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Journal of Translational Medicine|April 24, 2008
Foxp3 expression in human cancer cellsVaios Karanikas, Matthaios Speletas, Maria Zamanakou, et al.
Journal of Molecular Neuroscience : MN|November 9, 2019
A novel homozygous SACS mutation identified by whole exome sequencing-genotype phenotype correlations of all published casesGeorgia Xiromerisiou, Katerina Dadouli, Chrysoula Marogianni, et al.
BMJ Open|October 9, 2017
Fabry disease due to D313Y and novel GLA mutationsKonstantinos Koulousios, Konstantinos Stylianou, Panagiotis Pateinakis, et al.
International Archives of Allergy and Immunology|November 14, 2017
Genetic Determinants of C1 Inhibitor Deficiency Angioedema Age of OnsetPanagiota Gianni, Gedeon Loules, Maria Zamanakou, et al.
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.
Molecular Therapy. Oncology|July 5, 2024
CDKN2A copy number alteration in bladder cancer: Integrative analysis in patient-derived xenografts and cancer patientsMaria-Alexandra Papadimitriou, Katerina-Marina Pilala, Konstantina Panoutsopoulou, 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 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.
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