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 no BMC Pediatr (2018)

Analysis of possible genetic risk factors contributing to development of childhood acute lymphoblastic leukaemia in the Latvian population

Por Kreile, Madara, Piekuse, Linda, Rots, Dmitrijs, Dobele, Zane, Kovalova, Zhanna, Lace, Baiba
Publicado no Arch Med Sci (2016)

Association of ARID5B Genetic Variants with Risk of Childhood B Cell Precursor Acute Lymphoblastic Leukaemia in Latvia

Por Kreile, Madara, Rots, Dmitrijs, Zarina, Agnese, Rautiainen, Linda, Visnevska-Preciniece, Zelma, Kovalova, Zhanna, Gailite, Linda
Publicado no Asian Pac J Cancer Prev (2018)

Association between inherited monogenic liver disorders and chronic hepatitis C

Por Piekuse, Linda, Kreile, Madara, Zarina, Agnese, Steinberga, Zane, Sondore, Valentina, Keiss, Jazeps, Lace, Baiba, Krumina, Astrida
Publicado em 2014

Elevated Serum Levels of Homocysteine as an Early Prognostic Factor of Psychiatric Disorders in Children and Adolescents

Por Kevere, Laura, Purvina, Santa, Bauze, Daiga, Zeibarts, Marcis, Andrezina, Raisa, Rizevs, Arnis, Jelisejevs, Sergejs, Piekuse, Linda, Kreile, Madara, Purvins, Indulis
Publicado em 2012

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 no Mol Genet Genomic Med (2017)