Search Results - "BUT, Wai Man"
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Incidence and clinical characteristics of pediatric‐onset type 2 diabetes in Hong Kong: The Hong Kong childhood diabetes registry 2008 to 2017
Published in Pediatric diabetes (01-08-2022)“…Objective With increasing prevalence of childhood obesity worldwide, the incidence of pediatric‐onset type 2 diabetes (T2D) is also increasing in many…”
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Increasing incidence of type 1 diabetes among Hong Kong children and adolescents: The Hong Kong Childhood Diabetes Registry 2008 to 2017
Published in Pediatric diabetes (01-08-2020)“…Objective The incidence of childhood‐onset type 1 diabetes (T1D) has been reported to be rising but there is also evidence that it has been attenuated in…”
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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
Published in Annals of pediatric endocrinology & metabolism (01-06-2021)“…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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Growth charts for Chinese Down syndrome children from birth to 14 years
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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Asia‐Pacific Consensus Recommendations on X‐Linked Hypophosphatemia: Diagnosis, Multidisciplinary Management, and Transition From Pediatric to Adult Care
Published in JBMR plus (01-06-2023)“…ABSTRACT X‐linked hypophosphatemia (XLH) is a rare, inherited, multisystem disorder characterized by hypophosphatemia that occurs secondary to renal phosphate…”
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Current diagnosis and management of mucopolysaccharidosis VI in the Asia-Pacific region
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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24 h Activity Guidelines in Children and Adolescents: A Prevalence Survey in Asia-Pacific Cities
Published in International journal of environmental research and public health (19-07-2023)“…This study aimed to examine the prevalence of adherence to 24 h activity guidelines in children and adolescents from Asia-Pacific cities. In 1139 children aged…”
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A novel nonsense mutation in the LPL gene in a Chinese neonate with hypertriglyceridemia
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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Glucose-6-phosphatase gene (727G→T) splicing mutation is prevalent in Hong Kong Chinese patients with glycogen storage disease type la
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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Diagnosis of 5α-reductase 2 deficiency: is measurement of dihydrotestosterone essential?
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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Growth charts for Chinese Down syndrome children from birth to 14years
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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Medical Issues among Children and Teenagers with Down Syndrome in Hong Kong
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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Diagnosis of 5[alpha]-Reductase 2 Deficiency: Is Measurement of Dihydrotestosterone Essential?
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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Glucose-6-phosphatase gene (727G→T) splicing mutation is prevalent in Hong Kong Chinese patients with glycogen storage disease type 1a
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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Nephroptosis: The wandering kidney
Published in Kidney research and clinical practice (30-09-2018)Get full text
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Distributed Leadership in Hong Kong Early Childhood Education Sector
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
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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Distributed Leadership in Hong Kong Early Childhood Education Sector
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Vascular endothelial growth factor and pigment epithelium-derived factor in aqueous humor of patients with choroidal neovascularization
Published in Zhejiang da xue xue bao. Journal of Zhejiang University. Medical sciences. Yi xue ban (01-05-2006)“…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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Digenic association of RHO and RP1 genes with retinitis pigmentosa among Chinese population in Hong Kong
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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