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Allergology International : Official Journal of the Japanese Society of Allergology|January 22, 2020
A novel deep intronic SERPING1 variant as a cause of hereditary angioedema due to C1-inhibitor deficiencySofia Vatsiou, Maria Zamanakou, Gedeon Loules, et al.
Frontiers in Oncology|August 6, 2019
BAFF/APRIL System Is Functional in B-Cell Acute Lymphoblastic Leukemia in a Disease Subtype MannerEirini Sevdali, Eleni Katsantoni, Cristian R Smulski, et al.
Frontiers in Allergy|August 12, 2022
SERPING1 Variants and C1-INH Biological Function: A Close Relationship With C1-INH-HAEChristian Drouet, Alberto López-Lera, Arije Ghannam, et al.
The Journal of Allergy and Clinical Immunology. in Practice|November 1, 2019
International Consensus on the Use of Genetics in the Management of Hereditary AngioedemaAnastasios E Germenis, Maurizio Margaglione, João Bosco Pesquero, et al.
Frontiers in Immunology|January 30, 2018
An Activating Janus Kinase-3 Mutation Is Associated with Cytotoxic T Lymphocyte Antigen-4-Dependent Immune Dysregulation SyndromeHeiko Sic, Matthaios Speletas, Vanessa Cornacchione, et al.
Frontiers in Allergy|July 25, 2022
Searching for Genetic Biomarkers for Hereditary Angioedema Due to C1-Inhibitor Deficiency (C1-INH-HAE)Faidra Parsopoulou, Gedeon Loules, Maria Zamanakou, et al.
Journal of Clinical Medicine|October 29, 2020
Deciphering the Genetics of Primary Angioedema with Normal Levels of C1 InhibitorGedeon Loules, Faidra Parsopoulou, Maria Zamanakou, et al.
Frontiers in Allergy|August 4, 2026
Hereditary angioedema care across selected health systems in the Balkan Peninsula area: policy gaps, practice variation, and actionable recommendationsGeorge N Konstantinou, Sladjana Andrejevic, Natasha Angjeleska, et al.
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