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

Daniel G Healy

Showing results (21-30 of 50) with videos related to

Pageof 5
Sort By:
Annals of Neurology|September 4, 2003
The role of pathogenic DJ-1 mutations in Parkinson's diseasePatrick M Abou-Sleiman, Daniel G Healy, Niall Quinn, et al.
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.
Clinical and Experimental Dermatology|March 4, 2025
General dermatology & dermatology in primary health careLi Jie Helena Yoo, Stephanie L Ryan, Cristina Grechin, et al.
The British Journal of Psychiatry : the Journal of Mental Science|October 11, 2011
Anti-NMDA receptor encephalitis: an important differential diagnosis in psychosisHelen Barry, Orla Hardiman, Daniel G Healy, et al.
Journal of the Peripheral Nervous System : JPNS|September 17, 2019
Clinical spectrum of AIFM1-associated disease in an Irish family, from mild neuropathy to severe cerebellar ataxia with colour blindnessPetya Bogdanova-Mihaylova, Michael D Alexander, Raymond P Murphy, et al.
Infection Control and Hospital Epidemiology|June 11, 2014
Managing the consequences of neurosurgical intervention in a patient with previously undiagnosed Creutzfeldt-Jakob diseaseEdmond G Smyth, Michael Farrell, Daniel G Healy, et al.
Archives of Neurology|January 13, 2006
Apolipoprotein e genotype modifies the phenotype of Alzheimer diseaseJonathan M Schott, Basil H Ridha, Sebastian J Crutch, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 11, 2013
The endophenotype and the phenotype: temporal discrimination and adult-onset dystoniaMichael Hutchinson, Okka Kimmich, Anna Molloy, et al.
Brain : a Journal of Neurology|October 29, 2004
The spectrum of pathological involvement of the striatonigral and olivopontocerebellar systems in multiple system atrophy: clinicopathological correlationsTetsutaro Ozawa, Dominic Paviour, Niall P Quinn, et al.
Pageof 5

Showing results (21-30 of 50) with videos related to

Sort By:
Pageof 5
Annals of Neurology|September 4, 2003
The role of pathogenic DJ-1 mutations in Parkinson's diseasePatrick M Abou-Sleiman, Daniel G Healy, Niall Quinn, et al.
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.
Clinical and Experimental Dermatology|March 4, 2025
General dermatology & dermatology in primary health careLi Jie Helena Yoo, Stephanie L Ryan, Cristina Grechin, et al.
The British Journal of Psychiatry : the Journal of Mental Science|October 11, 2011
Anti-NMDA receptor encephalitis: an important differential diagnosis in psychosisHelen Barry, Orla Hardiman, Daniel G Healy, et al.
Journal of the Peripheral Nervous System : JPNS|September 17, 2019
Clinical spectrum of AIFM1-associated disease in an Irish family, from mild neuropathy to severe cerebellar ataxia with colour blindnessPetya Bogdanova-Mihaylova, Michael D Alexander, Raymond P Murphy, et al.
Infection Control and Hospital Epidemiology|June 11, 2014
Managing the consequences of neurosurgical intervention in a patient with previously undiagnosed Creutzfeldt-Jakob diseaseEdmond G Smyth, Michael Farrell, Daniel G Healy, et al.
Archives of Neurology|January 13, 2006
Apolipoprotein e genotype modifies the phenotype of Alzheimer diseaseJonathan M Schott, Basil H Ridha, Sebastian J Crutch, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 11, 2013
The endophenotype and the phenotype: temporal discrimination and adult-onset dystoniaMichael Hutchinson, Okka Kimmich, Anna Molloy, et al.
Brain : a Journal of Neurology|October 29, 2004
The spectrum of pathological involvement of the striatonigral and olivopontocerebellar systems in multiple system atrophy: clinicopathological correlationsTetsutaro Ozawa, Dominic Paviour, Niall P Quinn, et al.
Pageof 5