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Attention, Perception & Psychophysics|May 13, 2022
The relationships between reading fluency and different measures of holistic word processingPaulo Ventura, Helen W-Y Tse, José C Guerreiro, et al.Journal of Medical Genetics|August 16, 2003
Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSAP2 in the major neurological symptomsH L Wilson, A C C Wong, S R Shaw, et al.Clinical Genetics|June 18, 1998
Glucose-6-phosphatase gene (727G-->T) splicing mutation is prevalent in Hong Kong Chinese patients with glycogen storage disease type 1aC W Lam, W M But, C C Shek, et al.International Journal of Clinical Pharmacology and Therapeutics|August 1, 2015
Prescription patterns of psychotropic medications and use of electroconvulsive therapy in Chinese patients with dementiaLu Li, Zhi-Min Wang, Helen F K Chiu, et al.Journal of Affective Disorders|November 1, 2015
The 33-item Hypomania Checklist (HCL-33): A new self-completed screening instrument for bipolar disorderYuan Feng, Yu-Tao Xiang, Wei Huang, et al.East Asian Archives of Psychiatry : Official Journal of the Hong Kong College of Psychiatrists = Dong Ya Jing Shen Ke Xue Zhi : Xianggang Jing Shen Ke Yi Xue Yuan Qi Kan|September 30, 2021
Wilson Sims Fall Risk Assessment Tool Versus Morse Fall Scale in Psychogeriatric Inpatients: a Multicentre StudyM M C Wong, P F Pang, C F Chan, et al.Journal of Neurogastroenterology and Motility|June 11, 2010
Validation of Self-administrated Questionnaire for Psychiatric Disorders in Patients with Functional DyspepsiaAda W Y Tse, Larry H Lai, C C Lee, et al.Hong Kong Medical Journal = Xianggang Yi Xue Za Zhi|October 24, 2015
Aetiological bases of 46,XY disorders of sex development in the Hong Kong Chinese populationAngel O K Chan, W M But, C Y Lee, et al.Hong Kong Medical Journal = Xianggang Yi Xue Za Zhi|August 5, 2011
Enzyme replacement therapy for mucopolysaccharidosis VI (Maroteaux-Lamy syndrome): experience in Hong KongW M But, M Y Wong, J C K Chow, et al.Steroids|May 17, 2011
Molecular analysis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Hong Kong Chinese patientsAngel O K Chan, W M But, K L Ng, et al.Pageof 4