UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 47

Sortiert nach

Early lymphocyte collection for anti‐CD19 CART production improves T‐cell fitness in patients with relapsed/refractory diffuse large B‐cell lymphoma

British journal of haematology, 2023-07, Vol.202 (1), p.74-85

2023

Volltextzugriff (PDF)

Incidence and risk factors for moderate-to-severe veno-occlusive disease of the liver after allogeneic stem cell transplantation using a reduced intensity conditioning regimen

Bone marrow transplantation (Basingstoke), 2014-11, Vol.49 (11), p.1389-1392

2014

Volltextzugriff (PDF)

Inherited susceptibility to pre B-ALL caused by germline transmission of PAX5 c.547G>A

Leukemia, 2014-05, Vol.28 (5), p.1136-1138

2014

Volltextzugriff (PDF)

The use of whole exome sequencing for the diagnosis of autosomal recessive malignant infantile osteopetrosis

Clinical genetics, 2017-07, Vol.92 (1), p.80-85

2017

Volltextzugriff (PDF)

Management of XLP-1 and ITK deficiency: The challenges posed by PID with an unpredictable spectrum of disease manifestations

Clinical immunology (Orlando, Fla.), 2019-01, Vol.198, p.39-45

2019

Volltextzugriff (PDF)

The molecular rationale for steroid based therapy of leukemia: diagnostic and therapeutic implications

European journal of cancer (1990), 2016-07, Vol.61, p.S179-S180

2016

Volltextzugriff (PDF)

Extending the clinical and immunological phenotype of human interleukin-21 receptor deficiency

Haematologica (Roma), 2015-02, Vol.100 (2), p.e72

2015

Volltextzugriff (PDF)

Loss-of-function mutations within the IL-2 inducible kinase ITK in patients with EBV-associated lymphoproliferative diseases

Leukemia, 2012-05, Vol.26 (5), p.963-971

2012

Volltextzugriff (PDF)

Non-fermentative Gram-negative rods bacteremia in children with cancer: a 14-year single-center experience

Infection, 2017-06, Vol.45 (3), p.327-334

2017

Volltextzugriff (PDF)

Deregulation of Fas ligand expression as a novel cause of autoimmune lymphoproliferative syndrome-like disease

Haematologica (Roma), 2015-09, Vol.100 (9), p.1189

2015

Volltextzugriff (PDF)

P887: IN‐HOUSE ANTI BCMA CAR‐T THERAPY FOR THE TREATMENT OF RELAPSED REFRACTORY MULTIPLE MYELOMA: PHASE 1 RESULTS

HemaSphere, 2022-06, Vol.6 (Suppl), p.779-780

2022

Volltextzugriff (PDF)

Colistin is relatively safe in hematological malignancies and hematopoietic stem cell transplantation patients

Infection, 2013-10, Vol.41 (5), p.991-997

2013

Volltextzugriff (PDF)

Reduced-intensity conditioning and HLA-matched haemopoietic stem-cell transplantation in patients with chronic granulomatous disease: a prospective multicentre study

The Lancet (British edition), 2014-02, Vol.383 (9915), p.436-448

2014

Volltextzugriff (PDF)

Long-term outcome of LRBA deficiency in 76 patients after various treatment modalities as evaluated by the immune deficiency and dysregulation activity (IDDA) score

Journal of allergy and clinical immunology, 2020-05, Vol.145 (5), p.1452-1463

2020

Volltextzugriff (PDF)

Successful second haploidentical SCT in osteopetrosis

Bone marrow transplantation (Basingstoke), 2011-07, Vol.46 (7), p.1021-1022

2011

Volltextzugriff (PDF)

MSC for the improvement of hematopoietic engraftment

Bone marrow transplantation (Basingstoke), 2010-03, Vol.45 (3), p.605-606

2010

Volltextzugriff (PDF)

788 - The molecular rationale for steroid based therapy of leukemia: diagnostic and therapeutic implications

European journal of cancer (1990), 2016-07, Vol.61, p.S179-S180

2016

Volltextzugriff (PDF)

Treatment of severe forms of LPS-responsive beige-like anchor protein deficiency with allogeneic hematopoietic stem cell transplantation

Journal of allergy and clinical immunology, 2018-02, Vol.141 (2), p.770-775.e1

2018

Volltextzugriff (PDF)

IL-2-inducible T-cell kinase deficiency: clinical presentation and therapeutic approach

Haematologica (Roma), 2011-03, Vol.96 (3), p.472-476

2011

Volltextzugriff (PDF)

