UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 184

Sortiert nach

Biallelic RIPK1 mutations in humans cause severe immunodeficiency, arthritis, and intestinal inflammation

Science (American Association for the Advancement of Science), 2018-08, Vol.361 (6404), p.810-813

2018

Volltextzugriff (PDF)

Management of autoimmune diseases after haematopoietic stem cell transplantation

British journal of haematology, 2012-05, Vol.157 (3), p.281-290

2012

Volltextzugriff (PDF)

Biallelic hypomorphic mutations in a linear deubiquitinase define otulipenia, an early-onset autoinflammatory disease

Proceedings of the National Academy of Sciences - PNAS, 2016-09, Vol.113 (36), p.10127-10132

2016

Volltextzugriff (PDF)

Hematopoietic stem cell transplantation in 29 patients hemizygous for hypomorphic IKBKG/NEMO mutations

Blood, 2017-09, Vol.130 (12), p.1456-1467

2017

Volltextzugriff (PDF)

Hematopoietic stem cell transplant in patients with activated PI3K delta syndrome

Journal of allergy and clinical immunology, 2017-03, Vol.139 (3), p.1046-1049

2017

Volltextzugriff (PDF)

Hematopoietic stem cell transplantation for CTLA4 deficiency

Journal of allergy and clinical immunology, 2016-08, Vol.138 (2), p.615-619.e1

2016

Volltextzugriff (PDF)

Hematopoietic Stem Cell Transplantation Resolves the Immune Deficit Associated with STAT3-Dominant-Negative Hyper-IgE Syndrome

Journal of clinical immunology, 2021-07, Vol.41 (5), p.934-943

2021

Volltextzugriff (PDF)

Outcome of Hematopoietic Stem Cell Transplantation in patients with Mendelian Susceptibility to Mycobacterial Diseases

Journal of clinical immunology, 2021-11, Vol.41 (8), p.1774-1780

2021

Volltextzugriff (PDF)

Improved survival and graft function in ex vivo T-cell depleted haploidentical hematopoietic cell transplantation for primary immunodeficiency

Bone marrow transplantation (Basingstoke), 2021-05, Vol.56 (5), p.1200-1204

2021

Volltextzugriff (PDF)

Outcome of autoimmune cytopenia after hematopoietic cell transplantation in primary immunodeficiency

Journal of allergy and clinical immunology, 2020-08, Vol.146 (2), p.406-416

2020

Volltextzugriff (PDF)

Osteoclast-poor osteopetrosis

Bone (New York, N.Y.), 2022-11, Vol.164, p.116541-116541, Article 116541

2022

Volltextzugriff (PDF)

Allogeneic HSCT for Autoimmune Diseases: A Retrospective Study From the EBMT ADWP, IEWP, and PDWP Working Parties

Frontiers in immunology, 2019-07, Vol.10, p.1570-1570

2019

Volltextzugriff (PDF)

Osteoclast-poor human osteopetrosis due to mutations in the gene encoding RANKL

Nature genetics, 2007-08, Vol.39 (8), p.960-962

2007

Volltextzugriff (PDF)

Hematopoietic stem cell transplantation corrects osteopetrosis in a child carrying a novel homozygous mutation in the FERMT3 gene

Bone (New York, N.Y.), 2017-04, Vol.97, p.126-129

2017

Volltextzugriff (PDF)

Risks of serious infections in children treated with biologic response-modifying drugs

Rheumatology (Oxford, England), 2018-02, Vol.57 (2), p.211-212

Abinun, Mario

2018

Volltextzugriff (PDF)

Long-term survival and transplantation of haemopoietic stem cells for immunodeficiencies: report of the European experience 1968–99

The Lancet (British edition), 2003-02, Vol.361 (9357), p.553-560

2003

Volltextzugriff (PDF)

Infection-Related Death among Persons with Refractory Juvenile Idiopathic Arthritis

Emerging infectious diseases, 2016-10, Vol.22 (10), p.1720-1727

2016

Volltextzugriff (PDF)

Outcome of Non-hematological Autoimmunity After Hematopoietic Cell Transplantation in Children with Primary Immunodeficiency

Journal of clinical immunology, 2021, Vol.41 (1), p.171-184

2021

Volltextzugriff (PDF)

