Search Results - "Tse, Wing Yee"
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Improved Properties of the Big Five Inventory and the Rosenberg Self-Esteem Scale in the Expanded Format Relative to the Likert Format
Published in Frontiers in psychology (04-06-2019)“…Previous research by Zhang and Savalei (2015) proposed an alternative scale format to the Likert scale format: the Expanded format. Scale items in the Expanded…”
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Does strict invariance matter? Valid group mean comparisons with ordered-categorical items
Published in Behavior research methods (01-04-2024)“…Measurement invariance (MI) of a psychometric scale is a prerequisite for valid group comparisons of the measured construct. While the invariance of loadings…”
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Adjusting for partial invariance in latent parameter estimation: Comparing forward specification search and approximate invariance methods
Published in Behavior research methods (01-02-2022)“…Measurement invariance is the condition that an instrument measures a target construct in the same way across subgroups, settings, and time. In psychological…”
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Correcting for Unreliability and Partial Invariance: A Two-Stage Path Analysis Approach
Published in Structural equation modeling (04-03-2023)“…In path analysis, using composite scores without adjustment for measurement unreliability and violations of factorial invariance across groups lead to biased…”
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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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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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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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Long-term outcome of oxandrolone treatment in boys with constitutional delay of growth and puberty
Published in The Journal of pediatrics (01-10-1990)Get more information
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9
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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10
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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