K. Y. Chan

发表

Surveillance of acute flaccid paralysis in Hong Kong: 1997 to 2002.

T. Lam, Y. Lau, R. Lam, 2005, Hong Kong medical journal = Xianggang yi xue za zhi.

Pipeline embolisation device for wide-necked internal carotid artery aneurysms in a hospital in Hong Kong: preliminary experience.

T. Chan, J. Kwok, K. Y. Chan, 2011, Hong Kong medical journal = Xianggang yi xue za zhi.

Clinical Guidelines on Management of Prolonged Seizures, Serial Seizures and Convulsive Status Epilepticus in Children

K. Kwong, A. Yung, E. Fung, 2011 .

Multicentre study of hospitalised patients with sports- and recreational cycling-related traumatic brain injury in Hong Kong.

D. T. Chan, W. Lui, P. Tan, 2021, Hong Kong medical journal = Xianggang yi xue za zhi.

Genetic diagnosis of severe myoclonic epilepsy of infancy (Dravet syndrome) with SCN1A mutations in the Hong Kong Chinese patients.

C. Lam, C. Mak, A. Chan, 2011, Hong Kong medical journal = Xianggang yi xue za zhi.

Hereditary spastic paraplegia: identification of an SPG3A gene mutation in a Chinese family.

C. Lam, C. Mak, A. Chan, 2009, Hong Kong medical journal = Xianggang yi xue za zhi.

Effect of non-invasive prenatal testing as a contingent approach on the indications for invasive prenatal diagnosis and prenatal detection rate of Down's syndrome.

K. Y. Chan, A. Kan, K. Leung, 2016, Hong Kong medical journal = Xianggang yi xue za zhi.

Diagnosis of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes in a Chinese family by PCR/restriction enzyme analysis

C. Lam, Y. Chan, K. Y. Chan, 1995, Clinical molecular pathology.

Benign childhood epilepsy with centrotemporal spikes: a study of 50 Chinese children

K. Y. Chan, C. Ma, Ck Ma, 2003, Brain and Development.

A patient with congenital hyperlactataemia and Leigh syndrome: an uncommon mitochondrial variant.

K. Au, C. Mak, Y. Yuen, 2013, Hong Kong medical journal = Xianggang yi xue za zhi.

Infantile isolated sulphite oxidase deficiency in a Chinese family: a rare neurodegenerative disorder.

C. Lai, A. Chan, C. Li, 2002, Hong Kong medical journal = Xianggang yi xue za zhi.

Neurocysticercosis in a young Indian male.

P. Woo, K. Y. Chan, E. Ng, 2016, Hong Kong medical journal = Xianggang yi xue za zhi.

RYR1-related central core myopathy in a Chinese adolescent boy.

C. Mak, A. Chan, S. P. Chen, 2011, Hong Kong medical journal = Xianggang yi xue za zhi.

Spectrum of mutations in the MECP2 gene in patients with infantile autism and Rett syndrome

V. Wong, C. Pang, T. Fok, 2000, Journal of medical genetics.

Herpetic shoulder paresis in a Chinese elderly patient.

L. Chu, J. Luk, K. Y. Chan, 2005, Hong Kong medical journal = Xianggang yi xue za zhi.

Factors associated with common and atypical chromosome abnormalities after positive combined first-trimester screening in Chinese women: a retrospective cohort study

K. Leung, T. Ma, M. Tang, 2019, BMC Pregnancy and Childbirth.

Recurrent and novel mutations of GCDH gene in Chinese glutaric acidemia type I families

T. Fok, A. Chan, N. Tang, 2000, Human mutation.

patients with infantile autism and Rett syndrome gene in MECP2 Spectrum of mutations in the

V. Wong, C. Pang, C. Lam, 2006 .

Juvenile-onset glycogen storage disease type II with novel mutations in acid α-glucosidase gene

F. Martiniuk, C. Lam, C. Lai, 2003, Neurology.

A novel mitochondrial DNA deletion in a Chinese girl with Kearns-Sayre syndrome.

K. Au, Y. Chan, T. Chow, 2009, Hong Kong medical journal = Xianggang yi xue za zhi.

Biochemical and molecular characterization of tyrosine hydroxylase deficiency in Hong Kong Chinese.

V. Wong, S. Tam, C. Fung, 2010, Molecular genetics and metabolism.

Interferon treatment for multiple sclerosis patients in Hong Kong.

Y. Chan, K. Chin, K. Lau, 2000, Hong Kong medical journal = Xianggang yi xue za zhi.

Carnitine-acylcarnitine translocase deficiency in three neonates presenting with rapid deterioration and cardiac arrest.

C. Lam, C. Lai, C. Shek, 2007, Hong Kong medical journal = Xianggang yi xue za zhi.