Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Hadley Mahon"'
Autor:
Amanda Worker, Hadley Mahon, Jack Sams, Freya Boardman-Pretty, Elena Marchini, Rand Dubis, Alan Warren, Jez Stockdale, Jyothika Kumar, Elizabeth Varones, Daniel Ollerenshaw, Calum Grant, Peter Fish, Richard J. Kelly
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-11 (2024)
Abstract Background Paroxysmal Nocturnal Haemoglobinuria (PNH) is an ultra-rare, acquired disorder that is challenging to diagnose due to varied symptoms, heterogeneous patient presentations, and lack of awareness among healthcare professionals. This
Externí odkaz:
https://doaj.org/article/e788d01ac5f04052a0b45d8c9f5b7321
Is it possible to implement a rare disease case-finding tool in primary care? A UK-based pilot study
Autor:
Orlando Buendia, Sneha Shankar, Hadley Mahon, Connor Toal, Lara Menzies, Pradeep Ravichandran, Jane Roper, Jag Takhar, Rudy Benfredj, Will Evans
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-11 (2022)
Abstract Introduction This study implemented MendelScan, a primary care rare disease case-finding tool, into a UK National Health Service population. Rare disease diagnosis is challenging due to disease complexity and low physician awareness. The 202
Externí odkaz:
https://doaj.org/article/82a9b1d8fcb440f1a9947fd1b3b093cb
Is it Possible to Implement a Rare Disease Case-Finding Tool in Primary Care? A UK-Based Pilot Study
Autor:
Orlando Buendia, Sneha Shankar, Hadley Mahon, Connor Toal, Lara Menzies, Pradeep Ravichandran, Jane Roper, Jag Takhar, Rudy Benfredj, Will Evans
Introduction This study implemented MendelScan, a primary care rare disease case-finding tool, into a UK National Health Service population. Rare disease diagnosis is challenging due to disease complexity and low physician awareness. The 2021 UK Rare
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b2a5cc56149a7ceb4fc2b707eccef7e
https://doi.org/10.21203/rs.3.rs-638180/v2
https://doi.org/10.21203/rs.3.rs-638180/v2
Is It Possible to Implement a Rare Disease Case-finding Tool in Primary Care? A UK-based Pilot Study
Autor:
William Evans, Sneha Shankar, Rudy Benfredj, Connor Toal, Pradeep Ravichandran, Lara Menzies, Hadley Mahon, Orlando Buendia
Introduction:This study implemented MendelScan, a primary care rare disease case-finding tool, into a UK NHS population. Rare disease diagnosis is challenging due to disease complexity and low physician awareness. The 2021 UK Rare Diseases Framework
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::098e96e4360fd9c9bbdd5064099a583f
https://doi.org/10.21203/rs.3.rs-638180/v1
https://doi.org/10.21203/rs.3.rs-638180/v1