Search Results - "BUT, Wai Man"

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    Features of partial remission in children with type 1 diabetes using the insulin dose-adjusted A1c definition and risk factors associated with nonremission by Wong, Tsz Wai Catherine, Wong, Man Yee Shirley, But, Wai Man Betty

    “…PURPOSEWe sought to evaluate features of partial remission (PR) in children with type 1 diabetes mellitus (T1DM) using the insulin-dose adjusted A1c (IDAA1c)…”
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    Journal Article
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    Growth charts for Chinese Down syndrome children from birth to 14 years by Su, Xuefen, Lau, Joseph Tak Fai, Yu, Chak Man, Chow, Chun Bong, Lee, Lai Ping, But, Betty Wai Man, Yam, Winnie Ka Ling, Tse, Philomena Wan Ting, Fung, Eva Lai Wah, Choi, Kai Chow

    Published in Archives of disease in childhood (01-09-2014)
    “…Objective To establish Down syndrome (DS)-specific growth charts for Hong Kong Chinese children. Design and setting Growth data were collected from (1) members…”
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    Journal Article
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    Current diagnosis and management of mucopolysaccharidosis VI in the Asia-Pacific region by Hwu, Wuh-Liang, Okuyama, Torayuki, But, Wai Man, Estrada, Sylvia, Gu, Xuefan, Hui, Joannie, Kosuga, Motomichi, Lin, Shuan-Pei, Ngu, Lock-Hock, Shi, Huiping, Tanaka, Akemi, Thong, Meow-Keong, Wattanasirichaigoon, Duangrurdee, Wasant, Pornswan, McGill, Jim

    Published in Molecular genetics and metabolism (01-09-2012)
    “…Mucopolysaccharidosis (MPS) type VI (Maroteaux–Lamy syndrome) is a clinically heterogeneous lysosomal storage disorder. It presents significant diagnostic and…”
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    Journal Article
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    A novel nonsense mutation in the LPL gene in a Chinese neonate with hypertriglyceridemia by Chan, Angel On-kei, But, Wai-man, Lau, Gene Tze-chin, Tse, Wing-yee, Shek, Chi-chung

    Published in Clinica chimica acta (01-06-2006)
    “…Lipoprotein lipase (LPL) deficiency is a rare autosomal recessive disorder characterized by hypertriglyceridemia. The genetic defect lies in a mutation of the…”
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    Journal Article
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    Glucose-6-phosphatase gene (727G→T) splicing mutation is prevalent in Hong Kong Chinese patients with glycogen storage disease type la by Lam, Ching-Wan, But, Wai-Man, Shek, Chi-Chung, Tong, Sui-Fan, Chan, Yuen-Shan, Choy, Kwong-Wai, Tse, Wing-Yee, Pang, Chi-Pui, Hjelm, Nils Magnus

    Published in Clinical genetics (01-03-1998)
    “…Glycogen storage disease type la (GSD1a) is an autosomal recessive metabolic disorder caused by a deficiency in glucose‐6‐phosphatase (GóPase). We analyzed the…”
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    Journal Article
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    Diagnosis of 5α-reductase 2 deficiency: is measurement of dihydrotestosterone essential? by Chan, Angel On Kei, But, Betty Wai Man, Lee, Ching Yin, Lam, Yuen Yu, Ng, Kwok Leung, Tung, Joanna Yuet Ling, Kwan, Elaine Yin Wah, Chan, Yuk Kit, Tsui, Teresa Kam Chi, Lam, Almen Lai Na, Tse, Wing Yee, Cheung, Pik To, Shek, Chi Chung

    Published in Clinical chemistry (Baltimore, Md.) (01-05-2013)
    “…5α-Reductase 2 deficiency (5ARD) is a known cause of 46,XY disorders of sex development (DSD). Traditionally, the diagnosis relies on dihydrotestosterone (DHT)…”
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    Journal Article
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    Growth charts for Chinese Down syndrome children from birth to 14years by Su, Xuefen, Lau, Joseph Tak Fai, Yu, Chak Man, Chow, Chun Bong, Lee, Lai Ping, But, Betty Wai Man, Yam, Winnie Ka Ling, Tse, Philomena Wan Ting, Fung, Eva Lai Wah, Choi, Kai Chow

