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

O Riess

Showing results (131-140 of 144) with videos related to

Pageof 15
Sort By:
Journal of Neural Transmission (Vienna, Austria : 1996)|November 10, 2000
Genetic analysis of immunomodulating factors in sporadic Parkinson's diseaseR Krüger, C Hardt, F Tschentscher, et al.
Cell Death & Disease|April 19, 2014
Mitochondrial proteolytic stress induced by loss of mortalin function is rescued by Parkin and PINK1L F Burbulla, J C Fitzgerald, K Stegen, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|December 29, 2004
The role of alpha-synuclein gene multiplications in early-onset Parkinson's disease and dementia with Lewy bodiesA Hofer, D Berg, F Asmus, et al.
Journal of Medical Genetics|February 27, 2004
Trinucleotide repeat expansion in SCA17/TBP in white patients with Huntington's disease-like phenotypeP Bauer, F Laccone, A Rolfs, et al.
Cerebellum (London, England)|December 6, 2013
Consensus paper: pathological mechanisms underlying neurodegeneration in spinocerebellar ataxiasA Matilla-Dueñas, T Ashizawa, A Brice, et al.
Neurobiology of Disease|January 8, 2010
Expression profiling in peripheral blood reveals signature for penetrance in DYT1 dystoniaM Walter, M Bonin, R Saunders Pullman, et al.
Neurology|September 17, 1999
DNA analysis of Huntington's disease: five years of experience in Germany, Austria, and SwitzerlandF Laccone, U Engel, E Holinski-Feder, et al.
Neurology|February 12, 2004
DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson diseaseK Hedrich, A Djarmati, N Schäfer, et al.
Neurogenetics|May 1, 1997
SCA2 trinucleotide expansion in German SCA patientsO Riess, F A Laccone, S Gispert, et al.
Molecular Psychiatry|July 13, 2000
Allelic distribution of CTG18.1 in Caucasian populations: association studies in bipolar disorder, schizophrenia, and ataxiaM G McInnis, T Swift-Scanlanl, A T Mahoney, et al.
Pageof 15

Showing results (131-140 of 144) with videos related to

Sort By:
Pageof 15
Journal of Neural Transmission (Vienna, Austria : 1996)|November 10, 2000
Genetic analysis of immunomodulating factors in sporadic Parkinson's diseaseR Krüger, C Hardt, F Tschentscher, et al.
Cell Death & Disease|April 19, 2014
Mitochondrial proteolytic stress induced by loss of mortalin function is rescued by Parkin and PINK1L F Burbulla, J C Fitzgerald, K Stegen, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|December 29, 2004
The role of alpha-synuclein gene multiplications in early-onset Parkinson's disease and dementia with Lewy bodiesA Hofer, D Berg, F Asmus, et al.
Journal of Medical Genetics|February 27, 2004
Trinucleotide repeat expansion in SCA17/TBP in white patients with Huntington's disease-like phenotypeP Bauer, F Laccone, A Rolfs, et al.
Cerebellum (London, England)|December 6, 2013
Consensus paper: pathological mechanisms underlying neurodegeneration in spinocerebellar ataxiasA Matilla-Dueñas, T Ashizawa, A Brice, et al.
Neurobiology of Disease|January 8, 2010
Expression profiling in peripheral blood reveals signature for penetrance in DYT1 dystoniaM Walter, M Bonin, R Saunders Pullman, et al.
Neurology|September 17, 1999
DNA analysis of Huntington's disease: five years of experience in Germany, Austria, and SwitzerlandF Laccone, U Engel, E Holinski-Feder, et al.
Neurology|February 12, 2004
DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson diseaseK Hedrich, A Djarmati, N Schäfer, et al.
Neurogenetics|May 1, 1997
SCA2 trinucleotide expansion in German SCA patientsO Riess, F A Laccone, S Gispert, et al.
Molecular Psychiatry|July 13, 2000
Allelic distribution of CTG18.1 in Caucasian populations: association studies in bipolar disorder, schizophrenia, and ataxiaM G McInnis, T Swift-Scanlanl, A T Mahoney, et al.
Pageof 15