FUS-P525L Juvenile Amyotrophic Lateral Sclerosis and Intellectual Disability: Evidence for Association and Oligogenic Inheritance

por Goldstein, Orly, Inbar, Talya, Kedmi, Merav, Gana-Weisz, Mali, Abramovich, Beatrice, Orr-Urtreger, Avi, Drory, Vivian E.
Publicado 2022

C9orf72-G(4)C(2) Intermediate Repeats and Parkinson’s Disease; A Data-Driven Hypothesis

por Kobo, Hila, Goldstein, Orly, Gana-Weisz, Mali, Bar-Shira, Anat, Gurevich, Tanya, Thaler, Avner, Mirelman, Anat, Giladi, Nir, Orr-Urtreger, Avi
Publicado 2021

SPIKE – a database, visualization and analysis tool of cellular signaling pathways

por Elkon, Ran, Vesterman, Rita, Amit, Nira, Ulitsky, Igor, Zohar, Idan, Weisz, Mali, Mass, Gilad, Orlev, Nir, Sternberg, Giora, Blekhman, Ran, Assa, Jackie, Shiloh, Yosef, Shamir, Ron
Publicado 2008

The Effect of GBA Mutations and APOE Polymorphisms on Dementia with Lewy Bodies in Ashkenazi Jews

por Shiner, Tamara, Mirelman, Anat, Rosenblum, Yevgenia, Kavé, Gitit, Weisz, Mali Gana, Bar-Shira, Anat, Goldstein, Orly, Thaler, Avner, Gurevich, Tanya, Orr-Urtreger, Avi, Giladi, Nir, Bregman, Noa
Publicado 2021

R869C mutation in molecular motor KIF17 gene is involved in dementia with Lewy bodies

por Goldstein, Orly, Gana‐Weisz, Mali, Shiner, Tamara, Attar, Reut, Mordechai, Yael, Waldman, Yedael Y., Bar‐Shira, Anat, Thaler, Avner, Gurevich, Tanya, Mirelman, Anat, Giladi, Nir, Orr‐Urtreger, Avi
Publicado 2021

The natural history study of preclinical genetic Creutzfeldt-Jakob Disease (CJD): a prospective longitudinal study protocol

por Bregman, Noa, Shiner, Tamara, Kavé, Gitit, Alcalay, Roy, Gana-Weisz, Mali, Goldstein, Orly, Glinka, Tal, Aizenstein, Orna, Bashat, Dafna Ben, Alcalay, Yifat, Mirelman, Anat, Thaler, Avner, Giladi, Nir, Omer, Nurit
Publicado 2023

Correction: The natural history study of preclinical genetic Creutzfeldt-Jakob Disease (CJD): a prospective longitudinal study protocol

por Bregman, Noa, Shiner, Tamara, Kavé, Gitit, Alcalay, Roy, Gana-Weisz, Mali, Goldstein, Orly, Glinka, Tal, Aizenstein, Orna, Ben Bashat, Dafna, Alcalay, Yifat, Mirelman, Anat, Thaler, Avner, Giladi, Nir, Omer, Nurit
Publicado 2023

Hierarchical Data-Driven Analysis of Clinical Symptoms Among Patients With Parkinson's Disease

por Kozlovski, Tal, Mitelpunkt, Alexis, Thaler, Avner, Gurevich, Tanya, Orr-Urtreger, Avi, Gana-Weisz, Mali, Shachar, Netta, Galili, Tal, Marcus-Kalish, Mira, Bressman, Susan, Marder, Karen, Giladi, Nir, Benjamini, Yoav, Mirelman, Anat
Publicado 2019

Metabolic syndrome does not influence the phenotype of LRRK2 and GBA related Parkinson’s disease

por Thaler, Avner, Shenhar-Tsarfaty, Shani, Shaked, Yanay, Gurevich, Tanya, Omer, Nurit, Bar-Shira, Anat, Gana-Weisz, Mali, Goldstein, Orly, Kestenbaum, Meir, Cedarbaum, Jesse M., Orr-Urtreger, Avi, Giladi, Nir, Mirelman, Anat
Publicado 2020

Mutations in GBA and LRRK2 Are Not Associated with Increased Inflammatory Markers

por Thaler, Avner, Omer, Nurit, Giladi, Nir, Gurevich, Tanya, Bar-Shira, Anat, Gana-Weisz, Mali, Goldstein, Orly, Kestenbaum, Meir, Shirvan, Julia C., Cedarbaum, Jesse M., Orr-Urtreger, Avi, Regev, Keren, Shenhar-Tsarfaty, Shani, Mirelman, Anat
Publicado 2021

Glucocerebrosidase Activity is not Associated with Parkinson's Disease Risk or Severity

por Omer, Nurit, Giladi, Nir, Gurevich, Tanya, Bar‐Shira, Anat, Gana‐Weisz, Mali, Glinka, Tal, Goldstein, Orly, Kestenbaum, Meir, Cedarbaum, Jesse M., Mabrouk, Omar S., Fraser, Kyle B., Shirvan, Julia C., Orr‐Urtreger, Avi, Mirelman, Anat, Thaler, Avner
Publicado 2021