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FEATURES OF CHILDREN’S PSYCHO-EMOTIONAL STATE WITH NEWLY DIAGNOSED TYPE I DIABETES

Visnyk problem biolohiï i medyt︠s︡yny, 2020-12, Vol.4 (1), p.306-309

2020

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A CLINICAL CASE OF MULTISYSTEM INFLAMMATORY SYNDROME IN A 12-YEAR-OLD CHILD

Visnyk problem biolohiï i medyt︠s︡yny, 2022, Vol.2 (2), p.201

2022

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TO THE 60TH ANNIVERSARY OF THE BIRTH OF VALERII IVANOVYCH POKHYLKO

Visnyk problem biolohiï i medyt︠s︡yny, 2024, Vol.1 (1), p.8

2024

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CLINICAL CASE OF DIFFUSE TOXIC GOITER IN THREE YEARS OLD CHILD

Visnyk problem biolohiï i medyt︠s︡yny, 2019, Vol.3 (152), p.209

2019

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THE ROLE OF 4a4b POLYMORPHISM OF THE eNOS GENE IN THE DEVELOPMENT OF LETHAL OUTCOMES OF SEVERE INTRAVENTRICULAR HAEMORRHAGE IN PRETERM INFANTS

Visnyk problem biolohiï i medyt︠s︡yny, 2018, Vol.4.3 (141), p.95

2018

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CONTINUOUS TRAINING THE PREREQUISITE OF A DOCTOR S PROFESSIONALISM IN MODERN CONDITIONS

Visnyk problem biolohiï i medyt︠s︡yny, 2018, Vol.4, p.183

2018

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CONTINUOUS TRAINING - THE PREREQUISITE OF A DOCTORS PROFESSIONALISM IN MODERN CONDITIONS

Visnyk problem biolohiï i medyt︠s︡yny, 2018-11, Vol.1 (4), p.183-185

2018

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PRIMARY DIAGNOSTICS OF CYSTIC FIBROSIS IN A 10-YEARS-OLD CHILD (CASE REPORT)

Visnyk problem biolohiï i medyt︠s︡yny, 2018, Vol.1.2 (144), p.219

2018

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INTEGRATED MODEL FOR THE PREDICTION OF ORGANIC DYSFUNCTIONS DEVELOPMENT IN NEWBORNS WITH ASPHYXIA AND APPLIED POINTS OF ITS IMPLEMENTATION

Neonatolohii︠a︡, khirurhii︠a︡ ta perynatalʹna medyt︠s︡yna, 2017-12, Vol.7 (4(26)), p.24-30

2017

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Readiness of clinical laboratory diagnostics and cardiologists to implement the recommendations of the fourth universal definition of myocardial infarction

Russian Clinical Laboratory Diagnostics, 2021-11, Vol.66 (11), p.695-704

2021

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ELECTROCARDIOGRAPHIC CHANGES IN NEWBORNS FROM MOTHERS WITH METABOLIC SYNDROME

Wiadomości lekarskie (1960), 2021, Vol.74 (6), p.1349-1354

2021

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Bronchial fistula management. Is the exit found?

Hirurgija (Moskva), 2018 (3. Vyp. 2), p.33

2018

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Flow cytometric analysis of leukemic blast cells in pediatric B-cell precursor acute lymphoblastic leukemia with translocation t(12;21)(p13;q22)/ETV6-RUNX1

Onkogematologii͡a, 2019-01, Vol.13 (4), p.93-103

2019

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EXPERIENCE OF TREATMENT OF FISTULA OF RIGHT MAIN BRONCHUS STUMP WITH THE USE OF VASCULAR OCCLUDER

Tuberkulëz i bolezni lëgkikh, 2017-01, Vol.95 (1), p.51-55

2017

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SIGNIFICANCE OF ETV6-RUNX1 FUSION GENE TRANSCRIPT DETECTION IN PEDIATRIC B-CELL PRECURSOR ACUTE LYMPHOBLASTIC LEUKEMIA WITH TRANSLOCATION t(12;21)(p13;q22)

Onkogematologii͡a, 2018-02, Vol.12 (4), p.57-70

2018

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Prognostic value of the determination of bone marrow lesion in patients with neuroblastoma based on the gene PHOX2B and TH expression

Voprosy onkologij, 2014, Vol.60 (2), p.57

2014

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Methods of detection and prognostic significance of genetic material increase of the short arm of chromosome 2 and a deletion of the short arm of chromosome 1 in patients with neuroblastoma

Voprosy onkologij, 2013, Vol.59 (5), p.591

2013

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THE COMPARISON OF RESULTS OF DETECTION OF MINIMAL RESIDUAL DISEASE IN PERIPHERAL BLOOD AND MARROW IN CHILDREN OF THE FIRST YEAR OF LIFE WITH ACUTE LYMPHOBLASTIC LEUCOSIS

Klinicheskaia laboratornaia diagnostika, 2015-04, Vol.60 (4), p.14

2015

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Experience of tracheo-bronchoplastic surgery for lung cancer

