Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Lilia Lykopoulou"'
Autor:
Manthoula Valari, Martha Theodoraki, Ierotheos Loukas, Sylvia Gkantseva-Patsoura, Georgia Karavana, Vasiliki Falaina, Lilia Lykopoulou, Roser Pons, Ioannis Athanasiou, Katarzyna Wertheim-Tysarowska, Christina Kanaka-Gantenbein, Dimitra Kiritsi
Publikováno v:
Acta Dermato-Venereologica, Vol 99, Iss 13, Pp 1309-1310 (2019)
Externí odkaz:
https://doaj.org/article/75d97d886563485b97424d025e7ee1cb
Autor:
Meritxell Reverter, Carles Rentero, Ana Garcia-Melero, Monira Hoque, Sandra Vilà de Muga, Anna Álvarez-Guaita, James R.W. Conway, Peta Wood, Rose Cairns, Lilia Lykopoulou, Daniel Grinberg, Lluïsa Vilageliu, Marta Bosch, Joerg Heeren, Juan Blasi, Paul Timpson, Albert Pol, Francesc Tebar, Rachael Z. Murray, Thomas Grewal, Carlos Enrich
Publikováno v:
Cell Reports, Vol 7, Iss 3, Pp 883-897 (2014)
Inhibition of cholesterol export from late endosomes causes cellular cholesterol imbalance, including cholesterol depletion in the trans-Golgi network (TGN). Here, using Chinese hamster ovary (CHO) Niemann-Pick type C1 (NPC1) mutant cell lines and hu
Externí odkaz:
https://doaj.org/article/06a91864d03547b39c978ce313decb26
Autor:
Chrysoula Kosmeri, Dimitrios Rallis, Maria Baltogianni, Helen Bouza, Lilia Lykopoulou, Loukia Lianou, Eleni Papadopoulou, Marianna Tzanoudaki, Evangelia Farmaki, Vassilios Papadakis, Vasileios Giapros, Alexandros Makis
Publikováno v:
Journal of pediatric hematology/oncology.
A term neonate presented with persistent severe thrombocytopenia, elevated liver enzymes, conjugated hyperbilirubinemia, hepatosplenomegaly, and mild hypotonia.A thorough workup for infections, congenital thrombocytopenias, and neonatal malignancies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6539f43e3e70b88b10ca2322b9efbd72
https://pubmed.ncbi.nlm.nih.gov/36162002
https://pubmed.ncbi.nlm.nih.gov/36162002
Autor:
Athanasios Michos, Alexandra Palili, Emmanouil I. Koutouzis, Adina Sandu, Lilia Lykopoulou, Vassiliki P. Syriopoulou
Publikováno v:
IDCases, Vol 5, Iss C, Pp 27-28 (2016)
We report the use of FilmArray Blood Culture Identification (BCID) multiplex PCR system for pathogen detection from a child with septic arthritis that Streptococcus pyogenes was identified directly from synovial fluid and a child with complicated pne
Externí odkaz:
https://doaj.org/article/6f0dfa2a2610496b8ad17ea018da1ca5
Autor:
Konstantinos Salpasaranis, Lilia Lykopoulou, Aglaia Zellos, Paraskevi Galina, Maria Zarifi, Efthymia Alexopoulou, Anastasia Mentessidou, Amalia Patereli, Nikolaos Kelekis, Petros Mirilas
Publikováno v:
Pediatric radiology. 51(8)
Although fibrosis is the main determinant of liver stiffness, other disease-related factors usually disregarded in studies on liver elastography, such as inflammation and cholestasis, may influence liver stiffness. To evaluate the accuracy of two-dim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d86fbf6d04b6854088f37a65b41ff426
https://pubmed.ncbi.nlm.nih.gov/33755748
https://pubmed.ncbi.nlm.nih.gov/33755748
Autor:
Athanasios G. Kaditis, Lilia Lykopoulou, Christina Kanaka-Gantenbein, Evanthia Botsa, Elissavet Georgiadou, Adina Sandu, Theoni Petropoulou
Publikováno v:
Paediatric respiratory physiology and sleep.
Introduction and Aims: Current guidelines suggest that oxygen may not be administered to infants with bronchiolitis and SpO2 >90%. However, the pathophysiological consequences of acute hypoxemia in infants are unknown. We hypothesized that even mild
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::38e909fb9f4c22319c12a53235adc0ad
https://doi.org/10.1183/13993003.congress-2019.pa4982
https://doi.org/10.1183/13993003.congress-2019.pa4982
Autor:
Vasiliki Dermentzoglou, Christina Kanaka-Gantenbein, Athanasia Stelianidi, Elissavet Georgiadou, John Anastasopoulos, Artemis Doulgeraki, Lilia Lykopoulou
Publikováno v:
Bone Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f8994656cea437314e44e6ee2826caac
https://doi.org/10.1530/boneabs.7.p190
https://doi.org/10.1530/boneabs.7.p190
Publikováno v:
Pediatric Immunology ISBN: 9783030212612
RAG1/RAG2 mutations result in variable clinical manifestations, ranging from severe combined immunodeficiency (SCID) and Omenn Syndrome to milder forms
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed755f0908c12c7708449e23cc92d2a8
https://doi.org/10.1007/978-3-030-21262-9_148
https://doi.org/10.1007/978-3-030-21262-9_148
Autor:
Katarzyna Wertheim-Tysarowska, Vasiliki Falaina, Dimitra Kiritsi, Georgia Karavana, Ierotheos Loukas, Martha Theodoraki, Christina Kanaka-Gantenbein, Sylvia Gkantseva-Patsoura, Manthoula Valari, Roser Pons, Lilia Lykopoulou, Ioannis Athanasiou
Publikováno v:
Acta Dermato-Venereologica, Vol 99, Iss 13, Pp 1309-1310 (2019)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76704c14c0d5e5fa4dac14d088a4abeb
https://doi.org/10.2340/00015555-3317
https://doi.org/10.2340/00015555-3317
Autor:
Lorenzo D'Antiga, F. Papadia, Lorena Travaglini, Livia Pisciotta, Patricia Crock, Tiziano Lucchi, Maja Di Rocco, Giulia Tozzi, Stefano Bertolini, Giuseppe Indolfi, Roberta Taurisano, Anastasia Garoufi, Helen Michelakakis, Komal Vora, Lilia Lykopoulou, Scott Nightingale, Sebastiano Calandra
Background and aims Childhood/Adult-onset Lysosomal Acid Lipase Deficiency (LAL-D) is a recessive disorder due to loss of function variants of LAL, the enzyme which hydrolyses cholesteryl esters, derived from internalized apoB containing lipoproteins
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d1caad9b454355f5e14ad4b06e4edf2
http://hdl.handle.net/11567/892426
http://hdl.handle.net/11567/892426