UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Rediscovery of a forgotten disease: Hereditary Angioedema

Balkan medical journal, 2021-03, Vol.38 (2), p.68-72

2021

Volltextzugriff (PDF)

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

Frontiers in immunology, 2024, Vol.15, p.1342668-1342668

2024

Volltextzugriff (PDF)

Hereditary angioedema: Molecular and clinical differences among European populations

Journal of allergy and clinical immunology, 2015-02, Vol.135 (2), p.570-573.e10

2015

Volltextzugriff (PDF)

Persistent Activation of Innate Immunity in Patients with Primary Antibody Deficiencies

Journal of Immunology Research, 2020-11, Vol.2020 (2020), p.1-11

2020

Volltextzugriff (PDF)

Editorial: C1 inhibitor deficiency and angioedema

Frontiers in allergy, 2022-11, Vol.3, p.1065400-1065400

2022

Volltextzugriff (PDF)

Foxp3 expression in human cancer cells

Journal of translational medicine, 2008-04, Vol.6 (1), p.19-19, Article 19

2008

Volltextzugriff (PDF)

Genetics of Hereditary Angioedema Revisited

Clinical Reviews in Allergy & Immunology, 2016-10, Vol.51 (2), p.170-182

2016

Volltextzugriff (PDF)

Fabry disease due to D313Y and novel GLA mutations

BMJ open, 2017-10, Vol.7 (10), p.e017098-e017098

2017

Volltextzugriff (PDF)

SERPING1 Variants and C1-INH Biological Function: A Close Relationship With C1-INH-HAE

Frontiers in allergy, 2022-03, Vol.3, p.835503-835503

2022

Volltextzugriff (PDF)

A common single nucleotide polymorphism impairs B-cell activating factor receptor's multimerization, contributing to common variable immunodeficiency

Journal of allergy and clinical immunology, 2014-04, Vol.133 (4), p.1222-1225.e10

2014

Volltextzugriff (PDF)

An Activating Janus Kinase-3 Mutation Is Associated with Cytotoxic T Lymphocyte Antigen-4-Dependent Immune Dysregulation Syndrome

Frontiers in immunology, 2017-12, Vol.8, p.1824-1824

2017

Volltextzugriff (PDF)

A novel deep intronic SERPING1 variant as a cause of hereditary angioedema due to C1-inhibitor deficiency

Allergology International, 2020-07, Vol.69 (3), p.443-449

2020

Volltextzugriff (PDF)

Hereditary angioedema with normal C1 inhibitor associated with carboxypeptidase N deficiency

The journal of allergy and clinical immunology. Global, 2024-05, Vol.3 (2), p.100223, Article 100223

2024

Volltextzugriff (PDF)

Hereditary Angioedema in Greece: The First Results of the Greek Hereditary Angioedema Registry

International archives of allergy and immunology, 2014-01, Vol.164 (4), p.326-332

2014

Volltextzugriff (PDF)

Driving towards Precision Medicine for angioedema without wheals

Journal of autoimmunity, 2019-11, Vol.104, p.102312-102312, Article 102312

2019

Volltextzugriff (PDF)

Liver FOXP3 and PD1/PDL1 Expression is Down-Regulated in Chronic HBV Hepatitis on Maintained Remission Related to the Degree of Inflammation

Frontiers in immunology, 2013-01, Vol.4, p.207-207

2013

Volltextzugriff (PDF)

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

Frontiers in allergy, 2022-07, Vol.3, p.868185-868185

2022

Volltextzugriff (PDF)

BAFF/APRIL System Is Functional in B-Cell Acute Lymphoblastic Leukemia in a Disease Subtype Manner

Frontiers in oncology, 2019-07, Vol.9, p.594-594

2019

Volltextzugriff (PDF)

Toll-Like Receptor 4 Gene (TLR4), but Not TLR2, Polymorphisms Modify the Risk of Tonsillar Disease Due to Streptococcus pyogenes and Haemophilus influenzae

Clinical and Vaccine Immunology, 2011-02, Vol.18 (2), p.217-222

2011

Volltextzugriff (PDF)

MBL2 Genotypes and Their Associations with MBL Levels and NICU Morbidity in a Cohort of Greek Neonates

Journal of Immunology Research, 2015-01, Vol.2015 (2015), p.1-10

2015

Volltextzugriff (PDF)

SIAE Rare Variants in Juvenile Idiopathic Arthritis and Primary Antibody Deficiencies

Journal of immunology research, 2017-01, Vol.2017 (2017), p.1-11

2017

Volltextzugriff (PDF)

Hereditary Angioedema with Normal C1 Inhibitor: Update on Evaluation and Treatment

Immunology and allergy clinics of North America, 2017-08, Vol.37 (3), p.571-584

2017

Volltextzugriff (PDF)

Performance of Antibodies against Tissue Transglutaminase for the Diagnosis of Celiac Disease: Meta-Analysis

Clinical and Vaccine Immunology, 2006-02, Vol.13 (2), p.187-192

2006

Volltextzugriff (PDF)

1 – 25 von 101

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(97)
Mit Volltextzugriff
(92)

Publikationsform

Artikel
(100)
Berichte
(1)

Sprache

Englisch
(101)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Rediscovery of a forgotten disease: Hereditary Angioedema

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

Targeted next-generation sequencing for the molecular diagnosis of hereditary angioedema due to C1-inhibitor deficiency

Hereditary angioedema: Molecular and clinical differences among European populations

Persistent Activation of Innate Immunity in Patients with Primary Antibody Deficiencies

Editorial: C1 inhibitor deficiency and angioedema

Foxp3 expression in human cancer cells

Genetics of Hereditary Angioedema Revisited

Fabry disease due to D313Y and novel GLA mutations

SERPING1 Variants and C1-INH Biological Function: A Close Relationship With C1-INH-HAE

A common single nucleotide polymorphism impairs B-cell activating factor receptor's multimerization, contributing to common variable immunodeficiency

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

An Activating Janus Kinase-3 Mutation Is Associated with Cytotoxic T Lymphocyte Antigen-4-Dependent Immune Dysregulation Syndrome

A novel deep intronic SERPING1 variant as a cause of hereditary angioedema due to C1-inhibitor deficiency

Hereditary angioedema with normal C1 inhibitor associated with carboxypeptidase N deficiency

Hereditary Angioedema in Greece: The First Results of the Greek Hereditary Angioedema Registry

Driving towards Precision Medicine for angioedema without wheals

Liver FOXP3 and PD1/PDL1 Expression is Down-Regulated in Chronic HBV Hepatitis on Maintained Remission Related to the Degree of Inflammation

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

BAFF/APRIL System Is Functional in B-Cell Acute Lymphoblastic Leukemia in a Disease Subtype Manner

Toll-Like Receptor 4 Gene (TLR4), but Not TLR2, Polymorphisms Modify the Risk of Tonsillar Disease Due to Streptococcus pyogenes and Haemophilus influenzae

MBL2 Genotypes and Their Associations with MBL Levels and NICU Morbidity in a Cohort of Greek Neonates

SIAE Rare Variants in Juvenile Idiopathic Arthritis and Primary Antibody Deficiencies

Hereditary Angioedema with Normal C1 Inhibitor: Update on Evaluation and Treatment

Performance of Antibodies against Tissue Transglutaminase for the Diagnosis of Celiac Disease: Meta-Analysis

Suchergebnisse filtern