M.-P. Muriel

Mutations in the SPG3A gene encoding the GTPase atlastin interfere with vesicle trafficking in the ER/Golgi interface and Golgi morphogenesis

Michito Namekawa, M.-P. Muriel, Alexandre Janer et al. · Molecular and Cellular Neuroscience · 2007 · 75 citations

Signal Transduction, Cell Signaling, Genetics +11

Nondopaminergic neurons in Parkinson's disease.

Étienne C. Hirsch, Gaël Orieux, M.-P. Muriel et al. · PubMed · 2003 · 39 citations

Nondopaminergic Neurons, Neurodegenerative Diseases, Neurobiology Of Disease +8

Morphological and biochemical studies of a mouse mutant (fro/fro) with bone fragility

M.-P. Muriel, Jacky Bonaventure, R Stănescu et al. · Bone · 1991 · 36 citations

Mechanobiology, Bone Fragility, Developmental Biology +8

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

Type II collagen defect in two sibs with the Goldblatt syndrome, a chondrodysplasia with dentinogenesis imperfecta, and joint laxity

Jacky Bonaventure, R Stănescu, V. Stănescu et al. · American Journal of Medical Genetics · 1992 · 33 citations