Results 1 to 11 of 11
Page 1 of 1
TypeTitleAuthor(s)YearViews
Expanding phenotype and clinical analysis of tyrosine hydroxylase deficiency
Journal:
Journal of Child Neurology
Publisher:
Sage Publications, Inc.. The Journal's web site is located at http://jcn.sagepub.com
Yeung, WL; Wong, VCN; Chan, KY; Hui, J; Fung, CW; Yau, E; Ko, CH; Lam, CW; Mak, CM; Siu, S; Low, L2011266
 
Phenylketonuria in Hong Kong Chinese: A call for hyperphenylalaninemia newborn screening in the special administrative region, China
Journal:
Chinese Medical Journal
Publisher:
Zhonghua Yixuehui. The Journal's web site is located at http://www.cmj.org/
Mak, CM; Ko, CH; Lam, CW; Lau, WL; Siu, WK; Chen, SPL; Law, CY; Lai, CK; Yu, CM; Chan, AYW2011187
 
Biochemical and molecular characterization of tyrosine hydroxylase deficiency in Hong Kong Chinese
Journal:
Molecular Genetics and Metabolism
Publisher:
Academic Press. The Journal's web site is located at http://www.elsevier.com/locate/ymgme
Mak, CM; Lam, CW; Siu, TS; Chan, KY; Siu, WK; Yeung, WL; Hui, J; Wong, VCN; Low, LCK; Ko, CH; Fung, CW; Chen, SP; Yuen, YP; Lee, HC; Yau, E; Chan, B; Tong, SF; Tam, S; Chan, YW2010275
 
Mutational analysis of 65 Wilson disease patients in Hong Kong Chinese: Identification of 17 novel mutations and its genetic heterogeneity (Journal of Human Genetics (2008) 53 (55-63) DOI: 10.1007/s10038-007-0218-2)
Journal:
Journal of Human Genetics
Publisher:
Springer Japan. The Journal's web site is located at http://link.springer.de/link/service/journals/10038/index.htm
Mak, CM; Lam, CW; Tam, S; Lai, CL; Chan, LY; Fan, ST; Lau, YL; Lai, ST; Yuen, P; Hui, J; Fu, CC; Wong, KS; Mak, WL; Tze, K; Tong, SF; Lau, A; Leung, N; Hui, A; Cheung, KM; Ko, CH; Chan, YK; Ma, O; Chau, TN; Chiu, A; Chan, YW2008195
 
Mutational analysis of 65 Wilson disease patients in Hong Kong Chinese: Identification of 17 novel mutations and its genetic heterogeneity
Journal:
Journal of Human Genetics
Publisher:
Springer Japan. The Journal's web site is located at http://link.springer.de/link/service/journals/10038/index.htm
Mak, CM; Lam, CW; Tam, S; Lai, CL; Chan, LY; Fan, ST; Lau, YL; Lai, JY; Yuen, P; Hui, J; Fu, CC; Wong, KS; Mak, WL; Tze, K; Tong, SF; Lau, A; Leung, N; Hui, A; Cheung, KM; Ko, CH; Chan, YK; Ma, O; Chau, TN; Chiu, A; Chan, YW2008284
 
Improving the oral health of elders in a care and attention home
Publisher:
Faculty of Dentistry, The University of Hong Kong.
Lo, ECM; Lui, KC; Au Yeung, CO; Chan, PCY; Chan, RKP; Chu, SY; Ko, CH; Lai, FWS; Li, KWK; Lin, WWS; Tse, JYY2005124
 
Randomised control trial of tongue acupuncture versus sham acupuncture in improving functional outcome in cerebral palsy
Journal:
Journal of Neurology, Neurosurgery and Psychiatry
Publisher:
B M J Publishing Group. The Journal's web site is located at http://www.jnnp.com/
Sun, JG; Ko, CH; Wong, V; Sun, XR2004284
 
Magnetic resonance spectroscopy and analysis of MECP2 in Rett syndrome
Journal:
Pediatric Neurology
Publisher:
Elsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/pedneu
Khong, PL; Lam, CW; Ooi, CGC; Ko, CH; Wong, VCN2002169
 
Atypical presentation of dopa-responsive dystonia: Generalized hypotonia and proximal weakness
Journal:
Neurology
Publisher:
Lippincott Williams & Wilkins. The Journal's web site is located at http://www.neurology.org
Kong, CK; Ko, CH; Tong, SF; Lam, CW2001134
 
Two novel CLN2 gene mutations in an Chinese patient with classical late-infantile neuronal ceroid lipofuscinosis [2]
Journal:
American Journal of Medical Genetics
Lam, CW; Poon, PMK; Tong, SF; Ko, CH2001102
 
Spectrum of mutations in the MECP2 gene in patients with infantile autism and Rett syndrome.
Journal:
Journal of medical genetics
Publisher:
B M J Publishing Group. The Journal's web site is located at http://jmg.bmjjournals.com/
Lam, CW; Yeung, WL; Ko, CH; Poon, PM; Tong, SF; Chan, KY; Lo, IF; Chan, LY; Hui, J; Wong, V; Pang, CP; Lo, YM; Fok, TF2000360
 
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