Publications by authors named "Anastasios Germenis"

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Incidental findings related to genes associated to HAE-nC1INH: how to proceed?
Anastasios E Germenis, Despina Sanoudou

Front Immunol· July 2025

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Hereditary Angioedema with Normal C1 Inhibitor: an Updated International Consensus Paper on Diagnosis, Pathophysiology, and Treatment.
Bruce L Zuraw, Konrad Bork, Laurence Bouillet, Sandra C Christiansen, Henriette Farkas, Anastasios E Germenis

Clin Rev Allergy Immunol· March 2025

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TNFRSF11A variants contribute to systemic autoinflammatory diseases: A case series of 12 patients.
Vasileios Papatheodorou, Charalampos Gerodimos, Antonios Dimitrakopoulos, Efrosini Lada, Maria G Tektonidou, Anastasios Germenis

Semin Arthritis Rheum· October 2024

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Levels of Natural Antibodies Before and After Immunoglobulin Replacement Treatment Affect the Clinical Phenotype in Common Variable Immunodeficiency.
Ioannis Sarrigeorgiou, Gerasimina Tsinti, Fani Kalala, Anastasios Germenis, Matthaios Speletas

J Clin Immunol· September 2024

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Hereditary angioedema with normal C1 inhibitor associated with carboxypeptidase N deficiency.
Denis Vincent, Faidra Parsopoulou, Ludovic Martin, Christine Gaboriaud, Jacques Demongeot, Anastasios E Germenis

J Allergy Clin Immunol Glob· May 2024

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A Nationwide Study of the Delayed Diagnosis and the Clinical Manifestations of Predominantly Antibody Deficiencies and -Mediated Immune Dysregulation Syndrome in Greece.
Androniki Kapousouzi, Fani Kalala, Styliani Sarrou, Evangelia Farmaki, Nikolaos Antonakos, Anastasios E Germenis

Medicina (Kaunas)· May 2024

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The expanding clinical spectrum of autoinflammatory diseases with variants: a case series and literature review.
Anastasios Karamanakos, Olga Vougiouka, Evdoxia Sapountzi, Aliki I Venetsanopoulou, Maria G Tektonidou, Anastasios E Germenis

Front Immunol· February 2024

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Genetic Variants Leading to Urticaria and Angioedema and Associated Biomarkers.
Jonathan J Lyons, Henriette Farkas, Anastasios E Germenis, Matija Rijavec, Tukisa D Smith

J Allergy Clin Immunol Pract· August 2023

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Identification of the novel HLA-DRB1*11:308 allele in a Greek individual.
Maria Zamanakou, Sophia Vatsiou, Panagiota Batsaki, Sotirios P Fortis, Anastasios E Germenis

HLA· May 2023

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Editorial: C1 inhibitor deficiency and angioedema.
Henriette Farkas, Anastasios E Germenis, Hilary Longhurst

Front Allergy· November 2022

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Autoinflammatory syndromes with coexisting variants in Mediterranean FeVer and other genes: Utility of multiple gene screening and the possible impact of gene dosage.
Anastasios Karamanakos, Maria Tektonidou, Olga Vougiouka, Charalampos Gerodimos, Christina Katsiari, Anastasios Germenis

Semin Arthritis Rheum· October 2022

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Searching for Genetic Biomarkers for Hereditary Angioedema Due to C1-Inhibitor Deficiency (C1-INH-HAE).
Faidra Parsopoulou, Gedeon Loules, Maria Zamanakou, Dorottya Csuka, Agnes Szilagyi, Anastasios E Germenis

Front Allergy· July 2022

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Variants and C1-INH Biological Function: A Close Relationship With C1-INH-HAE.
Christian Drouet, Alberto López-Lera, Arije Ghannam, Margarita López-Trascasa, Sven Cichon, Anastasios E Germenis

Front Allergy· March 2022

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Significance of regional population HLA immunogenetic datasets in the efficacy of umbilical cord blood banks and marrow donor registries: a study of Cretan HLA genetic diversity.
Helen Latsoudis, Emmanouil Stylianakis, Irene Mavroudi, Alexandros Kanterakis, Pavlos Pavlidis, Anastasios E Germenis

Cytotherapy· February 2022

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Persistent Activation of Innate Immunity in Patients with Primary Antibody Deficiencies.
Gerasimina Tsinti, Demosthenes Makris, Anastasios E Germenis, Matthaios Speletas

J Immunol Res· August 2021

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The Global Registry for Hereditary Angioedema due to C1-Inhibitor Deficiency.
Andrea Zanichelli, Henriette Farkas, Laurance Bouillet, Noemi Bara, Anastasios E Germenis

Clin Rev Allergy Immunol· August 2021

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Leveraging Genetics for Hereditary Angioedema: A Road Map to Precision Medicine.
Anastasios E Germenis, Matija Rijavec, Camila Lopes Veronez

Clin Rev Allergy Immunol· June 2021

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Identification of two novel alleles, HLA-A*02:01:193 and -DQA1*02:17, in Greek individuals.
Maria Zamanakou, Sophia Vatsiou, Savvas Stokidis, Sotirios P Fortis, Anastasios E Germenis

HLA· June 2021

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Detection of two novel alleles, HLA-A*02:943 and -B*51:104:02, in Greek cord blood units.
Angeliki Xagorari, Maria Zamanakou, Sofia Vatsiou, Anastasios E Germenis, Damianos Sotiropoulos

HLA· March 2021

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Deep Intronic SERPING1 Gene Variants: Ending One Odyssey and Starting Another?
Anastasios E Germenis, Sofia Vatsiou, Dorottya Csuka, Maria Zamanakou, Henriette Farkas

J Clin Immunol· January 2021

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Deciphering the Genetics of Primary Angioedema with Normal Levels of C1 Inhibitor.
Gedeon Loules, Faidra Parsopoulou, Maria Zamanakou, Dorottya Csuka, Maria Bova, Anastasios E Germenis

J Clin Med· October 2020

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Plasminogen glycoforms alteration and activation susceptibility associated with the missense variant p.Lys330Glu in HAE-PLG patients.
Faidra Parsopoulou, Delphine Charignon, Maud Tengo, Fotis Psarros, Coen Maas, Anastasios E Germenis

Allergy· August 2020

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A novel deep intronic SERPING1 variant as a cause of hereditary angioedema due to C1-inhibitor deficiency.
Sofia Vatsiou, Maria Zamanakou, Gedeon Loules, Fotis Psarros, Faidra Parsopoulou, Anastasios E Germenis

Allergol Int· July 2020

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International Consensus on the Use of Genetics in the Management of Hereditary Angioedema.
Anastasios E Germenis, Maurizio Margaglione, João Bosco Pesquero, Henriette Farkas, Sven Cichon

J Allergy Clin Immunol Pract· March 2020

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TNFRSF13C/BAFFR P21R and H159Y polymorphisms in multiple sclerosis.
Panagiotis Ntellas, Efthimios Dardiotis, Eirini Sevdali, Vasileios Siokas, Athina-Maria Aloizou, Anastasios E Germenis

Mult Scler Relat Disord· January 2020

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