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...

Mutations in the X-Linked and Autosomal Recessive Forms of Chronic Granulomatous Disease

Blood, 1996-03, Vol.87 (5), p.1663-1681

1996

Volltextzugriff (PDF)

Mutations in the X-linked and autosomal recessive forms of chronic granulomatous disease

Blood, 1996-03, Vol.87 (5), p.1663-1681

1996

Volltextzugriff (PDF)

The effect of two different dosages of intravenous immunoglobulin on the incidence of recurrent infections in patients with primary hypogammaglobulinemia. A randomized, double-blind, multicenter crossover trial

Annals of internal medicine, 2001-08, Vol.135 (3), p.165

2001

Volltextzugriff (PDF)

BFM-oriented treatment for children with acute lymphoblastic leukemia without cranial irradiation and treatment reduction for standard risk patients: results of DCLSG protocol ALL-8 (1991-1996)

Leukemia, 2002-06, Vol.16 (6), p.1099-1111

2002

Volltextzugriff (PDF)

Treatment strategy and results in children treated on three Dutch Childhood Oncology Group acute myeloid leukemia trials

Leukemia, 2005-12, Vol.19 (12), p.2063-2071

2005

Volltextzugriff (PDF)

Point Mutations in the β-Subunit of Cytochrome b558 Leading to X-Linked Chronic Granulomatous Disease

Blood, 1991-06, Vol.77 (11), p.2482-2487

1991

Volltextzugriff (PDF)

Intensive Treatment of Children With Acute Lymphoblastic Leukemia According to ALL-BFM-86 Without Cranial Radiotherapy: Results of Dutch Childhood Leukemia Study Group Protocol ALL-7 (1988-1991)

Blood, 1999-08, Vol.94 (4), p.1226-1236

1999

Volltextzugriff (PDF)

Characterization of Two Monoclonal Antibodies Against Cytochrome b558 of Human Neutrophils

Blood, 1989-05, Vol.73 (6), p.1686-1694

1989

Volltextzugriff (PDF)

Genetic analysis of patients with leukocyte adhesion deficiency: Genomic sequencing reveals otherwise undetectable mutations

Experimental hematology, 2002-03, Vol.30 (3), p.252-261

2002

Volltextzugriff (PDF)

Fc gamma receptor IIa (CD32) polymorphism in fulminant meningococcal septic shock in children

The Journal of infectious diseases, 1994-10, Vol.170 (4), p.848

1994

Volltextzugriff (PDF)

A missense mutation in the heavy subunit of γ-glutamylcysteine synthetase gene causes hemolytic anemia

Blood, 2000-04, Vol.95 (7), p.2193-2197

2000

Volltextzugriff (PDF)

Clinical and laboratory work-up of patients with neutrophil shortage or dysfunction

Journal of immunological methods, 1999-12, Vol.232 (1), p.211-229

1999

Volltextzugriff (PDF)

Four novel mutations in the gene encoding gp91-phox of human NADPH oxidase : consequences for oxidase assembly

Blood, 2000-01, Vol.95 (2), p.666-673

2000

Volltextzugriff (PDF)

Intracellular Reactions in Single Human Granulocytes upon Phorbol Myristate Acetate Activation using Confocal Raman Microspectroscopy

Biophysical journal, 2000-05, Vol.78 (5), p.2606-2613

2000

Volltextzugriff (PDF)

Limitations on the use of dihydrorhodamine 123 for flow cytometric analysis of the neutrophil respiratory burst

Journal of immunological methods, 1996-05, Vol.191 (2), p.187-196

1996

Volltextzugriff (PDF)

Point mutations in the promoter region of the CYBB gene leading to mild chronic granulomatous disease

Clinical and experimental immunology, 2000-12, Vol.122 (3), p.410-417

2000

Volltextzugriff (PDF)

Phagocytosis of Staphylococcus aureus and Haemophilus influenzae type B opsonized with polyclonal human IgG1 and IgG2 antibodies. Functional hFc gamma RIIa polymorphism to IgG2

The Journal of immunology (1950), 1993-08, Vol.151 (3), p.1463-1472

1993

Volltextzugriff (PDF)

Enhanced thrombin generation in children with sickle cell disease

Thrombosis and haemostasis, 1994-02, Vol.71 (2), p.169

1994

Volltextzugriff (PDF)

A Single Dose of Granulocyte-Macrophage Colony-Stimulating Factor Induces Systemic Interleukin-8 Release and Neutrophil Activation in Healthy Volunteers

Blood, 1996-06, Vol.87 (12), p.5305-5313

1996

Volltextzugriff (PDF)

Increased risk of malignancy for patients with chronic granulomatous disease and its possible link to the pathogenesis of cancer

European journal of cancer (1990), 1996-04, Vol.32 (4), p.734-735

1996

Volltextzugriff (PDF)

