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Seizure
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October 24, 2022
Intolerance to quinidine in a n-of-1 trial for KCNT1 associated epilepsy of infancy with migrating focal seizures
Elaine Hughes, Stephanie Oates, Deb K Pal
European Journal of Human Genetics : EJHG
|
May 2, 2013
Pre-symptomatic genetic testing for inherited cardiac conditions: a qualitative exploration of psychosocial and ethical implications
Elizabeth Ormondroyd, Stephanie Oates, Michael Parker, et al.
Nursing Children and Young People
|
December 16, 2024
Caring for children and young people with inherited cardiac conditions: the evolving role of specialist nurses
Jennifer Tollit, Stephanie Oates, Alessia Odori, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition
|
June 6, 2025
Evaluation of infants born to a parent with gene-positive long QT syndrome: a retrospective single-centre review
Claire Margaret Lawley, Bernadette Khodaghalian, Nichola French, et al.
Open Heart
|
March 1, 2016
Inpatient detection of cardiac-inherited disease: the impact of improving family history taking
Kathryn E Waddell-Smith, Tom Donoghue, Stephanie Oates, et al.
NPJ Genomic Medicine
|
May 16, 2018
Incorporating epilepsy genetics into clinical practice: a 360°evaluation
Stephanie Oates, Shan Tang, Richard Rosch, et al.
European Journal of Human Genetics : EJHG
|
January 12, 2022
Complementing the phenotypical spectrum of TUBA1A tubulinopathy and its role in early-onset epilepsies
Julian Schröter, Bernt Popp, Heiko Brennenstuhl, et al.
International Journal of Cardiology
|
September 30, 2023
Sudden cardiac death in childhood RASopathy-associated hypertrophic cardiomyopathy: Validation of the HCM risk-kids model and predictors of events
Olga D Boleti, Sotirios Roussos, Gabrielle Norrish, et al.
Clinical Genetics
|
July 3, 2021
ZMYND11 variants are a novel cause of centrotemporal and generalised epilepsies with neurodevelopmental disorder
Stephanie Oates, Michael Absoud, Sushma Goyal, et al.
Neurology
|
February 10, 2019
Clinical spectrum of <i>STX1B</i>-related epileptic disorders
Stefan Wolking, Patrick May, Davide Mei, et al.
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Search research articles
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Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Seizure
|
October 24, 2022
Intolerance to quinidine in a n-of-1 trial for KCNT1 associated epilepsy of infancy with migrating focal seizures
Elaine Hughes, Stephanie Oates, Deb K Pal
European Journal of Human Genetics : EJHG
|
May 2, 2013
Pre-symptomatic genetic testing for inherited cardiac conditions: a qualitative exploration of psychosocial and ethical implications
Elizabeth Ormondroyd, Stephanie Oates, Michael Parker, et al.
Nursing Children and Young People
|
December 16, 2024
Caring for children and young people with inherited cardiac conditions: the evolving role of specialist nurses
Jennifer Tollit, Stephanie Oates, Alessia Odori, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition
|
June 6, 2025
Evaluation of infants born to a parent with gene-positive long QT syndrome: a retrospective single-centre review
Claire Margaret Lawley, Bernadette Khodaghalian, Nichola French, et al.
Open Heart
|
March 1, 2016
Inpatient detection of cardiac-inherited disease: the impact of improving family history taking
Kathryn E Waddell-Smith, Tom Donoghue, Stephanie Oates, et al.
NPJ Genomic Medicine
|
May 16, 2018
Incorporating epilepsy genetics into clinical practice: a 360°evaluation
Stephanie Oates, Shan Tang, Richard Rosch, et al.
European Journal of Human Genetics : EJHG
|
January 12, 2022
Complementing the phenotypical spectrum of TUBA1A tubulinopathy and its role in early-onset epilepsies
Julian Schröter, Bernt Popp, Heiko Brennenstuhl, et al.
International Journal of Cardiology
|
September 30, 2023
Sudden cardiac death in childhood RASopathy-associated hypertrophic cardiomyopathy: Validation of the HCM risk-kids model and predictors of events
Olga D Boleti, Sotirios Roussos, Gabrielle Norrish, et al.
Clinical Genetics
|
July 3, 2021
ZMYND11 variants are a novel cause of centrotemporal and generalised epilepsies with neurodevelopmental disorder
Stephanie Oates, Michael Absoud, Sushma Goyal, et al.
Neurology
|
February 10, 2019
Clinical spectrum of <i>STX1B</i>-related epileptic disorders
Stefan Wolking, Patrick May, Davide Mei, et al.
Page
of 1