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Hadj Salem, Ikhlass
20  Ergebnisse:
Personensuche X
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1

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/..
 
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2

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/..
 
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3

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/..
 
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4

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/..
 
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5

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/..
 
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6

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/..
 
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7

A whole mitochondrial genome screening in a MELAS patient: ..:

Mezghani, Najla ; Mnif, Mouna ; Kacem, Maha...
Biochemical and Biophysical Research Communications.  407 (2011)  4 - p. 747-752 , 2011
Link: https://doi.org/10.1016/..
 
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8

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/..
 
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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/..
 
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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/..
 
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11

Novel sequence variations in LAMA2 and SGCG genes modulatin..:

Olfa Siala ; Ikhlass Hadj Salem ; Abdelaziz Tlili...
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572010000100032.  , 2010
Link: https://doaj.org/article..
 
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12

Co-culture of human bronchial fibroblasts and CD4+ T cells ..:

Lionel Loubaki ; Ikhlass Hadj-Salem ; Raouia Fakhfakh...
http://europepmc.org/articles/PMC3857794?pdf=render.  , 2013
Link: https://doi.org/10.1371/..
 
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13

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/..
 
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14

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/..
 
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15

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/..
 
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