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Number of items: 4.

Looi, R.Y. and Goh, K.J. and Shahrizaila, N. and Thong, M.K. and Ahmad-Annuar, A. and Wong, K.T. (2010) Genetic mutations in dysferlinopathy in a Malaysian population. Neuromuscular Disorders, 20 (9-10). p. 606.

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.

Low, Soon-Chai and Md Sari, Nor Ashikin and Tan, Cheng-Yin and Ahmad-Annuar, Azlina and Wong, Kum-Thong and Law, Wan-Chung and Sim, Rachel Siew-Hung and Lin, Kon-Ping and Shahrizaila, Nortina and Goh, Khean-Jin (2021) Hereditary transthyretin amyloidosis in multi-ethnic Malaysians. Neuromuscular Disorders, 31 (7). pp. 642-650. ISSN 0960-8966, DOI https://doi.org/10.1016/j.nmd.2021.03.008.

Tan, Cheng Yin and Goh, Khean Jin and Oh, Ai-Wen and Devaux, Jerome and Shahrizaila, Nortina (2022) Autoantibody profile in a Malaysian cohort of chronic inflammatory demyelinating polyneuropathy. Neuromuscular Disorders, 32 (3). pp. 255-262. ISSN 0960-8966, DOI https://doi.org/10.1016/j.nmd.2022.01.006.

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