Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Simona Stojanovska-Jakimovska"'
Autor:
Nevenka Ridova, Sanja Trajkova, Biljana Chonevska, Zlate Stojanoski, Martin Ivanovski, Marija Popova-Labachevska, Simona Stojanovska-Jakimovska, Venko Filipche, Aspazija Sofijanova, Irina Panovska-Stavridis
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 32, Iss , Pp 100895- (2022)
The majority of Gaucher Disease (GD) cases result from pathologic mutations in the GBA1 gene. A rich mutational spectrum of about 500 identified variants has been recognized. The disease is characterized by phenotypic diversity. Data regarding the ge
Externí odkaz:
https://doaj.org/article/0642f2602258478da790e4e96a1e9e17
Autor:
Nevenka Ridova, Milche Cvetanoski, Sanja Trajkova, Martin Ivanovski, Aleksandra Pivkova Veljanovska, Zlate Stojanoski, Marija Popova Labachevska, Simona Stojanovska Jakimovska, Dushko Dukovski, Lazar Chadievski, Svetlana Krstevska - Balkanov, Mario Jakimovski, Arita Fazliu, Viktorija Kostojchinovska, Gordana Petrushevska, Irina Panovska-Stavridis
Publikováno v:
HemaSphere, Vol 7, p e33999e0 (2023)
Externí odkaz:
https://doaj.org/article/0f980654f77e455dafe3b68f37d99163
Autor:
Marija Popova Labachevska, Irina Panova Stavridis, Sanja Trajkova, Nevenka Ridova, Marija Staninova, Simona Stojanovska Jakimovska, Aleksandra Pivkova, Zlate Stojanoski, Velimir Stojkoski
Publikováno v:
Journal of Morphological Sciences. 6:8-16
Autor:
Irina Panovska-Stavridis, Nevenka Ridova, Martin Ivanovski, Sanja Trajkova, Aleksandra Pivkova-Veljanovska, Lazar Chadievski, Dushko Dukovski, Zlate Stojanoski, Marija Popova-Labachevska, Bozidar Kochoski, Simona Stojanovska-Jakimovska, Milche Cvetanoski, Milena Grivchevska, Viktorija Kostojchinoska, Mario Jakjimovski, Ilina Hamamdzieva, Aleksandar S. Dimovski
Publikováno v:
Clinical Lymphoma Myeloma and Leukemia. 22:S200-S201
Autor:
Nevenka Ridova, Sanja Trajkova, Marija Popova-Labachevska, Simona Stojanovska – Jakimovska, Filip Nikolov, Irina Panovska-Stavridis
Publikováno v:
European Journal of Case Reports in Internal Medicine.
Gaucher disease (GD) is a rare inherited lysosomal storage disease characterized by multi-system impairment. One of its main features is the over-expressed chronic stimulation and activation of the immune system, which may play a crucial role in the
Autor:
Nevenka Ridova, Martin Ivanovski, Sanja Trajkova, Aleksandra Pivkova-Veljanovska, Lazar Chadievski, Dushko Dukovski, Marija Popova-Labachevska, Svetlana Krstevska-Balkanov, Zlate Stojanoski, Simona Stojanovska-Jakimovska, Milche Cvetanoski, Dijana Milovska, Milena Grivchevska, Bozidar Kochoski, Viktorija Kostojchinoska, Mario Jakjimovski, Irina Panovska-Stavridis
Publikováno v:
Clinical Lymphoma Myeloma and Leukemia. 22:S346