Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Julia C Shirvan"'
Autor:
Jake DeBroff, Nurit Omer, Batsheva Cohen, Nir Giladi, Meir Kestenbaum, Julia C. Shirvan, Jesse M. Cedarbaum, Mali Gana‐Weisz, Orly Goldstein, Avi Orr‐Urtreger, Anat Mirelman, Avner Thaler
Publikováno v:
Movement Disorders Clinical Practice. 10:606-616
Autor:
Avner Thaler, Tamara Schejter-Margalit, Julia C Shirvan, Nir Giladi, Jesse M. Cedarbaum, Anat Mirelman, Rachel Kizony, Noa Bregman
Publikováno v:
Parkinsonism & Related Disorders. 90:84-89
Introduction The prevalence of subtle cognitive decline in the early stages of Parkinson's Disease (PD) is common and is thought to be even greater in patients carrying genetic mutations in the GBA gene. Current cognitive tests often lack sensitivity
Autor:
Mali Gana-Weisz, Meir Kestenbaum, Julia C Shirvan, Shani Shenhar-Tsarfaty, Tanya Gurevich, Avi Orr-Urtreger, Anat Bar-Shira, Avner Thaler, Nurit Omer, Orly Goldstein, Keren Regev, Jesse M. Cedarbaum, Nir Giladi, Anat Mirelman
Publikováno v:
Journal of Parkinson's Disease
Background: Inflammation is an integral part of neurodegeneration including in Parkinson’s disease (PD). Ashkenazi Jews have high rates of genetic PD with divergent phenotypes among GBA-PD and LRRK2-PD. The role of inflammation in the prodromal pha
Autor:
Jesse M. Cedarbaum, Theresa Ellis, Paolo Bonato, Lynn Rochester, Elisa Pelosin, Lena Granovsky, Nir Giladi, Michal Melamed, Quincy J. Almeida, Laura Avanzino, Chris J. Hass, Andrea Cereatti, Jamie L. Hamilton, Alice Nieuwboer, Avner Thaler, Mor Ben Or Frank, Bastiaan R. Bloem, Jeffrey M. Hausdorff, Maidan Inbal, Richard Camicioli, Anat Mirelman, Julia C Shirvan, Silvia Del Din, Ugo Della Croce
Publikováno v:
Movement Disorders, 36, 9, pp. 2144-2155
Movement Disorders, 36, 2144-2155
Movement Disorders, 36, 2144-2155
Contains fulltext : 238527.pdf (Publisher’s version ) (Closed access) BACKGROUND: It is not clear how specific gait measures reflect disease severity across the disease spectrum in Parkinson's disease (PD). OBJECTIVE: To identify the gait and mobil
Autor:
Nurit Omer, Tanya Gurevich, Nir Giladi, Julia C Shirvan, Avner Thaler, Jesse M. Cedarbaum, Orly Goldstein, Mali Gana-Weisz, Meir Kestenbaum, Avi Orr-Urtreger, Kyle B Fraser, Anat Bar-Shira, Tal Glinka, Anat Mirelman, Omar S Mabrouk
Publikováno v:
Movement Disorders. 37:651-652
Background Mutations in the GBA gene, which encodes the lysosomal enzyme glucocerebrosidase (GCase), are risk factors for Parkinson's disease (PD). Objective To explore the association between GCase activity, PD phenotype, and probability for prodrom