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Daniel G Healy

Showing results (41-50 of 50) with videos related to

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JAMA Neurology|March 6, 2013
Parkin disease: a clinicopathologic entity?Karen M Doherty, Laura Silveira-Moriyama, Laura Parkkinen, et al.
Biochemical and Biophysical Research Communications|November 12, 2013
Pathogenic Parkinson's disease mutations across the functional domains of LRRK2 alter the autophagic/lysosomal response to starvationClaudia Manzoni, Adamantios Mamais, Sybille Dihanich, et al.
Annals of Neurology|March 3, 2004
A functional polymorphism regulating dopamine beta-hydroxylase influences against Parkinson's diseaseDaniel G Healy, Patrick M Abou-Sleiman, Tetsutaro Ozawa, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 12, 2005
UCHL-1 gene in multiple system atrophy: a haplotype tagging approachDaniel G Healy, Patrick M Abou-Sleiman, Niall Quinn, et al.
Annals of Neurology|February 2, 2006
UCHL-1 is not a Parkinson's disease susceptibility geneDaniel G Healy, Patrick M Abou-Sleiman, Juan P Casas, et al.
Journal of Neurochemistry|June 30, 2006
Altered cleavage and localization of PINK1 to aggresomes in the presence of proteasomal stressMiratul M K Muqit, Patrick M Abou-Sleiman, Adrian T Saurin, et al.
Brain : a Journal of Neurology|December 10, 2003
The expression of DJ-1 (PARK7) in normal human CNS and idiopathic Parkinson's diseaseRina Bandopadhyay, Ann E Kingsbury, Mark R Cookson, et al.
Science (New York, N.Y.)|April 17, 2004
Hereditary early-onset Parkinson's disease caused by mutations in PINK1Enza Maria Valente, Patrick M Abou-Sleiman, Viviana Caputo, et al.
The Lancet. Neurology|June 10, 2008
Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control studyDaniel G Healy, Mario Falchi, Sean S O'Sullivan, et al.
Brain : a Journal of Neurology|November 8, 2005
Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic dataNaheed L Khan, Shushant Jain, John M Lynch, et al.
Pageof 5

Showing results (41-50 of 50) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 50 results.
JAMA Neurology|March 6, 2013
Parkin disease: a clinicopathologic entity?Karen M Doherty, Laura Silveira-Moriyama, Laura Parkkinen, et al.
Biochemical and Biophysical Research Communications|November 12, 2013
Pathogenic Parkinson's disease mutations across the functional domains of LRRK2 alter the autophagic/lysosomal response to starvationClaudia Manzoni, Adamantios Mamais, Sybille Dihanich, et al.
Annals of Neurology|March 3, 2004
A functional polymorphism regulating dopamine beta-hydroxylase influences against Parkinson's diseaseDaniel G Healy, Patrick M Abou-Sleiman, Tetsutaro Ozawa, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 12, 2005
UCHL-1 gene in multiple system atrophy: a haplotype tagging approachDaniel G Healy, Patrick M Abou-Sleiman, Niall Quinn, et al.
Annals of Neurology|February 2, 2006
UCHL-1 is not a Parkinson's disease susceptibility geneDaniel G Healy, Patrick M Abou-Sleiman, Juan P Casas, et al.
Journal of Neurochemistry|June 30, 2006
Altered cleavage and localization of PINK1 to aggresomes in the presence of proteasomal stressMiratul M K Muqit, Patrick M Abou-Sleiman, Adrian T Saurin, et al.
Brain : a Journal of Neurology|December 10, 2003
The expression of DJ-1 (PARK7) in normal human CNS and idiopathic Parkinson's diseaseRina Bandopadhyay, Ann E Kingsbury, Mark R Cookson, et al.
Science (New York, N.Y.)|April 17, 2004
Hereditary early-onset Parkinson's disease caused by mutations in PINK1Enza Maria Valente, Patrick M Abou-Sleiman, Viviana Caputo, et al.
The Lancet. Neurology|June 10, 2008
Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control studyDaniel G Healy, Mario Falchi, Sean S O'Sullivan, et al.
Brain : a Journal of Neurology|November 8, 2005
Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic dataNaheed L Khan, Shushant Jain, John M Lynch, et al.
Pageof 5