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Mitotic recombination of chromosome arm 17q as a cause of loss of heterozygosity of NF1 in neurofibromatosis type I-associated glomus tumors
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Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS
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Glomus tumors in neurofibromatosis type 1: genetic, functional, and clinical evidence of a novel association (vol 69, pg 7393, 2009)
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Glomus tumors in neurofibromatosis type 1: genetic, functional, and clinical evidence of a novel association
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Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS
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Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family
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Translocation of the HMGI-C (HMGA2) gene in a benign mesenchymoma (chondrolipoangioma)
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Deletion of the hypoxia-response element in the vascular endothelial growth factor promoter causes motor neuron degeneration
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Prominent axonopathy and disruption of axonal transport in transgenic mice expressing human apolipoprotein E4 in neurons of brain and spinal cord
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Familial Creutzfeldt-Jakob disease in a patient carrying both a presenilin 1 missense substitution and a prion protein gene insertion