    Published in Archives of disease in childhood (30-09-2014)
    “…ObjectiveTo establish Down syndrome (DS)-specific growth charts for Hong Kong Chinese children.Design and settingGrowth data were collected from (1) members of…”
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    Journal Article
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    Medical Issues among Children and Teenagers with Down Syndrome in Hong Kong by Yam, Winnie Ka-Ling, Tse, Philomena Wan Ting, Yu, Chak Man, Chow, Chun Bong, But, Wai Man, Li, Kit Yu, Lee, Lai Ping, Fung, Eva Lai Wah, Mak, Pauline Pui Yee, Lau, Joseph Tak Fai

    Published in Down's syndrome, research and practice (01-10-2008)
    “…We examined the prevalence of medical problems in children and teenagers with Down syndrome in Hong Kong. Methods: Children with Down syndrome receiving care…”
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    Journal Article
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    Diagnosis of 5[alpha]-Reductase 2 Deficiency: Is Measurement of Dihydrotestosterone Essential? by Chan, Angel OnKei, But, Betty Wai Man, Lee, Ching Yin, Lam, Yuen Yu, Ng, Kwok Leung, Tung, Joanna Yuet Ling, Kwan, Elaine Yin Wah, Chan, Yuk Kit, Tsui, Teresa Kam Chi, Lam, Almen Lai Na, Tse, Wing Yee, Cheung, Pik To, Shek, Chi Chung

    Published in Clinical chemistry (Baltimore, Md.) (01-05-2013)
    “…5α-Reductase 2 deficiency (5ARD) is a known cause of 46,XY disorders of sex development (DSD). Traditionally, the diagnosis relies on dihydrotestosterone (DHT)…”
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    Journal Article
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    Glucose-6-phosphatase gene (727G→T) splicing mutation is prevalent in Hong Kong Chinese patients with glycogen storage disease type 1a by LAM, C.-W, BUT, W.-M, SHEK, C.-C, TONG, S.-F, CHAN, Y.-S, CHOY, K.-W, TSE, W.-Y, PANG, C.-P, HJELM, N. M

    Published in Clinical genetics (01-03-1998)
    “…Glycogen storage disease type la (GSD1a) is an autosomal recessive metabolic disorder caused by a deficiency in glucose-6-phosphatase (G6Pase). We analyzed the…”
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    Journal Article
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    Distributed Leadership in Hong Kong Early Childhood Education Sector by Au, Wai Man

    Published 01-01-2012
    “…As an exploratory study, the influences from the Pre-primary School Voucher policy, market needs and educational philosophy upon the forms of leadership of the…”
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    Dissertation
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    Recent progress in molecular genetics and gene therapy for retinitis pigmentosa by Wang, Dan-Yi, Fan, Bao-Jian, Wu, Xiang-Qian, Chan, Wai-Man, Lam, Shun-Chiu, Pang, Chi-Pui

    Published in Chung-hua yen k'o tsa chih (01-02-2005)
    “…Retinitis pigmentosa (RP) is a common genetic eye disease affecting about 1 in 3500 people worldwide with pan-ethnic occurrence. So far there is no effective…”
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    Journal Article
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    Distributed Leadership in Hong Kong Early Childhood Education Sector by Au, Wai Man

    “…As an exploratory study, the influences from the Pre-primary School Voucher policy, market needs and educational philosophy upon the forms of leadership of the…”
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    Dissertation
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    Vascular endothelial growth factor and pigment epithelium-derived factor in aqueous humor of patients with choroidal neovascularization by Tong, Jian-ping, Shen, Ye, Chan, Wai-man, Lin, Shun-chao, Peng, Zhi-pei

    “…To detect the levels of vascular endothelial growth factor (VEGF) and pigment epithelium-derived factor (PEDF) in aqueous humor of patients with active…”
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    Journal Article
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    Digenic association of RHO and RP1 genes with retinitis pigmentosa among Chinese population in Hong Kong by Wang, Dan-yi, Fan, Bao-jian, Chan, Wai-man, Tam, Oi-sin, Chiang, Wai-yee, Lam, Shun-chiu, Pang, Chi-pui

    Published in Zhong hua yi xue za zhi (22-06-2005)
    “…To identify the mutation patterns of RHO and RP1 genes in the Chinese patients with retinitis pigmentosa (RP) and to explore their potential interactions in…”
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    Journal Article