UB Paderborn / Katalog / Suche / in CDI

1 – 23 von 23

Sortiert nach

More than trivial: strategies for using humor in palliative care

Cancer nursing, 2005-07, Vol.28 (4), p.292

2005

Volltextzugriff (PDF)

A qualitative study on African immigrant and refugee families' experiences of accessing primary health care services in Manitoba, Canada: it's not easy

International journal for equity in health, 2017-01, Vol.16 (1), p.5-5, Article 5

2017

Volltextzugriff (PDF)

Cultural competence: nursing in a multicultural society

Nursing for women's health, 2010-02, Vol.14 (1), p.50-59

Dean, Ruth Anne Kinsman

2010

Volltextzugriff (PDF)

Humor and laughter in palliative care: An ethnographic investigation

Palliative & supportive care, 2004-06, Vol.2 (2), p.139-148

2004

Volltextzugriff (PDF)

SLC12A2 variants cause a neurodevelopmental disorder or cochleovestibular defect

Brain (London, England : 1878), 2020-08, Vol.143 (8), p.2380-2387

2020

Volltextzugriff (PDF)

Genomic Diagnosis of Rare Pediatric Disease in the United Kingdom and Ireland

The New England journal of medicine, 2023-04, Vol.388 (17), p.1559-1571

2023

Volltextzugriff (PDF)

Community-Acquired Pneumonia Requiring Hospitalization among U.S. Children

The New England journal of medicine, 2015-02, Vol.372 (9), p.835-845

2015

Volltextzugriff (PDF)

Singing for people with aphasia (SPA): results of a pilot feasibility randomised controlled trial of a group singing intervention investigating acceptability and feasibility

BMJ open, 2021-01, Vol.11 (1), p.e040544-e040544

2021

Volltextzugriff (PDF)

Cerebral microbleeds and intracranial haemorrhage risk in patients anticoagulated for atrial fibrillation after acute ischaemic stroke or transient ischaemic attack (CROMIS-2): a multicentre observational cohort study

Lancet neurology, 2018-06, Vol.17 (6), p.539-547

2018

Volltextzugriff (PDF)

Coffin-Siris Syndrome and the BAF Complex: Genotype-Phenotype Study in 63 Patients

Human mutation, 2013-11, Vol.34 (11), p.1519-1528

2013

Volltextzugriff (PDF)

Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia

American journal of human genetics, 2019-05, Vol.104 (5), p.948-956

2019

Volltextzugriff (PDF)

Reliability and Minimal Detectable Change of Physical Performance Measures in Individuals With Pre-manifest and Manifest Huntington Disease

Physical therapy, 2013-07, Vol.93 (7), p.942-956

2013

Volltextzugriff (PDF)

Rapid intrapartum test for maternal group B streptococcal colonisation and its effect on antibiotic use in labouring women with risk factors for early-onset neonatal infection (GBS2): cluster randomised trial with nested test accuracy study

BMC medicine, 2022-01, Vol.20 (1), p.9-9, Article 9

2022

Volltextzugriff (PDF)

Health-Related Quality of Life After Community-Acquired Septic Shock in Children With Preexisting Severe Developmental Disabilities

Pediatric critical care medicine, 2021-05, Vol.22 (5), p.e302

2021

Volltextzugriff (PDF)

Variability in chest compression rate calculations during pediatric cardiopulmonary resuscitation

Resuscitation, 2020-04, Vol.149, p.127-133

2020

Volltextzugriff (PDF)

Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections

Genetics in medicine, 2024-02, Vol.26 (2), p.101023, Article 101023

2024

Volltextzugriff (PDF)

The Family Network Collaborative: engaging families in pediatric critical care research

Pediatric research, 2023-02, Vol.93 (3), p.453-456

2023

Volltextzugriff (PDF)

Clinical Characteristics and Factors Associated With Disability and Impaired Quality of Life in Children With Juvenile Systemic Sclerosis: Results From the Childhood Arthritis and Rheumatology Research Alliance Legacy Registry

Arthritis care & research (2010), 2018-12, Vol.70 (12), p.1806-1813

2018

Volltextzugriff (PDF)

