UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Sie befinden Sich nicht im Netzwerk der Universität Paderborn. Der Zugriff auf elektronische Ressourcen ist gegebenenfalls nur via VPN oder Shibboleth (DFN-AAI) möglich. mehr Informationen...

Smartphone app for non-invasive detection of anemia using only patient-sourced photos

Nature communications, 2018-12, Vol.9 (1), p.4924-10, Article 4924

2018

Link zum Volltext

Verfügbarkeit prüfen

Transfusion management in thalassemia

Annals of the New York Academy of Sciences, 2023-09, Vol.1527 (1), p.42-48

Boudreaux, Jeanne

2023

Link zum Volltext

Verfügbarkeit prüfen

Eculizumab for complement mediated thrombotic microangiopathy in sickle cell disease

Haematologica (Roma), 2020-12, Vol.105 (12), p.2887-2891

2020

Link zum Volltext

Verfügbarkeit prüfen

Decision-making about gene therapy in transfusion dependent thalassemia

BMC pediatrics, 2022-09, Vol.22 (1), p.536-536, Article 536

2022

Link zum Volltext

Verfügbarkeit prüfen

Chelation use and iron burden in North American and British thalassemia patients: a report from the Thalassemia Longitudinal Cohort

Blood, 2012-03, Vol.119 (12), p.2746-2753

2012

Link zum Volltext

Verfügbarkeit prüfen

Inadequate Dietary Intake in Patients with Thalassemia

Journal of the Academy of Nutrition and Dietetics, 2012-07, Vol.112 (7), p.980-990

2012

Link zum Volltext

Verfügbarkeit prüfen

Heterogeneity in myocardial iron content in pediatric and young adult patients

Journal of cardiovascular magnetic resonance, 2013-01, Vol.15 (S1), p.P287-P287, Article P287

2013

Link zum Volltext

Verfügbarkeit prüfen

Human T cell lymphotropic virus type 1 infection among U.S. thalassemia patients

AIDS research and human retroviruses, 2013-07, Vol.29 (7), p.1006

2013

Link zum Volltext

Verfügbarkeit prüfen

Fibroblast Growth Factor Receptor Signaling Activates the Human Interstitial Collagenase Promoter via the Bipartite Ets-AP1 Element

Molecular endocrinology (Baltimore, Md.), , Vol.11 (8), p.1129-1144

Link zum Volltext

Verfügbarkeit prüfen

Transfusion complications in thalassemia patients: a report from the Centers for Disease Control and Prevention (CME)

Transfusion (Philadelphia, Pa.), 2014-04, Vol.54 (4), p.972-981

2014

Link zum Volltext

Verfügbarkeit prüfen

An update on the US adult thalassaemia population: a report from the CDC thalassaemia treatment centres

British journal of haematology, 2022-01, Vol.196 (2), p.380-389

2022

Link zum Volltext

Verfügbarkeit prüfen

A synonymous coding variant that alters ALAS2 splicing and causes X‐linked sideroblastic anemia

Pediatric blood & cancer, 2022-01, Vol.69 (1), p.e29309-n/a

2022

Link zum Volltext

Verfügbarkeit prüfen

Nuclear localization of liver X receptor α and β is differentially regulated

Journal of cellular biochemistry, 2007-01, Vol.100 (1), p.69-85

2007

Link zum Volltext

Verfügbarkeit prüfen

Influence of user-centered clinical decision support on pediatric blood product ordering errors

Blood transfusion = Trasfusione del sangue, 2023-01, Vol.21 (1), p.3-12

2023

Link zum Volltext

Verfügbarkeit prüfen

Mutations in the iron-sulfur cluster biogenesis protein HSCB cause congenital sideroblastic anemia

The Journal of clinical investigation, 2020-10, Vol.130 (10), p.5245-5256

2020

Link zum Volltext

Verfügbarkeit prüfen

Guidelines for the Standard Monitoring of Patients With Thalassemia: Report of the Thalassemia Longitudinal Cohort

Journal of pediatric hematology/oncology, 2015-04, Vol.37 (3), p.e162-e169

2015

Link zum Volltext

Verfügbarkeit prüfen

Newly diagnosed immune thrombocytopenia in children and adults: a comparative prospective observational registry of the Intercontinental Cooperative Immune Thrombocytopenia Study Group

Haematologica (Roma), 2011-12, Vol.96 (12), p.1831

2011

Link zum Volltext

Verfügbarkeit prüfen

Red cell alloimmunization in a diverse population of transfused patients with thalassaemia

