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authIdHal_s : abdellatif-barakat

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 of Clinical Immunology, 2016, 36 (3), pp.187-194. ⟨10.1007/s10875-016-0251-z⟩
Journal articles pasteur-01374987v1

Molecular Defects in Moroccan Patients with Ataxia-Telangiectasia.

L. Jeddane , F. Ailal , C. Dubois-d'Enghien , O. Abidi , I. Benhsaien , et al.
NeuroMolecular Medicine, 2013, epub ahead of print. ⟨10.1007/s12017-013-8218-1⟩
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.
PLoS ONE, 2019, 14 (3), pp.e0214122. ⟨10.1371/journal.pone.0214122⟩
Journal articles hal-02080935v1

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.
Human Heredity, 2021, 85 (1), pp.35-39. ⟨10.1159/000512712⟩
Journal articles pasteur-03219602v1

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.
Gene, 2018, 659, pp.89-92. ⟨10.1016/j.gene.2018.03.042⟩
Journal articles pasteur-03219641v1

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.
International Journal of Pediatric Otorhinolaryngology, 2021, 140, pp.110481. ⟨10.1016/j.ijporl.2020.110481⟩
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.
BMC Neurology, 2015, 15 (1), pp.244. ⟨10.1186/s12883-015-0503-1⟩
Journal articles inserm-01264481v1

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.
Molecular Biology Reports, 2022, 49 (5), pp.3949-3954. ⟨10.1007/s11033-022-07245-z⟩
Journal articles pasteur-03985530v1

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.
Biochemical Genetics, 2014, 52 (9-10), pp.430-42. ⟨10.1007/s10528-014-9658-5⟩
Journal articles pasteur-01375062v1

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.
Human Mutation, 2015, 36 (11), pp.E2441-53. ⟨10.1002/humu.22835⟩
Journal articles istex pasteur-01375020v1

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.
Diabetes & Metabolic Syndrome: Clinical Research & Reviews, 2017, 11 (supplement 2), pp.S853-S857. ⟨10.1016/j.dsx.2017.07.005⟩
Journal articles hal-01571303v1

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.
Human Heredity, 2020, 84 (3), pp.109-116. ⟨10.1159/000503450⟩
Journal articles pasteur-03219615v1

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.
Archives of Dermatological Research, 2013, 305 (1), pp.53-7. ⟨10.1007/s00403-012-1299-0⟩
Journal articles istex pasteur-00796957v1

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.
Mitochondrial DNA, 2016, 27 (2), pp.1558--1563. ⟨10.3109/19401736.2014.953136⟩
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
Preprints, Working Papers, ... hal-02410685v1

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.
Mitochondrial DNA Part A, 2017, 29 (1), pp.9-13. ⟨10.1080/24701394.2016.1233530⟩
Journal articles pasteur-01966344v1