Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Sarah Meglaj"'
Autor:
Kristina Dominko, Ana Rastija, Sandra Sobocanec, Lea Vidatic, Sarah Meglaj, Andrea Lovincic Babic, Birgit Hutter-Paier, Alessio-Vittorio Colombo, Stefan F. Lichtenthaler, Sabina Tahirovic, Silva Hecimovic
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 24, p 13256 (2021)
Niemann-Pick type C disease (NPC) is a rare inherited neurodegenerative disorder characterized by an accumulation of intracellular cholesterol within late endosomes and lysosomes due to NPC1 or NPC2 dysfunction. In this work, we tested the hypothesis
Externí odkaz:
https://doaj.org/article/67ca3503d20b48539006972a0277bafd
Autor:
Antonela Blazekovic, Kristina Gotovac Jercic, Sarah Meglaj, Vlasta Duranovic, Igor Prpic, Bernarda Lozic, Masa Malenica, Silvana Markovic, Lucija Lujic, Zeljka Petelin Gadze, Romana Juraski, Nina Barišic, Ivo Baric, Fran Borovecki
Publikováno v:
Genes; Volume 13; Issue 8; Pages: 1466
Genes
Volume 13
Issue 8
Genes
Volume 13
Issue 8
Epilepsy is one of the most common neurological disorders with diverse phenotypic characteristics and high genetic heterogeneity. Epilepsy often occurs in childhood, so timely diagnosis and adequate therapy are crucial for preserving quality of life
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81a5f6c8738873530eaa110e22c1e7cf
https://doi.org/10.3390/genes13081466
https://doi.org/10.3390/genes13081466
