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...

Guidelines on the use of irradiated blood components

British journal of haematology, 2020-12, Vol.191 (5), p.704-724

2020

Volltextzugriff (PDF)

Rituximab Associated Hypogammaglobulinemia in Autoimmune Disease

Frontiers in immunology, 2021-05, Vol.12, p.671503-671503

2021

Volltextzugriff (PDF)

Respiratory infectious burden in a cohort of antibody deficiency patients treated with immunoglobulin replacement therapy: The impact of lung pathology and gastroesophageal reflux disease

The journal of allergy and clinical immunology. Global, 2023-11, Vol.2 (4), p.100133-100133, Article 100133

2023

Volltextzugriff (PDF)

Optimizing hereditary angioedema management through tailored treatment approaches

Expert review of clinical immunology, 2016-01, Vol.12 (1), p.19-31

2016

Volltextzugriff (PDF)

Use of recombinant C1 inhibitor in patients with resistant or frequent attacks of hereditary or acquired angioedema

EJD. European journal of dermatology, 2014, Vol.24 (1), p.28-34

2014

Volltextzugriff (PDF)

Evidence that a STAT3 Mutation Causing Hyper IgE Syndrome Leads to Repression of Transcriptional Activity

Case Reports in Immunology, 2019, Vol.2019 (2019), p.1-5

2019

Volltextzugriff (PDF)

The European Society for Immunodeficiencies (ESID) Registry Working Definitions for the Clinical Diagnosis of Inborn Errors of Immunity

The journal of allergy and clinical immunology in practice (Cambridge, MA), 2019-07, Vol.7 (6), p.1763-1770

2019

Volltextzugriff (PDF)

Anaphylaxis to Patent Blue V: a case series

Asia Pacific allergy, 2012-01, Vol.2 (1), p.86-89

2012

Volltextzugriff (PDF)

Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans

Journal of allergy and clinical immunology, 2018-10, Vol.142 (4), p.1285-1296

2018

Volltextzugriff (PDF)

Monogenic early-onset lymphoproliferation and autoimmunity: Natural history of STAT3 gain-of-function syndrome

Journal of allergy and clinical immunology, 2023-04, Vol.151 (4), p.1081-1095

2023

Volltextzugriff (PDF)

Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations

Journal of allergy and clinical immunology, 2020-10, Vol.146 (4), p.901-911

2020

Volltextzugriff (PDF)

1773. Complement level measurements for children in England suggest a possible unreported Post Streptococcal Glomerulonephritis Outbreak

Open forum infectious diseases, 2023-11, Vol.10 (Supplement_2)

2023

Volltextzugriff (PDF)

Guidelines on the use of irradiated blood components

British journal of haematology, 2020-12, Vol.191 (5), p.704-724

2020

Volltextzugriff (PDF)

A novel de novo activating mutation in STAT3 identified in a patient with common variable immunodeficiency (CVID)

Clinical immunology (Orlando, Fla.), 2018-02, Vol.187, p.132-136

2018

Volltextzugriff (PDF)

Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes

American journal of human genetics, 2018-07, Vol.103 (1), p.3-18

2018

Volltextzugriff (PDF)

Autosomal Dominant STAT6 Gain of Function Causes Severe Atopy Associated with Lymphoma

Journal of clinical immunology, 2023-10, Vol.43 (7), p.1611-1622

2023

Volltextzugriff (PDF)

Telomerecat: A ploidy-agnostic method for estimating telomere length from whole genome sequencing data

Scientific reports, 2018-01, Vol.8 (1), p.1300-17, Article 1300

2018

Volltextzugriff (PDF)

Skipping of Exon 9 of Human CFTR in YAC-Transgenic Mice

Genomics (San Diego, Calif.), 2001-10, Vol.77 (3), p.127-134

2001

Volltextzugriff (PDF)

Practical challenges for functional validation of STAT1 gain of function genetic variants

Clinical and experimental immunology, 2023-04, Vol.212 (2), p.166-169

2023

Volltextzugriff (PDF)

