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The Experience of Using Multipotent Mesenchymal Stromal Cells in the Treatment of Severe Recurrent Cholangitis in Children with Biliary Atresia after Kasai Surgery

Bulletin of experimental biology and medicine, 2022-11, Vol.174 (1), p.164-173

2022

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Visceral symptoms as a key diagnostic sign for the early infantile form of Niemann-Pick disease type C in a Russian patient: a case report

Journal of medical case reports, 2016-06, Vol.10 (1), p.143-143, Article 143

2016

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Mitochondrial DNA maintenance disorders in 102 patients from different parts of Russia: Mutational spectrum and phenotypes

Mitochondrion, 2021-03, Vol.57, p.205-212

2021

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Photoinduced Control of Phase State of Monolayers Based on Phospholipids and Spirocompounds

Bulletin of the Russian Academy of Sciences. Physics, 2023-12, Vol.87 (Suppl 3), p.S375-S379

2023

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UPSET RECOVERY TRAINING FOR CIVIL AVIATION PILOTS

Nauchnyĭ vestnik MGTU GA (Online), 2021-02, Vol.24 (1), p.8-15

2021

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Advantages of Kasai procedure through minimally invasive approach in children with biliary atresia

Hirurgija (Moskva), 2019 (3), p.48

2019

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Genetic aspects of biliary atresia etiology

Bulletin of Russian State Medical University, 2020-12 (2020(6))

2020

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CHOLESTASIS, HYPOGLYCEMIA AND UNUSUAL PHENOTYPE AS THE MANIFESTATIONS OF CONGENITAL HYPOPITUITARISM AS PART OF MONOSOMY 18P- SYNDROME

Medical Council, 2018-02 (2), p.233-237

2018

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ULTRASONIC POSSIBILITIES OF DIAGNOSING CHANGES IN KIDNEYS OF CHILDREN WITH ALAGILLE SYNDROME

Medicinskij sovet, 2017-07 (9), p.148-153

2017

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C-Reactive Protein and Procalcitonin Diagnostic Value in Congenital Infection in Newborns with Extremely Low and Very Low Birth Weight

Pediatricheskai͡a︡ farmakologii͡a︡ : nauchno-prakticheskiĭ zhurnal Soi͡u︡za pediatrov Rossii, 2015-11, Vol.12 (4), p.422-428

2015

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Peculiarities of development of deep-preterm infants by 12 months of adjusted age, depending on the rate of escalating enteral nutrition in the early neonatal period

Akusherstvo i ginekologiia, 2018-09, Vol.8_2018, p.152-159

2018

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A clinical case of Streptococcus equi subsp. ruminatorum infection in a 9-year-old child

Rossiĭskiĭ vestnik perinatologii i pediatrii, 2022-06, Vol.67 (2), p.127-131

2022

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Maralixibat is an alternative to liver transplantation in children with Alagille syndrome

Rossiĭskiĭ vestnik perinatologii i pediatrii, 2023-01, Vol.67 (6), p.123-130

2023

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Congenital hypopituitarism with monosomy of chromosome 18

Problemy ėndokrinologii, 2021-09, Vol.67 (4), p.57-67

2021

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Neonatal seizures in extremely preterm infants with very and extremely low birth weight: prevalence and transformation into structural epilepsy

Akusherstvo i ginekologiia, 2021-10, Vol.10_2021, p.134-142

2021

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Hyperammonemia in Neonatologist Practice

Rossiĭskiĭ vestnik perinatologii i pediatrii, 2021-01, Vol.65 (6), p.98-107

2021

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Severe galactosemia of type 1 in a premature baby: difficulties of differential diagnosis

Rossiĭskiĭ vestnik perinatologii i pediatrii, 2020-11, Vol.65 (5), p.73-82

2020

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Therapeutic effect of human umbilical cord-derived multipotent mesenchymal stromal cells in a patient with Crigler–Najjar syndrome type I

Rossiĭskiĭ vestnik perinatologii i pediatrii, 2019-09, Vol.64 (4), p.26-34

2019

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Remote results of treatment of biliary atresia in children

