M. Yahyaoui

Molecular and Clinical Correlations in Spinocerebellar Ataxia 2: A Study of 32 Families

Alexandra Dürr, Olivier Didierjean, G. Imbert et al. · Human Molecular Genetics · 1997 · 256 citations · Full text

The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12–p21.1

Ali Benomar, Luc Krols, Giovanni Stévanin et al. · Nature Genetics · 1995 · 159 citations

Neurodegenerative Diseases, Mendelian Disorder, Genetic Disorder +6

Autosomal‐dominant cerebellar ataxia with retinal degeneration (ADCA type II) is genetically different from ADCA type I

Ali Benomar, E. Le Guern, Alexandra Dürr et al. · Annals of Neurology · 1994 · 65 citations

Neurological manifestations of Behçet's disease: Evaluation of 40 patients treated by cyclophosphamide

El Hachmia Ait Ben Haddou, Fatima Imounan, Wafa Regragui et al. · Revue Neurologique · 2011 · 35 citations

Autoimmune Disease, Medicine, Pathology +4

Autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2): phenotype-genotype correlations in 13 Moroccan families

Ahmed Bouhouche, N. Birouk, H. Azzedine et al. · Brain · 2006 · 33 citations · Full text

Mendelian Disorder, Genetic Disorder, Charcot-marie-tooth Disease +13