Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Emna Ellouz"'
Autor:
Imen Ketata, Emna Ellouz
Publikováno v:
Rare, Vol 1, Iss , Pp 100010- (2023)
Background and purpose: Aceruloplasminemia is an uncommon genetic disorder with considerable diversity in clinical manifestations and tissue iron overload, whose underlying mechanisms are unclear. We aim to explain early and follow-up clinical/biolog
Externí odkaz:
https://doaj.org/article/0b52ab5109844166b662d192e47efa85
Publikováno v:
Revue Neurologique. 179:S46
Publikováno v:
Multiple Sclerosis and Related Disorders. 71:104344
Publikováno v:
Multiple Sclerosis and Related Disorders. 71:104305
Publikováno v:
Multiple Sclerosis and Related Disorders. 71:104308
Publikováno v:
Multiple Sclerosis and Related Disorders. 71:104325
Publikováno v:
Revue Neurologique. 178:S132
Autor:
Sondes Bader, Emna Ellouz
Publikováno v:
Multiple Sclerosis and Related Disorders. 59:103604
Publikováno v:
Multiple Sclerosis and Related Disorders. 59:103598
Publikováno v:
Multiple Sclerosis and Related Disorders. 59:103603