HKU Scholars Hub: Browsing DSpace

Browsing by Author Fung, CW

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 中

or enter first few letters:

Showing results 47 to 66 of 97 < previous next >

Title	Author(s)	Issue Date	Views
Kbg syndrome: Clinical features and specific dental findings Journal:Pediatric Dentistry	Almandey, HA Anthonappa, RP King, NM Fung, CW	2010	188
Lathosterolosis: A Disorder Of Cholesterol Biosynthesis Resembling Smith-lemli-opitz Syndrome Journal:Journal Of Inherited Metabolic Disease	Ho, CCA Fung, CW Siu, TS Ma, OCK Lam, CW Tam, S Wong, VCN	2014	84
MALDI-MS profiling of serum O-glycosylation and N-glycosylation in COG5-CDG Journal:Journal of Mass Spectrometry	Palmigiano, A Bua, RO Barone, R Rymen, D Legal, L Deconinck, N Dionisi-Vici, C Fung, CW Garozzo, D Jaeken, J Sturiale, L	2017	56
Megaconial Congenital Muscular Dystrophy: Same Novel Homozygous Mutation In Chkb Gene In Two Unrelated Chinese Patients Journal:Neuromuscular Disorders	Chan, HSS Ho, RSL Khong, PL Chung, BHY TSANG, MHY YU, MHC Yeung, MCY Chan, AOK Fung, CW	2020	46
Minimum Configuration Design for Digital Control of Power Converters Proceeding/Conference:International Exhibition and Conference for Power Electronics, Intelligent Motion and Power Quality (PCIM Europe 2007). Proceedings of a meeting held 22-24 May 2007, Nuremberg, Germany	Fung, CW Liu, CP Pong, MH	2007	123
A modified screening tool for autism (Checklist for Autism in Toddlers [CHAT-23]) for Chinese children. Journal:Pediatrics	Wong, V Hui, LH Lee, WC Leung, LS Ho, PK Lau, WL Fung, CW Chung, B	2004	190
MR imaging of spinal tumors in children with neurofibromatosis I Journal:American Journal of Roentgenology	Khong, PL Goh, WHS Wong, VCN Fung, CW Ooi, GC	2003	105
Mutation of the LDHD gene in a Chinese girl with global developmental delay, transient hepatomegaly, hyperlactataemia and mitochondrial complex IV deficiency Proceeding/Conference:The 16th Conference of Asian Society for Mitochondrial Research and Medicine (ASMRM) & The 19th Conference of Japanese Society of Mitochondrial Research and Medicine (J-mit), 2019	Kwong, KY RODENBURG, RJT SMEITINK, J Fung, CW	2019	2
Mycophenolate mofetil inhibits nitric oxide generation during renal ischemia repefusion injury Proceeding/Conference:Transplantation	Lui, SL Zhang, HX Chan, L Zhu, W Chan, DTM Fung, CW Lai, KN	1999	112
NDUFA9 point mutations cause a variable mitochondrial complex I assembly defect Journal:Clinical Genetics	Baertling, F Sánche-Caballero, L van den Brand, MAM Fung, CW Chan, HSS Wong, CNV Hellebrekers, DME de Coo, IFM Smeitink, JAN AM Rodnburg, RJT Nijtmans, LGJ	2018	70
Neurocognitive function, performance status, and quality of life in pediatric intracranial germ cell tumor survivors Journal:Journal of Neuro-Oncology	Tso, WYW Liu, APY Lee, TMC Cheuk, KL Shing, MK Luk, CW Ling, SC Ku, DTL Li, K Yung, A Fung, CW Chan, SHS Ho, ACC Ho, KWF Ip, P Chan, GCF	2019	108
Neuroimaging in Primary Coenzyme-Q10-Deficiency Disorders Journal:Antioxidants	Munch, J Prasuhn, J Laugwitz, L Fung, CW Chung, BHY Bellusci, M Mayatepek, E Klee, D Distelmaier, F	14-Mar-2023
Neuromuscular involvement in children with mitochondrial disease: A single centre experience Proceeding/Conference:14th Asian and Oceanian Congress of Child Neurology	Chiu, ATG Fung, CW Chan, HSS	2017	35
A new presentation of 6-pyruvoyl tetrahydropterin synthase (PTPS) deficiency - Dopa Responsive Dystonia (DRD) Proceeding/Conference:Journal of Inherited Metabolic Disease	Fung, CW Blau, N Siu, S Mak, CM Cheung, PT Tam, S Wong, VCN	2007	154
Novel POLG mutation in a patient with sensory ataxia, neuropathy, ophthalmoparesis and stroke Journal:Clinica Chimica Acta	Lam, CW Law, CY Siu, CWK Fung, CW Yau, MM Huen, KF Lee, HHC Mak, CM	2015	211
Paroxysmal non-epileptic movements in childhood Journal:HK Journal of Paediatrics (new series)	Fung, CW Wong, VCN	2012
Partnering role of FOXM1 and EPS8 in maintaining chemoresistance in human ovarian cancer Proceeding/Conference:Hong Kong Inter-University Postgraduate Symposium in Biochemical Sciences, 2017	Fung, CW Chan, DW Yao, KM	2017	45
Primary coenzyme Q10 deficiency-7: expanded phenotypic spectrum and a founder mutation in southern Chinese Journal:npj Genomic Medicine	YU, MHC TSANG, MHY Lai, S Ho, MSP Tse, DML Willis, B Kwong, AKY Chou, YY Lin, SP Quinzii, CM Hwu, WL Chien, YH Kuo, PL Chan, VCM Tsoi, C Chong, SC Rodenburg, RJT Smetinik, J Mak, CCY Yeung, KS Fung, LF Lam, W Hui, J Lee, NC Fung, CW Chung, BHY	2019	68
Program for Chinese children with developmental disabilities - The Hong Kong model Journal:Brain and Development	Fung, CW Wong, V	2005	154
Quality of life and symptom burden in children with neurodegenerative diseases: using PedsQL and SProND, a new symptom-based scale Journal:Orphanet Journal of Rare Diseases	Chiu, ATG Wong, SSN Wong, NWT Wong, WHS Tso, WYW Fung, CW	2022

Showing results 47 to 66 of 97 < previous next >