Items where Author is "Khoo, T.B."

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Number of items: 4.

Article

Chen, B.C. and McGown, I.N. and Thong, M.K. and Pitt, J. and Yunus, Z.M. and Khoo, T.B. and Ngu, L.H. and Duley, J.A. (2010) Adenylosuccinate lyase deficiency in a Malaysian patient, with novel adenylosuccinate lyase gene mutations. Journal of Inherited Metabolic Disease, 33 (3). S159-S162.

Looi, R.Y. and Thong, M.K. and Goh, K.J. and Ahmad-Annuar, A. and Shahrizaila, N. and Thomas, T. and Khoo, T.B. and Wong, K.T. (2010) Genetic mutations in sarcoglycanopathies in a Malaysian population. Neuromuscular Disorders, 20 (9-10). pp. 609-610.

Conference or Workshop Item

Fong, C.Y. and Chang, W.M. and Kong, A.N. and R., A.M. and Khoo, T.B. and Ong, L.C. (2018) Health-related quality of life in Malaysian children with epilepsy. In: British Paediatric Neurology Association (BPNA) 44th Annual Conference , 03-05 January 2018, King's College London, United Kingdom.

Choong Yi, F. and Kong, A.N. and Poh, B.K. and Mohamed, A.R. and Khoo, T.B. and Nadarajaw, T. and Ong, L.C. (2015) Vitamin D status & bone health lifestyle evaluation in Malaysian children with epilepsy. In: Asian and Oceanian Congress of Child Neurology, 13-17 May 2015, Taipei, Taiwan. (Submitted)

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