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Zornitza Stark

Showing results (1-10 of 270) with videos related to

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European Journal of Human Genetics : EJHG|November 8, 2021
Rapid genomic testing for critically ill children: time to become standard of care?Zornitza Stark, Sian Ellard
Clinical Chemistry|July 18, 2022
Can Rapid Nanopore Sequencing Bring Genomic Testing to the Bedside?Sebastian Lunke, Zornitza Stark
Orphanet Journal of Rare Diseases|February 24, 2009
OsteopetrosisZornitza Stark, Ravi Savarirayan
Nature Reviews. Genetics|June 29, 2023
Genomic newborn screening for rare diseasesZornitza Stark, Richard H Scott
Bioethics|November 27, 2019
Drugs, genes and screens: The ethics of preventing and treating spinal muscular atrophyChristopher Gyngell, Zornitza Stark, Julian Savulescu
Journal of Paediatrics and Child Health|January 4, 2020
Treatment limitation and advance planning: Hospital-wide audit of paediatric deathManon Audigé, Lynn Gillam, Zornitza Stark
European Journal of Human Genetics : EJHG|January 11, 2024
Reanalysis of genomic data, how do we do it now and what if we automate it? A qualitative studyZoe Fehlberg, Zornitza Stark, Stephanie Best
Journal of Inherited Metabolic Disease|January 13, 2025
Letter to the editor in response to Betzler et alLilian Downie, Sebastian Lunke, Zornitza Stark
Prenatal Diagnosis|March 8, 2025
The Intersection Between Genetic Reproductive Carrier Screening and Genomic Newborn Screening: Implications for Clinical PracticeLilian Downie, Sebastian Lunke, Zornitza Stark
Journal of Paediatrics and Child Health|July 22, 2008
Discussing withholding and withdrawing of life-sustaining medical treatment in paediatric inpatients: audit of current practiceZornitza Stark, Jenny Hynson, Mike Forrester
Pageof 27

Showing results (1-10 of 270) with videos related to

Sort By:
Pageof 27
European Journal of Human Genetics : EJHG|November 8, 2021
Rapid genomic testing for critically ill children: time to become standard of care?Zornitza Stark, Sian Ellard
Clinical Chemistry|July 18, 2022
Can Rapid Nanopore Sequencing Bring Genomic Testing to the Bedside?Sebastian Lunke, Zornitza Stark
Orphanet Journal of Rare Diseases|February 24, 2009
OsteopetrosisZornitza Stark, Ravi Savarirayan
Nature Reviews. Genetics|June 29, 2023
Genomic newborn screening for rare diseasesZornitza Stark, Richard H Scott
Bioethics|November 27, 2019
Drugs, genes and screens: The ethics of preventing and treating spinal muscular atrophyChristopher Gyngell, Zornitza Stark, Julian Savulescu
Journal of Paediatrics and Child Health|January 4, 2020
Treatment limitation and advance planning: Hospital-wide audit of paediatric deathManon Audigé, Lynn Gillam, Zornitza Stark
European Journal of Human Genetics : EJHG|January 11, 2024
Reanalysis of genomic data, how do we do it now and what if we automate it? A qualitative studyZoe Fehlberg, Zornitza Stark, Stephanie Best
Journal of Inherited Metabolic Disease|January 13, 2025
Letter to the editor in response to Betzler et alLilian Downie, Sebastian Lunke, Zornitza Stark
Prenatal Diagnosis|March 8, 2025
The Intersection Between Genetic Reproductive Carrier Screening and Genomic Newborn Screening: Implications for Clinical PracticeLilian Downie, Sebastian Lunke, Zornitza Stark
Journal of Paediatrics and Child Health|July 22, 2008
Discussing withholding and withdrawing of life-sustaining medical treatment in paediatric inpatients: audit of current practiceZornitza Stark, Jenny Hynson, Mike Forrester
Pageof 27