Author

Adnane Karkar

Observed name: A. Karkar

Institution: Hospital Fatuma Bourguiba Monastir

Observed institutions: Inserm, Sorbonne Paris Cité, Hôpital Robert-Debré, Hospital Fatuma Bourguiba Monastir, Université Paris Diderot, NeuroDiderot, University of Hassan II Casablanca

ORCID: 0000-0001-7025-299X

Observed ORCID: 0000-0001-7025-299X

OpenAlex ID: A5057427900

The polymorphism G894 T of endothelial nitric oxide synthase (eNOS) gene is associated with susceptibility to essential hypertension (EH) in Morocco

2018 · Sanaa Nassereddine, Hind Hassani Idrissi, et al. · BMC Medical Genetics · 35

Novel POLR1C mutation in RNA polymerase III‐related leukodystrophy with severe myoclonus and dystonia

2019 · Ichraf Kraoua, Adnane Karkar, et al. · Molecular Genetics & Genomic Medicine · 13

A novel mutation in the ABCD1 gene of a Moroccan patient with X-linked adrenoleukodystrophy: case report

2015 · Adnane Karkar, Abdelhamid Barakat, et al. · BMC Neurology · 9

Screening for SGCE mutations in Moroccan sporadic patients with Myoclonus-Dystonia syndrome

2019 · Laila Rachad, Hicham El Otmani, et al. · Neuroscience Letters · 2

Évaluation de la qualité de vie des aidants familiaux des sujets âgés présentant une fracture de l’extrémité supérieure du fémur

2023 · A. Fekih, A. Karkar, et al. · Revue du Rhumatisme

Genetic aspect of leukodystrophies in Moroccan population

2019 · Adnane Karkar, Imen Dorboz, et al. · IBRO Reports

Leucodystrophies : aspects génétiques et moléculaires au Maroc

2018 · Adnane Karkar · theses.fr (ABES)

A novel SGCE gene mutation in a Moroccan sporadic case with myoclonus-dystonia syndrome

2018 · Laila Rachad, Hicham El Otmani, et al. · Gene Reports

Works count: 8

Citation count: 59

H-index: 3

I10-index: 2