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Paula Byrne

Showing results (21-30 of 29) with videos related to

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Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin|February 4, 2022
Transmission of SARS-CoV-2 by children: a rapid review, 30 December 2019 to 10 August 2020Barbara Clyne, Karen Jordan, Susan Ahern, et al.
The International Journal on Drug Policy|June 23, 2022
Consensus recommendations for opioid agonist treatment following the introduction of emergency clinical guidelines in Ireland during the COVID-19 pandemic: A national Delphi studyLouise Durand, Eamon Keenan, Fiona Boland, et al.
BMJ Evidence-Based Medicine|June 30, 2022
Perspectives on the production, and use, of rapid evidence in decision making during the COVID-19 pandemic: a qualitative studyBarbara Clyne, Lisa Hynes, Colette Kirwan, et al.
The Journal of Infection|July 3, 2020
SARS-CoV-2 detection, viral load and infectivity over the course of an infectionKieran A Walsh, Karen Jordan, Barbara Clyne, et al.
Reviews in Medical Virology|September 23, 2020
Immune response following infection with SARS-CoV-2 and other coronaviruses: A rapid reviewEamon O Murchu, Paula Byrne, Kieran A Walsh, et al.
Journal of Clinical Epidemiology|April 22, 2026
Comparison of AI-assisted and human-produced podcasts derived from Cochrane PLSs: protocol for a randomised non-inferiority trial (HIET-2)Isabel O'Byrne, Johanna Pope, Paula Byrne, et al.
American Journal of Human Genetics|April 9, 2008
Identification of the SPG15 gene, encoding spastizin, as a frequent cause of complicated autosomal-recessive spastic paraplegia, including Kjellin syndromeSylvain Hanein, Elodie Martin, Amir Boukhris, et al.
Health Technology Assessment (Winchester, England)|June 27, 2017
Debt Counselling for Depression in Primary Care: an adaptive randomised controlled pilot trial (DeCoDer study)Mark B Gabbay, Adele Ring, Richard Byng, et al.
Brain : a Journal of Neurology|March 7, 2008
REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31Christian Beetz, Rebecca Schüle, Tine Deconinck, et al.
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Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin|February 4, 2022
Transmission of SARS-CoV-2 by children: a rapid review, 30 December 2019 to 10 August 2020Barbara Clyne, Karen Jordan, Susan Ahern, et al.
The International Journal on Drug Policy|June 23, 2022
Consensus recommendations for opioid agonist treatment following the introduction of emergency clinical guidelines in Ireland during the COVID-19 pandemic: A national Delphi studyLouise Durand, Eamon Keenan, Fiona Boland, et al.
BMJ Evidence-Based Medicine|June 30, 2022
Perspectives on the production, and use, of rapid evidence in decision making during the COVID-19 pandemic: a qualitative studyBarbara Clyne, Lisa Hynes, Colette Kirwan, et al.
The Journal of Infection|July 3, 2020
SARS-CoV-2 detection, viral load and infectivity over the course of an infectionKieran A Walsh, Karen Jordan, Barbara Clyne, et al.
Reviews in Medical Virology|September 23, 2020
Immune response following infection with SARS-CoV-2 and other coronaviruses: A rapid reviewEamon O Murchu, Paula Byrne, Kieran A Walsh, et al.
Journal of Clinical Epidemiology|April 22, 2026
Comparison of AI-assisted and human-produced podcasts derived from Cochrane PLSs: protocol for a randomised non-inferiority trial (HIET-2)Isabel O'Byrne, Johanna Pope, Paula Byrne, et al.
American Journal of Human Genetics|April 9, 2008
Identification of the SPG15 gene, encoding spastizin, as a frequent cause of complicated autosomal-recessive spastic paraplegia, including Kjellin syndromeSylvain Hanein, Elodie Martin, Amir Boukhris, et al.
Health Technology Assessment (Winchester, England)|June 27, 2017
Debt Counselling for Depression in Primary Care: an adaptive randomised controlled pilot trial (DeCoDer study)Mark B Gabbay, Adele Ring, Richard Byng, et al.
Brain : a Journal of Neurology|March 7, 2008
REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31Christian Beetz, Rebecca Schüle, Tine Deconinck, et al.
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