UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 149

Sortiert nach

PROMIS ® pediatric self-report scales distinguish subgroups of children within and across six common pediatric chronic health conditions

Quality of life research, 2015-09, Vol.24 (9), p.2195-2208

2015

Link zum Volltext

Verfügbarkeit prüfen

Estimating minimally important difference (MID) in PROMIS pediatric measures using the scale-judgment method

Quality of life research, 2016-01, Vol.25 (1), p.13-23

2016

Link zum Volltext

Verfügbarkeit prüfen

Impact of arginine therapy on mitochondrial function in children with sickle cell disease during vaso-occlusive pain

Blood, 2020-09, Vol.136 (12), p.1402-1406

2020

Link zum Volltext

Verfügbarkeit prüfen

A randomized clinical trial of the efficacy and safety of rivipansel for sickle cell vaso-occlusive crisis

Blood, 2023-01, Vol.141 (2), p.168-179

2023

Link zum Volltext

Verfügbarkeit prüfen

Definitions of the phenotypic manifestations of sickle cell disease

American journal of hematology, 2010-01, Vol.85 (1), p.6-13

2010

Link zum Volltext

Verfügbarkeit prüfen

Characterizing User Engagement With a Digital Intervention for Pain Self-management Among Youth With Sickle Cell Disease and Their Caregivers: Subanalysis of a Randomized Controlled Trial

Journal of medical Internet research, 2022-08, Vol.24 (8), p.e40096-e40096

2022

Link zum Volltext

Verfügbarkeit prüfen

iCanCope with Sickle Cell Pain: Design of a randomized controlled trial of a smartphone and web-based pain self-management program for youth with sickle cell disease

Contemporary clinical trials, 2018-11, Vol.74, p.88-96

2018

Link zum Volltext

Verfügbarkeit prüfen

Red blood cell alloimmunization in sickle cell disease: prevalence in 2010

Transfusion (Philadelphia, Pa.), 2013-04, Vol.53 (4), p.704-709

2013

Link zum Volltext

Verfügbarkeit prüfen

Clinical trial designs and models for analgesic medications for acute pain in neonates, infants, toddlers, children, and adolescents: ACTTION recommendations

Pain (Amsterdam), 2018-02, Vol.159 (2), p.193

2018

Link zum Volltext

Verfügbarkeit prüfen

Tissue factor-positive monocytes in children with sickle cell disease: correlation with biomarkers of haemolysis

British journal of haematology, 2012-05, Vol.157 (3), p.370-380

2012

Link zum Volltext

Verfügbarkeit prüfen

Pediatric analgesic clinical trial designs, measures, and extrapolation: report of an FDA scientific workshop

Pediatrics (Evanston), 2012-02, Vol.129 (2), p.354

2012

Link zum Volltext

Verfügbarkeit prüfen

Sickle Cell Disease Treatment with Arginine Therapy (STArT): study protocol for a phase 3 randomized controlled trial

Trials, 2023-08, Vol.24 (1), p.538-538, Article 538

2023

Link zum Volltext

Verfügbarkeit prüfen

Quality of life among adolescents with sickle cell disease: mediation of pain by internalizing symptoms and parenting stress

Health and quality of life outcomes, 2008-08, Vol.6 (1), p.60-60

2008

Link zum Volltext

Verfügbarkeit prüfen

New and emerging treatments for vaso-occlusive pain in sickle cell disease

Expert review of hematology, 2019-10, Vol.12 (10), p.857-872

Dampier, Carlton

2019

Link zum Volltext

Verfügbarkeit prüfen

Clinical trial implementation and recruitment: Lessons learned from the early closure of a randomized clinical trial

Contemporary clinical trials, 2012-03, Vol.33 (2), p.291-297

2012

Link zum Volltext

Verfügbarkeit prüfen

Characterizing Intracranial Hemodynamics in Sickle Cell Anemia: Impact of Patient-Specific Viscosity

Cardiovascular engineering and technology, 2022-02, Vol.13 (1), p.104-119

2022

Link zum Volltext

Verfügbarkeit prüfen

Reply to comment on: Hydroxyurea and pain history in relation to patient‐reported outcomes using PROMIS® measures and the frequency of assessments in sickle cell disease patients

Pediatric blood & cancer, 2017-01, Vol.64 (1), p.204-204

Dampier, Carlton

2017

Link zum Volltext

Verfügbarkeit prüfen

Inpatient management of sickle cell pain: A 'snapshot' of current practice

American journal of hematology, 2012-03, Vol.87 (3), p.333-336

2012

Link zum Volltext

Verfügbarkeit prüfen

Double-blind, randomized, multicenter phase 2 study of SC411 in children with sickle cell disease (SCOT trial)

Blood advances, 2018-08, Vol.2 (15), p.1969-1979

2018

Link zum Volltext

Verfügbarkeit prüfen

IMPROVE trial: A randomized controlled trial of patient-controlled analgesia for sickle cell painful episodes: rationale, design challenges, initial experience, and recommendations for future studies

