Nathalie Verpoorten
Janssen (Belgium)(BE)
Publications by Year
Research Areas
Hereditary Neurological Disorders, Cellular transport and secretion, Endoplasmic Reticulum Stress and Disease, Wnt/β-catenin signaling in development and cancer, Heat shock proteins research
Most-Cited Works
- → Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy(2004)581 cited
- → Mutations in the Small GTP-ase Late Endosomal Protein RAB7 Cause Charcot-Marie-Tooth Type 2B Neuropathy(2003)452 cited
- → Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathy(2004)417 cited
- → Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndrome(2004)377 cited
- → Mutations in SEPT9 cause hereditary neuralgic amyotrophy(2005)260 cited
- → Mutations in a Gene Encoding a Novel SH3/TPR Domain Protein Cause Autosomal Recessive Charcot-Marie-Tooth Type 4C Neuropathy(2003)210 cited
- → Astrocytes regulate GluR2 expression in motor neurons and their vulnerability to excitotoxicity(2007)207 cited
- → Slowed Conduction and Thin Myelination of Peripheral Nerves Associated with Mutant Rho Guanine-Nucleotide Exchange Factor 10(2003)118 cited
- → Experimental Charcot–Marie–Tooth type 1A: A cDNA microarrays analysis(2005)44 cited
- → Disease mechanisms in hereditary sensory and autonomic neuropathies(2005)44 cited