R. Zemmouri

Mutation analysis of the paraplegin gene ( <i>SPG7</i> ) in patients with hereditary spastic paraplegia

N. Elleuch, Christel Depienne, Ali Benomar et al. · Neurology · 2006 · 106 citations

Clinical Heterogeneity of Autosomal Recessive Spastic Paraplegias

Paula Coutinho, José Barros, R. Zemmouri et al. · Archives of Neurology · 1999 · 93 citations

A clinical, electrophysiologic, neuropathologic, and genetic study of two large Algerian families with an autosomal recessive demyelinating form of Charcot‐Marie‐Tooth disease

M. Kessali, R. Zemmouri, A. Guilbot et al. · Neurology · 1997 · 76 citations

Genetics, Pathology, Disease Gene Identification +21

Charcot–Marie–Tooth 2-like presentation of an Algerian family with giant axonal neuropathy

R. Zemmouri, Hamid Azzedine, Salima Assami et al. · Neuromuscular Disorders · 2000 · 37 citations

Peripheral Nerves, Charcot–marie–tooth 2-Like Presentation, Giant Axonal Neuropathy +8

Genetic heterogeneity in giant axonal neuropathy: an Algerian family not linked to chromosome 16q24.1

Mériem Tazir, Jean-Michel Vallat, Pascale Bomont et al. · Neuromuscular Disorders · 2002 · 26 citations

Neurodegenerative Diseases, Neuroregeneration, Mendelian Disorder +12