Riadh Gouider

Mutations in MTMR13, a New Pseudophosphatase Homologue of MTMR2 and Sbf1, in Two Families with an Autosomal Recessive Demyelinating Form of Charcot-Marie-Tooth Disease Associated with Early-Onset Glaucoma

Hamid Azzedine, Alessandra Bolino, T. Taïeb et al. · The American Journal of Human Genetics · 2003 · 301 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +9

Reducing the Risk of Cognitive Decline and Dementia: WHO Recommendations

Neerja Chowdhary, Corrado Barbui, Kaarin J. Anstey et al. · Frontiers in Neurology · 2022 · 185 citations · Full text

Aging, Geriatric Medicine, Epidemiology Of Aging +25

Spectrum of clinical and electrophysiologic features in HNPP patients with the 17p11.2 deletion

Philippe Mouton, Sandrine Tardieu, Riadh Gouider et al. · Neurology · 1999 · 184 citations

X-linked Charcot-Marie-Tooth disease with connexin 32 mutations

Nazha Birouk, Éric Leguern, Thierry Maisonobe et al. · Neurology · 1998 · 170 citations

Clinical, electrophysiologic, and molecular correlations in 13 families with hereditary neuropathy with liability to pressure palsies and a chromosome 17p11.2 deletion

Riadh Gouider, Éric Leguern, Michel Gugenheim et al. · Neurology · 1995 · 113 citations