期 |
栏目 |
标题 |
文件 |
卷 4, 编号 3 (2013) |
Articles |
Mucopolysaccharidosis type I: genetic variants and enzyme replacement therapy experience in Saint-Petersburg |
|
卷 5, 编号 4 (2014) |
Articles |
Higher-dose canakinumab therapy for refractory macrophage activation syndrome in children with systemic juvenile idiopathic arthritis: two case reports |
|
卷 12, 编号 3 (2021) |
Reviews |
Lysosomal storage diseases: mucopolysaccharidosis type I and II |
![PDF](/img/labels/pdf.png) (Rus)
![PDF](/img/labels/pdf.png) (Eng)
|
卷 12, 编号 6 (2021) |
Наследственные болезни обмена |
Lysosomal storage diseases. Mucopolysaccharidosis types IV, VI, and VII – Morquio, Maroto–Lamy and Sly syndrome |
|
卷 13, 编号 2 (2022) |
Наследственные болезни обмена |
Lysosomal storage diseases. Sphingolipidoses — Fabry, Gaucher and Farber diseases |
![PDF](/img/labels/pdf.png) (Rus)
|
卷 13, 编号 4 (2022) |
Editorial |
Lysosomal storage diseases. Sphingolipidoses — sphingomyelin lipidosis, or Niemann–Pick disease, Wolman disease |
|
卷 14, 编号 4 (2023) |
Наследственные болезни обмена |
Lysosomal storage diseases. Sphingolipidoses — gangliosidoses |
|
卷 14, 编号 6 (2023) |
Наследственные болезни обмена |
Lysosomal storage diseases. Sphingolipidoses – leukodystrophy |
|