Genetic <scp>Creutzfeldt‐Jakob</scp> disease in Turkish Jews—demographic and clinical features-Reference-Cited by-同舟云学术

Genetic Creutzfeldt‐Jakob disease in Turkish Jews—demographic and clinical features

Published:2022-08-16 Issue:5 Volume:146 Page:586-589
ISSN:0001-6314
Container-title:Acta Neurologica Scandinavica
language:en
Short-container-title:Acta Neuro Scandinavica

Author:

Menendez Leslie¹,Milo Ron¹²,Cohen Oren S.³⁴,Chapman Joab⁴⁵,Rosenmann Hanna⁶,Nitsan Zeev¹²,Kahana Esther¹²,Appel Shmuel¹²^ORCID

Affiliation:

1. Department of Neurology Barzilai University Medical Center Ashkelon Israel

2. Faculty of Health Sciences Ben Gurion University of the Negev Beer‐Sheva Israel

3. Department of Neurology Assaf Harofeh Medical Center Zerifin Israel

4. Robert and Martha Harden Chair in Mental and Neurological Diseases, Sackler Faculty of Medicine Tel Aviv University Tel Aviv Israel

5. Department of Neurology The Sagol Neuroscience Center, and Chaim Sheba Medical Center Ramat Gan Israel

6. Department of Neurology, The Agnes Ginges Center for Human Neurogenetics, Hadassah Medical Organization, Faculty of Medicine Hebrew University Jerusalem Israel

Publisher

Hindawi Limited

Subject

Neurology (clinical),Neurology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ane.13684

Reference27 articles.

1. Prion Disease

2. Rapidly progressive Creutzfeldt-Jakob disease in patients with Familial Mediterranean Fever

3. PRION DISEASES

4. Prion disease in Indigenous Australians

5. Mortality trend from sporadic Creutzfeldt-Jakob disease (CJD) in Italy, 1993–2000

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Updated global epidemiology atlas of human prion diseases;Frontiers in Public Health;2024-06-13