| Issue |
Section |
Title |
File |
| Vol 4, No 3 (2013) |
Articles |
Mucopolysaccharidosis type I: genetic variants and enzyme replacement therapy experience in Saint-Petersburg |
|
| Vol 5, No 4 (2014) |
Articles |
Higher-dose canakinumab therapy for refractory macrophage activation syndrome in children with systemic juvenile idiopathic arthritis: two case reports |
|
| Vol 12, No 3 (2021) |
Reviews |
Lysosomal storage diseases: mucopolysaccharidosis type I and II |
(Rus)
(Eng)
|
| Vol 12, No 6 (2021) |
Наследственные болезни обмена |
Lysosomal storage diseases. Mucopolysaccharidosis types IV, VI, and VII – Morquio, Maroto–Lamy and Sly syndrome |
|
| Vol 13, No 2 (2022) |
Наследственные болезни обмена |
Lysosomal storage diseases. Sphingolipidoses — Fabry, Gaucher and Farber diseases |
(Rus)
|
| Vol 13, No 4 (2022) |
Editorial |
Lysosomal storage diseases. Sphingolipidoses — sphingomyelin lipidosis, or Niemann–Pick disease, Wolman disease |
|
| Vol 14, No 4 (2023) |
Наследственные болезни обмена |
Lysosomal storage diseases. Sphingolipidoses — gangliosidoses |
|
| Vol 14, No 6 (2023) |
Наследственные болезни обмена |
Lysosomal storage diseases. Sphingolipidoses – leukodystrophy |
|
| Vol 15, No 5 (2024) |
Наследственные болезни обмена |
Lysosomal storage diseases. Mucolipidosis |
|
| Vol 16, No 1 (2025) |
Editorial |
Lysosomal storage diseases. Glycoproteinoses — oligosaccharidoses |
|
