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Nathalie Verpoorten

University of Antwerp

18

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Astrocytes regulate GluR2 expression in motor neurons and their vulnerability to excitotoxicity

2007 Proceedings of the National Academy of Sciences of the United States of America
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Corrigendum to “Synaptopodin and 4 novel genes identified in primary sensory neurons” [Mol. Cell. Neurosci. 30 (2005) 316–325]

2006 Molecular and Cellular Neuroscience
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Novel frameshift and splice site mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with hereditary sensory neuropathy type IV

2006 Neuromuscular Disorders
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Synaptopodin and 4 novel genes identified in primary sensory neurons

2005 Molecular and Cellular Neuroscience
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Mutations in the human septin 0 gene (SEPT9) cause hereditary neuralgic amyotrophy (HNA)

2005
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Mutations in SEPT9 cause hereditary neuralgic amyotrophy

2005 Nature Genetics
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Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndrome

2004 Nature Genetics
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The phenotype of motor neuropathies associated with BSCL2 mutations is broader than Silver syndrome and distal HMN type V

2004 Brain
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Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy

2004 Nature Genetics
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Autosomal dominant axonal Charcot-Marie-Tooth disease type 2 (CMT2G) maps to chromosome 12q12–q13.3

2004 Journal of Medical Genetics
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Citations (37)