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Mary M Reilly

Showing results (61-70 of 362) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|October 15, 2014
An observational study of asymmetry in CMT1AAna L Pelayo-Negro, Aisling S Carr, Matilde Laura, et al.
Neuromuscular Disorders : NMD|January 25, 2011
Conduction block and tonic pupils in Charcot-Marie-Tooth disease caused by a myelin protein zero p.Ile112Thr mutationSinéad M Murphy, Matilde Laurá, Julian Blake, et al.
Journal of the Peripheral Nervous System : JPNS|December 1, 2025
ITPR1 Deletion in a Patient With Sensory Ataxic Neuropathy and Sjögren SyndromeSaif Haddad, Roy Poh, Jason Hehir, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 14, 2010
Rituximab in the treatment of three coexistent neurological autoimmune diseases: chronic inflammatory demyelinating polyradiculoneuropathy, Morvan syndrome and myasthenia gravisAnna Sadnicka, Mary M Reilly, Cath Mummery, et al.
Journal of the Peripheral Nervous System : JPNS|March 2, 2021
A prospective study on surgical management of foot deformities in Charcot Marie tooth diseaseGita Ramdharry, Dishan Singh, Julia Gray, et al.
Neurology|July 15, 2016
Rydel-Seiffer fork revisited: Beyond a simple case of black and whiteFrancis B Panosyan, Joan M Mountain, Mary M Reilly, et al.
Journal of Neurology|July 12, 2015
Erratum to: Charcot-Marie-Tooth disease type 2C and scapuloperoneal muscular atrophy overlap syndrome in a patient with the R232C TRPV4 mutationGeorgios Koutsis, David Lynch, Andreea Manole, et al.
Journal of the Peripheral Nervous System : JPNS|May 16, 2020
A novel homozygous variant extending the peripheral myelin protein 22 by 9 amino acids causes early-onset Charcot-Marie-Tooth disease with predominant severe sensory ataxiaAlberto A Zambon, Matthew Pitt, Matilde Laurà, et al.
Journal of the Peripheral Nervous System : JPNS|May 26, 2017
A novel mutation in the FGD4 gene causing Charcot-Marie-Tooth diseasePanagiotis Zis, Mary M Reilly, Dasappaiah G Rao, et al.
Physiotherapy Research International : the Journal for Researchers and Clinicians in Physical Therapy|February 22, 2023
Incidence and risk factors for patellofemoral dislocation in adults with Charcot-Marie-Tooth disease: An observational studyEnza Leone, Sally Davenport, Claire Robertson, et al.
Pageof 37

Showing results (61-70 of 362) with videos related to

Sort By:
Pageof 37
Journal of Neurology, Neurosurgery, and Psychiatry|October 15, 2014
An observational study of asymmetry in CMT1AAna L Pelayo-Negro, Aisling S Carr, Matilde Laura, et al.
Neuromuscular Disorders : NMD|January 25, 2011
Conduction block and tonic pupils in Charcot-Marie-Tooth disease caused by a myelin protein zero p.Ile112Thr mutationSinéad M Murphy, Matilde Laurá, Julian Blake, et al.
Journal of the Peripheral Nervous System : JPNS|December 1, 2025
ITPR1 Deletion in a Patient With Sensory Ataxic Neuropathy and Sjögren SyndromeSaif Haddad, Roy Poh, Jason Hehir, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 14, 2010
Rituximab in the treatment of three coexistent neurological autoimmune diseases: chronic inflammatory demyelinating polyradiculoneuropathy, Morvan syndrome and myasthenia gravisAnna Sadnicka, Mary M Reilly, Cath Mummery, et al.
Journal of the Peripheral Nervous System : JPNS|March 2, 2021
A prospective study on surgical management of foot deformities in Charcot Marie tooth diseaseGita Ramdharry, Dishan Singh, Julia Gray, et al.
Neurology|July 15, 2016
Rydel-Seiffer fork revisited: Beyond a simple case of black and whiteFrancis B Panosyan, Joan M Mountain, Mary M Reilly, et al.
Journal of Neurology|July 12, 2015
Erratum to: Charcot-Marie-Tooth disease type 2C and scapuloperoneal muscular atrophy overlap syndrome in a patient with the R232C TRPV4 mutationGeorgios Koutsis, David Lynch, Andreea Manole, et al.
Journal of the Peripheral Nervous System : JPNS|May 16, 2020
A novel homozygous variant extending the peripheral myelin protein 22 by 9 amino acids causes early-onset Charcot-Marie-Tooth disease with predominant severe sensory ataxiaAlberto A Zambon, Matthew Pitt, Matilde Laurà, et al.
Journal of the Peripheral Nervous System : JPNS|May 26, 2017
A novel mutation in the FGD4 gene causing Charcot-Marie-Tooth diseasePanagiotis Zis, Mary M Reilly, Dasappaiah G Rao, et al.
Physiotherapy Research International : the Journal for Researchers and Clinicians in Physical Therapy|February 22, 2023
Incidence and risk factors for patellofemoral dislocation in adults with Charcot-Marie-Tooth disease: An observational studyEnza Leone, Sally Davenport, Claire Robertson, et al.
Pageof 37