Jellouli, Nadege Kammoun ; Hadj Salem, Ikhlass...
Journal of Human Genetics. 59 (2014) 4 - p. 216-222 , 2014

Link: https://doi.org/10.1038/..

14

A double mutation in AGXT gene in families with primary hyp..:

Kanoun, Houda ; Jarraya, Faiçal ; Hadj Salem, Ikhlass...
Gene. 531 (2013) 2 - p. 451-456 , 2013

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

15

Molecular confirmation of founder mutation c.-167A>G in Tun..:

Kammoun Jellouli, Nadege ; Hadj Salem, Ikhlass ; Ellouz, Emna...
Gene. 513 (2013) 2 - p. 233-238 , 2013

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