| Issue |
Section |
Title |
File |
| Vol 18, No 2 (2019) |
CLINICAL OBSERVATIONS |
The phenomenon of conversion of the donor-derived blood group to the patient’s original blood group after ABO-incompatible hematopoietic stem cell transplantation in a patient with Wiskott–Aldrich syndrome |
(Rus)
|
| Vol 19, No 1 (2020) |
CLINICAL SIGNIFICANCE OF BASIC RESEARCH |
Specific features of intracellular calcium signalling, distinctive for Wiskott-Aldrich syndrome patients |
(Rus)
|
| Vol 19, No 1 (2020) |
ШКОЛА ИММУНОЛОГА |
Rosay–Dorfman – like lymphadenopathy in a patient with Wiskott–Aldrich syndrome: diagnostic difficulties |
(Rus)
|
| Vol 19, No 2 (2020) |
ORIGINAL ARTICLES |
Development of flow cytometry assay for Wiskott–Aldrich syndrome diagnosis by WASP protein evaluation |
(Rus)
|
| Vol 19, No 4 (2020): supplement |
MATERIALS OF THE 3rd WORKING MEETING OF ALLERGISTS-IMMUNOLOGISTS |
The efficacy and safety of romiplostim in the treatment of thrombocytopenia in pediatric patients with Wiskott–Aldrich syndrome: the results of a retrospective study |
(Rus)
|
| Vol 19, No 4 (2020): supplement |
MATERIALS OF THE 3rd WORKING MEETING OF ALLERGISTS-IMMUNOLOGISTS |
Non-infectious complications in the group of pediatric patients with chronic granulomatous disease |
(Rus)
|
| Vol 19, No 4 (2020): supplement |
MATERIALS OF THE 3rd WORKING MEETING OF ALLERGISTS-IMMUNOLOGISTS |
Chromosomal aberrations as the cause of a complex phenotype in children with primary immunodeficiencies |
(Rus)
|
| Vol 20, No 2 (2021) |
SCHOOL OF IMMUNOLOGY – EXPERT OPINION |
Long-term persistent mixed chimerism in a patient with Wiskott–Aldrich syndrome after allogeneic hematopoietic stem cell transplantation |
(Rus)
|
| Vol 20, No 2 (2021) |
SCHOOL OF IMMUNOLOGY – EXPERT OPINION |
Long-term persistent mixed chimerism in a patient with Wiskott–Aldrich syndrome after allogeneic hematopoietic stem cell transplantation |
(Rus)
|
| Vol 20, No 3 (2021) |
SCHOOL OF IMMUNOLOGY – EXPERT OPINION |
Clinical case of type I interferonopathy: homozygous STAT2 gain-of-function mutation |
(Rus)
|
| Vol 21, No 4 (2022) |
SCHOOL OF IMMUNOLOGY – EXPERT OPINION |
A case report of autoinflammation and PLCy2-associated antibody deficiency and immune dysregulation |
(Rus)
|
| Vol 21, No 4 (2022) |
CLINICAL OBSERVATIONS |
Newborn screening for primary immunodeficiencies as a way to detect syndromal disorders in neonates: a clinical case of 22q11.2DS syndrome |
(Rus)
|
| Vol 22, No 3 (2023) |
ORIGINAL ARTICLES |
A single-center experience of using immunofluorescence staining of blood smears for the diagnosis of hereditary thrombocytopathies |
(Rus)
|
