相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。SERPING1 Variants and C1-INH Biological Function: A Close Relationship With C1-INH-HAE
Christian Drouet et al.
FRONTIERS IN ALLERGY (2022)
Overview of SERPING1 Variations Identified in Hungarian Patients With Hereditary Angioedema
Edina Szabo et al.
FRONTIERS IN ALLERGY (2022)
A robust multiplexed assay to quantify C1-inhibitor, C1q, and C4 proteins for in vitro diagnosis of hereditary angioedema from dried blood spot
Yongquan Lai et al.
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS (2021)
Deep Intronic Mutation in SERPING1 Caused Hereditary Angioedema Through Pseudoexon Activation
Pavla Hujova et al.
JOURNAL OF CLINICAL IMMUNOLOGY (2020)
A novel functional C1 inhibitor activity assay in dried blood spot for diagnosis of Hereditary angioedema
Yongquan Lai et al.
CLINICA CHIMICA ACTA (2020)
The Role of Complement in Hereditary Angioedema
Marcel Levi et al.
TRANSFUSION MEDICINE REVIEWS (2019)
Analysis of the Complement System in the Clinical Immunology Laboratory
Morris Ling et al.
CLINICS IN LABORATORY MEDICINE (2019)
Targeted next-generation sequencing for the molecular diagnosis of hereditary angioedema due to C1-inhibitor deficiency
Gedeon Loules et al.
GENE (2018)
Angioedema Due to Bradykinin Dysregulation
Marco Cicardi et al.
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE (2018)
Acquired C1 Inhibitor Deficiency
Iris M. Otani et al.
IMMUNOLOGY AND ALLERGY CLINICS OF NORTH AMERICA (2017)
Hereditary angioedema: Molecular and clinical differences among European populations
Matthaios Speletas et al.
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY (2015)
Classification, diagnosis, and approach to treatment for angioedema: consensus report from the Hereditary Angioedema International Working Group
M. Cicardi et al.
ALLERGY (2014)
Pharmacokinetics of plasma-derived C1-esterase inhibitor after subcutaneous versus intravenous administration in subjects with mild or moderate hereditary angioedema: the PASSION study
Inmaculada Martinez-Saguer et al.
TRANSFUSION (2014)
Less severe clinical manifestations in patients with hereditary angioedema with missense C1INH gene mutations
Andras Bors et al.
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY (2013)
Mutational spectrum of the C1INH (SERPING1) gene in patients with hereditary angioedema
T. Goesswein et al.
CYTOGENETIC AND GENOME RESEARCH (2008)
Complement analysis in the 21st century
Tom Eirik Mollnes et al.
MOLECULAR IMMUNOLOGY (2007)
Lymphoproliferative disease and acquired C1 inhibitor deficiency
Roberto Castelli et al.
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL (2007)
Hereditary anglioedema:: The mutation spectrum of SERPING1/C1NH in a large Spanish cohort
O Roche et al.
HUMAN MUTATION (2005)
Mutation Screening of the C1 Inhibitor Gene Among Hungarian Patients With Hereditary Angioedema
Lajos Kalmar et al.
HUMAN MUTATION (2003)
Increased expression of C1-inhibitor mRNA in patients with hereditary angioedema treated with Danazol
E Pappalardo et al.
IMMUNOLOGY LETTERS (2003)
Complement C4 inhibits systemic autoimmunity through a mechanism independent of complement receptors CR1 and CR2
ZB Chen et al.
JOURNAL OF EXPERIMENTAL MEDICINE (2000)