Rossiĭskiĭ vestnik perinatologii i pediatrii, 2019-03, Vol.64 (1), p.46-55

2019

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NEONATAL CHOLESTASIS – ONE OF THE EARLIEST MANIFESTATIONS OF NIEMANN–PICK DISEASE TYPE C

Pediatrija, 2017-01, Vol.96 (1), p.164-170

2017

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Clinical case of Mitochondrial DNA Depletion

Rossiĭskiĭ vestnik perinatologii i pediatrii, 2017-01, Vol.62 (5), p.55-62

2017

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687 Role of Intrauterine Cmv Infection in Formation of Biliary Atresia

Archives of disease in childhood, 2012-10, Vol.97 (Suppl 2), p.A198-A198

2012

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Congenital hypopituitarism with monosomy of chromosome 18

Problemy endokrinologii, 2021-07, Vol.67 (4), p.57

2021

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The experience of using multipotent mesenchymal stromal cells in the treatment of severe recurrent cholangitis in children with biliary atresia after Kasai surgery

Cell Technologies in Biology and Medicine, 2022 (3), p.189-199

2022

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The Y sub 2 Cu sub 2 O sub 5 --BaCuO sub 2 Polythermal Section of the Y sub 2 O sub 3 --BaO--CuO Ternary System

Russian journal of inorganic chemistry, 1990-01, Vol.35 (2), p.258-260

1990

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The Experience of Using Multipotent Mesenchymal Stromal Cells in the Treatment of Severe Recurrent Cholangitis in Children with Biliary Atresia after Kasai Surgery

Visceral symptoms as a key diagnostic sign for the early infantile form of Niemann-Pick disease type C in a Russian patient: a case report

Mitochondrial DNA maintenance disorders in 102 patients from different parts of Russia: Mutational spectrum and phenotypes

Photoinduced Control of Phase State of Monolayers Based on Phospholipids and Spirocompounds

UPSET RECOVERY TRAINING FOR CIVIL AVIATION PILOTS

Advantages of Kasai procedure through minimally invasive approach in children with biliary atresia

Genetic aspects of biliary atresia etiology

CHOLESTASIS, HYPOGLYCEMIA AND UNUSUAL PHENOTYPE AS THE MANIFESTATIONS OF CONGENITAL HYPOPITUITARISM AS PART OF MONOSOMY 18P- SYNDROME

ULTRASONIC POSSIBILITIES OF DIAGNOSING CHANGES IN KIDNEYS OF CHILDREN WITH ALAGILLE SYNDROME

C-Reactive Protein and Procalcitonin Diagnostic Value in Congenital Infection in Newborns with Extremely Low and Very Low Birth Weight

Peculiarities of development of deep-preterm infants by 12 months of adjusted age, depending on the rate of escalating enteral nutrition in the early neonatal period

A clinical case of Streptococcus equi subsp. ruminatorum infection in a 9-year-old child

Maralixibat is an alternative to liver transplantation in children with Alagille syndrome

Congenital hypopituitarism with monosomy of chromosome 18

Neonatal seizures in extremely preterm infants with very and extremely low birth weight: prevalence and transformation into structural epilepsy

Hyperammonemia in Neonatologist Practice

Severe galactosemia of type 1 in a premature baby: difficulties of differential diagnosis

Therapeutic effect of human umbilical cord-derived multipotent mesenchymal stromal cells in a patient with Crigler–Najjar syndrome type I

Remote results of treatment of biliary atresia in children

NEONATAL CHOLESTASIS – ONE OF THE EARLIEST MANIFESTATIONS OF NIEMANN–PICK DISEASE TYPE C

Clinical case of Mitochondrial DNA Depletion

687 Role of Intrauterine Cmv Infection in Formation of Biliary Atresia

Congenital hypopituitarism with monosomy of chromosome 18

The experience of using multipotent mesenchymal stromal cells in the treatment of severe recurrent cholangitis in children with biliary atresia after Kasai surgery

The Y sub 2 Cu sub 2 O sub 5 --BaCuO sub 2 Polythermal Section of the Y sub 2 O sub 3 --BaO--CuO Ternary System

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