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 ..

Methylcrotonyl-CoA carboxylase (MCC) deficiency associated with severe muscle pain and physical disability in an adult

A Boneh, M Baumgartner, M Hayman, H Peters

Journal article  |  2005  |  Journal of Inherited Metabolic Disease