Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Sofia Vatsiou"'
Autor:
Sofia Vatsiou, Maria Zamanakou, Gedeon Loules, Fotis Psarros, Faidra Parsopoulou, Dorottya Csuka, Anna Valerieva, Maria Staevska, Grzegorz Porebski, Krystyna Obtulowicz, Markus Magerl, Marcus Maurer, Matthaios Speletas, Henriette Farkas, Anastasios E. Germenis
Publikováno v:
Allergology International, Vol 69, Iss 3, Pp 443-449 (2020)
Background: In about 5% of patients with hereditary angioedema due to C1-inhibitor deficiency (C1-INH-HAE) no mutation in the SERPING1 gene is detected. Methods: C1-INH-HAE cases with no mutation in the coding region of SERPING1 after conventional ge
Externí odkaz:
https://doaj.org/article/f6bdd3722a2649f4adc561644d087638
Autor:
Faidra Parsopoulou, Grzegorz Porebski, Anna Valerieva, Krystyna Obtułowicz, Anastasios E. Germenis, Sofia Vatsiou, Gedeon Loules, Marcus Maurer, Maria Zamanakou, Matthaios Speletas, Markus Magerl, Henriette Farkas, Dorottya Csuka, Maria Staevska, Fotis Psarros
Publikováno v:
Allergology International, Vol 69, Iss 3, Pp 443-449 (2020)
Background In about 5% of patients with hereditary angioedema due to C1-inhibitor deficiency (C1-INH-HAE) no mutation in the SERPING1 gene is detected. Methods C1-INH-HAE cases with no mutation in the coding region of SERPING1 after conventional geno
Publikováno v:
Journal of Clinical Immunology. 41:248-250
Autor:
Damianos Sotiropoulos, Anastasios E. Germenis, Angeliki Xagorari, Maria Zamanakou, Sofia Vatsiou
Publikováno v:
HLAREFERENCES. 97(3)
The new alleles A*02:943 and B*51:104:02 were detected in Greek cord blood units.
Autor:
Maria Bova, Gregor Porebski, Fotis Psarros, Michael Makris, Anastasios E. Germenis, Faidra Parsopoulou, Stefano Del Giacco, Henriette Farkas, Davide Firinu, Maria Zamanakou, Matthaios Speletas, Dorottya Csuka, T González-Quevedo, Chiara Suffritti, Gedeon Loules, Sofia Vatsiou, Andrea Zanichelli
Publikováno v:
Journal of Clinical Medicine, Vol 9, Iss 3402, p 3402 (2020)
Journal of Clinical Medicine
Volume 9
Issue 11
Journal of Clinical Medicine
Volume 9
Issue 11
The genetic alteration underlying the great majority of primary angioedema with normal C1 inhibitor (nl-C1-INH-HAE) cases remains unknown. To search for variants associated with nl-C1-INH-HAE, we genotyped 133 unrelated nl-C1-INH-HAE patients using a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c076fcc21a138e9ea066d47960ef97de
https://ruj.uj.edu.pl/xmlui/handle/item/264574
https://ruj.uj.edu.pl/xmlui/handle/item/264574
Autor:
Henriette Farkas, Faidra Parsopoulou, Margarita López-Trascasa, Markus Magerl, Dumitru Moldovan, Maria Staevska, Anna Valerieva, Marcus Maurer, Krystyna Obtułowicz, Anastasios E. Germenis, Alberto López-Lera, Gedeon Loules, Fotis Psarros, Dorottya Csuka, Maria Zamanakou, Matthaios Speletas, Sofia Vatsiou, Grzegorz Porebski
SERPING1 genotyping of subjects suspicious for hereditary angioedema due to C1-INH deficiency (C1-INH-HAE) is important for clinical practice as well as for research reasons. Conventional approaches towards the detection of C1-INH-HAE-associated SERP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::113cae0ba1b594d9da2f2d885d9d2f0d
https://ruj.uj.edu.pl/xmlui/handle/item/94059
https://ruj.uj.edu.pl/xmlui/handle/item/94059