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pro vyhledávání: '"Madara K"'
Akademický článek
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Publikováno v:
International Journal of Abdominal Wall and Hernia Surgery, Vol 4, Iss 3, Pp 83-89 (2021)
BACKGROUND: Meckel’s diverticulum (MD) is the most prevalent congenital anomaly of the gastrointestinal tract with an estimated prevalence ranging from 2% to 4%. The diverticulum is a remnant of the vitelline duct, which leads to the formation of a
Externí odkaz:
https://doaj.org/article/bf60df80f7a247be8414aefe8bb78b84
Autor:
Lilite Sadovska, Jānis Auders, Laura Keiša, Nadezhda Romanchikova, Laila Silamiķele, Madara Kreišmane, Pawel Zayakin, Satoru Takahashi, Zane Kalniņa, Aija Linē
Publikováno v:
Frontiers in Molecular Biosciences, Vol 8 (2022)
Increasing evidence suggests that regular physical exercise not only reduces the risk of cancer but also improves functional capacity, treatment efficacy and disease outcome in cancer patients. At least partially, these effects are mediated by the se
Externí odkaz:
https://doaj.org/article/231e6456437640969a019fbaf142bb42
Autor:
Kristine Vaivode, Irina Verhovcova, Dace Skrastina, Ramona Petrovska, Madara Kreismane, Daira Lapse, Zane Kalnina, Kristine Salmina, Diana Rubene, Dace Pjanova
Publikováno v:
Pharmaceuticals, Vol 15, Iss 9, p 1053 (2022)
Bacteriophage-derived dsRNA, known as Larifan, is a nationally well-known broad-spectrum antiviral medication. This study aimed to ascertain the antiviral activity of Larifan against the novel SARS-CoV-2 virus. Larifan’s effect against SARS-CoV-2 i
Externí odkaz:
https://doaj.org/article/456452f86f3043da8f4a525dc0f91bbd
Autor:
Arta Katkevica, Madara Kreile, Ieva Grinfelde, Gita Taurina, Ieva Micule, Iveta Dzivite-Krisane, Arta Smite-Laguna, Ieva Malniece
Publikováno v:
Case Reports in Medicine, Vol 2021 (2021)
Leigh syndrome is a neurodegenerative disorder with an incidence of 1 : 40,000 live births. The clinical presentation of LS is highly variable with heterogeneity in the disease-associated symptoms of cerebellar, motor, and extrapyramidal dysfunction
Externí odkaz:
https://doaj.org/article/0a2a163ec95f41babe723e6e2379e8b8
Autor:
Linda Gailite, Alberto Valenzuela-Palomo, Lara Sanoguera-Miralles, Dmitrijs Rots, Madara Kreile, Eladio A. Velasco
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
A large fraction of DNA variants impairs pre-mRNA splicing in human hereditary disorders. Crigler-Najjar syndrome (CNS) is characterized by a severe unconjugated hyperbilirubinemia caused by variants in the UGT1A1 gene. We previously reported one CNS
Externí odkaz:
https://doaj.org/article/1c8b08301f3148cc96b7f111e1d9ec0f
Autor:
Ieva Nokalna, Madara Kreile, Dagnija Butane, Zhanna Kovalova, Zanda Daneberga, Edvins Miklasevics, Dace Gardovska, Linda Gailite
Publikováno v:
Case Reports in Medicine, Vol 2020 (2020)
X-linked lymphoproliferative disease (XLP) is a rare primary immunodeficiency. Affected individuals usually present with the Epstein–Barr virus infection and have no apparent disease prior to presentation. The most common clinical manifestations ar
Externí odkaz:
https://doaj.org/article/16ac6b382db74baeb4679d911066edcf
Publikováno v:
BMC Pediatrics, Vol 18, Iss 1, Pp 1-5 (2018)
Abstract Background Inherited unconjugated hyperbilirubinemia is caused by variants in the gene UGT1A1 leading to Gilbert’s syndrome and Crigler-Najjar syndrome types I and II. These syndromes are differentiated on the basis of UGT1A1 residual enzy
Externí odkaz:
https://doaj.org/article/fd47efeaec364158ab0b56e1e661ce60
Akademický článek
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Akademický článek
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