Clinical trials (London, England), 2013-04, Vol.10 (2), p.319-331

2013

Link zum Volltext

Verfügbarkeit prüfen

Psychosocial and Functional Outcomes in Youth With Chronic Sickle Cell Pain

The Clinical journal of pain, 2016-06, Vol.32 (6), p.527-533

2016

Link zum Volltext

Verfügbarkeit prüfen

AAPT Diagnostic Criteria for Chronic Sickle Cell Disease Pain

The journal of pain, 2017-05, Vol.18 (5), p.490-498

2017

Link zum Volltext

Verfügbarkeit prüfen

Opioid patient controlled analgesia use during the initial experience with the IMPROVE PCA trial: A phase III analgesic trial for hospitalized sickle cell patients with painful episodes

American journal of hematology, 2011-12, Vol.86 (12), p.E70-E73

2011

Link zum Volltext

Verfügbarkeit prüfen

Impact of PCA strategies on pain intensity and functional assessment measures in adults with sickle cell disease during hospitalized vaso-occlusive episodes

American journal of hematology, 2012-10, Vol.87 (10), p.E71-E74

2012

Link zum Volltext

Verfügbarkeit prüfen

Pediatric Pain Screening Identifies Youth at Risk for Chronic Pain in Sickle Cell Disease

Blood, 2017-12, Vol.130, p.3548-3548

2017

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 149

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(143)
Mit Volltextzugriff
(138)

Publikationsform

Sprache

Englisch
(149)
Japanisch
(2)

Erscheinungsjahr

n.n

Thema

Life Sciences & Biomedicine
(92)
Science & Technology
(92)
Humans
(85)
Child
(71)
Adolescent
(62)
Sickle Cell Disease
(60)
Anemia, Sickle Cell - Complications
(58)
Female
(55)
Male
(55)
Hematology
(51)
Pediatrics
(48)
Pain
(34)
Adult
(32)
Biological And Medical Sciences
(29)
Medical Sciences
(28)
Child, Preschool
(26)
Pain - Etiology
(22)
Oncology
(21)
Anemias. Hemoglobinopathies
(19)
Diseases Of Red Blood Cells
(19)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(3)

Menü

Weitere Dienste

Einstellungen

PROMIS ® pediatric self-report scales distinguish subgroups of children within and across six common pediatric chronic health conditions

Estimating minimally important difference (MID) in PROMIS pediatric measures using the scale-judgment method

Impact of arginine therapy on mitochondrial function in children with sickle cell disease during vaso-occlusive pain

A randomized clinical trial of the efficacy and safety of rivipansel for sickle cell vaso-occlusive crisis

Definitions of the phenotypic manifestations of sickle cell disease

Characterizing User Engagement With a Digital Intervention for Pain Self-management Among Youth With Sickle Cell Disease and Their Caregivers: Subanalysis of a Randomized Controlled Trial

iCanCope with Sickle Cell Pain: Design of a randomized controlled trial of a smartphone and web-based pain self-management program for youth with sickle cell disease

Red blood cell alloimmunization in sickle cell disease: prevalence in 2010

Clinical trial designs and models for analgesic medications for acute pain in neonates, infants, toddlers, children, and adolescents: ACTTION recommendations

Tissue factor-positive monocytes in children with sickle cell disease: correlation with biomarkers of haemolysis

Pediatric analgesic clinical trial designs, measures, and extrapolation: report of an FDA scientific workshop

Sickle Cell Disease Treatment with Arginine Therapy (STArT): study protocol for a phase 3 randomized controlled trial

Quality of life among adolescents with sickle cell disease: mediation of pain by internalizing symptoms and parenting stress

New and emerging treatments for vaso-occlusive pain in sickle cell disease

Clinical trial implementation and recruitment: Lessons learned from the early closure of a randomized clinical trial

Characterizing Intracranial Hemodynamics in Sickle Cell Anemia: Impact of Patient-Specific Viscosity

Reply to comment on: Hydroxyurea and pain history in relation to patient‐reported outcomes using PROMIS® measures and the frequency of assessments in sickle cell disease patients

Inpatient management of sickle cell pain: A 'snapshot' of current practice

Double-blind, randomized, multicenter phase 2 study of SC411 in children with sickle cell disease (SCOT trial)

IMPROVE trial: A randomized controlled trial of patient-controlled analgesia for sickle cell painful episodes: rationale, design challenges, initial experience, and recommendations for future studies

Psychosocial and Functional Outcomes in Youth With Chronic Sickle Cell Pain

AAPT Diagnostic Criteria for Chronic Sickle Cell Disease Pain

Opioid patient controlled analgesia use during the initial experience with the IMPROVE PCA trial: A phase III analgesic trial for hospitalized sickle cell patients with painful episodes

Impact of PCA strategies on pain intensity and functional assessment measures in adults with sickle cell disease during hospitalized vaso-occlusive episodes

Pediatric Pain Screening Identifies Youth at Risk for Chronic Pain in Sickle Cell Disease

Suchergebnisse filtern