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Novel finding of lissencephaly and severe osteopenia in a Chinese patient with SATB2‐associated syndrome and a brief review of literature

American journal of medical genetics. Part A, 2022-07, Vol.188 (7), p.2168-2172

2022

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Kawasaki disease with retropharyngeal edema: case series from a single center experience

Chinese medical journal, 2019-07, Vol.132 (14), p.1753-1754

2019

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Left ventricular stiffness in paediatric patients with end-stage kidney disease

Pediatric nephrology (Berlin, West), 2020-06, Vol.35 (6), p.1051-1060

2020

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Fatal viral infection-associated encephalopathy in two Chinese boys: a genetically determined risk factor of thermolabile carnitine palmitoyltransferase II variants

Journal of human genetics, 2011-08, Vol.56 (8), p.617-621

2011

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Clinical whole-exome sequencing reveals a common pathogenic variant in patients with CoQ10 deficiency: An underdiagnosed cause of mitochondriopathy

Clinica chimica acta, 2019-10, Vol.497, p.88-94

2019

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Centrosome-associated CDC25B is a novel disease-causing gene for a syndrome with cataracts, dilated cardiomyopathy, and multiple endocrinopathies

Clinica chimica acta, 2020-05, Vol.504, p.81-87

2020

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Clinical whole-exome sequencing reveals a novel missense pathogenic variant of GNAO1 in a patient with infantile-onset epilepsy

Clinica chimica acta, 2015-12, Vol.451 (Pt B), p.292-296

2015

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Early detection of Berry syndrome in a newborn with differential cyanosis

Chinese medical journal, 2006-09, Vol.119 (17), p.1485-1488

2006

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Cardiac ryanodine receptor gene (hRyR2) mutation underlying catecholaminergic polymorphic ventricular tachycardia in a Chinese adolescent presenting with sudden cardiac arrest and cardiac syncope

Chinese medical journal, 2006-12, Vol.119 (24), p.2129-2133

2006

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Diagnostic yield of array CGH in patients with autism spectrum disorder in Hong Kong

Clinical and translational medicine, 2016-05, Vol.5 (1), p.1-8

2016

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Kawasaki Disease with Rare Presentation Masquerading as Severe Infection in Children: A 10-year Retrospective Review in a Tertiary Hospital in Hong Kong SAR

American journal of internal medicine (Print), 2019, Vol.7 (6), p.175

2019

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Clinical whole-exome sequencing reveals a common pathogenic variant in patients with CoQ 10 deficiency: An underdiagnosed cause of mitochondriopathy

Clinica chimica acta, 2019-10, Vol.497, p.88

2019

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Prevalence and potential risk factors of hypokalemia in pediatric patients with diabetic ketoacidosis

International journal of pediatric endocrinology, 2015-04, Vol.2015 (S1), p.P8-P8, Article P8

2015

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Ten years’ experience of paediatrics acute drug poisoning in a tertiary center in Hong Kong

Journal of Emergency and Critical Care Medicine, 2024-09, Vol.8, p.18-18

2024

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Kawasaki Disease with Rare Presentation Masquerading as Severe Infection in Children: A 10-year Retrospective Review in a Tertiary Hospital in Hong Kong SAR

Advanced Biomedicine, 2020-08, Vol.2 (5)

2020

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Cardiac ryanodine receptor gene （hRyR2） mutation underlying catecholaminergic polymorphic ventricular tachycardia in a Chinese adolescent presenting with sudden cardiac arrest and cardiac syncope

Chinese medical journal, 2006, Vol.119 (24), p.2129-2133

Ngai-Shing Mok Ching-Wan Lam Nai-Chung Fong Yim-Wo Hui Yuen-Choi Choi Kwok-Yin Chan

2006

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Kawasaki Disease in Hong Kong, 1994-2000 Surveillance

Pediatric research, 2003-01, Vol.53 (1), p.159-159

2003

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Centrosome-associated CDC25B is a novel disease-causing gene for a syndrome with cataracts, dilated cardiomyopathy, and multiple endocrinopathies

Clinica chimica acta; international journal of clinical chemistry, 2020, Vol.504, p.81-87

2020

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Novel finding of lissencephaly and severe osteopenia in a Chinese patient with SATB2‐associated syndrome and a brief review of literature

Kawasaki disease with retropharyngeal edema: case series from a single center experience

Left ventricular stiffness in paediatric patients with end-stage kidney disease

Fatal viral infection-associated encephalopathy in two Chinese boys: a genetically determined risk factor of thermolabile carnitine palmitoyltransferase II variants

Clinical whole-exome sequencing reveals a common pathogenic variant in patients with CoQ10 deficiency: An underdiagnosed cause of mitochondriopathy

Centrosome-associated CDC25B is a novel disease-causing gene for a syndrome with cataracts, dilated cardiomyopathy, and multiple endocrinopathies

Clinical whole-exome sequencing reveals a novel missense pathogenic variant of GNAO1 in a patient with infantile-onset epilepsy

Early detection of Berry syndrome in a newborn with differential cyanosis

Cardiac ryanodine receptor gene (hRyR2) mutation underlying catecholaminergic polymorphic ventricular tachycardia in a Chinese adolescent presenting with sudden cardiac arrest and cardiac syncope

Diagnostic yield of array CGH in patients with autism spectrum disorder in Hong Kong

Kawasaki Disease with Rare Presentation Masquerading as Severe Infection in Children: A 10-year Retrospective Review in a Tertiary Hospital in Hong Kong SAR

Clinical whole-exome sequencing reveals a common pathogenic variant in patients with CoQ 10 deficiency: An underdiagnosed cause of mitochondriopathy

Prevalence and potential risk factors of hypokalemia in pediatric patients with diabetic ketoacidosis

Ten years’ experience of paediatrics acute drug poisoning in a tertiary center in Hong Kong

Kawasaki Disease with Rare Presentation Masquerading as Severe Infection in Children: A 10-year Retrospective Review in a Tertiary Hospital in Hong Kong SAR

Cardiac ryanodine receptor gene （hRyR2） mutation underlying catecholaminergic polymorphic ventricular tachycardia in a Chinese adolescent presenting with sudden cardiac arrest and cardiac syncope

Kawasaki Disease in Hong Kong, 1994-2000 Surveillance

Centrosome-associated CDC25B is a novel disease-causing gene for a syndrome with cataracts, dilated cardiomyopathy, and multiple endocrinopathies

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