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Alexander M Rossor

Showing results (41-50 of 97) with videos related to

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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|April 14, 2022
Unusual upper limb features in SORD neuropathyChristopher J Record, Menelaos Pipis, Julian Blake, 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.
Neuromuscular Disorders : NMD|November 7, 2016
Pilot phenotype and natural history study of hereditary neuropathies caused by mutations in the HSPB1 geneAlexander M Rossor, Jasper M Morrow, James M Polke, et al.
Practical Neurology|November 20, 2025
Severe lupus vasculitic neuropathyApoorva Anil Kumar, Victor Jia Wei Zhang, Carine J Moezinia, et al.
Neuromuscular Disorders : NMD|November 3, 2018
IGHMBP2 mutation associated with organ-specific autonomic dysfunctionPedro J Tomaselli, Alejandro Horga, Alexander M Rossor, et al.
Journal of the Peripheral Nervous System : JPNS|June 28, 2012
BAG3 mutations: another cause of giant axonal neuropathyFatima Jaffer, Sinéad M Murphy, Mariacristina Scoto, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 11, 2017
Peripheral neuropathy in complex inherited diseases: an approach to diagnosisAlexander M Rossor, Aisling S Carr, Helen Devine, et al.
Journal of the Peripheral Nervous System : JPNS|June 28, 2012
A novel p.Gln175X [corrected] premature stop mutation in the C-terminal end of HSP27 is a cause of CMT2Alexander M Rossor, Gabrielle L Davidson, Julian Blake, et al.
Journal of the Peripheral Nervous System : JPNS|December 22, 2023
Digenic FLNA and UCHL1 variants resulting in a complex phenotypeHelena F Pernice, Luke F O'Donnell, Alexander M Rossor, et al.
Pageof 10

Showing results (41-50 of 97) with videos related to

Sort By:
Pageof 10
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|April 14, 2022
Unusual upper limb features in SORD neuropathyChristopher J Record, Menelaos Pipis, Julian Blake, 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.
Neuromuscular Disorders : NMD|November 7, 2016
Pilot phenotype and natural history study of hereditary neuropathies caused by mutations in the HSPB1 geneAlexander M Rossor, Jasper M Morrow, James M Polke, et al.
Practical Neurology|November 20, 2025
Severe lupus vasculitic neuropathyApoorva Anil Kumar, Victor Jia Wei Zhang, Carine J Moezinia, et al.
Neuromuscular Disorders : NMD|November 3, 2018
IGHMBP2 mutation associated with organ-specific autonomic dysfunctionPedro J Tomaselli, Alejandro Horga, Alexander M Rossor, et al.
Journal of the Peripheral Nervous System : JPNS|June 28, 2012
BAG3 mutations: another cause of giant axonal neuropathyFatima Jaffer, Sinéad M Murphy, Mariacristina Scoto, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 11, 2017
Peripheral neuropathy in complex inherited diseases: an approach to diagnosisAlexander M Rossor, Aisling S Carr, Helen Devine, et al.
Journal of the Peripheral Nervous System : JPNS|June 28, 2012
A novel p.Gln175X [corrected] premature stop mutation in the C-terminal end of HSP27 is a cause of CMT2Alexander M Rossor, Gabrielle L Davidson, Julian Blake, et al.
Journal of the Peripheral Nervous System : JPNS|December 22, 2023
Digenic FLNA and UCHL1 variants resulting in a complex phenotypeHelena F Pernice, Luke F O'Donnell, Alexander M Rossor, et al.
Pageof 10