Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Ibrahim Alcan"'
Autor:
Lucas Jacobs, Bertil Delsaut, Marta Lamartine S. Monteiro, Audrey Cambier, Ibrahim Alcan, Evelyne Maillart, Maxime Taghavi
Publikováno v:
Neurology International, Vol 16, Iss 5, Pp 1112-1121 (2024)
Background. Froin’s syndrome (FS) is a rare entity with uncertain prevalence and prognosis, defined by a pathognomonic triad: cerebrospinal fluid (CSF) xanthochromia, elevated protein levels in the CSF, and hypercoagulated CSF, usually obtained thr
Externí odkaz:
https://doaj.org/article/cf50720035534b3a96fe7cc0fc2b4598
Publikováno v:
Oxford Medical Case Reports. 2022
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::63c88a6f5c0469f94660f833348282c3
https://doi.org/10.1093/omcr/omac011
https://doi.org/10.1093/omcr/omac011
Publikováno v:
Journal of Clinical Neurology (Korea), 10 (2
Journal of Clinical Neurology (Seoul, Korea)
Journal of Clinical Neurology (Seoul, Korea)
Background Inclusion-body myopathy with Paget's disease of the bone and frontotemporal dementia (IBMPFD) is a rare, late-onset autosomal disorder arising from missense mutations in a gene coding for valosin-containing protein. Case Report We report t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c952e967a26e3a4107b8763c0fdb303
https://doi.org/10.3988/jcn.2014.10.2.166
https://doi.org/10.3988/jcn.2014.10.2.166