I agree that this site is using cookies. You can find further informations
here
.
X
Login
My folder (
0
)
Home
About us
Home About us
Our history
Profile
Press & public relations
Friends
The library in figures
Exhibitions
Projects
Training, internships, careers
Films
Services & Information
Home Services & Information
Lending and interlibrary loans
Returns and renewals
Training and library tours
My Account
Library cards
New to the library?
Download Information
Opening hours
Learning spaces
PC, WLAN, copy, scan and print
Catalogs and collections
Home Catalogs and Collections
Rare books and manuscripts
Digital collections
Subject Areas
Our sites
Home Our sites
Central Library
Law Library (Juridicum)
BB Business and Economics (BB11)
BB Physics and Electrical Engineering
TB Engineering and Social Sciences
TB Economics and Nautical Sciences
TB Music
TB Art & Design
TB Bremerhaven
Contact the library
Home Contact the library
Staff Directory
Open access & publishing
Home Open access & publishing
Reference management: Citavi & RefWorks
Publishing documents
Open Access in Bremen
Show Desktop-Version
Toggle navigation
Salem, Ikhlass Haj
18
results:
Search for persons
X
Format
Online (18)
Mediatypes
Articles (Online) (16)
Bookchapter (Online) (1)
OpenAccess-fulltext (1)
Sorted by: Relevance
Sorted by: Year
?
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
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/..
?
15
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/..
1-15