Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Eleanor Gait-Carr"'
Autor:
Mahmoud Ali, Katie Hunt, Paul Clarke, Sarah Myers, Paul Cawley, Cora Doherty, Vennila Ponnusamy, Hemananda Muniraman, Jessica Hillyer, Adam Heathcote, Zoe Coleman, Kendall Hammonds, Chandni Raiyani, Eleanor Gait-Carr, Vinayak Govande, Anoo Jain, Reese Clark, Venkata Raju
Publikováno v:
BMJ Paediatrics Open, Vol 4, Iss 1 (2020)
Objectives To ascertain parental perceptions of the impact of restricted visiting policies to neonatal intensive care units during the current COVID-19 pandemic.Design Cross-sectional survey of parents impacted by visitation policies.Setting Six tert
Externí odkaz:
https://doaj.org/article/bcf0e1cd30cb447c8570fc18bffc22d3
Autor:
Kendall Hammonds, Paul Cawley, Cora Doherty, Reese Clark, Eleanor Gait-Carr, Katie Hunt, Hemananda Muniraman, Vennila Ponnusamy, Venkata Raju, Vinayak Govande, Adam Charles Heathcote, Paul Clarke, Jessica Hillyer, Zoe Coleman, Sarah Myers, Anoo Jain, Mahmoud Ali, Chandni Raiyani
Publikováno v:
BMJ Paediatrics Open
BMJ Paediatrics Open, Vol 4, Iss 1 (2020)
BMJ Paediatrics Open, Vol 4, Iss 1 (2020)
ObjectivesTo ascertain parental perceptions of the impact of restricted visiting policies to neonatal intensive care units during the current COVID-19 pandemic.DesignCross-sectional survey of parents impacted by visitation policies.SettingSix tertiar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5570a5330292ab8cd97250e8603b52e
Autor:
Mohammed Rahman, Jennifer Brooke, Janet Lewis, Gala Gutierrez Buey, Anna Scholz, Carolyn Tang, Eleanor Gait-Carr, Andrew Lansdown, Ruth Ellis-Owen, Aled Rees
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::752a19047fb61164dcf41a166a072c01
https://doi.org/10.1530/endoabs.59.p017
https://doi.org/10.1530/endoabs.59.p017
Publikováno v:
Journal of Pediatric Hematology/Oncology. 39:233-234
Moyamoya syndrome is an unusual cerebrovascular disorder, which has rarely been reported in association with hereditary spherocytosis. We present the case of a 6-year-old boy with hereditary spherocytosis who was diagnosed with Moyamoya syndrome foll
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d54a5d0cf432f198ff4c61a6803be361
https://doi.org/10.1097/mph.0000000000000789
https://doi.org/10.1097/mph.0000000000000789