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...

Combined immunodeficiency and atopy caused by a dominant negative mutation in caspase activation and recruitment domain family member 11 (CARD11)

Journal of allergy and clinical immunology, 2018-05, Vol.141 (5), p.1818-1830.e2

2018

Volltextzugriff (PDF)

Compound heterozygous mutations in the noncoding RNU4ATAC cause Roifman Syndrome by disrupting minor intron splicing

Nature communications, 2015-11, Vol.6 (1), p.8718-8718, Article 8718

2015

Volltextzugriff (PDF)

Ataxia Telangiectasia Diagnosed on Newborn Screening-Case Cohort of 5 Years' Experience

Frontiers in immunology, 2019-12, Vol.10, p.2940-2940

2019

Volltextzugriff (PDF)

Psychosocial Issues of the Adolescent PI Patient & The Development of the PI Teen Outreach Program

LymphoSign journal, 2018-03, Article lymphosign-2018-0002

2018

Volltextzugriff (PDF)

A Unique Comprehensive Model to Screen Newborns for Severe Combined Immunodeficiency-An Ontario Single-Centre Experience Spanning 2013-2023

Genes, 2024-07, Vol.15 (7), p.920

2024

Volltextzugriff (PDF)

Hematopoietic Stem Cell Transplantation For RelB Deficiency

Journal of allergy and clinical immunology, 2017-10, Vol.140 (4), p.1199-1201.e3

2017

Volltextzugriff (PDF)

Managing Newborn Screening for SCID in a Referral Centre

LymphoSign journal, 2017-06, Article lymphosign-2017-0005

2017

Volltextzugriff (PDF)

Strategies for managing paediatric patients in immunoglobulin clinical trials

LymphoSign journal, 2019-09, Vol.6 (3), p.113-116

Reid, Brenda

2019

Volltextzugriff (PDF)

PSV-15 Variability in the Oxidative Status of Fats and Oils Used in Livestock Diets in North America

Journal of animal science, 2021-05, Vol.99 (Supplement_1), p.197-198

2021

Volltextzugriff (PDF)

Combined immunodeficiency caused by a novel homozygous NFKB1 mutation

Journal of allergy and clinical immunology, 2021-02, Vol.147 (2), p.727-733.e2

2021

Volltextzugriff (PDF)

Identification of a novel RAG1 hypomorphic mutation in a child presenting with disseminated vaccine-strain varicella

LymphoSign journal, 2021-03, Vol.8 (1), p.5-10

2021

Volltextzugriff (PDF)

Novel heterozygous PIK3CD mutation presenting with only laboratory markers of combined immunodeficiency

LymphoSign journal, 2020-06, Vol.7 (2), p.49-55

2020

Volltextzugriff (PDF)

Long-Term Outcome of Adenosine Deaminase-Deficient Patients—a Single-Center Experience

Journal of clinical immunology, 2017-08, Vol.37 (6), p.582-591

2017

Volltextzugriff (PDF)

Isolation protocol for patients with severe combined immune deficiency

LymphoSign journal, 2015-09, Vol.2 (3), p.165-170

2015

Volltextzugriff (PDF)

Mutations in STAT3 and IL12RB1 impair the development of human IL-17-producing T cells

The Journal of experimental medicine, 2008-07, Vol.205 (7), p.1543-1550

2008

Volltextzugriff (PDF)

Morbidity in an adenosine deaminase-deficient patient during 27 years of enzyme replacement therapy

Clinical immunology (Orlando, Fla.), 2020-02, Vol.211, p.108321-108321, Article 108321

2020

Volltextzugriff (PDF)

Bone marrow transplantation for severe combined immune deficiency

JAMA : the journal of the American Medical Association, 2006-02, Vol.295 (5), p.508

2006

Volltextzugriff (PDF)

Time-dependent decline of T-cell receptor excision circle levels in ZAP-70 deficiency

The journal of allergy and clinical immunology in practice (Cambridge, MA), 2020-02, Vol.8 (2), p.806-808.e2

2020

Volltextzugriff (PDF)

