Search Results - "Chan, O.K."
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Formation of TiN Grid on NiTi by Laser Gas Nitriding for Improving Wear Resistance in Hanks' Solution
Published in Journal of materials science & technology (01-05-2016)“…Laser gas nitriding (LGN) is a common surface modification method to enhance the wear resistance of titanium (Ti) alloys, which are known to have poor…”
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2
Corticosterone Methyl Oxidase Deficiency Type 1 with Normokalemia in an Infant
Published in Journal of clinical research in pediatric endocrinology (01-09-2016)“…Isolated aldosterone synthase deficiency may result in life-threatening salt-wasting and failure to thrive. The condition involves hyperkalemia accompanying…”
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3
Hyperandrogenism, Elevated 17-Hydroxyprogesterone and Its Urinary Metabolites in a Young Woman with Ovarian Steroid Cell Tumor, Not Otherwise Specified: Case Report and Review of the Literature
Published in Case reports in endocrinology (2019)“…We describe a case of a 24-year-old overweight woman who presented with hirsutism, secondary amenorrhea, clitoromegaly, and symptoms of diabetes mellitus (DM)…”
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Perioperative Prophylactic Internal Iliac Artery Balloon Occlusion in the Prevention of Postpartum Hemorrhage in Placenta Previa: A Randomized Controlled Trial
Published in Obstetric anesthesia digest (01-06-2021)“…(Am J Obstet Gynecol. 2020;223:117.e1–13) Placenta previa is a major cause of postpartum hemorrhage (PPH) and maternal death worldwide. As cesarean delivery…”
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5
Knowledge on hepatitis B infection among pregnant women in a high endemicity area
Published in Patient education and counseling (01-12-2011)“…Abstract Objective To assess the knowledge on hepatitis B virus (HBV) infection and associated factors among expectant mothers in an endemic region. Methods A…”
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A rare cause of hyperandrogenism and elevated 17-OHP in a young woman
Published in Pathology (01-02-2020)Get full text
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Performance of in silico analysis in predicting the effect of non-synonymous variants in inherited steroid metabolic diseases
Published in Steroids (01-07-2013)“…•SIFT and PolyPhen-2 had high concordance in testing genes of steroidogenic diseases.•PON-P behaved differently from the other two programs.•The performance of…”
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Urinary steroid profiling in the diagnosis of congenital adrenal hyperplasia and disorders of sex development: Experience of a urinary steroid referral centre in Hong Kong
Published in Clinical biochemistry (01-03-2013)“…Deficiency in any one of the steroidogenic enzymes may result in congenital adrenal hyperplasia (CAH) and disorders of sex development (DSD). Urinary steroid…”
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New strategies for detecting steroid metabolic disorders--paneling vs profiling
Published in Clinical chemistry (Baltimore, Md.) (01-08-2012)Get full text
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10
Delayed diagnosis of adrenal insufficiency in a patient with severe penoscrotal hypospadias due to two novel P450 side-change cleavage enzyme (CYP11A1) mutations (p.R360W; p.R405X)
Published in European journal of endocrinology (01-12-2012)“…ContextCytochrome P450 side-chain cleavage enzyme (CYP11A1) catalyses the first and rate-limiting step of steroidogenesis, the conversion of cholesterol to…”
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Congenital adrenal hyperplasia presenting as a large adrenal incidentaloma in an elderly man
Published in ANZ journal of surgery (01-04-2017)Get full text
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12
The reference interval of thyroid-stimulating hormone in Hong Kong Chinese
Published in Journal of clinical pathology (01-05-2011)“…The upper reference limit of thyroid-stimulating hormone (TSH) is critical for defining patients with subclinical hypothyroidism, a condition which carries a…”
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13
The first case series of Chinese patients in Hong Kong with familial Alzheimer's disease compared with those with biomarker-confirmed sporadic late-onset Alzheimer's disease
Published in Hong Kong medical journal = Xianggang yi xue za zhi (01-12-2017)“…Patients with familial Alzheimer's disease are being increasingly reported in Hong Kong. The objectives of this study were to report the clinical features of…”
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Aetiological bases of 46,XY disorders of sex development in the Hong Kong Chinese population
Published in Hong Kong medical journal = Xianggang yi xue za zhi (01-12-2015)“…Disorders of sex development are due to congenital defects in chromosomal, gonadal, or anatomical sex development. The objective of this study was to determine…”
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A common PRRT2 mutation in familial paroxysmal kinesigenic dyskinesia in Hong Kong: a case series of 16 patients
Published in Hong Kong medical journal = Xianggang yi xue za zhi (01-12-2016)Get full text
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The clinical significance of aldosterone synthase deficiency: report of a novel mutation in the CYP11B2 gene
Published in BMC endocrine disorders (03-04-2014)“…Aldosterone synthase (CYP11B2) deficiency is a rare autosomal recessive disorder, usually presenting with severe salt-wasting in infancy or stress-induced…”
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Hypertriglyceridaemia-induced pancreatitis: a contributory role of capecitabine?
Published in Hong Kong medical journal = Xianggang yi xue za zhi (01-12-2012)“…Capecitabine is an orally administered pro-drug of 5-fluorouracil that confers superior disease-free survival and presumably has a more favourable side-effect…”
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Molecular analysis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Hong Kong Chinese patients
Published in Steroids (01-09-2011)“…► The frequency of CYP21A2 mutations in Hong Kong Chinese differs from other Asian populations. ► Testing for gross deletion is mandatory to avoid…”
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Reference intervals of common serum analytes of Hong Kong Chinese
Published in Journal of clinical pathology (01-05-2008)“…Setting up reference intervals from the local service populations is one of the major responsibilities of clinical laboratories. Yet, this task is difficult to…”
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Long-term outcome of kidney transplantation in a patient with coexisting lipoprotein glomerulopathy and fibrillary glomerulonephritis
Published in Clinical kidney journal (01-08-2014)“…Both lipoprotein glomerulopathy (LPG) and fibrillary glomerulonephritis (FGN) are rare causes of end-stage renal disease (ESRD), and the literature concerning…”
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