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M M Reilly

Showing results (51-60 of 61) with videos related to

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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 the Peripheral Nervous System : JPNS|October 11, 2024
Patient-reported disease burden in the Accelerate Clinical Trials in Charcot-Marie-Tooth Disease StudyT Rehbein, J Purks, N Dilek, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 25, 2014
Is overwork weakness relevant in Charcot-Marie-Tooth disease?G Piscosquito, M M Reilly, A Schenone, et al.
European Journal of Neurology|October 14, 2017
Altered TDP-43-dependent splicing in HSPB8-related distal hereditary motor neuropathy and myofibrillar myopathyA Cortese, M Laurà, C Casali, et al.
Neuromuscular Disorders : NMD|March 31, 2015
Transthyretin V122I amyloidosis with clinical and histological evidence of amyloid neuropathy and myopathyA S Carr, A L Pelayo-Negro, Z Jaunmuktane, et al.
European Journal of Neurology|August 1, 2015
Responsiveness of clinical outcome measures in Charcot-Marie-Tooth diseaseG Piscosquito, M M Reilly, A Schenone, et al.
Neurology|March 31, 2012
Mutations in the tail domain of DYNC1H1 cause dominant spinal muscular atrophyM B Harms, K M Ori-McKenney, M Scoto, et al.
Journal of Neurology|December 10, 2014
Oculoleptomeningeal Amyloidosis associated with transthyretin Leu12Pro in an African patientP McColgan, S Viegas, S Gandhi, 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.
Journal of Neurology, Neurosurgery, and Psychiatry|November 29, 2014
CMT subtypes and disease burden in patients enrolled in the Inherited Neuropathies Consortium natural history study: a cross-sectional analysisV Fridman, B Bundy, M M Reilly, et al.
Pageof 7

Showing results (51-60 of 61) with videos related to

Sort By:
Pageof 7
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 the Peripheral Nervous System : JPNS|October 11, 2024
Patient-reported disease burden in the Accelerate Clinical Trials in Charcot-Marie-Tooth Disease StudyT Rehbein, J Purks, N Dilek, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 25, 2014
Is overwork weakness relevant in Charcot-Marie-Tooth disease?G Piscosquito, M M Reilly, A Schenone, et al.
European Journal of Neurology|October 14, 2017
Altered TDP-43-dependent splicing in HSPB8-related distal hereditary motor neuropathy and myofibrillar myopathyA Cortese, M Laurà, C Casali, et al.
Neuromuscular Disorders : NMD|March 31, 2015
Transthyretin V122I amyloidosis with clinical and histological evidence of amyloid neuropathy and myopathyA S Carr, A L Pelayo-Negro, Z Jaunmuktane, et al.
European Journal of Neurology|August 1, 2015
Responsiveness of clinical outcome measures in Charcot-Marie-Tooth diseaseG Piscosquito, M M Reilly, A Schenone, et al.
Neurology|March 31, 2012
Mutations in the tail domain of DYNC1H1 cause dominant spinal muscular atrophyM B Harms, K M Ori-McKenney, M Scoto, et al.
Journal of Neurology|December 10, 2014
Oculoleptomeningeal Amyloidosis associated with transthyretin Leu12Pro in an African patientP McColgan, S Viegas, S Gandhi, 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.
Journal of Neurology, Neurosurgery, and Psychiatry|November 29, 2014
CMT subtypes and disease burden in patients enrolled in the Inherited Neuropathies Consortium natural history study: a cross-sectional analysisV Fridman, B Bundy, M M Reilly, et al.
Pageof 7