Ural Medical Journal, 2021-11, Vol.20 (4), p.46-52

2021

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The TH, ELAVL4 and GD2 gene expression as diagnostic markers of bone marrow lesions in patients with neuroblastoma

Voprosy onkologij, 2012, Vol.58 (4), p.514

2012

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The limited possibility of using a simplified approach to detect minimal residual disease by the flow cytometry technique in children with precursor B-lineage acute lymphoblastic leukemia

Klinicheskaia laboratornaia diagnostika, 2011-03 (3), p.25

2011

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Minimal residual disease monitoring by flow cytometry in children with acute lymphoblastic leukemia

Klinicheskaia laboratornaia diagnostika, 2010-08 (8), p.36

2010

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Application of cytogenetic risk factors and molecular markers, assessed by multiplex ligation-dependent probe amplification for prognosis of outcome in pediatric B-cell precursor acute lymphoblastic leukemia do not bring any advantage over detection of isolated IKZF1 deletion

Russian Journal of Children Hematology and Oncology, 2018-02, Vol.5 (1), p.34-43

2018

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Fluorescent method of studying the binding sites of serum albumin for assessing status of patients with purulent-septic diseases

Vestnik hirurgii im. I.I. Grekova, 2001, Vol.160 (4), p.87

2001

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FEATURES OF CHILDREN’S PSYCHO-EMOTIONAL STATE WITH NEWLY DIAGNOSED TYPE I DIABETES

A CLINICAL CASE OF MULTISYSTEM INFLAMMATORY SYNDROME IN A 12-YEAR-OLD CHILD

TO THE 60TH ANNIVERSARY OF THE BIRTH OF VALERII IVANOVYCH POKHYLKO

CLINICAL CASE OF DIFFUSE TOXIC GOITER IN THREE YEARS OLD CHILD

THE ROLE OF 4a4b POLYMORPHISM OF THE eNOS GENE IN THE DEVELOPMENT OF LETHAL OUTCOMES OF SEVERE INTRAVENTRICULAR HAEMORRHAGE IN PRETERM INFANTS

CONTINUOUS TRAINING THE PREREQUISITE OF A DOCTOR S PROFESSIONALISM IN MODERN CONDITIONS

CONTINUOUS TRAINING - THE PREREQUISITE OF A DOCTORS PROFESSIONALISM IN MODERN CONDITIONS

PRIMARY DIAGNOSTICS OF CYSTIC FIBROSIS IN A 10-YEARS-OLD CHILD (CASE REPORT)

INTEGRATED MODEL FOR THE PREDICTION OF ORGANIC DYSFUNCTIONS DEVELOPMENT IN NEWBORNS WITH ASPHYXIA AND APPLIED POINTS OF ITS IMPLEMENTATION

Readiness of clinical laboratory diagnostics and cardiologists to implement the recommendations of the fourth universal definition of myocardial infarction

ELECTROCARDIOGRAPHIC CHANGES IN NEWBORNS FROM MOTHERS WITH METABOLIC SYNDROME

Bronchial fistula management. Is the exit found?

Flow cytometric analysis of leukemic blast cells in pediatric B-cell precursor acute lymphoblastic leukemia with translocation t(12;21)(p13;q22)/ETV6-RUNX1

EXPERIENCE OF TREATMENT OF FISTULA OF RIGHT MAIN BRONCHUS STUMP WITH THE USE OF VASCULAR OCCLUDER

SIGNIFICANCE OF ETV6-RUNX1 FUSION GENE TRANSCRIPT DETECTION IN PEDIATRIC B-CELL PRECURSOR ACUTE LYMPHOBLASTIC LEUKEMIA WITH TRANSLOCATION t(12;21)(p13;q22)

Prognostic value of the determination of bone marrow lesion in patients with neuroblastoma based on the gene PHOX2B and TH expression

Methods of detection and prognostic significance of genetic material increase of the short arm of chromosome 2 and a deletion of the short arm of chromosome 1 in patients with neuroblastoma

THE COMPARISON OF RESULTS OF DETECTION OF MINIMAL RESIDUAL DISEASE IN PERIPHERAL BLOOD AND MARROW IN CHILDREN OF THE FIRST YEAR OF LIFE WITH ACUTE LYMPHOBLASTIC LEUCOSIS

Experience of tracheo-bronchoplastic surgery for lung cancer

The TH, ELAVL4 and GD2 gene expression as diagnostic markers of bone marrow lesions in patients with neuroblastoma

The limited possibility of using a simplified approach to detect minimal residual disease by the flow cytometry technique in children with precursor B-lineage acute lymphoblastic leukemia

Minimal residual disease monitoring by flow cytometry in children with acute lymphoblastic leukemia

Application of cytogenetic risk factors and molecular markers, assessed by multiplex ligation-dependent probe amplification for prognosis of outcome in pediatric B-cell precursor acute lymphoblastic leukemia do not bring any advantage over detection of isolated IKZF1 deletion

Fluorescent method of studying the binding sites of serum albumin for assessing status of patients with purulent-septic diseases

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