Intracerebral large artery disease in Aicardi–Goutières syndrome implicates SAMHD1 in vascular homeostasis

Developmental medicine and child neurology, 2010-08, Vol.52 (8), p.725-732

2010

Volltextzugriff (PDF)

Osteoclast rich osteopetrosis due to defects in TCIRG1 gene

Bone (New York, N.Y.), 2022-12, Vol.165, p.116519-116519, Article 116519

2022

Volltextzugriff (PDF)

Defects in TCIRG1 subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosis

Nature genetics, 2000-07, Vol.25 (3), p.343-346

2000

Volltextzugriff (PDF)

Autoimmunity in human primary immunodeficiency diseases

Blood, 2002-04, Vol.99 (8), p.2694-2702

2002

Volltextzugriff (PDF)

1 – 25 von 184

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(160)
Mit Volltextzugriff
(175)

Publikationsform

Artikel
(166)
Berichte
(12)
Buchkapitel
(5)
Bücher
(1)

Sprache

Englisch
(184)
Japanisch
(24)

Erscheinungsjahr

n.n

Thema

Science & Technology
(120)
Humans
(115)
Life Sciences & Biomedicine
(115)
Immunology
(64)
Male
(63)
Child
(59)
Female
(59)
Infant
(49)
Biological And Medical Sciences
(43)
Child, Preschool
(43)
Medical Sciences
(41)
Adolescent
(37)
Hematopoietic Stem Cell Transplantation
(29)
Pediatrics
(29)
Hematology
(28)
Infectious Diseases
(28)
Mutation
(28)
Patients
(24)
Stem Cells
(22)
Transplantation
(22)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Biallelic RIPK1 mutations in humans cause severe immunodeficiency, arthritis, and intestinal inflammation

Management of autoimmune diseases after haematopoietic stem cell transplantation

Biallelic hypomorphic mutations in a linear deubiquitinase define otulipenia, an early-onset autoinflammatory disease

Hematopoietic stem cell transplantation in 29 patients hemizygous for hypomorphic IKBKG/NEMO mutations

Hematopoietic stem cell transplant in patients with activated PI3K delta syndrome

Hematopoietic stem cell transplantation for CTLA4 deficiency

Hematopoietic Stem Cell Transplantation Resolves the Immune Deficit Associated with STAT3-Dominant-Negative Hyper-IgE Syndrome

Outcome of Hematopoietic Stem Cell Transplantation in patients with Mendelian Susceptibility to Mycobacterial Diseases

Improved survival and graft function in ex vivo T-cell depleted haploidentical hematopoietic cell transplantation for primary immunodeficiency

Outcome of autoimmune cytopenia after hematopoietic cell transplantation in primary immunodeficiency

Osteoclast-poor osteopetrosis

Allogeneic HSCT for Autoimmune Diseases: A Retrospective Study From the EBMT ADWP, IEWP, and PDWP Working Parties

Human Tyrosine Kinase 2 Deficiency Reveals Its Requisite Roles in Multiple Cytokine Signals Involved in Innate and Acquired Immunity

Osteoclast-poor human osteopetrosis due to mutations in the gene encoding RANKL

Hematopoietic stem cell transplantation corrects osteopetrosis in a child carrying a novel homozygous mutation in the FERMT3 gene

Risks of serious infections in children treated with biologic response-modifying drugs

Secondary autoimmune diseases occurring after HSCT for an autoimmune disease: a retrospective study of the EBMT Autoimmune Disease Working Party

Long-term survival and transplantation of haemopoietic stem cells for immunodeficiencies: report of the European experience 1968–99

Infection-Related Death among Persons with Refractory Juvenile Idiopathic Arthritis

Outcome of Non-hematological Autoimmunity After Hematopoietic Cell Transplantation in Children with Primary Immunodeficiency

New autoimmune diseases after cord blood transplantation: a retrospective study of EUROCORD and the Autoimmune Disease Working Party of the European Group for Blood and Marrow Transplantation

Intracerebral large artery disease in Aicardi–Goutières syndrome implicates SAMHD1 in vascular homeostasis

Osteoclast rich osteopetrosis due to defects in TCIRG1 gene

Defects in TCIRG1 subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosis

Autoimmunity in human primary immunodeficiency diseases

Suchergebnisse filtern