Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Evangelia Paschali"'
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 20, Iss , Pp - (2019)
Lysosomal Storage Diseases (LSDs) are rare genetic diseases, the majority of which are caused by specific lysosomal enzyme deficiencies and all are characterized by malfunctioning lysosomes. Lysosomes are key regulators of many different cellular pro
Externí odkaz:
https://doaj.org/article/71a5f8ef41ac44e7a3a4908468c490ea
Publikováno v:
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports, Vol 20, Iss, Pp-(2019)
Molecular Genetics and Metabolism Reports, Vol 20, Iss, Pp-(2019)
Lysosomal Storage Diseases (LSDs) are rare genetic diseases, the majority of which are caused by specific lysosomal enzyme deficiencies and all are characterized by malfunctioning lysosomes. Lysosomes are key regulators of many different cellular pro
Publikováno v:
Heritage, Vol 5, Iss 2, Pp 1066-1088 (2022)
The intensifying effects of climate change are becoming one of the main threats to cultural heritage, posing risks of degradation or destruction. Climate change is bringing complexity and uncertainty to ensuring the resilience of cultural heritage, a
Externí odkaz:
https://doaj.org/article/7f22f87830d94cee8d5a479c3d6d8fce
Autor:
Sofia Tantou, M. Liatsis, Nikki Constantinidou, Athanasios Michos, Kleopatra Spanou, Maria Kanariou, Maria Raptaki, Ioanna Varela, Marianna Tzanoudaki, Evangelia Paschali, Chryssa Bakoula, Olga Moraloglou
Publikováno v:
Journal of clinical immunology. 34(7)
Primary Immunodeficiencies (PID) represent a group of heterogeneous immune diseases with important biological significance. We reviewed the records of children diagnosed with PID in the Referral Center for PID in our country in order to describe the
Autor:
Kostas Kakleas, Evangelia Paschali, Maria Kanariou, Nikos Kefalas, Vassilis Petrou, Kyriaki Karavanaki, Ilias Konstantopoulos, Christina Karayianni
Publikováno v:
Hormone research. 71(4)
Background/Aims: Type 1 diabetes (T1DM) is associated with autoimmune thyroid, celiac, autoimmune gastric and Addison’s disease. Our aim was to investigate the prevalence of associated autoantibodies in relation to the demographic and β-cell autoa
Autor:
Maria Kanariou, Constantinos Mihas, Evangelia Paschali, Christina Kanaka-Gantenbein, Marianna Tzanoudaki, Flora Tzifi, George P. Chrousos
Publikováno v:
BMC Immunology
Background Data regarding the quantitative expression of TCR Vβ subpopulations in children with autoimmune diseases provided interesting and sometimes conflicting results. The aim of the present study was to assess by comparative flow cytometric ana