Sudden arrhythmia death syndrome in young victims: a five-year retrospective review and two-year prospective molecular autopsy study by next-generation sequencing and clinical eval... von Mak, C M, Mok, N S, Shum, H C, Siu, W K, Chong, Y K, Lee, H H C, Fong, N C, Tong, S F, Lee, K W, Ching, C K, Chen, S P L, Cheung, W L, Tso, C B, Poon, W M, Lau, C L, Lo, Y K, Tsui, P T, Shum, S F, Lee, K C

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A Comparison of Morbidity Patterns in Public and Private Primary Care Clinics in Malaysia von Mimi, O, Tong, SF, Nordin, S, Teng, CL, Khoo, EM, Abdul-Rahman, A, Zailinawati, AH, Lee, VKM, Chen, WS, Shihabudin, WM, Noridah, MS, Fauziah, ZE

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A YOUNG MAN WITH LOIN PAIN von Tong, SF

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The roles of men in family planning - a study of married men at the UKM primary care clinic von Ling, Jes, Tong, S F

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MECP2 mutation in male patients with non-specific X-linked mental retardation von Orrico, Alfredo, Lam, Ching-Wan, Galli, Lucia, Dotti, Maria Teresa, Hayek, Giuseppe, Tong, Sui-Fan, Poon, Priscilla M.K., Zappella, Michele, Federico, Antonio, Sorrentino, Vincenzo

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A Patient Who Refused Medical Advice: The Doctor And The Patient Should Look For A Common Ground von Tong, SF, Robert, Chen

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A patient with novel ABCB11 gene mutations with phenotypic transition between BRIC2 and PFIC2 von Lam, Ching-Wan, Cheung, Ka-Ming, Tsui, Man-Shan, Yan, Matthew Shu-Ching, Lee, Ching-Yin, Tong, Sui-Fan

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Poor blood pressure control and its associated factors among older people with hypertension: A cross-sectional study in six public primary care clinics in Malaysia von Cheong, A T, Sazlina, S G, Tong, S F, Azah, A S, Salmiah, S

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Identification of RASSF1A modulated genes in nasopharyngeal carcinoma von Chow, L S-N, Lam, C-W, Chan, S Y-Y, Tsao, S-W, To, K-F, Tong, S-F, Hung, W-K, Dammann, R, Huang, D P, Lo, K-W

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A frequent activated smoothened mutation in sporadic basal cell carcinomas von LAM, C.-W, JINGWU XIE, TO, K.-F, NG, H.-K, LEE, K.-C, YUEN, N. W.-F, LIM, P.-L, CHAN, L. Y.-S, TONG, S.-F, MCCORMICK, F

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Validity and reliability of the Malay version of the Hill-Bone compliance to high blood pressure therapy scale for use in primary healthcare settings in Malaysia: A cross-sectional... von Cheong, A T, Tong, S F, Sazlina, S G

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Heterogeneous mutations in the SLC3A1 and SLC7A9 genes in Chinese patients with cystinuria von Yuen, Y.-P., Lam, C.-W., Lai, C.-K., Tong, S-F, Li, P.-S., Tam, S., Kwan, E.Y-W., Chan, S.-Y., Tsang, W.-K., Chan, K.-Y., Mak, W.-L., Cheng, C.-W., Chan, Y.-W.

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Missense mutation Leu72Pro located on the carboxyl terminal amphipathic helix of apolipoprotein C-II causes familial chylomicronemia syndrome von Lam, Ching-Wan, Yuen, Yuet-Ping, Cheng, Wai-Fun, Chan, Yan-Wo, Tong, Sui-Fan

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Atypical presentation of dopa-responsive dystonia: Generalized hypotonia and proximal weakness von KONG, Chi-Keung, KO, Chun-Hung, SUI FAN TONG, LAM, Ching-Wan

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Galactorrhea—A strong clinical clue towards the diagnosis of neurotransmitter disease von Yeung, Wai Lan, Lam, Ching Wan, Hui, Joannie, Tong, Sui Fan, Wu, Shun Ping

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Mutation of Proline 409 to Arginine in the Meander Region of Cytochrome P450c17 Causes Severe 17α-Hydroxylase Deficiency von Lam, Ching-Wan, Arlt, Wiebke, Chan, Chi-Kwok, Honour, John W., Lin, Chin Jia, Tong, Sui-Fan, Choy, Kwong-Wai, Miller, Walter L.

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Genome-wide detection of allelic imbalance in renal cell carcinoma using high-density single-nucleotide polymorphism microarrays von Lam, Ching-Wan, To, Ka-Fai, Tong, Sui-Fan

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Novel missense mutation (Y279S) in the GLRA1 gene causing hyperekplexia von Poon, Wing-Tat, Chan, Kwok-Yin, Au, Kam-Ming, Tong, Sui-Fan, Chan, Yan-Wo, Lam, Ching-Wan, Chow, Chun-Bong

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Novel missense mutation in the CASR gene in a Chinese family with familial hypocalciuric hypercalcemia von Lam, Ching-Wan, Lee, Ka-Fai, Chan, Angel On-Kei, Poon, Priscilla Miu-Kuen, Law, Tak-Yin, Tong, Sui-Fan

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Juvenile-onset glycogen storage disease type II with novel mutations in acid α-glucosidase gene von LAM, C. W, YUEN, Y. P, CHAN, K. Y, TONG, S. F, LAI, C. K, CHOW, T. C, LEE, K. C, CHAN, Y. W, MARTINIUK, F

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