| Issue | 
	Section | 
        Title | 
	File | 
											
				| Vol 16, No 1 (2017) | 
		Статьи | 
		MYH9-related inherited thrombocytopenia | 
		
																		  (Rus)
														 | 
		
												
				| Vol 16, No 1 (2017) | 
		Статьи | 
		Modern approach to diagnosis of inherited functional platelet disorders | 
		
																		  (Rus)
														 | 
		
												
				| Vol 14, No 4 (2015) | 
		CLINICAL OBSERVATIONS | 
		Methemoglobinemias in children (Review of literature and a clinical case report of a child with hemoglobin M Saskatoon) | 
		
																		  (Rus)
														 | 
		
												
				| Vol 17, No 4 (2018) | 
		CLINICAL OBSERVATIONS | 
		The case of rare hereditary thrombocytopenia with a predisposition to the development of acute myeloid leukemia in twin children | 
		
																		  (Rus)
														 | 
		
												
				| Vol 18, No 3 (2019) | 
		ORIGINAL ARTICLES | 
		Fisher-Evans Syndrome in Children: an Analysis of Genetic Defects and Therapy Response | 
		
																		  (Rus)
														 | 
		
												
				| Vol 18, No 3 (2019) | 
		CLINICAL OBSERVATIONS | 
		Clericusio syndrome (poikiloderm with neutropenia) | 
		
																		  (Rus)
														 | 
		
												
				| Vol 19, No 3 (2020) | 
		ORIGINAL ARTICLES | 
		Assessment of informative value of calculated red blood cell indices in the primary diagnosis of thalassemia | 
		
																		  (Rus)
														 | 
		
												
				| Vol 19, No 4 (2020): supplement | 
		MATERIALS OF THE 3rd WORKING MEETING OF ALLERGISTS-IMMUNOLOGISTS | 
		Characteristics of a group of patients with WHIM syndrome | 
		
																		  (Rus)
														 | 
		
												
				| Vol 20, No 1 (2021) | 
		ORIGINAL ARTICLES | 
		Immunophenotypic characterization of pediatric acute myeloid leukemia with inv(16)(p13.1q22)/t(16;16)(p13.1;q22)/CBFb-MYH11 | 
		
																		  (Rus)
														 | 
		
												
				| Vol 20, No 3 (2021) | 
		CLINICAL OBSERVATIONS | 
		Hemorrhagic thrombocytopathy with defective signal transduction CalDAG-GEFI | 
		
																		  (Rus)
														 | 
		
												
				| Vol 21, No 1 (2022) | 
		ORIGINAL ARTICLES | 
		Low specificity of HLA-DR expression for diagnosis of acute promyelocytic leukemia | 
		
																		  (Rus)
														 | 
		
												
				| Vol 21, No 3 (2022) | 
		ORIGINAL ARTICLES | 
		Unstable abnormal hemoglobins found in Russia in the past 10 years | 
		
																		  (Rus)
														 | 
		
												
				| Vol 21, No 3 (2022) | 
		CLINICAL OBSERVATIONS | 
		Rare unstable hemoglobin Hakkari in Russia: a case report and literature review | 
		
																		  (Rus)
														 | 
		
												
				| Vol 22, No 3 (2023) | 
		CLINICAL OBSERVATIONS | 
		Age-dependent changes in platelet function of a patient with SLFN14-related macrothrombocytopenia | 
		
																		  (Rus)
														 | 
		
												
				| Vol 22, No 3 (2023) | 
		ORIGINAL ARTICLES | 
		Using immature platelet fraction as a factor in deciding on the need for platelet transfusions | 
		
																		  (Rus)
														 | 
		
												
				| Vol 23, No 1 (2024) | 
		ORIGINAL ARTICLES | 
		Flow cytometric and cytomorphological definition of remission achievement in children with acute myeloid leukemia | 
		
																		  (Rus)
														 | 
		
												
				| Vol 23, No 2 (2024) | 
		ORIGINAL ARTICLES | 
		Red blood cell filterability measurement in the diagnosis of hereditary spherocytosis | 
		
																		  (Rus)
														 | 
		
												
				| Vol 24, No 1 (2025) | 
		ORIGINAL ARTICLES | 
		The prognostic value of FLT3-ITD in different cytogenetic and molecular genetic subgroups of pediatric acute myeloid leukemia | 
		
																		  (Rus)
														 | 
		
												
				| Vol 24, No 1 (2025) | 
		ORIGINAL ARTICLES | 
		Leukemia with L3 morphology: cytogenetic characterization and diagnostic challenges | 
		
																		  (Rus)
														 | 
		
												
				| Vol 24, No 1 (2025) | 
		ORIGINAL ARTICLES | 
		Pediatric non-Down syndrome acute megakaryoblastic leukemia with GATA1 mutations | 
		
																		  (Rus)
														 | 
		
												
				| Vol 24, No 1 (2025) | 
		ORIGINAL ARTICLES | 
		Preliminary results of treatment of intermediate-risk patients according to the AML-MRD-2018 protocol | 
		
																		  (Rus)
														 |