Author

AFRICAN RESEARCH NEXUS

SHINING A SPOTLIGHT ON AFRICAN RESEARCH

Marzouki, Naima

Exome Sequencing Can Improve Diagnosis and Alter Patient Management
Science Translational Medicine, Volume 4, No. 138, Article 138ra78, Year 2012, Citations 267
Vitamin E deficiency ataxia with (744 del A) mutation on α-TTP gene: Genetic and clinical peculiarities in Moroccan patients
European Journal of Medical Genetics, Volume 48, No. 1, Year 2005, Citations 42
Homozygosity mapping of giant axonal neuropathy gene to chromosome 16q24.1
Neurogenetics, Volume 1, No. 2, Year 1997, Citations 12
Vitamin E deficiency ataxia associated with adenoma
Journal of the Neurological Sciences, Volume 162, No. 1, Year 1999, Citations 12
Clinical heterogeneity of Moroccan patients with hemoglobin C disease
International Journal of Chemical and Biochemical Sciences, Volume 21, Year 2022, Citations 7

Institution	Country	Start Year	End Year	Affiliated Years
CHU Med VI	Morocco	2022	2022	1
El Razi Hospital	Morocco	2012	2012	1
Univ. of Fez Sidi Med Benabdellah	Morocco	2005	2005	1
Université Sidi Mohamed Ben Abdellah	Morocco	2001	2001	1
Faculté des Sciences Dhar El Mahraz, Université Sidi Mohamed Ben Abdellah	Morocco	2001	2001	1
Institut National de Neurologie Mongi-Ben Hamida	Tunisia	1997	1997	1