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...

Sensitivity and Specificity of Soluble Triggering Receptor Expressed on Myeloid Cells-1, Midregional Proatrial Natriuretic Peptide and Midregional Proadrenomedullin for Distinguishing Etiology and to Assess Severity in Community-Acquired Pneumonia

PloS one, 2016-11, Vol.11 (11), p.e0163262-e0163262

2016

Volltextzugriff (PDF)

Prevention of food and airway allergy: consensus of the Italian Society of Preventive and Social Paediatrics, the Italian Society of Paediatric Allergy and Immunology, and Italian Society of Pediatrics

The World Allergy Organization journal, 2016-08, Vol.9 (1), p.28-28, Article 28

2016

Volltextzugriff (PDF)

Missense mutations in the Fas gene resulting in autoimmune lymphoproliferative syndrome : A molecular and immunological analysis

Blood, 1997-02, Vol.89 (3), p.902-909

1997

Volltextzugriff (PDF)

One-step NGS molecular analysis of the CFTR gene on newborn dried blood spots gives a higher diagnostic sensitivity in affected and carrier subjects: A pilot study

Clinica chimica acta, 2024-01, Vol.552, p.117625-117625, Article 117625

2024

Volltextzugriff (PDF)

Multifocal lymphangioendotheliomatosis with thrombocytopenia

Minerva Pediatrics, 2022-08, Vol.74 (4)

2022

Volltextzugriff (PDF)

Multifocal lymphangioendotheliomatosis with thrombocytopenia

Minerva Pediatrics, 2021-01

2021

Volltextzugriff (PDF)

Shwachman-Diamond syndrome with autoimmune-like liver disease and enteropathy mimicking celiac disease

Clinics and research in hepatology and gastroenterology, 2015-02, Vol.39 (1), p.e1-e4

2015

Volltextzugriff (PDF)

Neonatal malpractice claims in Italy: how big is the problem and which are the causes?

The journal of maternal-fetal & neonatal medicine, 2012-05, Vol.25 (5), p.493-497

2012

Volltextzugriff (PDF)

Pediatric claims in Italy during a 8-years survey

Italian journal of pediatrics, 2014-08, Vol.40 (S1), p.A87-A87, Article A87

2014

Volltextzugriff (PDF)

Five human phenylalanine hydroxylase proteins identified in mild hyperphenylalaninemia patients are disease-causing variants

Biochimica et biophysica acta, 2008-06, Vol.1782 (6), p.378-384

2008

Volltextzugriff (PDF)

Propranolol for severe hemangioma of infancy

Journal of cardiovascular medicine (Hagerstown, Md.), 2011-01, Vol.12 (1), p.5

2011

Volltextzugriff (PDF)

Deficiency of the Fas apoptosis pathway without Fas gene mutations in pediatric patients with autoimmunity/lymphoproliferation

Blood, 1997-04, Vol.89 (8), p.2871-2879

1997

Volltextzugriff (PDF)

Infantile facial haemangioma and subclinical left ventricular dysfunction: the importance of z score in the diagnostic and therapeutic process

Journal of cardiovascular medicine (Hagerstown, Md.), 2010-09, Vol.11 (9), p.692-694

2010

Volltextzugriff (PDF)

Propranolol for severe hemangioma of infancy

Journal of cardiovascular medicine (Hagerstown, Md.), 2011-01, Vol.12 (1), p.73

2011

Volltextzugriff (PDF)

Reduction of inappropriate hospital admissions of children with influenza-like illness through the implementation of specific guidelines: a case-controlled study

Pediatrics (Evanston), 2005-10, Vol.116 (4), p.e506-e511

2005

Volltextzugriff (PDF)

Radiotherapy of a pseudotumor in a hemophiliac with Factor VIII inhibitor

Journal of pediatric hematology/oncology, 1984, Vol.6 (3), p.325-326

1984

Volltextzugriff (PDF)

Prediction of intellectual deficits in children with acute lymphoblastic leukemia

Journal of developmental and behavioral pediatrics, 1988-06, Vol.9 (3), p.122-128

1988

Volltextzugriff (PDF)

Inappropriately Low Red Cell 2,3-Diphosphoglycerate and p50 in Transfused β-Thalassemia

Blood, 1984-04, Vol.63 (4), p.803-806

1984

Volltextzugriff (PDF)

Relationship between weight gain and serum level of alkaline phosphatasein malnourished infants treated by total parenteral nutrition

The Journal of pediatrics, 1977, Vol.90 (1), p.160-161

1977

Volltextzugriff (PDF)