Long-term immune reconstitution after matched unrelated hematopoietic stem cell transplantation for immunodeficiency

Journal of allergy and clinical immunology, 2018-03, Vol.141 (3), p.1154-1157.e3

2018

Volltextzugriff (PDF)

Home gammaglobulin therapy: a patient survey of intravenous and subcutaneous options in Canada

LymphoSign journal, 2014-09, Vol.1 (1), p.27-37

2014

Volltextzugriff (PDF)

Coronin 1A deficiency identified by newborn screening for severe combined immunodeficiency

LymphoSign journal, 2019-03, Vol.6 (1), p.17-25

2019

Volltextzugriff (PDF)

Development of an ambulatory infusion protocol for Abatacept

LymphoSign journal, 2018-06, Vol.5 (2), p.61-65

2018

Volltextzugriff (PDF)

Successful hematopoietic stem cell transplantation in a patient with a novel mutation in coronin 1A

LymphoSign journal, 2019-06, Vol.6 (2), p.52-60

2019

Volltextzugriff (PDF)

Report of the Canadian Expert Committee on the management of ADA deficiency

LymphoSign journal, 2020-09, Vol.7 (3), p.109-115

2020

Volltextzugriff (PDF)

A Novel Mutation in Roifman Syndrome Redefines the Boundaries of the Sm Protein-Binding Site

LymphoSign journal, 2016-11, Article lymphosign-2016-0015

2016

Volltextzugriff (PDF)

1 – 25 von 315

Suche als RSS-Feed

Aktive Filter

ThemaChild

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(288)
Mit Volltextzugriff
(251)

Publikationsform

3 weitere anzeigen...

Weniger anzeigen...

Sprache

Englisch
(315)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

Menü

Weitere Dienste

Einstellungen

Combined immunodeficiency and atopy caused by a dominant negative mutation in caspase activation and recruitment domain family member 11 (CARD11)

Compound heterozygous mutations in the noncoding RNU4ATAC cause Roifman Syndrome by disrupting minor intron splicing

Ataxia Telangiectasia Diagnosed on Newborn Screening-Case Cohort of 5 Years' Experience

Psychosocial Issues of the Adolescent PI Patient & The Development of the PI Teen Outreach Program

A Unique Comprehensive Model to Screen Newborns for Severe Combined Immunodeficiency-An Ontario Single-Centre Experience Spanning 2013-2023

Hematopoietic Stem Cell Transplantation For RelB Deficiency

Managing Newborn Screening for SCID in a Referral Centre

Strategies for managing paediatric patients in immunoglobulin clinical trials

PSV-15 Variability in the Oxidative Status of Fats and Oils Used in Livestock Diets in North America

Combined immunodeficiency caused by a novel homozygous NFKB1 mutation

Identification of a novel RAG1 hypomorphic mutation in a child presenting with disseminated vaccine-strain varicella

Novel heterozygous PIK3CD mutation presenting with only laboratory markers of combined immunodeficiency

Long-Term Outcome of Adenosine Deaminase-Deficient Patients—a Single-Center Experience

Isolation protocol for patients with severe combined immune deficiency

Mutations in STAT3 and IL12RB1 impair the development of human IL-17-producing T cells

Morbidity in an adenosine deaminase-deficient patient during 27 years of enzyme replacement therapy

Bone marrow transplantation for severe combined immune deficiency

Time-dependent decline of T-cell receptor excision circle levels in ZAP-70 deficiency

Long-term immune reconstitution after matched unrelated hematopoietic stem cell transplantation for immunodeficiency

Home gammaglobulin therapy: a patient survey of intravenous and subcutaneous options in Canada

Coronin 1A deficiency identified by newborn screening for severe combined immunodeficiency

Development of an ambulatory infusion protocol for Abatacept

Successful hematopoietic stem cell transplantation in a patient with a novel mutation in coronin 1A

Report of the Canadian Expert Committee on the management of ADA deficiency

A Novel Mutation in Roifman Syndrome Redefines the Boundaries of the Sm Protein-Binding Site

Aktive Filter

Suchergebnisse filtern