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Paediatric multisystem inflammatory syndrome temporally associated with SARS-CoV-2: a case report

Hong Kong medical journal = Xianggang yi xue za zhi, 2022-02, Vol.28 (1), p.76

2022

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Aetiological bases of 46,XY disorders of sex development in the Hong Kong Chinese population

Hong Kong medical journal = Xianggang yi xue za zhi, 2015-12, Vol.21 (6), p.499-510

2015

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MECP2 mutation in male patients with non-specific X-linked mental retardation

FEBS letters, 2000-09, Vol.481 (3), p.285-288

2000

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Genetic basis of channelopathies and cardiomyopathies in Hong Kong Chinese patients: a 10-year regional laboratory experience

Hong Kong medical journal = Xianggang yi xue za zhi, 2018-08, Vol.24 (4), p.340-349

2018

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Atypical focal cortical dysplasia in a patient with Cowden syndrome

Hong Kong medical journal = Xianggang yi xue za zhi, 2014-04, Vol.20 (2), p.165-167

2014

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A Comparison of Nasendoscopy and Multiview Videofluoroscopy in Assessing Velopharyngeal Insufficiency

Otolaryngology-head and neck surgery, 2006-03, Vol.134 (3), p.394-402

2006

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Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) triggered by valproate therapy

European journal of pediatrics, 1997-07, Vol.156 (7), p.562-564

1997

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Ocular manifestations of Seckel syndrome

American journal of ophthalmology, 2001-10, Vol.132 (4), p.596-597

2001

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Galactorrhea—A strong clinical clue towards the diagnosis of neurotransmitter disease

Brain & development (Tokyo. 1979), 2006-07, Vol.28 (6), p.389-391

2006

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Quantitative Analysis of Pleural Fluid Cell-free DNA as a Tool for the Classification of Pleural Effusions

Clinical chemistry (Baltimore, Md.), 2003-05, Vol.49 (5), p.740-745

2003

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Is the timing of exposure to infection a major determinant of acute lymphoblastic leukaemia in Hong Kong?

Paediatric and perinatal epidemiology, 2002-04, Vol.16 (2), p.154-165

2002

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Genetic variation of glycoproteins B and H of human herpesvirus 7 in Hong Kong

Journal of medical virology, 2003-11, Vol.71 (3), p.429-433

2003

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Novel mutations in the PATCHED gene in basal cell nevus syndrome

Molecular genetics and metabolism, 2002-05, Vol.76 (1), p.57-61

2002

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Early-onset primary torsional dystonia in a 4-generation Chinese family with a mutation in the DYT1 gene

Chinese medical journal, 2005-05, Vol.118 (10), p.873-876

2005

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Magnetic resonance spectroscopy and analysis of MECP2 in Rett syndrome

Pediatric neurology, 2002-03, Vol.26 (3), p.205-209

2002

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Insight and General Public Attitude on Psychotic Experiences in Hong Kong

International journal of social psychiatry, 1996-04, Vol.42 (1), p.10-17

1996

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De novo mutation in the mitochondrial tRNALeu(UUR) gene (A3243G) with rapid segregation resulting in MELAS in the offspring

Journal of paediatrics and child health, 2001-02, Vol.37 (1), p.87-90

2001

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Paediatric multisystem inflammatory syndrome temporally associated with SARS-CoV-2: a case report

Aetiological bases of 46,XY disorders of sex development in the Hong Kong Chinese population

MECP2 mutation in male patients with non-specific X-linked mental retardation

Genetic basis of channelopathies and cardiomyopathies in Hong Kong Chinese patients: a 10-year regional laboratory experience

Atypical focal cortical dysplasia in a patient with Cowden syndrome

A Comparison of Nasendoscopy and Multiview Videofluoroscopy in Assessing Velopharyngeal Insufficiency

Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) triggered by valproate therapy

Ocular manifestations of Seckel syndrome

Galactorrhea—A strong clinical clue towards the diagnosis of neurotransmitter disease

Quantitative Analysis of Pleural Fluid Cell-free DNA as a Tool for the Classification of Pleural Effusions

Is the timing of exposure to infection a major determinant of acute lymphoblastic leukaemia in Hong Kong?

Genetic variation of glycoproteins B and H of human herpesvirus 7 in Hong Kong

Novel mutations in the PATCHED gene in basal cell nevus syndrome

Early-onset primary torsional dystonia in a 4-generation Chinese family with a mutation in the DYT1 gene

Magnetic resonance spectroscopy and analysis of MECP2 in Rett syndrome

Insight and General Public Attitude on Psychotic Experiences in Hong Kong

De novo mutation in the mitochondrial tRNALeu(UUR) gene (A3243G) with rapid segregation resulting in MELAS in the offspring

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