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

1

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/..

2

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/..

3

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/..

4

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/..

5

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/..

6

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/..

7

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/..

8

Dysregulated invertebrate tropomyosin–dectin-1 interaction ..:

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

Link: https://escholarship.org..

9

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/..

10

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/..

11

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/..

12

Co-Culture of Human Bronchial Fibroblasts and CD4+ T Cells ..:

Loubaki, Lionel ; Hadj-Salem, Ikhlass ; Fakhfakh, Raouia...
PLoS ONE. 8 (2013) 12 - p. e81983 , 2013

Link: https://doi.org/10.1371/..

13

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/..

14

Impact of single-nucleotide polymorphisms at the TP53-bindi..:

Hadj Salem, Ikhlass ; Kamoun, Fatma ; Louhichi, Nacim...
Molecular Biology Reports. 39 (2012) 7 - p. 7479-7486 , 2012

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

15

Retracted: Genotyping of Tunisian azoospermic men with Sert..:

Hadjkacem-Loukil, Lobna ; Hadj-kacem, Hassen ; Hadj Salem, Ikhlass...
Andrologia. 50 (2011) 4 - p. e1088 , 2011

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