Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Audrone Muleviciene"'
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:
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:
Audrone Muleviciene, Takuya Sekine, Timo Zondag, Yenan T. Bryceson, Bianca Tesi, Jelena Rascon
Publikováno v:
Pediatric bloodcancer. 69(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f1fe574e89dbad9ccc21862e08f01b7
https://pubmed.ncbi.nlm.nih.gov/34913575
https://pubmed.ncbi.nlm.nih.gov/34913575
Iron deficiency anemia-related gut microbiota dysbiosis in infants and young children: A pilot study
Publikováno v:
Acta Microbiologica et Immunologica Hungarica. 65:551-564
Nutritional iron deficiency (ID) causes not only anemia but also malfunction of the entire human organism. Recently, a role of the gut microbiota has been hypothesized, but limited data are available especially in infants. Here, we performed a pilot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::459839c0c252fbf5c99756006aa1888c
https://doi.org/10.1556/030.65.2018.045
https://doi.org/10.1556/030.65.2018.045
Autor:
Sigita Stankeviciene, Audrone Muleviciene, Natalija Sestel, Daiva Sniukaite-Adner, Roma Bartkeviciute, Augustina Jankauskiene, Jelena Rascon
Publikováno v:
Breastfeeding Medicine. 13:493-499
Iron deficiency anemia (IDA) is common in children aged 0-35 months in Lithuania. Nevertheless, there are no studies investigating IDA in this age group. We aimed to identify the major risk factors for disease development focusing on medical history
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f30c53c46b1ab99ff65feaa1d1f7643
https://doi.org/10.1089/bfm.2018.0083
https://doi.org/10.1089/bfm.2018.0083
Autor:
Yenan T. Bryceson, Samuel C. C. Chiang, Ruta Samaitiene, Audrone Muleviciene, Sigita Stankeviciene, Carsten Speckmann, Birute Burnyte, Miriam Heizmann, Sandra Juozapaite, Nerija Vaiciene-Magistris, Valdone Miseviciene, Marie Meeths, Jan-Inge Henter, Vytautas Zekas, Matthias Voss, Stephan Ehl, Alexandra Löfstedt, Reda Matuzeviciene, Jelena Rascon, Egle Kvedaraite, Bianca Tesi, Anders Fasth, Martha-Lena Müller, Rosita Kiudeliene, Magnus Nordenskjöld
Publikováno v:
The Journal of Allergy and Clinical Immunology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77beda991beb1f2c11b33a6d3a354ee3
https://doi.org/10.1016/j.jaci.2018.02.031
https://doi.org/10.1016/j.jaci.2018.02.031