Search Results - "Surkov, Andrey N."

Sodium-Dependent Glucose Transporter Type 2 Inhibitors as a Breakthrough in Neutropenia and Neutrophil Dysfunction Management in Patients with Glycogen Storage Disease Type Ib by Surkov, Andrey N., Namazova-Baranova, Leyla S., Arakelyan, Anna L., Bessonov, Evgeny E., Zhurkova, Natalia V.

“…Glycogen storage disease type Ib (GSD Ib) is a rare and extremely severe disease included in the group of hereditary carbohydrate metabolism disorders. The…”
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Modern View on Very Early Onset and Early Onset Inflammatory Bowel Diseases in Children by Khavkin, Anatoly I., Permyakova, Anastasiya A., Tsepilova, Mariya O., Kaplina, Aleksandra V., Sitkin, Stanislav I., Surkov, Andrey N., Getmanov, Stanislav D.

“…Nowadays, an urgent problem of pediatric gastroenterology is the study of inflammatory bowel diseases with very early onset (VEO-IBD), which have unique…”
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Niemann-Pick Disease, Type A: Clinical Case of 5 Months Old Patient by Zhurkova, Nataliya V., Vashakmadze, Nato V., Surkov, Andrey N., Turti, Tatiana V., Bogdanova, Kristina V., Kotalevskaya, Yuliya Yu, Zakharova, Ekaterina Yu, Namazova-Baranova, Leyla S.

“…Background . Niemann-Pick disease, type A is a rare hereditary disease from the group of lysosomal storage diseases, it is characterized by early onset and…”
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Hereditary Amino Acid Metabolism Disorders and Urea Cycle Disorders: to Practicing Physician by Zhurkova, Nataliya V., Vashakmadze, Nato V., Sergienko, Nataliya S., Dudina, Anastasiya N., Karaseva, Mariya S., Selimzyanova, Liliya R., Rachkova, Anna Yu, Kotalevskaya, Yuliya Yu, Surkov, Andrey N.

“…Hereditary amino acid metabolism disorders (aminoacidopathies) are clinically and genetically heterogeneous group of hereditary metabolic diseases caused by…”
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TNF-α Inhibitor-Induced Psoriasis and Psoriatic Alopecia in Adolescent with Ulcerative Colitis: Clinical Case by Ambarchyan, Eduard T., Ivanchikov, Vladislav V., Arakelyan, Anna L., Surkov, Andrey N., Kuzminova, Anastasia D., Bessonov, Evgeny E., Komarova, Elena V.

“…Background . Genetically engineered biological therapy has revolutionized the treatment of many chronic inflammatory diseases. It often allows to achieve…”
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Linguistic accuracy and authenticity of the content of the Russian version of the module of gastrointestinal symptoms of the PedsQL™ questionnaire for pediatric patients by Arakelyan, Anna L., Surkov, Andrey N., Baranov, Aleksander A., Namazova-Baranova, Leyla S., Gorev, Valeri V., Moskvina, Elena B., Skvorcova, Tamara A., Nikitin, Artem V., Chernikov, Vladislav V.

“…Background. Health Related Quality of Life (HRQL) is a person’s perception of the effect of a disease on physical, social and psychological functioning and…”
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Mitochondrial Fatty Acid Beta-Oxidation Disorders in Children: Literature Review by Zhurkova, Natalia V., Vashakmadze, Nato V., Surkov, Andrey N., Smirnova, Olga Ya, Sergienko, Natalia S., Ovsyanik, Natallia G., Selimzyanova, Lilia R.

“…Congenital mitochondrial fatty acid beta-oxidation disorders are a heterogeneous group of metabolic disorders characterized by impaired fatty acid metabolism…”
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Current Clinical Guidelines for the Management of Patients with Glycogen Storage Disease by Averkina, Natalia A., Bagaeva, Madlena E., Baranov, Aleksander A., Vashakmadze, Nato D., Vishneva, Elena A., Gundobina, Olga S., Zhurkova, Nataliya V., Kaitukova, Elena V., Komarova, Elena V., Margieva, Tea V., Namazova-Baranova, Leyla S., Novikova, Valeria P., Petryaykina, Elena E., Platonova, Mariya M., Potapov, Aleksander S., Smirnova, Olga Ya, Strokova, Tatiana V., Surkov, Andrey N., Taran, Nataliya N., Fedoseenko, Marina V., Semenova, Nataliya A., Anisimova, Inga V., Repina, Svetlana A., Subbotin, Dmitriy M., Sviridova, Valeria V., Havkin, Anatoliy I., Yablokova, Ekaterina A., Volynets, Galina V., Sadovnikova, Irina V., Tumanova, Elena L.

