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...

Alpha-1-antitrypsin-deficiency is associated with lower cardiovascular risk: an approach based on federated learning

Respiratory research, 2024-01, Vol.25 (1), p.38-38, Article 38

2024

Volltextzugriff (PDF)

DQAgui: a graphical user interface for the MIRACUM data quality assessment tool

BMC medical informatics and decision making, 2022-08, Vol.22 (1), p.1-213, Article 213

2022

Volltextzugriff (PDF)

The German Chronic Kidney Disease (GCKD) study: design and methods

Nephrology, dialysis, transplantation, 2012-04, Vol.27 (4), p.1454-1460

2012

Volltextzugriff (PDF)

Evaluating and Enhancing the Fitness-for-Purpose of Electronic Health Record Data: Qualitative Study on Current Practices and Pathway to an Automated Approach Within the Medical Informatics for Research and Care in University Medicine Consortium

JMIR medical informatics, 2024-08, Vol.12, p.e57153

2024

Volltextzugriff (PDF)

Shift of radiotherapy use during the first wave of the COVID-19 pandemic? An analysis of German inpatient data

Strahlentherapie und Onkologie, 2022-04, Vol.198 (4), p.334-345

2022

Volltextzugriff (PDF)

Linking a Consortium-Wide Data Quality Assessment Tool with the MIRACUM Metadata Repository

Applied clinical informatics, 2021-08, Vol.12 (4), p.826-835

2021

Volltextzugriff (PDF)

Early and Differential Diagnosis of Dementia and Mild Cognitive Impairment

Dementia and geriatric cognitive disorders, 2009-06, Vol.27 (5), p.404-417

2009

Volltextzugriff (PDF)

Early and differential diagnosis of dementia and mild cognitive impairment: design and cohort baseline characteristics of the German Dementia Competence Network

Dementia and geriatric cognitive disorders, 2009, Vol.27 (5), p.404

2009

Volltextzugriff (PDF)

Genetic risk variants for membranous nephropathy: extension of and association with other chronic kidney disease aetiologies

Nephrology, dialysis, transplantation, 2017-02, Vol.32 (2), p.325-332

2017

Volltextzugriff (PDF)

Circulating dendritic cell precursors in chronic kidney disease: a cross-sectional study

BMC nephrology, 2013-12, Vol.14 (1), p.274-274, Article 274

2013

Volltextzugriff (PDF)

Heart failure in a cohort of patients with chronic kidney disease: the GCKD study

PloS one, 2015-04, Vol.10 (4), p.e0122552-e0122552

2015

Volltextzugriff (PDF)

The effect of misspecifying allele frequencies in incompletely typed families

Genetic epidemiology, 1993, Vol.10 (6), p.413-418

1993

Volltextzugriff (PDF)

Complex segregation analysis of families ascertained through Gilles de la Tourette syndrome

Genetic epidemiology, 2000-01, Vol.18 (1), p.33-47

2000

Volltextzugriff (PDF)

Rates for tic disorders and obsessive compulsive symptomatology in families of children and adolescents with Gilles de la Tourette syndrome

Journal of psychiatric research, 1997-09, Vol.31 (5), p.519-530

1997

Volltextzugriff (PDF)

Major histocompatibility complex haplotypes and complement C4 alleles in systemic lupus erythematosus : results of a multicenter study

The Journal of clinical investigation, 1992-10, Vol.90 (4), p.1346-1351

1992

Volltextzugriff (PDF)

Testing for association in SLE families

Genetic epidemiology, 1991, Vol.8 (6), p.409-416

1991

Volltextzugriff (PDF)

Methods for predictor analysis of repeated measurements: application to psychiatric data

Methods of information in medicine, 2004-01, Vol.43 (2), p.184-191

2004

Volltextzugriff (PDF)

The dysplastic melanocytic nevus: A prevalent lesion that correlates poorly with clinical phenotype

