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X-Linked Agammagobulinemia in a Large Series of North African Patients: Frequency, Clinical Features and Novel BTK Mutations
Zahra Aadam
,
Nadia Kechout
,
Abdelhamid Barakat
,
Koon-Wing Chan
,
Meriem Ben-Ali
,
et al.
Journal articles
pasteur-01374987v1
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Molecular Defects in Moroccan Patients with Ataxia-Telangiectasia.
L. Jeddane
,
F. Ailal
,
C. Dubois-d'Enghien
,
O. Abidi
,
I. Benhsaien
,
et al.
Journal articles
pasteur-00796956v1
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Fine-scale haplotype mapping of MUT, AACS, SLC6A15 and PRKCA genes indicates association with insulin resistance of metabolic syndrome and relationship with branched chain amino acid metabolism or regulation
Sara Haydar
,
Florin Grigorescu
,
Mădălina Vintilă
,
Yannick Cogne
,
Corinne Lautier
,
et al.
Journal articles
hal-02080935v1
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Novel Mutation in AIFM1 Gene Associated with X-Linked Deafness in a Moroccan Family
Soukaina Elrharchi
,
Zied Riahi
,
Sara Salime
,
Hicham Charoute
,
Lamiae Elkhattabi
,
et al.
Journal articles
pasteur-03219602v1
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A novel mutation in SLITRK6 causes deafness and myopia in a Moroccan family
Sara Salime
,
Zied Riahi
,
Soukaina Elrharchi
,
Lamiae Elkhattabi
,
Hicham Charoute
,
et al.
Journal articles
pasteur-03219641v1
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A homozygous MPZL2 deletion is associated with non syndromic hearing loss in a moroccan family
Ghita Amalou
,
Crystel Bonnet
,
Zied Riahi
,
Aymane Bouzidi
,
Soukaina Elrharchi
,
et al.
Journal articles
pasteur-03215242v1
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A novel mutation in the ABCD1 gene of a Moroccan patient with X-linked adrenoleukodystrophy: case report
Adnane Karkar
,
Abdelhamid Barakat
,
Amina Bakhchane
,
Houda Fettah
,
Ilham Slassi
,
et al.
Journal articles
inserm-01264481v1
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Genetic heterogeneity in GJB2, COL4A3, ATP6V1B1 and EDNRB variants detected among hearing impaired families in Morocco
Imane Aitraise
,
Ghita Amalou
,
Amale Bousfiha
,
Hicham Charoute
,
Hassan Rouba
,
et al.
Journal articles
pasteur-03985530v1
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Association analysis of IGF2BP2, KCNJ11, and CDKAL1 polymorphisms with type 2 diabetes mellitus in a Moroccan population: a case-control study and meta-analysis.
Houda Benrahma
,
Hicham Charoute
,
Khaled Lasram
,
Redouane Boulouiz
,
Rym Kefi-Ben Atig
,
et al.
Journal articles
pasteur-01375062v1
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Mediterranean Founder Mutation Database (MFMD): Taking Advantage from Founder Mutations in Genetics Diagnosis, Genetic Diversity and Migration History of the Mediterranean Population.
Hassan Charoute
,
Amina Bakhchane
,
Houda Benrahma
,
Lilia Romdhane
,
Khalid Gabi
,
et al.
Journal articles
istex
pasteur-01375020v1
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Association study of HNF1A polymorphisms with metabolic syndrome in the Moroccan population.
Imane Morjane
,
Rym Kefi
,
Hicham Charoute
,
Fouzia Lakbakbi El Yaagoubi
,
Meryem Hechmi
,
et al.
Journal articles
hal-01571303v1
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Further Evidence for the Implication of the MET Gene in Non-Syndromic Autosomal Recessive Deafness
Amale Bousfiha
,
Zied Riahi
,
Lamiae Elkhattabi
,
Amina Bakhchane
,
Hicham Charoute
,
et al.
Journal articles
pasteur-03219615v1
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c.1643_1644delTG XPC mutation is more frequent in Moroccan patients with xeroderma pigmentosum.
Mohamed Amine Senhaji
,
Omar Abidi
,
Sellama Nadifi
,
Hakima Benchikhi
,
Khadija Khadir
,
et al.
Journal articles
istex
pasteur-00796957v1
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Study of the T16189C variant and mitochondrial lineages in Tunisian and overall Mediterranean region
Sana Hsouna
,
Nizar Ben Halim
,
Khaled Lasram
,
Ghlana Meiloud
,
Imen Arfa
,
et al.
Journal articles
hal-01356506v1
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Influence of pulsatile blood flow on allometry of aortic wall shear stress
G Croizat
,
A Kehren
,
H Roux de Bézieux
,
A. Barakat
2018
Preprints, Working Papers, ...
hal-02410685v1
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Novel variants of mitochondrial DNA associated with Type 2 diabetes mellitus in Moroccan population
Hicham Charoute
,
Rym Kefi
,
Safaa Bounaceur
,
Houda Benrahma
,
Ahmed Reguig
,
et al.
Journal articles
pasteur-01966344v1
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