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...

Chronic granulomatous disease: the European experience

PloS one, 2009-04, Vol.4 (4), p.e5234-e5234

2009

Volltextzugriff (PDF)

ROHHAD syndrome – A still unrecognized cause of childhood obesity: report of three cases

Journal of Pediatric Endocrinology and Metabolism, 2020-10, Vol.33 (10), p.1341-1348

2020

Volltextzugriff (PDF)

425 A case of a 13-year-old boy with parapneumonic effusion caused by Streptococcus constellatus

Archives of disease in childhood, 2021-10, Vol.106 (Suppl 2), p.A177-A178

2021

Volltextzugriff (PDF)

Hematopoietic stem cell gene therapy for adenosine deaminase-deficient severe combined immunodeficiency leads to long-term immunological recovery and metabolic correction

Science translational medicine, 2011-08, Vol.3 (97), p.97ra80

2011

Volltextzugriff (PDF)

Mild nocturnal hypoxaemia and elevated pulse rate in infants with viral bronchiolitis: An oximetry‐based study

Acta Paediatrica, 2022-03, Vol.111 (3), p.642-643

2022

Volltextzugriff (PDF)

A Syndrome with Congenital Neutropenia and Mutations in G6PC3

The New England journal of medicine, 2009-01, Vol.360 (1), p.32-43

2009

Volltextzugriff (PDF)

Teeth and tongue discoloration after linezolid treatment in children

The Pediatric infectious disease journal, 2013-11, Vol.32 (11), p.1284-1285

2013

Volltextzugriff (PDF)

Autoinflammation with Infantile Enterocolitis Associated with Recurrent Perianal Abscesses

Journal of clinical immunology, 2019-04, Vol.39 (3), p.237-240

2019

Volltextzugriff (PDF)

Thyroid Function in Greek Patients with Thalassemia Major

Blood, 2012-11, Vol.120 (21), p.5176-5176

2012

Volltextzugriff (PDF)

Longitudinal Changes in Iron Overload Parameters and Iron Chelation Therapy in Young Patients with Thalassemia Major

Blood, 2011-11, Vol.118 (21), p.3202-3202

2011

Volltextzugriff (PDF)

Iron Chelation Therapy in Transfusion Dependent Patients with Thalassemia and Minimal Liver Iron Load

Blood, 2010-11, Vol.116 (21), p.4270-4270

2010

Volltextzugriff (PDF)

Traffic Load Prediction in SDN/OpenFlow Networks

2016

Volltextzugriff (PDF)

Long-term follow-up and outcome of 39 patients with chronic granulomatous disease

The Journal of pediatrics, 2000-11, Vol.137 (5), p.687-693

2000

Volltextzugriff (PDF)

Cases of Tinea capitis due to pale isolates of Trichophyton violaceum (Trichophyton glabrum) in South-East Europe. A challenge to the clinical laboratory

Medical mycology case reports, 2012-01, Vol.1 (1), p.66-68

2012

Volltextzugriff (PDF)

A novel syndrome with congenital neutropenia caused by mutations in G6PC3

The New England journal of medicine, 2009-01, Vol.360 (1), p.32-43

2009

Volltextzugriff (PDF)

Changes in hypervariable region 1 of the envelope 2 glycoprotein of hepatitis C virus in children and adults with humoral immune defects

Journal of medical virology, 2003-03, Vol.69 (3), p.350-356

2003

Volltextzugriff (PDF)

Deletion of leucine 61 in glucose-6-phosphate dehydrogenase leads to chronic nonspherocytic anemia, granulocyte dysfunction, and increased susceptibility to infections

Blood, 2002-08, Vol.100 (3), p.1026-1030

2002

Volltextzugriff (PDF)

Comparison of two antiretroviral triple combinations including the protease inhibitor indinavir in children infected with human immunodeficiency virus

The Pediatric infectious disease journal, 1998-06, Vol.17 (6), p.495-499

1998

Volltextzugriff (PDF)

Lupus erythematosus tumidus and chronic discoid lupus erythematosus in carriers of X-linked chronic granulomatous disease

EJD. European journal of dermatology, 2000-04, Vol.10 (3), p.184-189

2000

Volltextzugriff (PDF)

Impact of prematurity, stress and sepsis on the neutrophil respiratory burst activity of neonates

Biology of the neonate, 1997, Vol.72 (4), p.201-209

1997

Volltextzugriff (PDF)

