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Mary M Reilly

Showing results (121-130 of 363) with videos related to

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Journal of the Peripheral Nervous System : JPNS|December 20, 2011
c-Jun expression in human neuropathies: a pilot studyElspeth J Hutton, Lucy Carty, Matilde Laurá, et al.
Practical Neurology|December 13, 2016
Leprosy in a patient infected with HIVClare M Galtrey, Hamid Modarres, Zane Jaunmuktane, et al.
Neurology|December 1, 2017
Neurofascin antibodies in autoimmune, genetic, and idiopathic neuropathiesElisabeth Burnor, Li Yang, Hao Zhou, et al.
Journal of the Peripheral Nervous System : JPNS|June 4, 2023
Recruiting for an International Rare Disease Clinical Trial Readiness Study during the COVID-19 pandemic: Challenges and solutionsKaty Eichinger, Steffen Behrens-Spraggins, Janet E Sowden, et al.
Journal of the Peripheral Nervous System : JPNS|October 5, 2019
Plasma neurofilament light chain concentration is increased and correlates with the severity of neuropathy in hereditary transthyretin amyloidosisMahima Kapoor, Martha Foiani, Amanda Heslegrave, et al.
Neurobiology of Disease|May 21, 2018
Hereditary sensory neuropathy type 1-associated deoxysphingolipids cause neurotoxicity, acute calcium handling abnormalities and mitochondrial dysfunction in vitroEmma R Wilson, Umaiyal Kugathasan, Andrey Y Abramov, et al.
Human Molecular Genetics|December 24, 2009
Mistargeting of SH3TC2 away from the recycling endosome causes Charcot-Marie-Tooth disease type 4CRhys C Roberts, Andrew A Peden, Folma Buss, et al.
Neuromuscular Disorders : NMD|March 11, 2009
The phenotype of Charcot-Marie-Tooth disease type 4C due to SH3TC2 mutations and possible predisposition to an inflammatory neuropathyHenry Houlden, Matilde Laura, Lionel Ginsberg, et al.
Neurogenetics|December 23, 2016
SBF1 mutations associated with autosomal recessive axonal neuropathy with cranial nerve involvementAndreea Manole, Alejandro Horga, Josep Gamez, et al.
Neuromuscular Disorders : NMD|August 2, 2025
ADGRG6-related disorder: a novel mutation resulting in distal arthrogryposis and a patchy neuropathyValentine Perrain, Christopher J Record, Mariola Skorupinska, et al.
Pageof 37

Showing results (121-130 of 363) with videos related to

Sort By:
Pageof 37
Journal of the Peripheral Nervous System : JPNS|December 20, 2011
c-Jun expression in human neuropathies: a pilot studyElspeth J Hutton, Lucy Carty, Matilde Laurá, et al.
Practical Neurology|December 13, 2016
Leprosy in a patient infected with HIVClare M Galtrey, Hamid Modarres, Zane Jaunmuktane, et al.
Neurology|December 1, 2017
Neurofascin antibodies in autoimmune, genetic, and idiopathic neuropathiesElisabeth Burnor, Li Yang, Hao Zhou, et al.
Journal of the Peripheral Nervous System : JPNS|June 4, 2023
Recruiting for an International Rare Disease Clinical Trial Readiness Study during the COVID-19 pandemic: Challenges and solutionsKaty Eichinger, Steffen Behrens-Spraggins, Janet E Sowden, et al.
Journal of the Peripheral Nervous System : JPNS|October 5, 2019
Plasma neurofilament light chain concentration is increased and correlates with the severity of neuropathy in hereditary transthyretin amyloidosisMahima Kapoor, Martha Foiani, Amanda Heslegrave, et al.
Neurobiology of Disease|May 21, 2018
Hereditary sensory neuropathy type 1-associated deoxysphingolipids cause neurotoxicity, acute calcium handling abnormalities and mitochondrial dysfunction in vitroEmma R Wilson, Umaiyal Kugathasan, Andrey Y Abramov, et al.
Human Molecular Genetics|December 24, 2009
Mistargeting of SH3TC2 away from the recycling endosome causes Charcot-Marie-Tooth disease type 4CRhys C Roberts, Andrew A Peden, Folma Buss, et al.
Neuromuscular Disorders : NMD|March 11, 2009
The phenotype of Charcot-Marie-Tooth disease type 4C due to SH3TC2 mutations and possible predisposition to an inflammatory neuropathyHenry Houlden, Matilde Laura, Lionel Ginsberg, et al.
Neurogenetics|December 23, 2016
SBF1 mutations associated with autosomal recessive axonal neuropathy with cranial nerve involvementAndreea Manole, Alejandro Horga, Josep Gamez, et al.
Neuromuscular Disorders : NMD|August 2, 2025
ADGRG6-related disorder: a novel mutation resulting in distal arthrogryposis and a patchy neuropathyValentine Perrain, Christopher J Record, Mariola Skorupinska, et al.
Pageof 37