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J M Polke

Showing results (1-10 of 5) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|April 1, 2009
Autosomal-dominant GTPCH1-deficient DRD: clinical characteristics and long-term outcome of 34 patientsI Trender-Gerhard, M G Sweeney, P Schwingenschuh, et al.
Neuromuscular Disorders : NMD|January 4, 2011
Variable phenotypes are associated with PMP22 missense mutationsM Russo, M Laurá, J M Polke, et al.
Neurology|July 1, 2011
Recessive axonal Charcot-Marie-Tooth disease due to compound heterozygous mitofusin 2 mutationsJ M Polke, M Laurá, D Pareyson, et al.
Journal of Neurology|February 4, 2012
Frequency of mutations in the genes associated with hereditary sensory and autonomic neuropathy in a UK cohortG L Davidson, S M Murphy, J M Polke, et al.
Molecular Psychiatry|October 4, 2018
Predictors for a dementia gene mutation based on gene-panel next-generation sequencing of a large dementia referral seriesC Koriath, J Kenny, G Adamson, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Journal of Neurology, Neurosurgery, and Psychiatry|April 1, 2009
Autosomal-dominant GTPCH1-deficient DRD: clinical characteristics and long-term outcome of 34 patientsI Trender-Gerhard, M G Sweeney, P Schwingenschuh, et al.
Neuromuscular Disorders : NMD|January 4, 2011
Variable phenotypes are associated with PMP22 missense mutationsM Russo, M Laurá, J M Polke, et al.
Neurology|July 1, 2011
Recessive axonal Charcot-Marie-Tooth disease due to compound heterozygous mitofusin 2 mutationsJ M Polke, M Laurá, D Pareyson, et al.
Journal of Neurology|February 4, 2012
Frequency of mutations in the genes associated with hereditary sensory and autonomic neuropathy in a UK cohortG L Davidson, S M Murphy, J M Polke, et al.
Molecular Psychiatry|October 4, 2018
Predictors for a dementia gene mutation based on gene-panel next-generation sequencing of a large dementia referral seriesC Koriath, J Kenny, G Adamson, et al.
Pageof 1