Combination of umbilical cord blood with BM from a 2-month-old sibling as lifesaving BMT for very severe aplastic anemia

Bone marrow transplantation (Basingstoke), 2008-10, Vol.42 (8), p.563-564

2008

Volltextzugriff (PDF)

Assessment of disease activity and management of patients with NFkB1 insufficiency

CLINICAL IMMUNOLOGY, 2023-05, Vol.250, p.109420, Article 109420

2023

Volltextzugriff (PDF)

Cutaneous Chronic Graft Versus Host Disease Following Allogeneic Haematopoietic Stem Cell Transplantation in Children: A Retrospective Study

Acta dermato-venereologica, 2018-02, Vol.98 (2), p.206-211

2018

Volltextzugriff (PDF)

Frequency and natural history of inherited bone marrow failure syndromes: the Israeli Inherited Bone Marrow Failure Registry

Haematologica (Roma), 2010-08, Vol.95 (8), p.1300-1307

2010

Volltextzugriff (PDF)

1 – 25 von 47

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(45)
Mit Volltextzugriff
(45)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Life Sciences & Biomedicine
(30)
Science & Technology
(30)
Humans
(27)
Male
(18)
Immunology
(17)
Hematology
(16)
Female
(15)
Child, Preschool
(13)
Medicin Och Hälsovetenskap
(12)
Biological And Medical Sciences
(11)
Child
(11)
Medical Sciences
(11)
Adolescent
(10)
Infant
(9)
Adult
(8)
Mutation
(8)
Stem Cell Transplantation
(8)
Patients
(7)
Hematologic And Hematopoietic Diseases
(6)
Hematopoietic Stem Cell Transplantation
(6)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Early lymphocyte collection for anti‐CD19 CART production improves T‐cell fitness in patients with relapsed/refractory diffuse large B‐cell lymphoma

Incidence and risk factors for moderate-to-severe veno-occlusive disease of the liver after allogeneic stem cell transplantation using a reduced intensity conditioning regimen

Inherited susceptibility to pre B-ALL caused by germline transmission of PAX5 c.547G>A

The use of whole exome sequencing for the diagnosis of autosomal recessive malignant infantile osteopetrosis

Management of XLP-1 and ITK deficiency: The challenges posed by PID with an unpredictable spectrum of disease manifestations

The molecular rationale for steroid based therapy of leukemia: diagnostic and therapeutic implications

Extending the clinical and immunological phenotype of human interleukin-21 receptor deficiency

Loss-of-function mutations within the IL-2 inducible kinase ITK in patients with EBV-associated lymphoproliferative diseases

Non-fermentative Gram-negative rods bacteremia in children with cancer: a 14-year single-center experience

Deregulation of Fas ligand expression as a novel cause of autoimmune lymphoproliferative syndrome-like disease

P887: IN‐HOUSE ANTI BCMA CAR‐T THERAPY FOR THE TREATMENT OF RELAPSED REFRACTORY MULTIPLE MYELOMA: PHASE 1 RESULTS

Colistin is relatively safe in hematological malignancies and hematopoietic stem cell transplantation patients

Reduced-intensity conditioning and HLA-matched haemopoietic stem-cell transplantation in patients with chronic granulomatous disease: a prospective multicentre study

Long-term outcome of LRBA deficiency in 76 patients after various treatment modalities as evaluated by the immune deficiency and dysregulation activity (IDDA) score

Hematopoietic cell transplantation in chronic granulomatous disease: a study of 712 children and adults

Successful second haploidentical SCT in osteopetrosis

MSC for the improvement of hematopoietic engraftment

788 - The molecular rationale for steroid based therapy of leukemia: diagnostic and therapeutic implications

Treatment of severe forms of LPS-responsive beige-like anchor protein deficiency with allogeneic hematopoietic stem cell transplantation

IL-2-inducible T-cell kinase deficiency: clinical presentation and therapeutic approach

Allogeneic Hematopoietic Cell Transplantation for Fanconi Anemia in Patients With Pretransplantation Cytogenetic Abnormalities, Myelodysplastic Syndrome, or Acute Leukemia

Combination of umbilical cord blood with BM from a 2-month-old sibling as lifesaving BMT for very severe aplastic anemia

Assessment of disease activity and management of patients with NFkB1 insufficiency

Cutaneous Chronic Graft Versus Host Disease Following Allogeneic Haematopoietic Stem Cell Transplantation in Children: A Retrospective Study

Frequency and natural history of inherited bone marrow failure syndromes: the Israeli Inherited Bone Marrow Failure Registry

Suchergebnisse filtern