Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Ieva Puķīte"'
Publikováno v:
Proceedings of the Latvian Academy of Sciences. Section B. Natural, Exact, and Applied Sciences.. 74:75-82
The MR activity indices used for quantification and follow-up of Crohn’s disease are composed of a number of subjectively determinable components with equivocal repeatability. The purpose of this article was to assess the repeatability of measureme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f7c36deaf8646064498319c6d6105332
https://doi.org/10.2478/prolas-2020-0012
https://doi.org/10.2478/prolas-2020-0012
Autor:
Antonella Lezo, Antonella Diamanti, Evelyne M. Marinier, Merit Tabbers, Anat Guz-Mark, Paolo Gandullia, Maria I. Spagnuolo, Sue Protheroe, Noel Peretti, Laura Merras-Salmio, Jessie M. Hulst, Sanja Kolaček, Looi C. Ee, Joanna Lawrence, Jonathan Hind, Lorenzo D’Antiga, Giovanna Verlato, Ieva Pukite, Grazia Di Leo, Tim Vanuytsel, Maryana K. Doitchinova-Simeonova, Lars Ellegard, Luisa Masconale, María Maíz-Jiménez, Sheldon C. Cooper, Giorgia Brillanti, Elena Nardi, Anna S. Sasdelli, Simon Lal, Loris Pironi
Publikováno v:
Nutrients, Vol 14, Iss 9, p 1889 (2022)
Background: The European Society for Clinical Nutrition and Metabolism database for chronic intestinal failure (CIF) was analyzed to investigate factors associated with nutritional status and the intravenous supplementation (IVS) dependency in childr
Externí odkaz:
https://doaj.org/article/6acbbad37d9d4b37ad092b7f87057d86
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