Pascal Laforêt
Assistance Publique – Hôpitaux de Paris(FR)Hôpital Raymond-Poincaré(FR)
Publications by Year
Research Areas
Glycogen Storage Diseases and Myoclonus, Lysosomal Storage Disorders Research, Muscle Physiology and Disorders, Mitochondrial Function and Pathology, Metabolism and Genetic Disorders
Most-Cited Works
- → A Randomized Study of Alglucosidase Alfa in Late-Onset Pompe's Disease(2010)737 cited
- → The gene encoding adipose triglyceride lipase (PNPLA2) is mutated in neutral lipid storage disease with myopathy(2006)457 cited
- → Mutations in dynamin 2 cause dominant centronuclear myopathy(2005)456 cited
- → Electromyography guides toward subgroups of mutations in muscle channelopathies(2004)306 cited
- → Multiple Phenotypes in Phosphoglucomutase 1 Deficiency(2014)284 cited
- → Anti-HMGCR Autoantibodies in European Patients With Autoimmune Necrotizing Myopathies(2014)268 cited
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