Association Francaise contre les Myopathies

Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy

Jing Liu, Masashi Aoki, Isabel Illa et al. · Nature Genetics · 1998 · 914 citations

Miyoshi Myopathy, Rare Diseases, Mendelian Disorder +6

Pediatric Mastocytosis Is a Clonal Disease Associated with D816V and Other Activating c-KIT Mutations

Christine Bodemer, Olivier Hermine, Fabienne Palmérini et al. · Journal of Investigative Dermatology · 2009 · 386 citations

Pediatric Mastocytosis, Genetic Disorder, Mast Cell Disorder +8

Striatal progenitors derived from human ES cells mature into DARPP32 neurons<i>in vitro</i>and in quinolinic acid-lesioned rats

Laëtitia Aubry, Aurore Bugi, Nathalie Lefort et al. · Proceedings of the National Academy of Sciences · 2008 · 290 citations · Full text

Fetal Cells, Substitutive Cell Therapy, Cellular Neurobiology +25

Swallowing problems in neuromuscular disorders

T.N. Willig, Jacques Paulus, J. Lacau Saint Guily et al. · Archives of Physical Medicine and Rehabilitation · 1994 · 178 citations

Phoniatrics, Medicine, Larynx +8

Case-Control Cohort Study of Patients' Perceptions of Disability in Mastocytosis

Olivier Hermine, Olivier Lortholary, Phillip S. Leventhal et al. · PLoS ONE · 2008 · 168 citations · Full text