about
Transient risk factors for acute traumatic hand injuries: a case-crossover study in Hong KongInborn errors of metabolism and expanded newborn screening: review and update.Clinical manifestation of late onset Pompe disease patients in Hong Kong.Fatal viral infection-associated encephalopathy in two Chinese boys: a genetically determined risk factor of thermolabile carnitine palmitoyltransferase II variants.Adulteration of proprietary Chinese medicines and health products with undeclared drugs: experience of a tertiary toxicology laboratory in Hong Kong.Hyperekplexia: a Chinese adolescent with 2 novel mutations of the GLRA1 gene.Cost-benefit analysis of hyperphenylalaninemia due to 6-pyruvoyl-tetrahydropterin synthase (PTPS) deficiency: for consideration of expanded newborn screening in Hong Kong.Novel POLG mutation in a patient with sensory ataxia, neuropathy, ophthalmoparesis and stroke.Genetic basis of channelopathies and cardiomyopathies in Hong Kong Chinese patients: a 10-year regional laboratory experience.Performance evaluation of five commercial assays for detection of acetaminophenRenal oligo- and anhydramnios with normal-looking fetal kidneys2,4-Dinitrophenol: A threat to Chinese body-conscious groupsHyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome: a treatable genetic liver disease warranting urgent diagnosisNon-invasive urinary screening for aromatic l-amino acid decarboxylase deficiency in high-prevalence areas: A pilot studySerotonin syndrome following overdose of a non-prescription slimming product containing sibutramine: A case reportDevelopment of a galactose biosensor with galactose oxidase-immobilized epidermis of Solanum lycopersicum: Potential point-of-care testing for citrin deficiency in high-prevalence areasYoung-Onset Parkinsonism in a Hong Kong Chinese Man With Adult-Onset Hallervorden–Spatz SyndromeThe co-occurrence of serologically proven myasthenia gravis and Miller Fisher/Guillain Barré overlap syndrome — A case reportClinical and pathological characterization of FLNC-related myofibrillar myopathy caused by founder variant c.8129G>A in Hong Kong ChineseCase Report: The first probable Hong Kong Chinese case of LPIN1-related acute recurrent rhabdomyolysis in a boy with two novel variantsPractical Aspects in Genetic Testing for Cardiomyopathies and ChannelopathiesFounder Mutation c.1516A>C in KLHL40 Is a Frequent Cause of Nemaline Myopathy With Hyponatremia in Ethnic Chinese
P50
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P50
description
researcher ORCID id 0000-0002-0162-5681
@en
wetenschapper
@nl
name
Han-Chih Hencher Lee
@ast
Han-Chih Hencher Lee
@en
Han-Chih Hencher Lee
@es
Han-Chih Hencher Lee
@nl
type
label
Han-Chih Hencher Lee
@ast
Han-Chih Hencher Lee
@en
Han-Chih Hencher Lee
@es
Han-Chih Hencher Lee
@nl
prefLabel
Han-Chih Hencher Lee
@ast
Han-Chih Hencher Lee
@en
Han-Chih Hencher Lee
@es
Han-Chih Hencher Lee
@nl
P106
P31
P496
0000-0002-0162-5681