Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Mary M Reilly

Showing results (91-100 of 362) with videos related to

Pageof 37
Sort By:
Journal of Neurology, Neurosurgery, and Psychiatry|March 8, 2022
Novel approaches to diagnosis and management of hereditary transthyretin amyloidosisAntonia Carroll, P James Dyck, Mamede de Carvalho, et al.
Journal of Neurology|September 21, 2002
Mutation of the sterol 27-hydroxylase gene ( CYP27A1) in a Taiwanese family with cerebrotendinous xanthomatosisMing-Jen Lee, Yuan-Chung Huang, Mary G Sweeney, et al.
Practical Neurology|March 1, 2017
Wisdom tooth extraction causing lingual nerve and styloglossus muscle damage: a mimic of multiple cranial nerve palsiesAisling S Carr, Matthew Evans, Sachit Shah, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|September 4, 2018
Raised VEGF: High sensitivity and specificity in the diagnosis of POEMS syndromeMorgane Pihan, Stephen Keddie, Shirley D'Sa, et al.
Neurology|January 12, 2018
Plasma neurofilament light chain concentration in the inherited peripheral neuropathiesÅsa Sandelius, Henrik Zetterberg, Kaj Blennow, et al.
Journal of the Peripheral Nervous System : JPNS|August 24, 2017
A de novo dominant mutation in KIF1A associated with axonal neuropathy, spasticity and autism spectrum disorderPedro J Tomaselli, Alexander M Rossor, Alejandro Horga, et al.
Acta Neuropathologica Communications|March 19, 2020
Loss of BICD2 in muscle drives motor neuron loss in a developmental form of spinal muscular atrophyAlexander M Rossor, James N Sleigh, Michael Groves, et al.
Journal of the Peripheral Nervous System : JPNS|December 12, 2025
Impact of High-Dose Tafamidis on Hereditary ATTR (ATTRv) Amyloidosis With Central Nervous System Involvement: Two Case Reports With Clinical, Radiological and Cerebrospinal Fluid Follow UpVictor Jia Wei Zhang, Laura Mantoan Ritter, Chandrashekar Hoskote, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 13, 2025
Role of ambulatory blood pressure monitoring as a non-invasive autonomic screening tool in hereditary transthyretin amyloidosisLaura Sander, Giacomo Chiaro, Domenico Abelardo, et al.
Acta Neuropathologica Communications|October 16, 2020
A dysfunctional endolysosomal pathway common to two sub-types of demyelinating Charcot-Marie-Tooth diseaseJames R Edgar, Anita K Ho, Matilde Laurá, et al.
Pageof 37

Showing results (91-100 of 362) with videos related to

Sort By:
Pageof 37
Journal of Neurology, Neurosurgery, and Psychiatry|March 8, 2022
Novel approaches to diagnosis and management of hereditary transthyretin amyloidosisAntonia Carroll, P James Dyck, Mamede de Carvalho, et al.
Journal of Neurology|September 21, 2002
Mutation of the sterol 27-hydroxylase gene ( CYP27A1) in a Taiwanese family with cerebrotendinous xanthomatosisMing-Jen Lee, Yuan-Chung Huang, Mary G Sweeney, et al.
Practical Neurology|March 1, 2017
Wisdom tooth extraction causing lingual nerve and styloglossus muscle damage: a mimic of multiple cranial nerve palsiesAisling S Carr, Matthew Evans, Sachit Shah, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|September 4, 2018
Raised VEGF: High sensitivity and specificity in the diagnosis of POEMS syndromeMorgane Pihan, Stephen Keddie, Shirley D'Sa, et al.
Neurology|January 12, 2018
Plasma neurofilament light chain concentration in the inherited peripheral neuropathiesÅsa Sandelius, Henrik Zetterberg, Kaj Blennow, et al.
Journal of the Peripheral Nervous System : JPNS|August 24, 2017
A de novo dominant mutation in KIF1A associated with axonal neuropathy, spasticity and autism spectrum disorderPedro J Tomaselli, Alexander M Rossor, Alejandro Horga, et al.
Acta Neuropathologica Communications|March 19, 2020
Loss of BICD2 in muscle drives motor neuron loss in a developmental form of spinal muscular atrophyAlexander M Rossor, James N Sleigh, Michael Groves, et al.
Journal of the Peripheral Nervous System : JPNS|December 12, 2025
Impact of High-Dose Tafamidis on Hereditary ATTR (ATTRv) Amyloidosis With Central Nervous System Involvement: Two Case Reports With Clinical, Radiological and Cerebrospinal Fluid Follow UpVictor Jia Wei Zhang, Laura Mantoan Ritter, Chandrashekar Hoskote, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 13, 2025
Role of ambulatory blood pressure monitoring as a non-invasive autonomic screening tool in hereditary transthyretin amyloidosisLaura Sander, Giacomo Chiaro, Domenico Abelardo, et al.
Acta Neuropathologica Communications|October 16, 2020
A dysfunctional endolysosomal pathway common to two sub-types of demyelinating Charcot-Marie-Tooth diseaseJames R Edgar, Anita K Ho, Matilde Laurá, et al.
Pageof 37