Case report: multiple UGT1A1 gene variants in a patient with Crigler-Najjar syndrome

por Gailite, Linda, Rots, Dmitrijs, Pukite, Ieva, Cernevska, Gunta, Kreile, Madara
Publicado 2018

Genetic variation spectrum in ATP7B gene identified in Latvian patients with Wilson disease

por Zarina, Agnese, Tolmane, Ieva, Kreile, Madara, Chernushenko, Aleksandrs, Cernevska, Gunta, Pukite, Ieva, Micule, Ieva, Krumina, Zita, Krumina, Astrida, Rozentale, Baiba, Piekuse, Linda
Publicado 2017

Chronic Intestinal Failure in Children: An International Multicenter Cross-Sectional Survey

por Lezo, Antonella, Diamanti, Antonella, Marinier, Evelyne M., Tabbers, Merit, Guz-Mark, Anat, Gandullia, Paolo, Spagnuolo, Maria I., Protheroe, Sue, Peretti, Noel, Merras-Salmio, Laura, Hulst, Jessie M., Kolaček, Sanja, Ee, Looi C., Lawrence, Joanna, Hind, Jonathan, D’Antiga, Lorenzo, Verlato, Giovanna, Pukite, Ieva, Di Leo, Grazia, Vanuytsel, Tim, Doitchinova-Simeonova, Maryana K., Ellegard, Lars, Masconale, Luisa, Maíz-Jiménez, María, Cooper, Sheldon C., Brillanti, Giorgia, Nardi, Elena, Sasdelli, Anna S., Lal, Simon, Pironi, Loris
Publicado 2022