The management of chronic granulomatous disease

European journal of pediatrics, 1993-11, Vol.152 (11), p.896-899

1993

Volltextzugriff (PDF)

Recombinant human interferon-gamma in patients with chronic granulomatous disease ? European follow up study

European journal of pediatrics, 1995-04, Vol.154 (4), p.295-298

1995

Volltextzugriff (PDF)

Chronic bullous disease of childhood and a paecilomyces lung infection in chronic granulomatous disease

Archives of disease in childhood, 1997-08, Vol.77 (2), p.150-152

1997

Volltextzugriff (PDF)

Purified protein kinase C phosphorylates a 47-kDa protein in control neutrophil cytoplasts but not in neutrophil cytoplasts from patients with the autosomal form of chronic granulomatous disease

The Journal of biological chemistry, 1988-02, Vol.263 (5), p.2352-2357

1988

Volltextzugriff (PDF)

1 – 25 von 90

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(81)
Mit Volltextzugriff
(64)

Publikationsform

Artikel
(89)
Tagungsberichte
(1)

Sprache

Englisch
(90)

Erscheinungsjahr

n.n

Thema

Science & Technology
(75)
Humans
(74)
Life Sciences & Biomedicine
(74)
Biological And Medical Sciences
(40)
Male
(38)
Female
(31)
Hematology
(28)
Medical Sciences
(28)
Child
(19)
Adult
(17)
Phagocytosis
(17)
Child, Preschool
(15)
Immunology
(15)
Adolescent
(14)
Granulomatous Disease, Chronic - Genetics
(14)
Fundamental And Applied Biological Sciences. Psychology
(12)
Infant
(12)
Medicine, Research & Experimental
(11)
Pediatrics
(11)
Research & Experimental Medicine
(11)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Mutations in the X-Linked and Autosomal Recessive Forms of Chronic Granulomatous Disease

Mutations in the X-linked and autosomal recessive forms of chronic granulomatous disease

The effect of two different dosages of intravenous immunoglobulin on the incidence of recurrent infections in patients with primary hypogammaglobulinemia. A randomized, double-blind, multicenter crossover trial

BFM-oriented treatment for children with acute lymphoblastic leukemia without cranial irradiation and treatment reduction for standard risk patients: results of DCLSG protocol ALL-8 (1991-1996)

Treatment strategy and results in children treated on three Dutch Childhood Oncology Group acute myeloid leukemia trials

Point Mutations in the β-Subunit of Cytochrome b558 Leading to X-Linked Chronic Granulomatous Disease

Intensive Treatment of Children With Acute Lymphoblastic Leukemia According to ALL-BFM-86 Without Cranial Radiotherapy: Results of Dutch Childhood Leukemia Study Group Protocol ALL-7 (1988-1991)

Characterization of Two Monoclonal Antibodies Against Cytochrome b558 of Human Neutrophils

Molecular Basis and Enzymatic Properties of Glucose 6-Phosphate Dehydrogenase Volendam, Leading to Chronic Nonspherocytic Anemia, Granulocyte Dysfunction, and Increased Susceptibility to Infections

Genetic analysis of patients with leukocyte adhesion deficiency: Genomic sequencing reveals otherwise undetectable mutations

Fc gamma receptor IIa (CD32) polymorphism in fulminant meningococcal septic shock in children

A missense mutation in the heavy subunit of γ-glutamylcysteine synthetase gene causes hemolytic anemia

Clinical and laboratory work-up of patients with neutrophil shortage or dysfunction

Four novel mutations in the gene encoding gp91-phox of human NADPH oxidase : consequences for oxidase assembly

Intracellular Reactions in Single Human Granulocytes upon Phorbol Myristate Acetate Activation using Confocal Raman Microspectroscopy

Limitations on the use of dihydrorhodamine 123 for flow cytometric analysis of the neutrophil respiratory burst

Point mutations in the promoter region of the CYBB gene leading to mild chronic granulomatous disease

Phagocytosis of Staphylococcus aureus and Haemophilus influenzae type B opsonized with polyclonal human IgG1 and IgG2 antibodies. Functional hFc gamma RIIa polymorphism to IgG2

Enhanced thrombin generation in children with sickle cell disease

A Single Dose of Granulocyte-Macrophage Colony-Stimulating Factor Induces Systemic Interleukin-8 Release and Neutrophil Activation in Healthy Volunteers

Increased risk of malignancy for patients with chronic granulomatous disease and its possible link to the pathogenesis of cancer

The management of chronic granulomatous disease

Recombinant human interferon-gamma in patients with chronic granulomatous disease ? European follow up study

Chronic bullous disease of childhood and a paecilomyces lung infection in chronic granulomatous disease

Purified protein kinase C phosphorylates a 47-kDa protein in control neutrophil cytoplasts but not in neutrophil cytoplasts from patients with the autosomal form of chronic granulomatous disease

Suchergebnisse filtern