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Neurology. Genetics|September 29, 2025
Peripheral Neuropathy in p.Val142Ile (Val122Ile) Variant Hereditary Transthyretin-Mediated Amyloidosis: United Kingdom ExperienceVictor Jia Wei Zhang, Luke F O'Donnell, Mariola Skorupinska, et al.
Human Molecular Genetics|August 15, 2019
Gene replacement therapy after neuropathy onset provides therapeutic benefit in a model of CMT1XA Kagiava, J Richter, C Tryfonos, et al.
Journal of the Peripheral Nervous System : JPNS|May 27, 2025
A Case Series of Unilateral Peripheral NeuropathyCaroline Kramarz, Marion Masingue, Françoise Bouhour, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 17, 2021
IgG<sub>1</sub> pan-neurofascin antibodies identify a severe yet treatable neuropathy with a high mortalityJanev Fehmi, Alexander J Davies, Jon Walters, et al.
European Journal of Neurology|February 10, 2025
Heterozygous PNPT1 Variants Cause a Sensory Ataxic NeuropathySaif Haddad, Christopher J Record, Eleanor Self, et al.
Journal of Acquired Immune Deficiency Syndromes (1999)|October 26, 1999
Prospective study of HTLV-I infection in an initially asymptomatic cohortG P Taylor, J H Tosswill, E Matutes, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|February 13, 2024
Serum neurofilament light chain in hereditary transthyretin amyloidosis: validation in real-life practiceAntonia S Carroll, Yousuf Razvi, Luke O'Donnell, et al.
Annals of Neurology|April 20, 2001
Patterns of temporal lobe atrophy in semantic dementia and Alzheimer's diseaseD Chan, N C Fox, R I Scahill, et al.
Journal of the Peripheral Nervous System : JPNS|June 28, 2025
Skin Biopsy as a Diagnostic Tool for ATTRv Amyloid Neuropathy in the UKLuke F O'Donnell, Victor Zhang, Roy Carganillo, et al.
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