Author

К. В. Савостьянов

Observed names: K V Savost'ianov, K. Savostianov, K. V. Savostianov, K. V. Savostyanov, KV Savostyanov, Kirill Savostianov, Kirill Savost’ianov, Kirill V Savostianov, Kirill V. Savostianov, К. V. Savostianov, К.В. Савостьянов, Кирилл Викторович Савостьянов, Кирилл Савостьянов, Савостьянов К. В., Савостьянов Кирилл Викторович, Савостьянов, К.В.

Institution: Ministry of Health of the Russian Federation

Observed institutions: Sechenov University, Ministry of Health of the Russian Federation, Scientific Center of Children's Health, Genetika

ORCID: 0000-0003-4885-4171

Observed ORCID: 0000-0003-4885-4171

OpenAlex ID: A5113482707

Руководство по интерпретации данных последовательности ДНК человека, полученных методами массового параллельного секвенирования (MPS) (редакция 2018, версия 2)

2020 · О.П. Рыжкова, О.Л. Кардымон, et al. · Nauchno-prakticheskii zhurnal «Medicinskaia genetika» · 132

Deficiency of Lysosomic Acid Lipase: Clinical Recommendations for Child Health Care Delivery

2016 · A. A. Baranov, L. S. Namazova-Baranova, et al. · Педиатрическая фармакология · 20

Methylmalonic Aciduria in Children: Clinical Recommendations

2017 · Alexander A. Baranov, Leyla S. Namasova-Baranova, et al. · Педиатрическая фармакология · 10

[Polymorphic locus D6S392 near the Mn-dependent superoxide dismutase gene is associated with diabetes mellitus in the Moscow population].

2002 · K V Savost'ianov, D A Chistiakov, et al. · PubMed · 9

Clinical Recommendation to the Diagnostics and Treatment of Hypophosphatasia in Children

2016 · A. A. Baranov, L. S. Namazova-Baranova, et al. · Педиатрическая фармакология · 8

Federal Clinical Guidelines on Rendering Help to Children with Hemolytic Uremic Syndrome

2015 · A. N. Tsygin, T. V. Vashurina, et al. · Педиатрическая фармакология · 7

A kinetic assay of total lipase activity for detecting lysosomal acid lipase deficiency (LAL‐D) and the molecular characterization of 18 LAL‐D patients from Russia

2019 · Nikolay Mayanskiy, Ekaterina Brzhozovskaya, et al. · JIMD Reports · 6

Genetic Determination of Bronchopulmonary Dysplasia Formation: Pros and Cons

2017 · V. K. Pozharishchenskaya, I. V. Davydova, et al. · Педиатрическая фармакология · 5

Neurogenetic Aspects of Perinatal Hypoxic-ischemic Affections of the Central Nervous System

2016 · G. A. Karkashadze, K. V. Savostianov, et al. · Вопросы современной педиатрии · 3

The role of globotriaosylsphingosine in the diagnosis of Fabry disease in Russian patients

2020 · Н.Н. Мазанова, А.А. Пушков, et al. · Nauchno-prakticheskii zhurnal «Medicinskaia genetika» · 2

High Efficiency of Kanakinumabum for a Patient with a Late Diagnosed Chronic Infantile Neurological Cutaneous Articular Syndrome (CINCA)

2015 · T. V. Sleptsova, E. I. Alekseeva, et al. · Педиатрическая фармакология · 2

Common variants of the mineralocorticoid and glucocorticoid receptor genes may contribute to pregnancy-related anxiety: a pilot study

2012 · Natalia Chistiakova, Elena Sergienko, et al. · Open Medicine · 2

423 Genetic predictors of a new form of bronchopulmonary dysplasia

2021 · VA Bondar, IV Davydova, et al. · Abstracts · 1

Two siblings with attenuated MPS II form: Long term enzyme replacement therapy

2021 · Nato Vashakmadze, Leyla Namazova-Baranova, et al. · Molecular Genetics and Metabolism · 1

Case of Enteropathic Acrodermatitis Due To Genetic Mutations Not Previously Described in Literature

2016 · T. V. Kulichenko, Yu. S. Lashkova, et al. · Вопросы современной педиатрии · 1

Trans-2,3-enoyl-CoA reductase-like-related catecholaminergic polymorphic ventricular tachycardia in a child: Clinical course and management outcomes

2026 · E. K. Kulbachinskaya, A. A. Pushkov, et al. · Annals of Pediatric Cardiology

Dilated cardiomyopathy in the structure of a familial form of TOP3A-related Bloom-like syndrome

2026 · Yu. S. Burykina, L. A. Gandaeva, et al. · L O Badalyan Neurological Journal

Clinical and genetic characteristics of Russian children with Dent's disease and Lowe syndrome: a single-center experience

2026 · A. M. Milovanova, P. V. Ananin, et al. · Nephrology and Dialysis

Clinical, laboratory, and radiological characteristics of lung damage in pediatric patients hospitalized with bronchial asthma and bronchiectasis

2025 · N. I. Kolganova, D. Yu. Ovsyannikov, et al. · Archives of Pediatrics and Pediatric Surgery

2025 · Милана Александровна Басаргина, Кирилл Викторович Савостьянов, et al. · Russian Pediatric Journal

Bronchial asthma in children with primary ciliary dyskinesia: two clinical cases

2025 · Maxim A Karpenko, Dmitriy Yu Ovsyannikov, et al. · Clinical review for general practice

Клинико-генетическая характеристика рестриктивной кардиомиопатии у детей, обусловленной патогенными вариантами в гене TNNI3

2024 · Н.А. Сдвигова, Е.Н. Басаргина, et al. · CHILDREN’S HEART AND VASCULAR DISEASES

Гипертрофическая кардиомиопатия в структуре RAS-патий у детей

2022 · Л.А. Гандаева, В.Г. Каверина, et al. · CHILDREN’S HEART AND VASCULAR DISEASES

Clinical heterogenity of Russian children with a CRB2 gene defect

2021 · Милованова, А.М., Вашурина, Т.В., et al. · Nauchno-prakticheskii zhurnal «Medicinskaia genetika»

94 Clinical and Genetic Spectrum of Dystroglycanopathy Due to POMGNT1 Mutations in Russian Patients

2021 · OB Kondakova, KV Savostyanov, et al. · Abstracts

Works count: 49

Citation count: 210

H-index: 6

I10-index: 3