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Mary M Reilly

Showing results (171-180 of 363) with videos related to

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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.
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.
Neuromuscular Disorders : NMD|July 2, 2013
Muscle MRI reveals distinct abnormalities in genetically proven non-dystrophic myotoniasJasper M Morrow, Emma Matthews, Dipa L Raja Rayan, et al.
Journal of the Peripheral Nervous System : JPNS|February 7, 2023
Validation of the parent-proxy pediatric Charcot-Marie-Tooth disease quality of life outcome measureTong Tong Wu, Richard S Finkel, Carly E Siskind, et al.
Neuromuscular Disorders : NMD|April 10, 2012
X inactivation in females with X-linked Charcot-Marie-Tooth diseaseSinéad M Murphy, Richard Ovens, James Polke, et al.
Advances in Therapy|April 14, 2022
Clinical and Genetic Evaluation of People with or at Risk of Hereditary ATTR Amyloidosis: An Expert Opinion and Consensus on Best Practice in Ireland and the UKJulian D Gillmore, Mary M Reilly, Caroline J Coats, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|April 25, 2019
Correlative SICM-FCM reveals changes in morphology and kinetics of endocytic pits induced by disease-associated mutations in dynaminTayyibah Ali, Joanna Bednarska, Stéphane Vassilopoulos, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 7, 2012
Tremor in inflammatory neuropathiesTabish Aziz Saifee, Petra Schwingenschuh, Mary M Reilly, et al.
The Journal of Biological Chemistry|January 26, 2010
Hereditary sensory neuropathy type 1 is caused by the accumulation of two neurotoxic sphingolipidsAnke Penno, Mary M Reilly, Henry Houlden, et al.
Annals of Clinical and Translational Neurology|February 17, 2025
Twelve-month change in quantitative MRI calf muscle fat fraction in CMT1A predicts clinical change over 4 yearsMatthew R B Evans, Hamza A Salhab, Christopher D J Sinclair, et al.
Pageof 37

Showing results (171-180 of 363) with videos related to

Sort By:
Pageof 37
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.
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.
Neuromuscular Disorders : NMD|July 2, 2013
Muscle MRI reveals distinct abnormalities in genetically proven non-dystrophic myotoniasJasper M Morrow, Emma Matthews, Dipa L Raja Rayan, et al.
Journal of the Peripheral Nervous System : JPNS|February 7, 2023
Validation of the parent-proxy pediatric Charcot-Marie-Tooth disease quality of life outcome measureTong Tong Wu, Richard S Finkel, Carly E Siskind, et al.
Neuromuscular Disorders : NMD|April 10, 2012
X inactivation in females with X-linked Charcot-Marie-Tooth diseaseSinéad M Murphy, Richard Ovens, James Polke, et al.
Advances in Therapy|April 14, 2022
Clinical and Genetic Evaluation of People with or at Risk of Hereditary ATTR Amyloidosis: An Expert Opinion and Consensus on Best Practice in Ireland and the UKJulian D Gillmore, Mary M Reilly, Caroline J Coats, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|April 25, 2019
Correlative SICM-FCM reveals changes in morphology and kinetics of endocytic pits induced by disease-associated mutations in dynaminTayyibah Ali, Joanna Bednarska, Stéphane Vassilopoulos, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 7, 2012
Tremor in inflammatory neuropathiesTabish Aziz Saifee, Petra Schwingenschuh, Mary M Reilly, et al.
The Journal of Biological Chemistry|January 26, 2010
Hereditary sensory neuropathy type 1 is caused by the accumulation of two neurotoxic sphingolipidsAnke Penno, Mary M Reilly, Henry Houlden, et al.
Annals of Clinical and Translational Neurology|February 17, 2025
Twelve-month change in quantitative MRI calf muscle fat fraction in CMT1A predicts clinical change over 4 yearsMatthew R B Evans, Hamza A Salhab, Christopher D J Sinclair, et al.
Pageof 37