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Rare disease in Malaysia: Challenges and solutions.
Shafie AA, Supian A, Ahmad Hassali MA, Ngu LH, Thong MK, Ayob H, Chaiyakunapruk N. Shafie AA, et al. Among authors: ngu lh. PLoS One. 2020 Apr 2;15(4):e0230850. doi: 10.1371/journal.pone.0230850. eCollection 2020. PLoS One. 2020. PMID: 32240232 Free PMC article.
Current diagnosis and management of mucopolysaccharidosis VI in the Asia-Pacific region.
Hwu WL, Okuyama T, But WM, Estrada S, Gu X, Hui J, Kosuga M, Lin SP, Ngu LH, Shi H, Tanaka A, Thong MK, Wattanasirichaigoon D, Wasant P, McGill J. Hwu WL, et al. Among authors: ngu lh. Mol Genet Metab. 2012 Sep;107(1-2):136-44. doi: 10.1016/j.ymgme.2012.07.019. Epub 2012 Jul 20. Mol Genet Metab. 2012. PMID: 22864057
Correction: Rare disease in Malaysia: Challenges and solutions.
Shafie AA, Supian A, Hassali MAA, Ngu LH, Thong MK, Ayob H, Chaiyakunapruk N. Shafie AA, et al. Among authors: ngu lh. PLoS One. 2022 Aug 26;17(8):e0273939. doi: 10.1371/journal.pone.0273939. eCollection 2022. PLoS One. 2022. PMID: 36018891 Free PMC article.
Clinical, biochemical and genetic profiles of patients with mucopolysaccharidosis type IVA (Morquio A syndrome) in Malaysia: the first national natural history cohort study.
Leong HY, Abdul Azize NA, Chew HB, Keng WT, Thong MK, Mohd Khalid MKN, Hung LC, Mohamed Zainudin N, Ramlee A, Md Haniffa MA, Yakob Y, Ngu LH. Leong HY, et al. Among authors: ngu lh. Orphanet J Rare Dis. 2019 Jun 14;14(1):143. doi: 10.1186/s13023-019-1105-6. Orphanet J Rare Dis. 2019. PMID: 31200731 Free PMC article.
61 results