Author Details

Сметанина, Н. С.

Issue Section Title File
Vol 14, No 3 (2015) CLINICAL OBSERVATIONS A clinical case report of acute intermittent porphyria in a patient aged 9 years PDF
(Rus)
Vol 18, No 3 (2019) ORIGINAL ARTICLES Epilemiological characteristics of Diamond–Blackfen anemia in pediatric population of the Russian Federation PDF
(Rus)
Vol 18, No 3 (2019) ORIGINAL ARTICLES Fisher-Evans Syndrome in Children: an Analysis of Genetic Defects and Therapy Response PDF
(Rus)
Vol 19, No 3 (2020) LITERATURE REVIEW Pyruvat kinase deficiency and nonspherocytic hemolytic anemia PDF
(Rus)
Vol 19, No 4 (2020): supplement MATERIALS OF THE 3rd WORKING MEETING OF ALLERGISTS-IMMUNOLOGISTS Fisher–Evans syndrome in children: an analysis of data from the D. Rogachev NMRCPHOI PDF
(Rus)
Vol 20, No 1 (2021) ШКОЛА ИММУНОЛОГА Rare CVID-like phenotype of autoimmune lymphoproliferative syndrome PDF
(Rus)
Vol 20, No 2 (2021) ORIGINAL ARTICLES Evans syndrome in children: the results of a retrospective study of 54 patients PDF
(Rus)
Vol 20, No 2 (2021) ORIGINAL ARTICLES Non-spherocytic hemolytic anemia caused by erythrocyte pyruvate kinase defiiency: the analysis of genetic defects in pediatric patients, living in Russian Federation PDF
(Rus)
Vol 20, No 3 (2021) ORIGINAL ARTICLES Endothelial dysfunction in patients with hereditary spherocytosis and b-thalassemia PDF
(Rus)
Vol 21, No 3 (2022) ORIGINAL ARTICLES Unstable abnormal hemoglobins found in Russia in the past 10 years PDF
(Rus)
Vol 23, No 2 (2024) ORIGINAL ARTICLES Red blood cell filterability measurement in the diagnosis of hereditary spherocytosis PDF
(Rus)
Vol 24, No 1 (2025) ORIGINAL ARTICLES Von Willebrand factor multimer profile and function in children and young adults with essential thrombocythemia PDF
(Rus)
Vol 24, No 1 (2025) ORIGINAL ARTICLES Selective enrichment of rare bone marrow cell populations for electron microscopy PDF
(Rus)