Subcutaneous implantable cardioverter defibrillator in children and adolescents: results from the S-ICD “Monaldi care” registry

Journal of interventional cardiac electrophysiology, 2022-03, Vol.63 (2), p.283-293

2022

Volltextzugriff (PDF)

Clinical presentation and genetic characterization of early‐onset atrial fibrillation in patients affected by long QT syndrome: A single‐center experience

Journal of cardiovascular electrophysiology, 2024-10, Vol.35 (10), p.1941-1951

2024

Volltextzugriff (PDF)

Antiarrhythmic therapy for narrow QRS supraventricular tachyarrhythmias in newborns and infants in the first year of life: Potent tools to be handled with care

Indian pacing and electrophysiology journal, 2024-09, Vol.24 (5), p.271-281

2024

Volltextzugriff (PDF)

The LLAMA Brazilian-Argentinian radiotelescope project: progress in Brazil and BRICS collaboration

Anais da Academia Brasileira de Ciências, 2021-01, Vol.93 (suppl 1), p.e20200846-e20200846

2021

Volltextzugriff (PDF)

Single-Chamber and Dual-Chamber Pacemaker Devices in Adults with Moderate and Complex Congenital Heart Disease: A Single Tertiary Referral Center Experience

Pediatric cardiology, 2024-02

2024

Volltextzugriff (PDF)

Treatments, prognostic factors, and genetic heterogeneity in advanced cholangiocarcinoma: A multicenter real‐world study

Cancer medicine (Malden, MA), 2024-02, Vol.13 (4), p.e6892-n/a

2024

Volltextzugriff (PDF)

1 – 25 von 32

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(32)
Mit Volltextzugriff
(23)

Publikationsform

Artikel
(32)

Sprache

Englisch
(32)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Sensitivity and Specificity of Soluble Triggering Receptor Expressed on Myeloid Cells-1, Midregional Proatrial Natriuretic Peptide and Midregional Proadrenomedullin for Distinguishing Etiology and to Assess Severity in Community-Acquired Pneumonia

Prevention of food and airway allergy: consensus of the Italian Society of Preventive and Social Paediatrics, the Italian Society of Paediatric Allergy and Immunology, and Italian Society of Pediatrics

Missense mutations in the Fas gene resulting in autoimmune lymphoproliferative syndrome : A molecular and immunological analysis

One-step NGS molecular analysis of the CFTR gene on newborn dried blood spots gives a higher diagnostic sensitivity in affected and carrier subjects: A pilot study

Multifocal lymphangioendotheliomatosis with thrombocytopenia

Multifocal lymphangioendotheliomatosis with thrombocytopenia

Shwachman-Diamond syndrome with autoimmune-like liver disease and enteropathy mimicking celiac disease

Neonatal malpractice claims in Italy: how big is the problem and which are the causes?

Pediatric claims in Italy during a 8-years survey

Five human phenylalanine hydroxylase proteins identified in mild hyperphenylalaninemia patients are disease-causing variants

Propranolol for severe hemangioma of infancy

Deficiency of the Fas apoptosis pathway without Fas gene mutations in pediatric patients with autoimmunity/lymphoproliferation

Infantile facial haemangioma and subclinical left ventricular dysfunction: the importance of z score in the diagnostic and therapeutic process

Propranolol for severe hemangioma of infancy

Reduction of inappropriate hospital admissions of children with influenza-like illness through the implementation of specific guidelines: a case-controlled study

Radiotherapy of a pseudotumor in a hemophiliac with Factor VIII inhibitor

Prediction of intellectual deficits in children with acute lymphoblastic leukemia

Inappropriately Low Red Cell 2,3-Diphosphoglycerate and p50 in Transfused β-Thalassemia

Relationship between weight gain and serum level of alkaline phosphatasein malnourished infants treated by total parenteral nutrition

Subcutaneous implantable cardioverter defibrillator in children and adolescents: results from the S-ICD “Monaldi care” registry

Clinical presentation and genetic characterization of early‐onset atrial fibrillation in patients affected by long QT syndrome: A single‐center experience

Antiarrhythmic therapy for narrow QRS supraventricular tachyarrhythmias in newborns and infants in the first year of life: Potent tools to be handled with care

The LLAMA Brazilian-Argentinian radiotelescope project: progress in Brazil and BRICS collaboration

Single-Chamber and Dual-Chamber Pacemaker Devices in Adults with Moderate and Complex Congenital Heart Disease: A Single Tertiary Referral Center Experience

Treatments, prognostic factors, and genetic heterogeneity in advanced cholangiocarcinoma: A multicenter real‐world study

Suchergebnisse filtern