The association of neurodevelopmental abnormalities, congenital heart and renal defects in a tuberous sclerosis complex patient cohort von Robinson, Jessica, Uzun, Orhan, Loh, Ne Ron, Harris, Isabelle Rose, Woolley, Thomas E, Harwood, Adrian J, Gardner, Jennifer Frances, Syed, Yasir Ahmed

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A genetic cause for neonatal encephalopathy: incontinentia pigmenti with NEMO mutation von Loh, Ne-Ron, Jadresic, Lyda P, Whitelaw, Andrew

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Untreated recurrent acute necrotising encephalopathy associated with RANBP2 mutation, and normal outcome in a Caucasian boy von Loh, Ne-Ron, Appleton, Donald Barry

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Interpretation and implementation of the revised European Society for Paediatric Gastroenterology Hepatology and Nutrition (ESPGHAN) guidelines on pediatric celiac disease amongst... von Paul, Siba Prosad, Adams, Helen Louise, Basude, Dharamveer

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Unravelling the Clinical Co-Morbidity and Risk Factors Associated with Agenesis of the Corpus Callosum von Smith, Callum J, Smith, Zoey G, Rasool, Hania, Cullen, Katie, Ghosh, Meghana, Woolley, Thomas E, Uzun, Orhan, Loh, Ne Ron, Tucker, David, Syed, Yasir Ahmed

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