British journal of haematology, 2011-04, Vol.153 (1), p.121-128

2011

Link zum Volltext

Verfügbarkeit prüfen

Lessons Learned from OpenNotes Learning Mode and Subsequent Implementation across a Pediatric Health System

Applied clinical informatics, 2022-01, Vol.13 (1), p.113-122

2022

Link zum Volltext

Verfügbarkeit prüfen

Disposable platform provides visual and color-based point-of-care anemia self-testing

The Journal of clinical investigation, 2014-10, Vol.124 (10), p.4387-4394

2014

Link zum Volltext

Verfügbarkeit prüfen

Hscb, a Mitochondrial Iron-Sulfur Cluster Assembly Co-Chaperone, Is a Novel Candidate Gene for Congenital Sideroblastic Anemia

Blood, 2017-12, Vol.130 (Suppl_1), p.79-79

2017

Link zum Volltext

Verfügbarkeit prüfen

Relationship among chelator adherence, change in chelators, and quality of life in Thalassemia

Quality of life research, 2014-10, Vol.23 (8), p.2277-2288

2014

Link zum Volltext

Verfügbarkeit prüfen

Formative Usability Testing Reduces Severe Blood Product Ordering Errors

Applied clinical informatics, 2019-10, Vol.10 (5), p.981-990

2019

Link zum Volltext

Verfügbarkeit prüfen

Class I and II HLA antibodies in pediatric patients with thalassemia major

Transfusion (Philadelphia, Pa.), 2016-04, Vol.56 (4), p.878-884

2016

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 47

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(47)
Mit Volltextzugriff
(45)

Publikationsform

Artikel
(47)

Sprache

Englisch
(47)
Japanisch
(4)

Erscheinungsjahr

n.n

Thema

Science & Technology
(32)
Life Sciences & Biomedicine
(30)
Humans
(25)
Female
(17)
Child
(16)
Male
(15)
Hematology
(14)
Adolescent
(13)
Adult
(12)
Biological And Medical Sciences
(11)
Medical Sciences
(11)
Child, Preschool
(9)
Young Adult
(9)
Hematologic And Hematopoietic Diseases
(8)
Middle Aged
(8)
Thalassemia
(8)
Anemias. Hemoglobinopathies
(7)
Diseases Of Red Blood Cells
(7)
Blood Transfusion
(6)
Longitudinal Studies
(6)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Smartphone app for non-invasive detection of anemia using only patient-sourced photos

Transfusion management in thalassemia

Eculizumab for complement mediated thrombotic microangiopathy in sickle cell disease

Decision-making about gene therapy in transfusion dependent thalassemia

Chelation use and iron burden in North American and British thalassemia patients: a report from the Thalassemia Longitudinal Cohort

Inadequate Dietary Intake in Patients with Thalassemia

Heterogeneity in myocardial iron content in pediatric and young adult patients

Human T cell lymphotropic virus type 1 infection among U.S. thalassemia patients

Fibroblast Growth Factor Receptor Signaling Activates the Human Interstitial Collagenase Promoter via the Bipartite Ets-AP1 Element

Transfusion complications in thalassemia patients: a report from the Centers for Disease Control and Prevention (CME)

An update on the US adult thalassaemia population: a report from the CDC thalassaemia treatment centres

A synonymous coding variant that alters ALAS2 splicing and causes X‐linked sideroblastic anemia

Nuclear localization of liver X receptor α and β is differentially regulated

Influence of user-centered clinical decision support on pediatric blood product ordering errors

Mutations in the iron-sulfur cluster biogenesis protein HSCB cause congenital sideroblastic anemia

MUTATION UPDATE SLC25A38: SLC25A38 Congenital Sideroblastic Anemia: Phenotypes and genotypes of 31 individuals from 24 families, including 11 novel mutations, and a review of the literature

Guidelines for the Standard Monitoring of Patients With Thalassemia: Report of the Thalassemia Longitudinal Cohort

Newly diagnosed immune thrombocytopenia in children and adults: a comparative prospective observational registry of the Intercontinental Cooperative Immune Thrombocytopenia Study Group

Red cell alloimmunization in a diverse population of transfused patients with thalassaemia

Lessons Learned from OpenNotes Learning Mode and Subsequent Implementation across a Pediatric Health System

Disposable platform provides visual and color-based point-of-care anemia self-testing

Hscb, a Mitochondrial Iron-Sulfur Cluster Assembly Co-Chaperone, Is a Novel Candidate Gene for Congenital Sideroblastic Anemia

Relationship among chelator adherence, change in chelators, and quality of life in Thalassemia

Formative Usability Testing Reduces Severe Blood Product Ordering Errors

Class I and II HLA antibodies in pediatric patients with thalassemia major

Suchergebnisse filtern