Jean-Michel Vallat
Centre Hospitalier Universitaire de Limoges(FR)Université de Limoges(FR)
Publications by Year
Research Areas
Hereditary Neurological Disorders, Peripheral Neuropathies and Disorders, Genetic Neurodegenerative Diseases, Botulinum Toxin and Related Neurological Disorders, Skin and Cellular Biology Research
Most-Cited Works
- → Homozygous Defects in LMNA, Encoding Lamin A/C Nuclear-Envelope Proteins, Cause Autosomal Recessive Axonal Neuropathy in Human (Charcot-Marie-Tooth Disorder Type 2) and Mouse(2002)548 cited
- → Intravenous immunoglobulin expands regulatory T cells via induction of cyclooxygenase-2–dependent prostaglandin E2 in human dendritic cells(2013)158 cited
- → Skin biopsies in myelin-related neuropathies: bringing molecular pathology to the bedside(2005)114 cited
- → Pathological findings in the x-linked form of Charcot-Marie-Tooth disease: a morphometric and ultrastructural analysis(2001)90 cited
- → Absence of P0 leads to the dysregulation of myelin gene expression and myelin morphogenesis(2000)65 cited
- → Effect of megazol on Trypanosoma brucei brucei acute and subacute infections in Swiss mice(1995)61 cited
- → Myelin widenings and MGUS-IgA: An immunoelectron microscopic study(2000)51 cited
- → Autosomal-Recessive Charcot-Marie-Tooth Diseases(2005)39 cited
- → Genetic heterogeneity in giant axonal neuropathy: an Algerian family not linked to chromosome 16q24.1(2002)27 cited
- → Phenotypic expression of a Pro 87 to Leu mutation in the connexin 32 gene in a large Swiss family with Charcot–Marie–Tooth neuropathy(2003)24 cited