Search Results - "Fisenko, Andrey"

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    The Use of Thoracoscopic Release in the Surgical Correction of Thoracic Scoliosis in Children by Chelpachenko, Oleg B., Gusev, Aleksey A., Pimbursky, Ivan P., Butenko, Andrey S., Samokhin, Konstantin A., Zherdev, Konstantin V., Yatsyk, Sergey P., Fisenko, Andrey P., Dyakonova, Elena Yu

    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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    Journal Article
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    Signatures of Dermal Fibroblasts from RDEB Pediatric Patients by Beilin, Arkadii K, Evtushenko, Nadezhda A, Lukyanov, Daniil K, Murashkin, Nikolay N, Ambarchian, Eduard T, Pushkov, Alexander A, Savostyanov, Kirill V, Fisenko, Andrey P, Rogovaya, Olga S, Vasiliev, Andrey V, Vorotelyak, Ekaterina A, Gurskaya, Nadya G

    “…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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    Chromosome and Molecular Analyses Reveal Significant Karyotype Diversity and Provide New Evidence on the Origin of Aegilops columnaris by Badaeva, Ekaterina D, Chikida, Nadezhda N, Fisenko, Andrey N, Surzhikov, Sergei A, Belousova, Maria K, Özkan, Hakan, Dragovich, Alexandra Y, Kochieva, Elena Z

    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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    Pediatric bacteremia and CNS infections associated with klebsiella pneumoniae: molecular genetic characteristics and clinical features by Sadeeva, Zulfirya Z., Novikova, Irina E., Lazareva, Anna V., Alyabyeva, Natalya M., Karaseva, Olga V., Yanushkina, Olga G., Verschinina, Marina G., Fisenko, Andrey P.

    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 by Chudakova, Daria, Kuzenkova, Ludmila, Fisenko, Andrey, Savostyanov, Kirill

    “…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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    Smell Status in Children Infected with SARS‐CoV‐2 by Rusetsky, Yury, Meytel, Irina, Mokoyan, Zhanna, Fisenko, Andrey, Babayan, Anna, Malyavina, Ulyana

    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 by Oldakovskiy, Vladislav, Murashkin, Nikolay, Lokhmatov, Maksim, Gusev, Aleksey, Tupylenko, Artem, Budkina, Tatiana, Yatzik, Sergey, Dyakonova, Elena, Abaykhanov, Rasul, Fisenko, Andrey

    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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    Sliding tracheoplasty of complete tracheal cartilage rings in children by Alkhasov, Abdumanap, Ratnikov, Sergey, Lezhnev, Alexandr, Razumovskiy, Aleksandr, Sergeeva, Irina, Kuzin, Sergey, Komina, Elena, Gusev, Aleksey, Yatzik, Sergey, Romanova, Ekaterina, Savelieva, Maria, Fisenko, Andrey

    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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    Genotype-Phenotype Correlations in 293 Russian Patients with Causal Fabry Disease Variants by Savostyanov, Kirill, Pushkov, Alexander, Zhanin, Ilya, Mazanova, Natalya, Pakhomov, Alexander, Trufanova, Elena, Alexeeva, Alina, Sladkov, Dmitry, Kuzenkova, Ludmila, Asanov, Aliy, Fisenko, Andrey

    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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