日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Editorial: Genetic and immunological insights into angioedema without wheals

社论:无风团血管性水肿的遗传学和免疫学见解

Rijavec, Matija; Margaglione, Maurizio; Germenis, Anastasios E

Hereditary Angioedema with Normal C1 Inhibitor: an Updated International Consensus Paper on Diagnosis, Pathophysiology, and Treatment

遗传性血管性水肿伴正常C1抑制剂:诊断、病理生理学和治疗的最新国际共识文件

Zuraw, Bruce L; Bork, Konrad; Bouillet, Laurence; Christiansen, Sandra C; Farkas, Henriette; Germenis, Anastasios E; Grumach, Anete S; Kaplan, Allen; López-Lera, Alberto; Magerl, Markus; Riedl, Marc A; Adatia, Adil; Banerji, Aleena; Betschel, Stephen; Boccon-Gibod, Isabelle; Bova, Maria; Boysen, Henrik Balle; Caballero, Teresa; Cancian, Mauro; Castaldo, Anthony J; Cohn, Danny M; Corcoran, Deborah; Drouet, Christian; Fukunaga, Atsushi; Hide, Michihiro; Katelaris, Constance H; Li, Philip H; Longhurst, Hilary; Peter, Jonny; Psarros, Fotis; Reshef, Avner; Ritchie, Bruce; Selva, Christine N; Zanichelli, Andrea; Maurer, Marcus

Incidental findings related to genes associated to HAE-nC1INH: how to proceed?

与 HAE-nC1INH 相关的基因的意外发现:如何处理?

Germenis, Anastasios E; Sanoudou, Despina

Levels of Natural Antibodies Before and After Immunoglobulin Replacement Treatment Affect the Clinical Phenotype in Common Variable Immunodeficiency

免疫球蛋白替代治疗前后的天然抗体水平影响常见变异性免疫缺陷的临床表型

Ioannis Sarrigeorgiou, Gerasimina Tsinti, Fani Kalala, Anastasios Germenis, Matthaios Speletas #, Peggy Lymberi #

The expanding clinical spectrum of autoinflammatory diseases with NOD2 variants: a case series and literature review

NOD2变异体相关自身炎症性疾病临床谱的扩展:病例系列及文献综述

Karamanakos, Anastasios; Vougiouka, Olga; Sapountzi, Evdoxia; Venetsanopoulou, Aliki I; Tektonidou, Maria G; Germenis, Anastasios E; Sfikakis, Petros P; Laskari, Katerina

A Nationwide Study of the Delayed Diagnosis and the Clinical Manifestations of Predominantly Antibody Deficiencies and CTLA4-Mediated Immune Dysregulation Syndrome in Greece

希腊一项关于抗体缺乏症和CTLA4介导的免疫失调综合征的延迟诊断和临床表现的全国性研究

Kapousouzi, Androniki; Kalala, Fani; Sarrou, Styliani; Farmaki, Evangelia; Antonakos, Nikolaos; Kakkas, Ioannis; Kourakli, Alexandra; Labropoulou, Vassiliki; Kelaidi, Charikleia; Tsiouma, Georgia; Dimou, Maria; Vassilakopoulos, Theodoros P; Voulgarelis, Michael; Onoufriadis, Ilias; Papadimitriou, Eleni; Polychronopoulou, Sophia; Giamarellos-Bourboulis, Evangelos J; Symeonidis, Argiris; Hadjichristodoulou, Christos; Germenis, Anastasios E; Speletas, Matthaios

Hereditary angioedema with normal C1 inhibitor associated with carboxypeptidase N deficiency

伴有羧肽酶N缺乏症的C1抑制剂正常的遗传性血管性水肿

Vincent, Denis; Parsopoulou, Faidra; Martin, Ludovic; Gaboriaud, Christine; Demongeot, Jacques; Loules, Gedeon; Fischer, Sascha; Cichon, Sven; Germenis, Anastasios E; Ghannam, Arije; Drouet, Christian

Genetic Variants Leading to Urticaria and Angioedema and Associated Biomarkers

导致荨麻疹和血管性水肿的遗传变异及相关生物标志物

Lyons, Jonathan J; Farkas, Henriette; Germenis, Anastasios E; Rijavec, Matija; Smith, Tukisa D; Valent, Peter

Editorial: C1 inhibitor deficiency and angioedema

社论:C1抑制剂缺乏与血管性水肿

Farkas, Henriette; Germenis, Anastasios E; Longhurst, Hilary

Searching for Genetic Biomarkers for Hereditary Angioedema Due to C1-Inhibitor Deficiency (C1-INH-HAE)

寻找C1抑制剂缺乏引起的遗传性血管性水肿(C1-INH-HAE)的遗传生物标志物

Parsopoulou, Faidra; Loules, Gedeon; Zamanakou, Maria; Csuka, Dorottya; Szilagyi, Agnes; Kompoti, Maria; Porebski, Grzegorz; Psarros, Fotis; Magerl, Markus; Valerieva, Anna; Staevska, Maria; Obtulowicz, Krystyna; Maurer, Marcus; Speletas, Matthaios; Farkas, Henriette; Germenis, Anastasios E