Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Tamara, Shiner"'
Autor:
Noa Bregman, Tamara Shiner, Gitit Kavé, Roy Alcalay, Mali Gana-Weisz, Orly Goldstein, Tal Glinka, Orna Aizenstein, Dafna Ben Bashat, Yifat Alcalay, Anat Mirelman, Avner Thaler, Nir Giladi, Nurit Omer
Publikováno v:
BMC Neurology, Vol 23, Iss 1, Pp 1-11 (2023)
Abstract Background Creutzfeldt-Jakob Disease (CJD) is the most common prion disease in humans causing a rapidly progressive neurological decline and dementia and is invariably fatal. The familial forms (genetic CJD, gCJD) are caused by mutations in
Externí odkaz:
https://doaj.org/article/ba96f32651c941c3803b22eb71035d6d
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-9 (2022)
Abstract The prevalence and severity of Multiple Sclerosis (MS) varies across different ethnicities, with a tendency to a more severe phenotype in non-Caucasian populations. Our objective was to evaluate the differences in disease phenotype between A
Externí odkaz:
https://doaj.org/article/e7d53b0137c247d4bc5f73eb39acf8af
Autor:
Noa Bregman, Tamara Shiner, Gitit Kavé, Roy Alcalay, Mali Gana-Weisz, Orly Goldstein, Tal Glinka, Orna Aizenstein, Dafna Ben Bashat, Yifat Alcalay, Anat Mirelman, Avner Thaler, Nir Giladi, Nurit Omer
Publikováno v:
BMC Neurology, Vol 23, Iss 1, Pp 1-1 (2023)
Externí odkaz:
https://doaj.org/article/f93d9ffb6f884497892b2e6226cc357a
Publikováno v:
Journal of Integrative Neuroscience, Vol 19, Iss 3, Pp 489-494 (2020)
Autonomic involvement, including cardiac denervation, may precede the motor symptoms of Parkinson’s disease by several years. L-3,4-dihydroxy-6-[18F] fluoro-phenylalanine is a positron emitter and a true analog of L-dopa, used in clinical practice
Externí odkaz:
https://doaj.org/article/819f30af107f4b49908462cd26663089
Autor:
Orly Goldstein, Mali Gana‐Weisz, Tamara Shiner, Reut Attar, Yael Mordechai, Yedael Y. Waldman, Anat Bar‐Shira, Avner Thaler, Tanya Gurevich, Anat Mirelman, Nir Giladi, Avi Orr‐Urtreger
Publikováno v:
Alzheimer’s & Dementia: Diagnosis, Assessment & Disease Monitoring, Vol 13, Iss 1, Pp n/a-n/a (2021)
Abstract Introduction: The GBA‐N370S mutation is one of the most frequent risk factors for dementia with Lewy bodies (DLB) and Parkinson's disease (PD). We looked for genetic variations that contribute to the outcome in N370S‐carriers, whether PD
Externí odkaz:
https://doaj.org/article/45796b003325402b8743a98f0170fd9b
Autor:
Yevgenia, Rosenblum, Inbal, Maidan, Orly, Goldstein, Mali, Gana-Weisz, Avi, Orr-Urtreger, Noa, Bregman, Nir, Giladi, Anat, Mirelman, Tamara, Shiner
Publikováno v:
Clinical Neurophysiology. 143:14-20
To compare event-related oscillations in patients with dementia with Lewy bodies (DLB) who are carriers and non-carriers of glucocerebrosidase (GBA) mutations.EEG was recorded during a visual oddball task in eight Ashkenazi Jewish DLB patients with t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf94098f13bbed283e153a8155169985
https://doi.org/10.1016/j.clinph.2022.08.011
https://doi.org/10.1016/j.clinph.2022.08.011
Autor:
Yevgenia Rosenblum, Tamara Shiner, Noa Bregman, Nir Giladi, Inbal Maidan, Firas Fahoum, Anat Mirelman
Publikováno v:
Journal of Neurology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::88184e95a6169f6982fa1786b032400d
https://doi.org/10.1007/s00415-023-11728-9
https://doi.org/10.1007/s00415-023-11728-9
Autor:
Noa, Bregman, Tamara, Shiner, Gitit, Kavé, Roy, Alcalay, Mali, Gana-Weisz, Orly, Goldstein, Tal, Glinka, Orna, Aizenstein, Dafna, Ben Bashat, Yifat, Alcalay, Anat, Mirelman, Avner, Thaler, Nir, Giladi, Nurit, Omer
Supplementary Material 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::927d4d84bf9924f256d1a057a7cf22fe
Autor:
Noa, Bregman, Tamara, Shiner, Gitit, Kavé, Roy, Alcalay, Mali, Gana-Weisz, Orly, Goldstein, Tal, Glinka, Orna, Aizenstein, Dafna, Ben Bashat, Yifat, Alcalay, Anat, Mirelman, Avner, Thaler, Nir, Giladi, Nurit, Omer
Supplementary Material 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cfecf52517ddcccf6b26a69fdf41fa5
Autor:
Martine Lederkremer, Orly Goldstein, Avi Orr-Urtreger, Avner Thaler, Nir Giladi, Mali Gana-Weisz, Reut Attar, Anat Bar-Shira, Tamara Shiner, Anat Mirelman
Publikováno v:
Molecular Genetics and Metabolism. 133:109-112
GBA variations are common risk factors for Parkinson's disease (PD), and are found in 21.7% of Ashkenazi PD patients (AJ-PD), 4.23% of them carry an allele, 370Rec, which is different from the common GBA-N370S allele. Using whole-genome-sequencing of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::946108cf85a18043240ab6f6a8275666
https://doi.org/10.1016/j.ymgme.2021.03.012
https://doi.org/10.1016/j.ymgme.2021.03.012