Suchergebnisse - "Carbo, Ellen C"

PubPharm (10)

1

No Remdesivir Resistance Observed in the Phase 3 Severe and Moderate COVID-19 SIMPLE Trials

enthalten in: Viruses | 2024

von Hedskog, C. | Spinner, C. | Protzer, U. | +24

2

Viral metagenomic sequencing in a cohort of international travellers returning with febrile illness

enthalten in: Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology | 2021

von Reyes, A. | Carbo, E. | Harinxma Thoe Slooten, J. | +6

3

STROBE-metagenomics : a STROBE extension statement to guide the reporting of metagenomics studies

enthalten in: The Lancet. Infectious diseases | 2020

von Bharucha, T. | Oeser, C. | Balloux, F. | +24

ErratumIn: Lancet Infect Dis. 2020 Dec;20(12):e298. - PMID 33120055

4

Improved diagnosis of viral encephalitis in adult and pediatric hematological patients using viral metagenomics

enthalten in: Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology | 2020

von Carbo, E. | Buddingh, E. | Karelioti, E. | +7

5

Retrospective Validation of a Metagenomic Sequencing Protocol for Combined Detection of RNA and DNA Viruses Using Respiratory Samples from Pediatric Patients

enthalten in: The Journal of molecular diagnostics : JMD | 2020

von van Boheemen, S. | van Rijn, A. | Pappas, N. | +8

6

Gene Mosaicism Screening Using Single-Molecule Molecular Inversion Probes in Routine Diagnostics for Systemic Autoinflammatory Diseases

enthalten in: The Journal of molecular diagnostics : JMD | 2019

von Kant, B. | Carbo, E. | Kokmeijer, I. | +7

7

Assessment of parental mosaicism in SCN1A-related epilepsy by single-molecule molecular inversion probes and next-generation sequencing

enthalten in: Journal of medical genetics | 2019

von de Lange, I. | Koudijs, M. | van 't Slot, R. | +10

8

The respiratory virome and exacerbations in patients with chronic obstructive pulmonary disease

enthalten in: PloS one | 2019

von van Rijn, A. | van Boheemen, S. | Sidorov, I. | +11

9

Mosaicism of de novo pathogenic SCN1A variants in epilepsy is a frequent phenomenon that correlates with variable phenotypes

enthalten in: Epilepsia | 2018

von de Lange, I. | Koudijs, M. | van 't Slot, R. | +13

10

Effectiveness of whole-exome sequencing and costs of the traditional diagnostic trajectory in children with intellectual disability

enthalten in: Genetics in medicine : official journal of the American College of Medical Genetics | 2016

von Monroe, G. | Frederix, G. | Savelberg, S. | +15

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