Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Tal, Glinka"'
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
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
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:
Nurit Omer, Rawan Silbak, Noa Trabulus, Mali Gana‐Weisz, Orly Goldstein, Tal Glinka, Avi Orr‐Urterger, Nir Giladi, Amgad Droby, Noa Bregman
Publikováno v:
Alzheimer's & Dementia. 17
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::79bd948a76f1cbe32bdcdaf4b869e68e
https://doi.org/10.1002/alz.057783
https://doi.org/10.1002/alz.057783
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11f2104ad5b0a986e2043d7eff032c72
https://doi.org/10.1002/mds.28929
https://doi.org/10.1002/mds.28929
Autor:
Lolita Tzach, Chia Wei Sheng, Mariola J. Edelmann, Ariel Stanhill, Ilana Braunstein, Tal Glinka, Benedikt M. Kessler, Joel Alter, Susana Geifman
Protein homoeostasis is a fundamental requirement for all living cells in order to survive in a dynamic surrounding. Proper levels of AIRAPL (arsenite-inducible RNA-associated protein-like protein) (ZFAND2B) are required in order to maintain cellular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10d3208733b8d432e463b2b69e9493f4
https://ora.ox.ac.uk/objects/uuid:a5b55e32-ad7b-4f9e-8ff3-96f1e0384983
https://ora.ox.ac.uk/objects/uuid:a5b55e32-ad7b-4f9e-8ff3-96f1e0384983