Search Results - "Fisenko, Andrey"
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The Use of Thoracoscopic Release in the Surgical Correction of Thoracic Scoliosis in Children
Published in Journal of pediatric surgery (17-09-2024)“…Recently, the use of thoracoscopic methods in spinal deformity surgery has increased, however, the issue of the effectiveness of combining anterior release…”
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90 The first clinical case of rare form of focal epilepsy caused by the novel mutation in the NPRL3 gene in Russian federation and kazakhstan
Published in Archives of disease in childhood (11-10-2021)“…ObjectiveMutations in the NPRL3 gene (OMIM 600928) are described predominantly in patients with autosomal dominant focal epilepsy according to the HGMD…”
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Targeted NGS in Diagnostics of Genodermatosis Characterized by the Epidermolysis Bullosa Symptom Complex in 268 Russian Children
Published in International journal of molecular sciences (18-11-2022)“…The pathogenic variants of genes encoding proteins, participating in the formation and functioning of epidermis and dermo-epidermal junctions, create a large…”
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Signatures of Dermal Fibroblasts from RDEB Pediatric Patients
Published in International journal of molecular sciences (11-02-2021)“…The recessive form of dystrophic epidermolysis bullosa (RDEB) is a debilitating disease caused by impairments in the junctions of the dermis and the basement…”
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Lipopolysaccharide From E. coli Increases Glutamate-Induced Disturbances of Calcium Homeostasis, the Functional State of Mitochondria, and the Death of Cultured Cortical Neurons
Published in Frontiers in molecular neuroscience (05-01-2022)“…Lipopolysaccharide (LPS), a fragment of the bacterial cell wall, specifically interacting with protein complexes on the cell surface, can induce the production…”
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Somatostatin analog (octreotide) and sirolimus immunosuppressive therapy in the treatment of chyloperitoneum and chylothorax in newborns and infants
Published in Journal of neonatal surgery (03-01-2024)“…Background: Chyloperitoneum (CP) and chylothorax (CT) are rare conditions that have a high mortality rate and unclear treatment options. Their incidence in…”
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Chromosome and Molecular Analyses Reveal Significant Karyotype Diversity and Provide New Evidence on the Origin of Aegilops columnaris
Published in Plants (Basel) (11-05-2021)“…Zhuk. is tetraploid grass species (2n = 4x = 28, U U X X ) closely related to and growing in Western Asia and a western part of the Fertile Crescent. Genetic…”
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Genetic diversity of storage protein genes in common wheat (Triticum aestivum L.) cultivars from China and its comparison with genetic diversity of cultivars from other countries
Published in Genetic resources and crop evolution (01-04-2011)“…Contemporary trends and perspectives of Chinese winter wheat breeding programs were explored using multiple alleles of gliadin (Gli) and glutenin (Glu)-coding…”
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Pediatric bacteremia and CNS infections associated with klebsiella pneumoniae: molecular genetic characteristics and clinical features
Published in Infekt͡s︡ii͡a︡ i immunitet (02-02-2024)“…Klebsiella pneumoniae is one of the most significant and life-threatening pathogen of nosocomial infections. This opportunistic microorganism can cause…”
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In Search of Spinal Muscular Atrophy Disease Modifiers
Published in International journal of molecular sciences (18-10-2024)“…The 5q Spinal Muscular Atrophy (SMA) is a hereditary autosomal recessive disease caused by defects in the survival motor neuron ( ) gene encoding survival…”
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Clinical Features and Management of the Disease Caused by New Coronaviral Infection (COVID-19) in Children. Version 2
Published in Pediatricheskai͡a︡ farmakologii͡a︡ : nauchno-prakticheskiĭ zhurnal Soi͡u︡za pediatrov Rossii (20-08-2020)“…The Ministry of Health of the Russian Federation jointly with professional association and experts in the field of pediatrics, infectious diseases and…”
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Smell Status in Children Infected with SARS‐CoV‐2
Published in The Laryngoscope (01-08-2021)“…Objectives/Hypothesis This study aimed to evaluate the olfactory status in children with laboratory confirmed SARS‐CoV‐2 using subjective and psychophysical…”
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Our experience of using Losartan for esophageal stenosis in children with dystrophic form of congenital epidermolysis bullosa
Published in Journal of pediatric surgery (01-04-2023)“…Dystrophic epidermolysis bullosa (DEB) is one of the most severe forms of congenital epidermolysis bullosa and characterized by the formation of many surgical…”
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Regulatory Peptide Pro-Gly-Pro Accelerates Neuroregeneration of Primary Neuroglial Culture after Mechanical Injury in Scratch Test
Published in International journal of molecular sciences (10-10-2024)“…The scratch test is used as an experimental in vitro model of mechanical damage to primary neuronal cultures to study the mechanisms of cell death in damaged…”
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Sliding tracheoplasty of complete tracheal cartilage rings in children
Published in Journal of pediatric surgery (01-04-2023)“…Complete tracheal rings are a rare malformation that occurs in 1 out of 100,000 live births. It is rare, isolated tracheal or tracheobronchial anomaly…”
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Clinical features of pediatric Danon disease and the importance of early diagnosis
Published in International journal of cardiology (15-10-2023)“…Successful therapy in a cohort with early onset Danon disease (DD) highlights the potential importance of earlier disease recognition. We present experience…”
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Next generation sequencing is useful for the diagnosis of mucopolysaccharidosis type III in Russian patients
Published in Molecular genetics and metabolism (01-02-2020)Get full text
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Selective screening for nephropathic cystinosis among high-risk contingents of the children population in Russia
Published in Molecular genetics and metabolism (01-02-2020)Get full text
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Genotype-Phenotype Correlations in 293 Russian Patients with Causal Fabry Disease Variants
Published in Genes (28-10-2023)“…Fabry disease (FD) is a rare hereditary multisystem disease caused by variants of the gene. Determination of gene variants and identification of…”
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