Successful Hematopoietic Stem Cell Transplantation in 2 Children with X-Linked Chronic Granulomatous Disease from Their Unaffected HLA-Identical Siblings Selected Using Preimplantation Genetic Diagnosis Combined with HLA Typing

Biology of blood and marrow transplantation, 2010-03, Vol.16 (3), p.344-349

2010

Volltextzugriff (PDF)

DNA, FISH and complementation studies in ICF syndrome : DNA hypomethylation of repetitive and single copy loci and evidence for a trans acting factor

Human genetics, 1995-11, Vol.96 (5), p.562-571

1995

Volltextzugriff (PDF)

Experimental validation of autonomic traffic engineering

2015 European Conference on Networks and Communications (EuCNC), 2015, p.533-537

2015

Volltextzugriff (PDF)

Autoinflammation with Infantile Enterocolitis Associated with Recurrent Perianal Abscesses

Journal of clinical immunology, 2019, Vol.39 (3), p.237-240

2019

Volltextzugriff (PDF)

1 – 25 von 26

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(22)
Mit Volltextzugriff
(17)

Publikationsform

Sprache

Englisch
(26)

Erscheinungsjahr

n.n

Thema

Science & Technology
(16)
Life Sciences & Biomedicine
(15)
Humans
(14)
Biological And Medical Sciences
(10)
Medical Sciences
(10)
Child, Preschool
(9)
Female
(9)
Male
(9)
Pediatrics
(8)
Adolescent
(7)
Child
(7)
Infant
(6)
Infectious Diseases
(6)
Adult
(5)
Immunology
(5)
Children
(3)
Granulomatous Disease, Chronic - Genetics
(3)
Immunodeficiencies
(3)
Immunodeficiencies. Immunoglobulinopathies
(3)
Immunopathology
(3)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Chronic granulomatous disease: the European experience

ROHHAD syndrome – A still unrecognized cause of childhood obesity: report of three cases

425 A case of a 13-year-old boy with parapneumonic effusion caused by Streptococcus constellatus

Hematopoietic stem cell gene therapy for adenosine deaminase-deficient severe combined immunodeficiency leads to long-term immunological recovery and metabolic correction

Mild nocturnal hypoxaemia and elevated pulse rate in infants with viral bronchiolitis: An oximetry‐based study

A Syndrome with Congenital Neutropenia and Mutations in G6PC3

Teeth and tongue discoloration after linezolid treatment in children

Autoinflammation with Infantile Enterocolitis Associated with Recurrent Perianal Abscesses

Thyroid Function in Greek Patients with Thalassemia Major

Longitudinal Changes in Iron Overload Parameters and Iron Chelation Therapy in Young Patients with Thalassemia Major

Iron Chelation Therapy in Transfusion Dependent Patients with Thalassemia and Minimal Liver Iron Load

Traffic Load Prediction in SDN/OpenFlow Networks

Long-term follow-up and outcome of 39 patients with chronic granulomatous disease

Cases of Tinea capitis due to pale isolates of Trichophyton violaceum (Trichophyton glabrum) in South-East Europe. A challenge to the clinical laboratory

A novel syndrome with congenital neutropenia caused by mutations in G6PC3

A Novel Clinical Syndrome Associating Severe Congenital Neutropenia and Complex Developmental Aberrations Caused by Deficiency of G6PC3

Changes in hypervariable region 1 of the envelope 2 glycoprotein of hepatitis C virus in children and adults with humoral immune defects

Deletion of leucine 61 in glucose-6-phosphate dehydrogenase leads to chronic nonspherocytic anemia, granulocyte dysfunction, and increased susceptibility to infections

Comparison of two antiretroviral triple combinations including the protease inhibitor indinavir in children infected with human immunodeficiency virus

Lupus erythematosus tumidus and chronic discoid lupus erythematosus in carriers of X-linked chronic granulomatous disease

Impact of prematurity, stress and sepsis on the neutrophil respiratory burst activity of neonates

Successful Hematopoietic Stem Cell Transplantation in 2 Children with X-Linked Chronic Granulomatous Disease from Their Unaffected HLA-Identical Siblings Selected Using Preimplantation Genetic Diagnosis Combined with HLA Typing

DNA, FISH and complementation studies in ICF syndrome : DNA hypomethylation of repetitive and single copy loci and evidence for a trans acting factor

Experimental validation of autonomic traffic engineering

Autoinflammation with Infantile Enterocolitis Associated with Recurrent Perianal Abscesses

Suchergebnisse filtern