Association Francaise contre les Myopathies

Institution (Funder)

Homepage ROR

Also Known As

AFM-Téléthon, Association Francaise contre les Myopathies, French Muscular Dystrophy Association · Acronym: AFM

397

Publications

17.2K

Citations

Authors

195

Concepts

About

Association Francaise contre les Myopathies is a funder institution in Rungis, France known for medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	27	79	9.2K
2	Engineering	5	12	397
3	Health Sciences	5	9	962
4	Education	2	2	124
5	Arts	1	1	77

Association Francaise contre les Myopathies

397

Publications

17.2K

Citations

Page 1

	Year	Citations
Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy Jing Liu, Masashi Aoki, Isabel Illa, Nature Genetics Miyoshi MyopathyRare DiseasesMendelian DisorderSkeletal MuscleGenetic Disorder	1998	914
Pediatric Mastocytosis Is a Clonal Disease Associated with D816V and Other Activating c-KIT Mutations Christine Bodemer, Olivier Hermine, Fabienne Palmérini, Journal of Investigative Dermatology Pediatric MastocytosisGenetic DisorderMast Cell DisorderImmunodeficienciesPathogenesis	2009	386
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, Proceedings of the National Academy of Sciences Fetal CellsSubstitutive Cell TherapyCellular NeurobiologySynaptic SignalingCellular Physiology	2008	290
Swallowing problems in neuromuscular disorders T.N. Willig, Jacques Paulus, J. Lacau Saint Guily, Archives of Physical Medicine and Rehabilitation PhoniatricsMedicineLarynxRehabilitationAnatomy	1994	178
Case-Control Cohort Study of Patients' Perceptions of Disability in Mastocytosis Olivier Hermine, Olivier Lortholary, Phillip S. Leventhal, PLoS ONE	2008	168
Limb-girdle muscular dystrophy in Guipuzcoa (Basque Country, Spain) Miguel Urtasun Brain Calpain-3 Gene MutationsGeneticsGenetic EpidemiologyPathologyDisease Gene Identification	1998	167
Phenotypic and Genotypic Characteristics of Mastocytosis According to the Age of Onset Fanny Lanternier, Annick Cohen-Akenine, Fabienne Palmérini, PLoS ONE Primary ImmunodeficiencyAutoimmune DiseaseMedicineMast Cell DisorderPathogenesis	2008	165
Differentiation In Vivo of Cardiac Committed Human Embryonic Stem Cells in Postmyocardial Infarcted Rats André Tomescot, Julia Leschik, Valérie Bellamy, Stem Cells Adult Stem CellCardiac Progenitor CellsCardiac RegenerationCell DifferentiationCell Specialization	2007	154
Analysis of Dp71 contribution in the severity of mental retardation through comparison of Duchenne and Becker patients differing by mutation consequences on Dp71 expression F. Daoud, Nathalie Angeard, B. Demerre, Human Molecular Genetics	2009	151
Gender as a Modifying Factor Influencing Myotonic Dystrophy Type 1 Phenotype Severity and Mortality: A Nationwide Multiple Databases Cross-Sectional Observational Study Céline Dogan, Marie De Antonio, Dalil Hamroun, PLoS ONE	2016	145

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