20 results on '"Lam, Ching Wan"'
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2. Optimal pooling strategy for liquid chromatography-high resolution mass spectrometry (LC-HR-MS) urine drug screening
3. Application of pharmacogenetics: UGT1A1*28 and nilotinib-induced unconjugated hyperbilirubinaemia in a patient with chronic myeloid leukaemia
4. Genotype-confirmed alanine aminotransferase deficiency in a Chinese patient with acute liver failure: a potential diagnostic pitfall
5. Cross reactivity between fibrinogen and epsilon heavy chain antiserum in immunofixation electrophoresis
6. Urine Organic Acid (UOA) Analysis for the diagnosis of Aromatic L-Amino Acid Decarboxylase (AADC) deficiency
7. ‘Silver man’ – A first case report of silver associated steatohepatitis (SASH) and discussion of its pathomechanism
8. A common COQ4 mutation in undiagnosed mitochondrial disease: a local case series
9. Pleural fluid total free fatty acids as cancer biomarkers in malignant pleural effusions: a preliminary study
10. Urine ‘total triglyceride’ for diagnosis of a rare cause of hypoglycemia: a novel, rapid and simple test
11. The first territory-wide expanded newborn screening for inborn errors of metabolism in Hong Kong: a pilot study
12. Ending a 40-year-diagnostic odyssey by clinical whole exome sequencing for a treatable neurological disease
13. Identifying the disease gene for a new locus of congenital myasthenic syndrome
14. A metabonomic approach for biomarker discovery for diagnosis of malignant pleural effusions (MPE)
15. New lights in light's criteria
16. NMR-based urinalysis for rapid diagnosis of inborn errors of metabolism
17. Neogenin mutations in autism spectrum disorders
18. Clinical classification of pleural effusion using 1H NMR spectroscopy
19. Nuclear magnetic resonance spectroscopy-based urinalysis for a young girl with extreme hypoglycaemia
20. A common COQ4mutation in undiagnosed mitochondrial disease: a local case series
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