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

Andreas Puschmann

Showing results (51-60 of 90) with videos related to

Pageof 9
Sort By:
American Journal of Human Genetics|November 30, 2023
Exonic trinucleotide repeat expansions in ZFHX3 cause spinocerebellar ataxia type 4: A poly-glycine diseaseJoel Wallenius, Efthymia Kafantari, Emma Jhaveri, et al.
Parkinsonism & Related Disorders|December 14, 2011
First neuropathological description of a patient with Parkinson's disease and LRRK2 p.N1437H mutationAndreas Puschmann, Elisabet Englund, Owen A Ross, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 30, 2010
LRRK2 variation and Parkinson's disease in African AmericansOwen A Ross, Greggory J Wilhoite, Justin A Bacon, et al.
Neurology. Genetics|August 31, 2017
Ataxia-pancytopenia syndrome with <i>SAMD9L</i> mutationsSorina Gorcenco, Jonna Komulainen-Ebrahim, Karin Nordborg, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 2, 2017
PBB3 imaging in Parkinsonian disorders: Evidence for binding to tau and other proteinsAlexandra Perez-Soriano, Julieta E Arena, Katie Dinelle, et al.
Neurobiology of Aging|June 4, 2016
Strong association between glucocerebrosidase mutations and Parkinson's disease in SwedenCaroline Ran, Lovisa Brodin, Lars Forsgren, et al.
American Journal of Neurodegenerative Disease|December 10, 2013
GWAS risk factors in Parkinson's disease: LRRK2 coding variation and genetic interaction with PARK16Alexandra I Soto-Ortolaza, Michael G Heckman, Catherine Labbé, et al.
Parkinsonism & Related Disorders|July 28, 2009
A Swedish family with de novo alpha-synuclein A53T mutation: evidence for early cortical dysfunctionAndreas Puschmann, Owen A Ross, Carles Vilariño-Güell, et al.
Cells|September 27, 2024
Structural and Functional Characterization of the Most Frequent Pathogenic PRKN Substitution p.R275WBernardo A Bustillos, Liam T Cocker, Mathew A Coban, et al.
Parkinsonism & Related Disorders|August 19, 2019
Low prevalence of known pathogenic mutations in dominant PD genes: A Swedish multicenter studyAndreas Puschmann, Itzia Jiménez-Ferrer, Elin Lundblad-Andersson, et al.
Pageof 9

Showing results (51-60 of 90) with videos related to

Sort By:
Pageof 9
American Journal of Human Genetics|November 30, 2023
Exonic trinucleotide repeat expansions in ZFHX3 cause spinocerebellar ataxia type 4: A poly-glycine diseaseJoel Wallenius, Efthymia Kafantari, Emma Jhaveri, et al.
Parkinsonism & Related Disorders|December 14, 2011
First neuropathological description of a patient with Parkinson's disease and LRRK2 p.N1437H mutationAndreas Puschmann, Elisabet Englund, Owen A Ross, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 30, 2010
LRRK2 variation and Parkinson's disease in African AmericansOwen A Ross, Greggory J Wilhoite, Justin A Bacon, et al.
Neurology. Genetics|August 31, 2017
Ataxia-pancytopenia syndrome with <i>SAMD9L</i> mutationsSorina Gorcenco, Jonna Komulainen-Ebrahim, Karin Nordborg, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 2, 2017
PBB3 imaging in Parkinsonian disorders: Evidence for binding to tau and other proteinsAlexandra Perez-Soriano, Julieta E Arena, Katie Dinelle, et al.
Neurobiology of Aging|June 4, 2016
Strong association between glucocerebrosidase mutations and Parkinson's disease in SwedenCaroline Ran, Lovisa Brodin, Lars Forsgren, et al.
American Journal of Neurodegenerative Disease|December 10, 2013
GWAS risk factors in Parkinson's disease: LRRK2 coding variation and genetic interaction with PARK16Alexandra I Soto-Ortolaza, Michael G Heckman, Catherine Labbé, et al.
Parkinsonism & Related Disorders|July 28, 2009
A Swedish family with de novo alpha-synuclein A53T mutation: evidence for early cortical dysfunctionAndreas Puschmann, Owen A Ross, Carles Vilariño-Güell, et al.
Cells|September 27, 2024
Structural and Functional Characterization of the Most Frequent Pathogenic PRKN Substitution p.R275WBernardo A Bustillos, Liam T Cocker, Mathew A Coban, et al.
Parkinsonism & Related Disorders|August 19, 2019
Low prevalence of known pathogenic mutations in dominant PD genes: A Swedish multicenter studyAndreas Puschmann, Itzia Jiménez-Ferrer, Elin Lundblad-Andersson, et al.
Pageof 9