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The Journal of Clinical Endocrinology and Metabolism|February 9, 2024
The Diagnostic Odyssey in Children and Adolescents With X-linked Hypophosphatemia: Population-Based, Case-Control StudyFreya Boardman-Pretty, Ashley Kieran Clift, Hadley Mahon, et al.
Orphanet Journal of Rare Diseases|February 17, 2022
Is it possible to implement a rare disease case-finding tool in primary care? A UK-based pilot studyOrlando Buendia, Sneha Shankar, Hadley Mahon, et al.
Orphanet Journal of Rare Diseases|October 13, 2024
A machine learning algorithm for the detection of paroxysmal nocturnal haemoglobinuria (PNH) in UK primary care electronic health recordsAmanda Worker, Hadley Mahon, Jack Sams, et al.
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