Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Audronė Mulevičienė"'
Autor:
Svetlana O. Sharapova, Małgorzata Skomska-Pawliszak, Yulia A. Rodina, Beata Wolska-Kuśnierz, Nel Dabrowska-Leonik, Bozena Mikołuć, Olga E. Pashchenko, Srdjan Pasic, Tomáš Freiberger, Tomáš Milota, Renata Formánková, Anna Szaflarska, Maciej Siedlar, Tadej Avčin, Gašper Markelj, Peter Ciznar, Krzysztof Kalwak, Sylwia Kołtan, Teresa Jackowska, Katarzyna Drabko, Alenka Gagro, Małgorzata Pac, Elissaveta Naumova, Snezhina Kandilarova, Katarzyna Babol-Pokora, Dzmitry S. Varabyou, Barbara H. Barendregt, Elena V. Raykina, Tatiana V. Varlamova, Anna V. Pavlova, Hana Grombirikova, Maruša Debeljak, Irina V. Mersiyanova, Anastasiia V. Bondarenko, Liudmyla I. Chernyshova, Larysa V. Kostyuchenko, Marina N. Guseva, Jelena Rascon, Audrone Muleviciene, Egle Preiksaitiene, Christoph B. Geier, Alexander Leiss-Piller, Yasuhiro Yamazaki, Tomoki Kawai, Jolan E. Walter, Irina V. Kondratenko, Anna Šedivá, Mirjam van der Burg, Natalia B. Kuzmenko, Luigi D. Notarangelo, Ewa Bernatowska, Olga V. Aleinikova
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
Background: Variants in recombination-activating genes (RAG) are common genetic causes of autosomal recessive forms of combined immunodeficiencies (CID) ranging from severe combined immunodeficiency (SCID), Omenn syndrome (OS), leaky SCID, and CID wi
Externí odkaz:
https://doaj.org/article/9b03aece41064fa7ac129d44af5c221a
Publikováno v:
Journal of Pediatric and Neonatal Individualized Medicine, Vol 9, Iss 1, Pp e090104-e090104 (2019)
Transient abnormal myelopoiesis (TAM) is a unique entity that usually occurs in children with Down syndrome (DS) or with trisomy 21 mosaicism. The somatic GATA1 mutation is a distinct feature of TAM. At presentation, TAM can resemble congenital leuke
Externí odkaz:
https://doaj.org/article/6f1934676fe04acbbe7e36199287627e
Autor:
Zanna Kovalova, Anda Kivite-Urtane, Jelena Rascon, Audronė Mulevičienė, Goda Elizabeta Vaitkevičienė, Kajus Merkevičius, Eglė Stukaitė-Ruibienė, Sonata Šaulytė Trakymienė
Publikováno v:
Acta Medica Lituanica, Vol 29, Iss 2 (2022)
Hematopoietic stem cell transplantation (HSCT) is a complex procedure that is curative for several fatal pediatric malignancies and non-malignant diseases. Despite its complexity, potential toxicity, and high costs HSCT has become a standard procedur
Externí odkaz:
https://doaj.org/article/e87464e775b14ae8964754da66614173
Autor:
Jelena Rascon, Ignė Kairienė, Goda Vaitkevičienė, Audronė Mulevičienė, Dovilė Rimkutė, Rimantė Čerkauskienė
Publikováno v:
Medicinos teorija ir praktika. 21:117-122
Chronic granulomatous disease (CGD) is an inherited X-linked or, less frequently, with somatic mutations linked disorder of phagocytic cells which presents in early childhood as recurrent granulomatous lesions and atypical bacterial or fungal infecti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9a6f7bf6e856c0e211b5ffdacfe65810
https://doi.org/10.15591/mtp.2015.017
https://doi.org/10.15591/mtp.2015.017
Autor:
Lina Ragelienė, Audronė Mulevičienė
Publikováno v:
Medicinos teorija ir praktika. 21:65-72
Iron deficiency is one of the most common micronutrient deficiency in infancy and childhood. The main long lasting effect of iron deficiency anemia in infancy is poor neurocognitive development. Despite early treatment with iron supplements, lower co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d90eb82b47a6f44e13c1e3c706401df
https://doi.org/10.15591/mtp.2015.009
https://doi.org/10.15591/mtp.2015.009