Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Christina Sidira"'
Autor:
Efthymia Vargiami, Stella Stabouli, Christina Sidira, Maria Kyriazi, Athanasia Anastasiou, Athanasios Notopoulos, Dimitrios Zafeiriou
Publikováno v:
European journal of pediatrics. 181(4)
Renal involvement is very common in tuberous sclerosis complex (TSC) and is characterized by the development of angiomyolipoma and cysts. The aims of the present study were to assess kidney function and clinical features of renal involvement in TSC,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0b1af5fbf97604c93e3dc05aaafaec1
https://pubmed.ncbi.nlm.nih.gov/34988664
https://pubmed.ncbi.nlm.nih.gov/34988664
Autor:
Christina Sidira, Athanasios Notopoulos, D.I. Zafeiriou, Kyriazi M, Vargiami E, Stella Stabouli, Anastasiou A
Background Renal involvement is very common in tuberous sclerosis complex (TSC) and is characterised by the development of angiomyolipoma and cysts. The aims of the present study were to assess kidney function and clinical features of renal involveme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e7a4dd84ffa626b99a951fa918e5ae38
https://doi.org/10.21203/rs.3.rs-444696/v1
https://doi.org/10.21203/rs.3.rs-444696/v1
Autor:
M. Kyriazi, Efterpi Dalpa, Argirios Ntinopoulos, Maria Spanou, Persefoni Talimtzi, Christina Sidira, Athanasia Anastasiou, P. Dragoumi, Athanasios Evangeliou, Dimitrios I. Zafeiriou, E. Vargiami
Publikováno v:
Pediatric neurology. 123
Background The neurodevelopmental impairment in tuberous sclerosis complex (TSC) has a multifactorial origin. Various factors have been proposed as predictors of neurological outcome such as tuber load, seizure onset, and TSC2 mutation. Cerebellar le
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0d56c9f701a54bc5c9ffa64a15ef57b
https://pubmed.ncbi.nlm.nih.gov/34399109
https://pubmed.ncbi.nlm.nih.gov/34399109
Publikováno v:
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society. 30
Hemimegalencephaly is a rare malformation of cortical development characterised by enlargement of one cerebral hemisphere. The association between hemimegalencephaly and tuberous sclerosis complex, an autosomal dominant genetic disorder, is uncommon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6769340a3a5c6acd5fd5b6b2d3f4af9
https://pubmed.ncbi.nlm.nih.gov/33387903
https://pubmed.ncbi.nlm.nih.gov/33387903
Autor:
Christina Sidira, Fotios Papachristou, Nikoleta Printza, John Dotis, Stella Stabouli, Ireni Georeli
Publikováno v:
Expert Review of Clinical Pharmacology. 11:459-461
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af32a62e3c37736719cd73eab59563c2
https://doi.org/10.1080/17512433.2018.1466414
https://doi.org/10.1080/17512433.2018.1466414
Autor:
E. Papathanasiou, A.-K. Giese, M. Kyriazi, H. Michelakakis, Dimitrios I. Zafeiriou, Spyros Batzios, E. Vargiami, Athanasios Anastasiou, Christina Sidira
Publikováno v:
European Journal of Paediatric Neurology. 19:S40
Objective Krabbe disease is an autosomal recessive neurodegenerative disorder due to a defect of the lysosomal enzyme galactocerebrosidase (GALC) and is classified into infantile and late-onset form, depending on the age of onset. Methods and results
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::adfe6a8b49fd82c9dc4b101b4febfb24
https://doi.org/10.1016/s1090-3798(15)30129-x
https://doi.org/10.1016/s1090-3798(15)30129-x