Zobrazeno 1 - 10
of 63
pro vyhledávání: '"Lucy Mckay"'
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-10 (2024)
Abstract Background An estimated 3.5 million people in the UK live with a rare disease however due to the rarity of each individual condition this is not currently reflected in mainstream medical education. As a result, common features of living with
Externí odkaz:
https://doaj.org/article/995f3c9bd65c489db68db5ac3810ba59
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-12 (2024)
Abstract Background The ‘diagnostic odyssey’ is a common challenge faced by patients living with rare diseases and poses a significant burden for patients, their families and carers, and the healthcare system. The diagnosis of rare diseases in cl
Externí odkaz:
https://doaj.org/article/edbd33cd79654d41b1c72b742b2b8067
Autor:
Birute Tumiene, Harm Peters, Bela Melegh, Borut Peterlin, Algirdas Utkus, Natalja Fatkulina, György Pfliegler, Holm Graessner, Sanja Hermanns, Maurizio Scarpa, Jean-Yves Blay, Sharon Ashton, Lucy McKay, Gareth Baynam
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-20 (2022)
Abstract People living with rare diseases (PLWRD) still face huge unmet needs, in part due to the fact that care systems are not sufficiently aligned with their needs and healthcare workforce (HWF) along their care pathways lacks competencies to effi
Externí odkaz:
https://doaj.org/article/6407632929da40bb8a36b39315418770
Autor:
S. Christy Rohani-Montez, Jennifer Bomberger, Cong Zhang, Jacob Cohen, Lucy McKay, William R.H. Evans
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100808- (2023)
Purpose: Recognizing rare diseases (RDs) and initiating appropriate investigation and referral is critical for timely diagnosis. Unfortunately, patients with RDs experience significant diagnostic delays, potentially leading to inappropriate or harmfu
Externí odkaz:
https://doaj.org/article/da36d6666aea43b5813eeda7ac04212c
Publikováno v:
European Medical Journal (2022)
Rare diseases are individually rare but collectively common, with a combined prevalence of 3.5–5.9%. A common feature of many diseases is a substantial delay in patients receiving a correct diagnosis; this protracted path to diagnosis is termed ‘
Externí odkaz:
https://doaj.org/article/709974bbf43b4e71b949b63cfe6f3d98
Autor:
Lucy McKay
Publikováno v:
New Zealand Medical Student Journal, Vol 0, Iss 29 (2019)
Over 7000 rare diseases have been described in accordance with the European Union definition of a condition that affects fewer than one in 2000 people. An initial browse of Orphanet’s Rare Disease Directory reveals a plethora of disparate condition
Externí odkaz:
https://doaj.org/article/f4397a3e909d425894ca9992aff92334
Publikováno v:
InnovAiT: Education and inspiration for general practice. 14:92-99
Rare diseases (RDs) are defined as diseases that affect less than 1 in 2000 people, 71.9% are genetic and 69.9% have symptom onset in childhood. There are an estimated 8000 rare diseases, and although individually rare, collectively they are common,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d763719a1c1342eed56445bd449995b8
https://doi.org/10.1177/1755738020974411
https://doi.org/10.1177/1755738020974411
Publikováno v:
Solid Earth, Vol 11, Pp 2119-2140 (2020)
Fault architecture and fracture network evolution (and resulting bulk hydraulic properties) are highly dependent on the mechanical properties of the rocks at the time the structures developed. This paper investigates the role of mechanical layering a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c46c04e42c5e42d8c4cf0a724fd7d7ba
https://doi.org/10.5194/se-11-2119-2020
https://doi.org/10.5194/se-11-2119-2020
Publikováno v:
Geoscientist
Despite the fact that 90% of global seismicity occurs at plate boundary faults, our understanding of their internal structure is lacking. It’s not easy to see inside a plate boundary fault – typically composed of a high-strain fault core surround
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c80ace54fda8c67560ab8588ee9ae2c
https://strathprints.strath.ac.uk/73156/1/McKay_etal_Geoscientist_2020_Core_surprise_whats_inside_a_plate_boundary.pdf
https://strathprints.strath.ac.uk/73156/1/McKay_etal_Geoscientist_2020_Core_surprise_whats_inside_a_plate_boundary.pdf
The Highland Boundary fault near Stonehaven, NE Scotland, provides a rare opportunity to study the internal fault structure of a well-exposed, along-strike section of an ancient plate boundary fault. As in many plate boundaries, serpentinite juxtapos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f16e6e0d575b823cf0d93c4201375288
https://strathprints.strath.ac.uk/69944/1/McKay_etal_JGS_2019_Detailed_internal_structure_and_along_strike_variability.pdf
https://strathprints.strath.ac.uk/69944/1/McKay_etal_JGS_2019_Detailed_internal_structure_and_along_strike_variability.pdf