Evaluation of the Clinical Performance of the HPV-Risk Assay Using the VALGENT-3 Panel.

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Triage of high-risk HPV-positive women in population-based screening by miRNA expression analysis in cervical scrapes; a feasibility study.Clinical Evaluation of INNO-LiPA HPV Genotyping II Assay Using the VALGENT Framework

P2860

Q55365141-030A0805-5B28-437C-A001-1B712F427FC0 Q58749448-7444C931-B1F4-4730-BF9A-5713FEBDB4F0

P2860

Evaluation of the Clinical Performance of the HPV-Risk Assay Using the VALGENT-3 Panel.

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http://www.wikidata.org/entity/Q47097439

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

@wuu

2017年学术文章

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2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

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@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh-hant

name

Evaluation of the Clinical Performance of the HPV-Risk Assay Using the VALGENT-3 Panel.

@en

Evaluation of the Clinical Performance of the HPV-Risk Assay Using the VALGENT-3 Panel.

@nl

type

Item

label

Evaluation of the Clinical Performance of the HPV-Risk Assay Using the VALGENT-3 Panel.

@en

Evaluation of the Clinical Performance of the HPV-Risk Assay Using the VALGENT-3 Panel.

@nl

prefLabel

Evaluation of the Clinical Performance of the HPV-Risk Assay Using the VALGENT-3 Panel.

@en

Evaluation of the Clinical Performance of the HPV-Risk Assay Using the VALGENT-3 Panel.

@nl

P1476

Evaluation of the Clinical Performance of the HPV-Risk Assay Using the VALGENT-3 Panel.

@en

P2093

A Oštrbenk

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C J L M Meijer

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D A M Heideman

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L Xu

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M Arbyn

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N J Polman

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P J F Snijders

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P2860

Comparative evaluation of first- and second-generation digene hybrid capture assays for detection of human papillomaviruses associated with high or intermediate risk for cervical cancer.

Clinical evaluation of a GP5+/6+-based luminex assay having full high-risk human papillomavirus genotyping capability and an internal control.

Comparison of clinical and analytical performance of the Abbott Realtime High Risk HPV test to the performance of hybrid capture 2 in population-based cervical cancer screening.

Which high-risk HPV assays fulfil criteria for use in primary cervical cancer screening?

Clinical and Analytical Performance of the Onclarity HPV Assay Using the VALGENT Framework.

Performance of a Cartridge-Based Assay for Detection of Clinically Significant Human Papillomavirus (HPV) Infection: Lessons from VALGENT (Validation of HPV Genotyping Tests)

Guidelines for human papillomavirus DNA test requirements for primary cervical cancer screening in women 30 years and older.

Clinical validation of the HPV-risk assay, a novel real-time PCR assay for detection of high-risk human papillomavirus DNA by targeting the E7 region.

Evidence regarding human papillomavirus testing in secondary prevention of cervical cancer.

Efficacy of HPV-based screening for prevention of invasive cervical cancer: follow-up of four European randomised controlled trials.

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3544-3551

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scholarly article

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10.1128/JCM.01282-17

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English

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Mario Poljak

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2017-10-11T00:00:00Z

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29021152

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5703818

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Evaluation of the Clinical Performance of the HPV-Risk Assay Using the VALGENT-3 Panel.

about

P2860

P2860

Evaluation of the Clinical Performance of the HPV-Risk Assay Using the VALGENT-3 Panel.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932