Complementation of null CF mice with a human CFTR YAC transgene

The EMBO journal, 1997-07, Vol.16 (14), p.4238-4249

1997

Volltextzugriff (PDF)

Liver disease is common in patients with common variable immunodeficiency and predicts mortality in the presence of cirrhosis or portal hypertension

The journal of allergy and clinical immunology in practice (Cambridge, MA), 2019-09, Vol.7 (7), p.2484-2486.e3

2019

Volltextzugriff (PDF)

Loss‐of‐function mutations in CSF3R cause moderate neutropenia with fully mature neutrophils: two novel pedigrees

British journal of haematology, 2020-12, Vol.191 (5), p.930-934

2020

Volltextzugriff (PDF)

A National Survey of Hereditary Angioedema and Acquired C1 Inhibitor Deficiency in the United Kingdom

The journal of allergy and clinical immunology in practice (Cambridge, MA), 2023-08, Vol.11 (8), p.2476-2483

2023

Volltextzugriff (PDF)

Human Amniotic Fluid Stem Cells Have Hematopoietic Potential In Vivo

Blood, 2016-12, Vol.128 (22), p.5719-5719

2016

Volltextzugriff (PDF)

1 – 25 von 38

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(34)
Mit Volltextzugriff
(35)

Publikationsform

Sprache

Englisch
(37)
Portugiesisch
(1)

Erscheinungsjahr

n.n

Thema

Science & Technology
(23)
Life Sciences & Biomedicine
(21)
Humans
(16)
Immunology
(13)
Allergy
(8)
Female
(7)
Adult
(6)
Male
(6)
Mutation
(6)
Common Variable Immunodeficiency
(5)
Gene Expression
(5)
Animals
(4)
Mice
(4)
Middle Aged
(4)
Aged
(3)
Autoimmunity
(3)
Biochemistry & Molecular Biology
(3)
Chromosomes, Artificial, Yeast
(3)
Cystic Fibrosis Transmembrane Conductance Regulator - Genetics
(3)
Gain Of Function Mutation
(3)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Guidelines on the use of irradiated blood components

Rituximab Associated Hypogammaglobulinemia in Autoimmune Disease

Respiratory infectious burden in a cohort of antibody deficiency patients treated with immunoglobulin replacement therapy: The impact of lung pathology and gastroesophageal reflux disease

Optimizing hereditary angioedema management through tailored treatment approaches

Use of recombinant C1 inhibitor in patients with resistant or frequent attacks of hereditary or acquired angioedema

Evidence that a STAT3 Mutation Causing Hyper IgE Syndrome Leads to Repression of Transcriptional Activity

The European Society for Immunodeficiencies (ESID) Registry Working Definitions for the Clinical Diagnosis of Inborn Errors of Immunity

Anaphylaxis to Patent Blue V: a case series

Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans

Monogenic early-onset lymphoproliferation and autoimmunity: Natural history of STAT3 gain-of-function syndrome

Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations

1773. Complement level measurements for children in England suggest a possible unreported Post Streptococcal Glomerulonephritis Outbreak

Guidelines on the use of irradiated blood components

A novel de novo activating mutation in STAT3 identified in a patient with common variable immunodeficiency (CVID)

Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes

Berotralstat for the prophylaxis of hereditary angioedema—Real‐world evidence data from the United Kingdom

Autosomal Dominant STAT6 Gain of Function Causes Severe Atopy Associated with Lymphoma

Telomerecat: A ploidy-agnostic method for estimating telomere length from whole genome sequencing data

Skipping of Exon 9 of Human CFTR in YAC-Transgenic Mice

Practical challenges for functional validation of STAT1 gain of function genetic variants

Complementation of null CF mice with a human CFTR YAC transgene

Liver disease is common in patients with common variable immunodeficiency and predicts mortality in the presence of cirrhosis or portal hypertension

Loss‐of‐function mutations in CSF3R cause moderate neutropenia with fully mature neutrophils: two novel pedigrees

A National Survey of Hereditary Angioedema and Acquired C1 Inhibitor Deficiency in the United Kingdom

Human Amniotic Fluid Stem Cells Have Hematopoietic Potential In Vivo

Suchergebnisse filtern