“…Glycogen storage disease refers to hereditary pathologies of carbohydrate metabolism, its cause is mutations of various genes encoding enzymes responsible for…”
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Correlation of Inflammatory Bowel Diseases with Liver Involvement Severity in Autoimmune Hepatobiliary Pathology: Cross-Sectional Study by Usoltseva, Olga V., Surkov, Andrey N., Movsisyan, Goar B., Potapov, Alexander S., Kulebina, Elena A., Kulikov, Кirill A., Chernikov, Vladislav V.

“…Background. Inflammatory bowel diseases (IBD) often occur with hepatobiliary system involvement, including autoimmune ones. The role of IBD in development and…”
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Children with disabilities during the COVID-19 pandemic: medical and social comparative study by Namazova-Baranova, Leyla S., Vishneva, Elena A., Kaytukova, Elena V., Ustinova, Natalia V., Alekseeva, Anna A., Karkashadze, George A., Belyaeva, Irina A., Levina, Julia G., Vashakmadze, Nato D., Fedoseenko, Marina V., Revunenkov, Grigory V., Mamedieiarov, Aiaz M., Surkov, Andrey N., Zelenkova, Irina V., Slipka, Maria I., Pashkov, Aleksandr V., Gordeeva, Olga B., Gorbunova, Elena A., Sadilloeva, Safarbegim H., Katalkina, Kseniya S.

“…Background. The COVID-19 pandemic is a global challenge to States and health systems. The pandemic and its consequences can have a devastating impact on the…”
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Clinical guidelines for the management of children with lysosomal acid lipase deficiency by Anisimova, Inga V., Albegova, Marina B., Bagaeva, Madlena E., Baidakova, Galina V., Baranov, Aleksandr A., Vashakmadze, Nato D., Vishneva, Elena A., Gundobina, Olga S., Degtiareva, Anna V., Ezhov, Marat V., Zharkova, Maria S., Zhurkova, Nataliia V., Zaharova, Ekaterina Yu, Ivashkin, Vladimir T., Kamenets, Elena A., Kutzev, Sergey I., Lavrova, Alla E., Matinian, Irina A., Mikhailova, Svetlana V., Namazova-Baranova, Leyla S., Pashkova, Irina E., Petriaykina, Elena E., Pervunina, Tatiana M., Pechatnikova, Nataliia L., Pogosian, Nelia S., Repina, Svetlana A., Selimzianova, Lilia R., Skvortsova, Tamara A., Strokova, Tatiana V., Subbotin, Dmitriy M., Surkov, Andrey N., Tumanova, Elena L., Tzimbalova, Ekaterina G.

“…Lysosomal acid lipase deficiency is s a rare hereditary enzymopathy. The article presents epidemiological data and features of etiopathogenesis of two…”
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Diagnostic value of anti-GP2 antibodies determined in serum and coprofiltrates in children with inflammatory bowel disease by Toptygina, A. P., Semikina, E. L., Petrichuk, S. V., Potapov, A. S., Surkov, Andrey N.

“…Inflammatory bowel diseases (IBD), such  as Crohn’s disease (CD) and  ulcerative colitis (UC), are characterized by chronically recurring inflammation of…”
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Management of Children with Glycogen Storage Disease (Liver Involvement Forms). Best Practice Guidelines by Baranov, Alexander A., Namazova-Baranova, Leyla S., Surkov, Andrey N., Gundobina, Olga S., Vishneva, Elena A., Margieva, Tea V., Vashakmadze, Nato D., Selimzyanova, Liliya R.

“…Glycogen storage disease is the hereditary carbohydrate metabolism pathology which is caused by mutations in various genes encoding enzymes responsible for…”
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Lysosomal acid lipase deficiency by Zhurkova, Natalya V., Vashakmadze, Nato D., Bokova, Tatyana A., Rykunova, Anastasia I., Surkov, Andrey N., Gundobina, Olga S., Kotalevskaya, Yulia Y., Namazova-Baranova, Leyla S.

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Transient elastographic follow-up hepatic fibrosis stage estimability in children with mucopolysaccharidoses by Surkov, Andrey N., Gevorkyan, Anait K., Vashakmadze, Nato D., Kuzenkova, Ludmila M., Podkletnova, Tatyana V., Babaykina, Marina A., Chernavina, Ekaterina G., Namazova-Baranova, Leyla S.

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