Showing results 1786 to 1805 of 2344
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| Title | Author(s) | Issue Date | |
|---|---|---|---|
Radiological features of PIK3CA-related overgrowth spectrum (PROS) Proceeding/Conference:Annual Scientific Meeting of Hong Kong College of Radiologists, HKCR 2016 | 2016 | ||
Randomisation, controls and sample size Proceeding/Conference:Journal of Gastroenterology and Hepatology | 2000 | ||
| 2006 | |||
Ranking variant pathogenicity using Exomiser facilitated the identification of the missing second mutation in three recessive cases of congenital myopathy Proceeding/Conference:The 20th Asian and Oceanian Myopathy Center (AOMC) Meeting in conjunction with the National Scientific Meeting of Indonesian Neurological Association (PERDOSSI) Jun 9th-12th 2022 | 2022 | ||
Rapid diagnosis of primary HHV-6 and HHV-7 infections Proceeding/Conference:Asia Pacific Congress of Medical Virology, APCMV 1997 | 1997 | ||
Rapid diagnosis of viral respiratory tract infections in paediatric patients is cost effective Proceeding/Conference:Meeting of the European Society for Clinical Virology, ESCV 1997 | 1997 | ||
Rapid induction of preproendothelin-1 mRNA in both astrocytes and cerebral endothelial cells of hypoxic-ischemic mouse brain Proceeding/Conference:Society for Neuroscience Abstracts | 1996 | ||
Rapid induction of preproendothelin-1 mRNA in both astrocytes and cerebral endothelial cells of hypoxic-ischemic mouse brain Proceeding/Conference:Proceedings of the Frontiers in Molecular & Cellular Biology | 1996 | ||
Rapid whole exome sequencing facilitates precision medicine in Paediatric rare disease patients and reduces healthcare costs Proceeding/Conference:HA Professional Training Program for Scientific Officer (Medical 2020/2021): Technology Advancement | 2020 | ||
A rare cause of hepatosplenomegaly - transaldolase deficiency Proceeding/Conference:Journal of Inherited Metabolic Disease | 2007 | ||
A rare cause of hepatosplenomegaly - transaldolase deficiency Proceeding/Conference:Annual Symposium of Society for the Study of Inborn Errors of Metabolism, SSIEM 2007 | 2007 | ||
A rare cause of hepatosplenomegaly transaldolase deficiency Proceeding/Conference:Joint Annual Scientific Meeting for Paediatricians & Paediatric Nurses | 2007 | ||
Rare genetic disease by using NGS Proceeding/Conference:Illumina Sequencing Symposium = 次世代定序與罕見疾病應用研討會 | 2018 | ||
A rare presentation of 6-pyruvoyl tetrahydropterin synthase (PTPS) deficiency - Dopa Responsive Dystronia (DRD) Proceeding/Conference:Joint Annual Scientific Meeting for Paediatricians & Paediatric Nurses | 2007 | ||
Rates of hospitalization for respiratory disease among children with no underlying conditions during influenza seasons Proceeding/Conference:International Congress of Pediatrics, IPA 2001 | 2001 | ||
Rational Choice of the New Vaccines in Asia Proceeding/Conference:Paediatric Share Care Programme in conjunction with the 3rd NUH Annual Scientific Meeting | 1999 | ||
Reading NGS Test Report: What a clinician needs to know Proceeding/Conference:HA 2016 Commissioned Training Programme - Genetics in O&G | 2016 | ||
Reanalyzing clinical whole exome sequencing (WES) data aprovides additional diagnosis in paediatric-onset undiagnosed diseases – a Yale-HKU collaborative study Proceeding/Conference:Joint Annual Scientific Meeting 2019 of The Hong Kong Paediatric Society, Hong Kong College of Paediatricians, Hong Kong Paediatric Nurses Association, &
Hong Kong College of Paediatric Nursing | 2019 | ||
Reanalyzing clinical whole exome sequencing (WES) data provides additional diagnosis in paediatric-onset undiagnowed diseases – A Yale-HKU collaboration Proceeding/Conference:Asia-Pacific Conference on Human Genetics (APCHG) 2019 | 2019 | ||
Recent Advances in Management of Paediatric Malignancies Proceeding/Conference:Hong Kong Shenzhen International Cancer Congress | 2014 |