S. Kearney

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Markers of cognitive function in individuals with metabolic disease: Morquio syndrome and tyrosinemia type III

S. Frisson, C. Hendriksz, P. Gissen, 2018, Cognitive neuropsychology.

Dorris, L. et al. (2017) A randomized controlled trial of a manual-based Psychosocial group Intervention for young people with Epilepsy

Nadia, Turton, G. Baker, 2018 .

A randomized controlled trial of a manual-based psychosocial group intervention for young people with epilepsy [PIE]

G. Baker, Helen Broome, L. Dorris, 2017, Epilepsy & Behavior.

The complete European guidelines on phenylketonuria: diagnosis and treatment

N. Blau, S. Huijbregts, A. Macdonald, 2017, Orphanet Journal of Rare Diseases.

Issues with European guidelines for phenylketonuria - Authors' reply.

N. Blau, S. Huijbregts, A. Burlina, 2017, The lancet. Diabetes & endocrinology.

Long-term open-label phase I/II extension study of intrathecal idursulfase-IT in the treatment of neuronopathic mucopolysaccharidosis II.

J. Muenzer, Margot B. Stein, S. Kearney, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

Therapy development for the mucopolysaccharidoses: Updated consensus recommendations for neuropsychological endpoints.

J. H. van der Lee, J. Eisengart, R. Giugliani, 2020, Molecular genetics and metabolism.

European guidelines for the diagnosis and management of patients with phenylketonuria

N. Blau, S. Huijbregts, A. Burlina, 2017 .

Management of the behavioural manifestations of Hunter syndrome.

Jane Roberts, S. Kearney, C. Stewart, 2016, British journal of nursing.

Cognitive endpoints for therapy development for neuronopathic mucopolysaccharidoses: Results of a consensus procedure.

J. H. van der Lee, Darren T. Janzen, R. Giugliani, 2017, Molecular genetics and metabolism.

Intellectual and neurological functioning in Morquio syndrome (MPS IVa)

C. Hendriksz, K. Foster, J. Davison, 2013, Journal of Inherited Metabolic Disease.

Defining tetrahydrobiopterin responsiveness in phenylketonuria: Survey results from 38 countries.

M. Langeveld, T. Coşkun, S. Huijbregts, 2021, Molecular genetics and metabolism.

Putting children forward for epilepsy surgery: A qualitative study of UK parents' and health professionals' decision-making experiences

G. Heath, S. Kearney, R. Begum, 2016, Epilepsy & Behavior.

Mapping language networks and their association with verbal abilities in paediatric epilepsy using MEG and graph analysis

A. Hillebrand, P. Furlong, S. Seri, 2020, NeuroImage: Clinical.