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 (81-90 of 362) with videos related to

Pageof 37
Sort By:
BMJ (Clinical Research Ed.)|April 14, 2010
Copper deficiency as a treatable cause of poor balanceZhaleh Khaleeli, Daniel G Healy, Anthony Briddon, et al.
Praxis|September 23, 2010
[Copper deficiency as a treatable cause of poor balance]Zhaleh Khaleeli, Daniel G Healy, Anthony Briddon, et al.
Journal of the Peripheral Nervous System : JPNS|October 12, 2022
Conduction block and temporal dispersion in a SIGMAR1-related neuropathyRodrigo Siqueira Soares Frezatti, Pedro José Tomaselli, Fernanda Barbosa Figueiredo, et al.
Journal of Neurology|August 22, 2016
Severe axonal neuropathy is a late manifestation of SPG11Andreea Manole, Viorica Chelban, Nourelhoda A Haridy, et al.
Journal of the Peripheral Nervous System : JPNS|January 13, 2016
A proposed dosing algorithm for the individualized dosing of human immunoglobulin in chronic inflammatory neuropathiesMichael P Lunn, Lauren Ellis, Robert D Hadden, et al.
The Lancet. Neurology|October 20, 2023
Hereditary transthyretin amyloid neuropathies: advances in pathophysiology, biomarkers, and treatmentDavid Adams, Yoshiki Sekijima, Isabel Conceição, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 21, 2007
New mutations, genotype phenotype studies and manifesting carriers in giant axonal neuropathyHenry Houlden, Mike Groves, Zosia Miedzybrodzka, et al.
Brain : a Journal of Neurology|November 14, 2002
Clinical and genetic characterization of families with triple A (Allgrove) syndromeHenry Houlden, Stephen Smith, Mamede De Carvalho, et al.
Journal of Neurology|June 7, 2015
Charcot-Marie-Tooth disease type 2C and scapuloperoneal muscular atrophy overlap syndrome in a patient with the R232C TRPV4 mutationGeorgios Koutsis, David Lynch, Andreea Manole, et al.
Journal of Neurology|September 3, 2011
Rituximab responsive multiple radiculopathies and cranial nerve palsies in association with chronic lymphocytic leukaemiaJasper M Morrow, Shirley D'Sa, Rupert A Page, et al.
Pageof 37

Showing results (81-90 of 362) with videos related to

Sort By:
Pageof 37
BMJ (Clinical Research Ed.)|April 14, 2010
Copper deficiency as a treatable cause of poor balanceZhaleh Khaleeli, Daniel G Healy, Anthony Briddon, et al.
Praxis|September 23, 2010
[Copper deficiency as a treatable cause of poor balance]Zhaleh Khaleeli, Daniel G Healy, Anthony Briddon, et al.
Journal of the Peripheral Nervous System : JPNS|October 12, 2022
Conduction block and temporal dispersion in a SIGMAR1-related neuropathyRodrigo Siqueira Soares Frezatti, Pedro José Tomaselli, Fernanda Barbosa Figueiredo, et al.
Journal of Neurology|August 22, 2016
Severe axonal neuropathy is a late manifestation of SPG11Andreea Manole, Viorica Chelban, Nourelhoda A Haridy, et al.
Journal of the Peripheral Nervous System : JPNS|January 13, 2016
A proposed dosing algorithm for the individualized dosing of human immunoglobulin in chronic inflammatory neuropathiesMichael P Lunn, Lauren Ellis, Robert D Hadden, et al.
The Lancet. Neurology|October 20, 2023
Hereditary transthyretin amyloid neuropathies: advances in pathophysiology, biomarkers, and treatmentDavid Adams, Yoshiki Sekijima, Isabel Conceição, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 21, 2007
New mutations, genotype phenotype studies and manifesting carriers in giant axonal neuropathyHenry Houlden, Mike Groves, Zosia Miedzybrodzka, et al.
Brain : a Journal of Neurology|November 14, 2002
Clinical and genetic characterization of families with triple A (Allgrove) syndromeHenry Houlden, Stephen Smith, Mamede De Carvalho, et al.
Journal of Neurology|June 7, 2015
Charcot-Marie-Tooth disease type 2C and scapuloperoneal muscular atrophy overlap syndrome in a patient with the R232C TRPV4 mutationGeorgios Koutsis, David Lynch, Andreea Manole, et al.
Journal of Neurology|September 3, 2011
Rituximab responsive multiple radiculopathies and cranial nerve palsies in association with chronic lymphocytic leukaemiaJasper M Morrow, Shirley D'Sa, Rupert A Page, et al.
Pageof 37