Journal of the American Academy of Dermatology, 1989-03, Vol.20 (3), p.407-415

1989

Volltextzugriff (PDF)

HGDBMS: A human genetics database management system

Computers and biomedical research, 1988-10, Vol.21 (5), p.478-487

1988

Volltextzugriff (PDF)

The "possible triangle" test for extreme discordant sib pairs

Genetic epidemiology, 1997, Vol.14 (6), p.833-838

1997

Volltextzugriff (PDF)

Genetik und Epidemiologic

Journal of public health, 1993-09, Vol.1 (3), p.245-248

1993

Volltextzugriff (PDF)

Genetic and Epidemiologic Evaluation of Dysplastic Nevi

Pigment cell research, 1988-12, Vol.1 (s1), p.144-151

1988

Volltextzugriff (PDF)

1 – 25 von 26

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(24)
Mit Volltextzugriff
(23)

Publikationsform

Artikel
(26)

Sprache

Englisch
(25)
Deutsch
(1)

Erscheinungsjahr

n.n

Thema

Science & Technology
(20)
Life Sciences & Biomedicine
(19)
Humans
(17)
Biological And Medical Sciences
(9)
Female
(9)
Male
(9)
Medical Sciences
(8)
Adult
(7)
Adolescent
(6)
Aged
(6)
Middle Aged
(6)
Risk Factors
(6)
Germany - Epidemiology
(5)
Genetics & Heredity
(4)
Germany
(4)
Mathematical & Computational Biology
(4)
Medical Informatics
(4)
Urology & Nephrology
(4)
Angina Pectoris
(3)
Cardiovascular Diseases
(3)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Alpha-1-antitrypsin-deficiency is associated with lower cardiovascular risk: an approach based on federated learning

DQAgui: a graphical user interface for the MIRACUM data quality assessment tool

The German Chronic Kidney Disease (GCKD) study: design and methods

Evaluating and Enhancing the Fitness-for-Purpose of Electronic Health Record Data: Qualitative Study on Current Practices and Pathway to an Automated Approach Within the Medical Informatics for Research and Care in University Medicine Consortium

Reduced Rate of Inpatient Hospital Admissions in 18 German University Hospitals During the COVID-19 Lockdown

Shift of radiotherapy use during the first wave of the COVID-19 pandemic? An analysis of German inpatient data

Linking a Consortium-Wide Data Quality Assessment Tool with the MIRACUM Metadata Repository

Early and Differential Diagnosis of Dementia and Mild Cognitive Impairment

Early and differential diagnosis of dementia and mild cognitive impairment: design and cohort baseline characteristics of the German Dementia Competence Network

Eosinopenia as Predictor of Disease Severity in Patients With Community-Acquired Pneumonia

Genetic risk variants for membranous nephropathy: extension of and association with other chronic kidney disease aetiologies

Circulating dendritic cell precursors in chronic kidney disease: a cross-sectional study

Eosinopenia as Predictor of Disease Severity in Patients With Community-Acquired Pneumonia: An Observational Study

Heart failure in a cohort of patients with chronic kidney disease: the GCKD study

The effect of misspecifying allele frequencies in incompletely typed families

Complex segregation analysis of families ascertained through Gilles de la Tourette syndrome

Rates for tic disorders and obsessive compulsive symptomatology in families of children and adolescents with Gilles de la Tourette syndrome

Major histocompatibility complex haplotypes and complement C4 alleles in systemic lupus erythematosus : results of a multicenter study

Testing for association in SLE families

Methods for predictor analysis of repeated measurements: application to psychiatric data

The dysplastic melanocytic nevus: A prevalent lesion that correlates poorly with clinical phenotype

HGDBMS: A human genetics database management system

The "possible triangle" test for extreme discordant sib pairs

Genetik und Epidemiologic

Genetic and Epidemiologic Evaluation of Dysplastic Nevi

Suchergebnisse filtern