Zobrazeno 1 - 3
of 3
pro vyhledávání: '"L. P. Smertina"'
Publikováno v:
Нервно-мышечные болезни, Vol 9, Iss 2, Pp 43-49 (2019)
Pompe disease is an orphan hereditary accumulation disease associated with a deficiency of the lysosomal enzyme alglucosidase alpha. Manifestations of the disease are associated with pathological deposition of glycogen in body tissues as a result of
Externí odkaz:
https://doaj.org/article/8201702c85ed42e8b8237c24b190c6e3
Autor:
L. P. Smertina, V. Z. Movsumov
Publikováno v:
Сибирский научный медицинский журнал, Vol 38, Iss 4, Pp 98-104 (2019)
Objective - to assess the own experience of human normal immunoglobulin (Privigen, CSL Behring) administration in patients with Guillain - Barre syndrome. Material and methods. Clinical cases of patients with Guillain - Barre syndrome treated with hu
Externí odkaz:
https://doaj.org/article/365dd22bd72f4a8499ec91b0a0edef58
Autor:
V A, Karlov, A A, Savin, L P, Smertina, E G, Redchits, A N, Seleznev, L Iu, Svetaĭlo, N V, Margosiuk, I D, Stulin
Publikováno v:
Zhurnal nevropatologii i psikhiatrii imeni S.S. Korsakova (Moscow, Russia : 1952). 90(11)
As many as 45 patients with multiple sclerosis were examined for rheological blood properties. As compared to controls, the group under examination manifested the rise of plasma viscosity, acceleration of red blood cell aggregation. 26.2% of patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7c701c3487f26c463570ce72024813e2
https://pubmed.ncbi.nlm.nih.gov/1706550
https://pubmed.ncbi.nlm.nih.gov/1706550