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Displaying the 3 most recent scholarly works by Michael Hayman.
Severe childhood speech disorder: Gene discovery highlights transcriptional dysregulation
Michael S Hildebrand, Victoria E Jackson, Thomas S Scerri, Olivia Van Reyk, Matthew Coleman, Ruth O Braden, Samantha Turner, Kristin A Rigbye, Amber Boys, Sarah Barton, Richard Webster, Michael Fahey, Kerryn Saunders, Bronwyn Parry-Fielder, Georgia Paxton, Michael Hayman, David Coman, Himanshu Goel, Anne Baxter, Alan Ma, et al.
Journal article | 2020 | Neurology
OBJECTIVE: Determining the genetic basis of speech disorders provides insight into the neurobiology of human communication. Despit..
Punctate white-matter lesions in the full-term newborn: Underlying aetiology and outcome.
Michael Hayman, Gerda van Wezel-Meijler, Henrica van Straaten, Eva Brilstra, Floris Groenendaal, Linda S de Vries
Journal article | 2019 | European Journal of Paediatric Neurology
BACKGROUND: Punctate white matter lesions (PWMLs) are small focal patches of increased signal intensity (SI) on T1- and decreased ..
Paediatrics Royal Children's Hospital