Katalog der Deutschen Nationalbibliothek

Neuigkeiten

Leichte Bedienung, intuitive Suche: Die Betaversion unseres neuen Katalogs ist online! → Zur Betaversion des neuen DNB-Katalogs

 
 
Neuigkeiten Ihr Suchergebnis enthält zu viele Treffer. Bitte schränken Sie Ihre Suche weiter ein.
 


Ergebnis der Suche nach: "a"
im Bestand: Gesamter Bestand

100001 - 100010 von 6760121
<< < > >>


Artikel 100001 Optimizing Documentation Integrity of Ophthalmic Diagnostic Test Interpretation through Electronic Health Record Clinical Decision Support
Enthalten in Applied clinical informatics Bd. 16, 2025, Nr. 04: 786-795
Online Ressource
Artikel 100002 Mobile Admission Process and Administrative Turnaround Time for Hospitalization of Outpatients: A Retrospective Study
Enthalten in Applied clinical informatics Bd. 16, 2025, Nr. 04: 769-776
Online Ressource
Artikel 100003 Lessons Learned from the Usability Assessment of an EHR-Based Tool to Support Adherence to Antihypertensive Medications
Enthalten in Applied clinical informatics Bd. 16, 2025, Nr. 04: 760-768
Online Ressource
Artikel 100004 From Steps to Mobility Levels: Validating a Consumer-Grade Activity Monitor for Automated Recording of Patient Mobility in Hospitals
Enthalten in Applied clinical informatics Bd. 16, 2025, Nr. 04: 753-759
Online Ressource
Artikel 100005 Exploring Provider Perceptions and Attitudes toward Copy–Paste and Copy–Forward in Clinical Documentation
Enthalten in Applied clinical informatics Bd. 16, 2025, Nr. 04: 736-746
Online Ressource
Artikel 100006 Missense Variant Met119Val in ACTB in a Patient with Baraitser-Winter Syndrome Type 1 and Mild Intellectual Disability
Enthalten in Molecular syndromology Bd. 16, 2025, Nr. 4: 390-396. 7 S.
Online Ressource
Artikel 100007 A Novel NOTCH3 Variant Leading to Lateral Meningocele Syndrome: Prenatal Diagnosis and Possible Expansion of the Phenotype
Enthalten in Molecular syndromology Bd. 16, 2025, Nr. 4: 384-389. 6 S.
Online Ressource
Artikel 100008 Co-Occurrence of Variants in 3 Genes in a Patient with Congenital Skeletal Dysplasia and Cardiac Anomalies: Diagnostic Challenge Posed by a Blended Phenotype
Enthalten in Molecular syndromology Bd. 16, 2025, Nr. 4: 374-383. 10 S.
Online Ressource
Artikel 100009 A Report of Dual Presentations of Pseudo-TORCH Syndrome 1 and MCC2 Deficiency and Review of the Literature
Enthalten in Molecular syndromology Bd. 16, 2025, Nr. 4: 366-373. 8 S.
Online Ressource
Artikel 100010 Cerebrotendinous Xanthomatosis Disease Prevalence in Patients with Autism Spectrum Disorder: A Prospective Observational Study
Enthalten in Molecular syndromology Bd. 16, 2025, Nr. 4: 354-365. 12 S.
Online Ressource


100001 - 100010 von 6760121
<< < > >>


E-Mail-IconAdministration