Cell-surface Notch1 expression identifies a primitive phenotype within CD34+CD38− haematopoietic cells

European journal of haematology, 2014-01, Vol.92 (1), p.26-34

2014

Volltextzugriff (PDF)

The JDRF CCTN CGM TIME Trial: Timing of Initiation of continuous glucose Monitoring in Established pediatric type 1 diabetes: study protocol, recruitment and baseline characteristics

BMC pediatrics, 2014-07, Vol.14 (1), p.183-183, Article 183

2014

Volltextzugriff (PDF)

The finished DNA sequence of human chromosome 12

Nature, 2006-03, Vol.440 (7082), p.346-351

2006

Volltextzugriff (PDF)

1 – 23 von 23

Suche als RSS-Feed

Aktive Filter

ThemaHumans

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(23)
Mit Volltextzugriff
(20)

Publikationsform

Artikel
(23)

Sprache

Englisch
(23)
Japanisch
(3)

Erscheinungsjahr

n.n

Thema

Science & Technology
(21)
Life Sciences & Biomedicine
(20)
Female
(11)
Child
(10)
Male
(10)
Adolescent
(6)
General & Internal Medicine
(6)
Child, Preschool
(5)
Pediatrics
(5)
Children
(4)
Infant
(4)
Medicine, General & Internal
(4)
Adult
(3)
Aged
(3)
Genetics & Heredity
(3)
Middle Aged
(3)
Neurodevelopmental Disorders - Genetics
(3)
Phenotype
(3)
Prospective Studies
(3)

14 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

More than trivial: strategies for using humor in palliative care

A qualitative study on African immigrant and refugee families' experiences of accessing primary health care services in Manitoba, Canada: it's not easy

Cultural competence: nursing in a multicultural society

Humor and laughter in palliative care: An ethnographic investigation

Vorinostat in patients with advanced malignant pleural mesothelioma who have progressed on previous chemotherapy (VANTAGE-014): a phase 3, double-blind, randomised, placebo-controlled trial

SLC12A2 variants cause a neurodevelopmental disorder or cochleovestibular defect

Genomic Diagnosis of Rare Pediatric Disease in the United Kingdom and Ireland

Community-Acquired Pneumonia Requiring Hospitalization among U.S. Children

Singing for people with aphasia (SPA): results of a pilot feasibility randomised controlled trial of a group singing intervention investigating acceptability and feasibility

Cerebral microbleeds and intracranial haemorrhage risk in patients anticoagulated for atrial fibrillation after acute ischaemic stroke or transient ischaemic attack (CROMIS-2): a multicentre observational cohort study

Childhood Asthma Incidence, Early and Persistent Wheeze, and Neighborhood Socioeconomic Factors in the ECHO/CREW Consortium

Coffin-Siris Syndrome and the BAF Complex: Genotype-Phenotype Study in 63 Patients

Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia

Reliability and Minimal Detectable Change of Physical Performance Measures in Individuals With Pre-manifest and Manifest Huntington Disease

Rapid intrapartum test for maternal group B streptococcal colonisation and its effect on antibiotic use in labouring women with risk factors for early-onset neonatal infection (GBS2): cluster randomised trial with nested test accuracy study

Health-Related Quality of Life After Community-Acquired Septic Shock in Children With Preexisting Severe Developmental Disabilities

Variability in chest compression rate calculations during pediatric cardiopulmonary resuscitation

Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections

The Family Network Collaborative: engaging families in pediatric critical care research

Clinical Characteristics and Factors Associated With Disability and Impaired Quality of Life in Children With Juvenile Systemic Sclerosis: Results From the Childhood Arthritis and Rheumatology Research Alliance Legacy Registry

Cell-surface Notch1 expression identifies a primitive phenotype within CD34+CD38− haematopoietic cells

The JDRF CCTN CGM TIME Trial: Timing of Initiation of continuous glucose Monitoring in Established pediatric type 1 diabetes: study protocol, recruitment and baseline characteristics

The finished DNA sequence of human chromosome 12

Aktive Filter

Suchergebnisse filtern