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Showing results 56 to 75 of 97 < previous next >

Title	Author(s)	Issue Date	Views
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
Radboud Centre for Mitochondrial Medicine Pediatric MRI score Journal:Mitochondrion	Wong, SSN Goraj, B Fung, CW Vister, J de Boer, L Koene, S Smeitink, J	2017	57
A rare cause of hepatosplenomegaly - transaldolase deficiency Proceeding/Conference:Annual Symposium of Society for the Study of Inborn Errors of Metabolism, SSIEM 2007	Fung, CW Siu, S Mak, C Poon, GWK Cheung, PT Low, LCK Tam, S Wong, VCN	2007
A rare cause of hepatosplenomegaly - transaldolase deficiency Proceeding/Conference:Journal of Inherited Metabolic Disease	Fung, CW Siu, S Mak, CM Poon, GWK Wong, KY Cheung, PT Low, LCK Tam, S Wong, VCN	2007	156
A rare cause of hepatosplenomegaly transaldolase deficiency Proceeding/Conference:Joint Annual Scientific Meeting for Paediatricians & Paediatric Nurses	Fung, CW Siu, S Mak, CM Poon, GWK Wong, KY Cheung, PT Low, LCK Tam, S Wong, VCN	2007
A rare presentation of 6-pyruvoyl tetrahydropterin synthase (PTPS) deficiency - Dopa Responsive Dystronia (DRD) Proceeding/Conference:Joint Annual Scientific Meeting for Paediatricians & Paediatric Nurses	Fung, CW Blau, N Siu, S Mak, CM Cheung, PT Tam, S Wong, VCN	2007	108
Review of 17 children with cyclic vomiting syndrome Proceeding/Conference:Chinese Paediatric Forum	Liu, SKY Fung, CW Chiu, SSS Wong, VCN	1996	88
Review of evolution of clinical, training and educational services and research program for autism spectrum disorders in Hong Kong Journal:Science China Life Sciences	Wong, VCN Fung, CW Lee, SL Wong, PT	2015	196
Revisiting ischaemia and reperfusion injury as a possible cause for necrotising enterocolitis Proceeding/Conference:Annual Scientific Meeting of the Australasian Association of Paediatric Surgeons	Chan, KL Chan, KW Hui, C Wo, JYH Tipoe, GL Fung, CW Tam, PKH	2001	119
SCN2A mutation in a Chinese boy with infantile spasm - response to Modified Atkins Diet Journal:Brain and Development	Wong, VCN Fung, CW Kwong, KY	2015	75

Showing results 56 to 75 of 97 < previous next >