Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Kathleen Dady"'
Autor:
Olga Boleti, Gabrielle Norrish, Ella Field, Kathleen Dady, Kim Summers, Gauri Nepali, Vinay Bhole, Orhan Uzun, Amos Wong, Piers E. F. Daubeney, Graham Stuart, Precylia Fernandes, Karen McLeod, Maria Ilina, Muhammad Najih Liaqath Ali, Tara Bharucha, Grazia Delle Donne, Elspeth Brown, Katie Linter, Caroline B. Jones, Jonathan Searle, William Regan, Sujeev Mathur, Nicola Boyd, Zdenka Reinhardt, Sophie Duignan, Terence Prendiville, Satish Adwani, Juan Pablo Kaski
Publikováno v:
ESC Heart Failure, Vol 11, Iss 2, Pp 923-936 (2024)
Abstract Aims This study aimed to describe the natural history and predictors of all‐cause mortality and sudden cardiac death (SCD)/equivalent events in children with a RASopathy syndrome and hypertrophic cardiomyopathy (HCM). Methods and results T
Externí odkaz:
https://doaj.org/article/774801a5c3044f99889a58c53cfad13e
Autor:
Gabrielle Norrish, Gali Kolt, Elena Cervi, Ella Field, Kathleen Dady, Lidia Ziółkowska, Iacopo Olivotto, Silvia Favilli, Silvia Passantino, Giuseppe Limongelli, Martina Caiazza, Marta Rubino, Anwar Baban, Fabrizio Drago, Karen Mcleod, Maria Ilina, Ruth McGowan, Graham Stuart, Vinay Bhole, Orhan Uzun, Amos Wong, Laz Lazarou, Elspeth Brown, Piers E.F. Daubeney, Amrit Lota, Grazia Delle Donne, Katie Linter, Sujeev Mathur, Tara Bharucha, Satish Adwani, Jon Searle, Anca Popoiu, Caroline B. Jones, Zdenka Reinhardt, Juan Pablo Kaski
Publikováno v:
ESC Heart Failure, Vol 8, Iss 6, Pp 5057-5067 (2021)
Abstract Aims Children presenting with hypertrophic cardiomyopathy (HCM) in infancy are reported to have a poor prognosis, but this heterogeneous group has not been systematically characterized. This study aimed to describe the aetiology, phenotype,
Externí odkaz:
https://doaj.org/article/606e02324a3e411484c1c9f074115236
Publikováno v:
Circulation: Genomic and Precision Medicine. 15
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::07f52c932be7e9061de83ee5120db4fe
https://doi.org/10.1161/circgen.121.003667
https://doi.org/10.1161/circgen.121.003667
Autor:
Katie Linter, Gali S. Kolt, Satish Adwani, Gabrielle Norrish, Fabrizio Drago, Marta Rubino, Maria Ilina, Vinay Bhole, Kathleen Dady, Tara Bharucha, Elspeth Brown, Iacopo Olivotto, Laz Lazarou, Graham Stuart, Martina Caiazza, Amos Wong, Caroline Jones, Amrit Lota, Grazia Delle Donne, Orhan Uzun, Anca Popoiu, Silvia Passantino, Jon Searle, Juan Pablo Kaski, Silvia Favilli, Lidia Ziółkowska, Giuseppe Limongelli, Ella Field, Karen McLeod, Elena Cervi, Piers E.F. Daubeney, Ruth McGowan, Zdenka Reinhardt, Anwar Baban, Sujeev Mathur
Publikováno v:
ESC Heart Failure, Vol 8, Iss 6, Pp 5057-5067 (2021)
ESC Heart Failure
ESC Heart Failure
Aims: Children presenting with hypertrophic cardiomyopathy (HCM) in infancy are reported to have a poor prognosis, but this heterogeneous group has not been systematically characterized. This study aimed to describe the aetiology, phenotype, and outc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc3cbee9430cbfd3d5464c3cda2be5a4
https://eprints.soton.ac.uk/453432/
https://eprints.soton.ac.uk/453432/
Autor:
Laia Brunet-Garcia, Johnson Ja, Ella Field, Gabrielle Norrish, Jenny Tollit, Jessica Shoshan, Nichola French, Amy Addis, Kathleen Dady, Elena Cervi, Luke Starling, Juan Pablo Kaski
Publikováno v:
Pediatric cardiology. 43(5)
Idiopathic ventricular fibrillation (IVF) is diagnosed in out-of-hospital VF survivors after comprehensive investigations have excluded structural heart disease or inherited channelopathies. Current guidelines recommend clinical screening of first-de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::485ca5a295ebded2197bdfddb96d06d0
https://pubmed.ncbi.nlm.nih.gov/35092457
https://pubmed.ncbi.nlm.nih.gov/35092457
Autor:
Petros Syrris, Juan Pablo Kaski, Hannah Fell, Juan Pablo Ochoa, Marcos Cicerchia, Vanessa Acquaah, Gabrielle Norrish, Karen McLeod, Ruth McGowan, Kathleen Dady, Ella Field, Luis R. Lopes, Elena Cervi
Publikováno v:
J Med Genet
BackgroundVariants in the cardiac myosin-binding protein C gene (MYBPC3) are a common cause of hypertrophic cardiomyopathy (HCM) in adults and have been associated with late-onset disease, but there are limited data on their role in paediatric-onset
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f7201eba8c69d9d9c9da9854464bbd1
https://pubmed.ncbi.nlm.nih.gov/34400558
https://pubmed.ncbi.nlm.nih.gov/34400558