Jean-Michel Vallat

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

Annachiara De Sandre‐Giovannoli, Malika Chaouch, Serguei Kozlov et al. · The American Journal of Human Genetics · 2002 · 542 citations · Full text

Neurodegenerative Diseases, Homozygous Defects, Molecular Neuroscience +8

Intravenous immunoglobulin expands regulatory T cells via induction of cyclooxygenase-2–dependent prostaglandin E2 in human dendritic cells

Jamma Trinath, Pushpa Hegde, Meenu Sharma et al. · Blood · 2013 · 158 citations · Full text

Skin biopsies in myelin-related neuropathies: bringing molecular pathology to the bedside

Jun Li, Yunhong Bai, Khaled Ghandour et al. · Brain · 2005 · 114 citations

Skin Biopsies, Pathology, Peripheral Nerve +17

Pathological findings in the x-linked form of Charcot-Marie-Tooth disease: a morphometric and ultrastructural analysis

Angelika F. Hahn, Peter Ainsworth, Charles F. Bolton et al. · Acta Neuropathologica · 2001 · 90 citations

Gross Anatomy, Charcot-marie-tooth Disease, X-linked Form +4

Absence of P0 leads to the dysregulation of myelin gene expression and myelin morphogenesis

Wenbo Xu, Daniela Manichella, Huiyuan Jiang et al. · Journal of Neuroscience Research · 2000 · 65 citations