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

Steven Frucht

Showing results (51-60 of 61) with videos related to

Pageof 7
Sort By:
Movement Disorders : Official Journal of the Movement Disorder Society|January 5, 2008
Phenotypic spectrum and sex effects in eleven myoclonus-dystonia families with epsilon-sarcoglycan mutationsDeborah Raymond, Rachel Saunders-Pullman, Patricia de Carvalho Aguiar, et al.
The Journal of Clinical Psychiatry|July 8, 2011
An international consensus study of neuroleptic malignant syndrome diagnostic criteria using the Delphi methodRonald J Gurrera, Stanley N Caroff, Abigail Cohen, et al.
Clinical Parkinsonism & Related Disorders|July 28, 2021
Targeting neurons in the gastrointestinal tract to treat Parkinson's diseaseRobert A Hauser, Dean Sutherland, Juan A Madrid, et al.
Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
Integrated Stress Response Signatures Drive Monocyte Dysfunction in <i>GBA1</i>- and <i>LRRK2</i>-Linked Parkinson's DiseaseDaniele Mattei, Erica Brophy, Mikaela Rosen, et al.
Research Square|February 27, 2026
Integrated Stress Response Signatures Drive Monocyte Dysfunction in GBA1- and LRRK2-Linked Parkinson's DiseaseDaniele Mattei, Erica Brophy, Mikaela Rosen, et al.
American Journal of Human Genetics|November 27, 2012
Exome sequencing reveals de novo WDR45 mutations causing a phenotypically distinct, X-linked dominant form of NBIATobias B Haack, Penelope Hogarth, Michael C Kruer, et al.
Archives of Neurology|September 15, 2010
Frequency of known mutations in early-onset Parkinson disease: implication for genetic counseling: the consortium on risk for early onset Parkinson disease studyRoy N Alcalay, Elise Caccappolo, Helen Mejia-Santana, et al.
Journal of the International Neuropsychological Society : JINS|November 25, 2010
Neuropsychological Profile of Parkin Mutation Carriers with and without Parkinson Disease: The CORE-PD StudyElise Caccappolo, Roy N Alcalay, Helen Mejia-Santana, et al.
Archives of Neurology|June 19, 2010
Predictors of parkin mutations in early-onset Parkinson disease: the consortium on risk for early-onset Parkinson disease studyKaren S Marder, Ming X Tang, Helen Mejia-Santana, et al.
Nature Aging|January 10, 2022
Dysregulation of mitochondrial and proteolysosomal genes in Parkinson's disease myeloid cellsElisa Navarro, Evan Udine, Katia de Paiva Lopes, et al.
Pageof 7

Showing results (51-60 of 61) with videos related to

Sort By:
Pageof 7
Movement Disorders : Official Journal of the Movement Disorder Society|January 5, 2008
Phenotypic spectrum and sex effects in eleven myoclonus-dystonia families with epsilon-sarcoglycan mutationsDeborah Raymond, Rachel Saunders-Pullman, Patricia de Carvalho Aguiar, et al.
The Journal of Clinical Psychiatry|July 8, 2011
An international consensus study of neuroleptic malignant syndrome diagnostic criteria using the Delphi methodRonald J Gurrera, Stanley N Caroff, Abigail Cohen, et al.
Clinical Parkinsonism & Related Disorders|July 28, 2021
Targeting neurons in the gastrointestinal tract to treat Parkinson's diseaseRobert A Hauser, Dean Sutherland, Juan A Madrid, et al.
Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
Integrated Stress Response Signatures Drive Monocyte Dysfunction in <i>GBA1</i>- and <i>LRRK2</i>-Linked Parkinson's DiseaseDaniele Mattei, Erica Brophy, Mikaela Rosen, et al.
Research Square|February 27, 2026
Integrated Stress Response Signatures Drive Monocyte Dysfunction in GBA1- and LRRK2-Linked Parkinson's DiseaseDaniele Mattei, Erica Brophy, Mikaela Rosen, et al.
American Journal of Human Genetics|November 27, 2012
Exome sequencing reveals de novo WDR45 mutations causing a phenotypically distinct, X-linked dominant form of NBIATobias B Haack, Penelope Hogarth, Michael C Kruer, et al.
Archives of Neurology|September 15, 2010
Frequency of known mutations in early-onset Parkinson disease: implication for genetic counseling: the consortium on risk for early onset Parkinson disease studyRoy N Alcalay, Elise Caccappolo, Helen Mejia-Santana, et al.
Journal of the International Neuropsychological Society : JINS|November 25, 2010
Neuropsychological Profile of Parkin Mutation Carriers with and without Parkinson Disease: The CORE-PD StudyElise Caccappolo, Roy N Alcalay, Helen Mejia-Santana, et al.
Archives of Neurology|June 19, 2010
Predictors of parkin mutations in early-onset Parkinson disease: the consortium on risk for early-onset Parkinson disease studyKaren S Marder, Ming X Tang, Helen Mejia-Santana, et al.
Nature Aging|January 10, 2022
Dysregulation of mitochondrial and proteolysosomal genes in Parkinson's disease myeloid cellsElisa Navarro, Evan Udine, Katia de Paiva Lopes, et al.
Pageof 7