N. Loh

The association of neurodevelopmental abnormalities, congenital heart and renal defects in a tuberous sclerosis complex patient cohort

A. Harwood, T. Woolley, O. Uzun, 2022, BMC Medicine.

Untreated recurrent acute necrotising encephalopathy associated with RANBP2 mutation, and normal outcome in a Caucasian boy

D. B. Appleton, N. Loh, 2010, European Journal of Pediatrics.

Focal epilepsy presenting as a bath-induced paroxysmal event/breath-holding attack

N. Loh, C. Stutchfield, 2014, Epilepsy & Behavior Case Reports.

What is new in migraine management in children and young people?

W. Whitehouse, R. Howells, N. Loh, 2022, Archives of Disease in Childhood.

Unravelling the Clinical Co-Morbidity and Risk Factors Associated with Agenesis of the Corpus Callosum

D. Tucker, T. Woolley, O. Uzun, 2023, Journal of clinical medicine.

A genetic cause for neonatal encephalopathy: incontinentia pigmenti with NEMO mutation

A. Whitelaw, L. Jadresić, N. Loh, 2008, Acta paediatrica.