Personal Information
Ching-Wan
Lam, Clinical
Professor, Department
of Pathology, Faculty of Medicine, The UniversityofHong Kong, Hong Kong, China.
Publications
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Lai
CK, Lam CW, Chan YW. High performance thin-layer chromatography of free
porphyrins for diagnosis of porphyria. Clin Chem 1994; 40: 2026-2029
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Lolin
YL, Lam CW, Lo WH, Au KL, Masarei JRL. IgD multiple myeloma with thoracic
spinal cord compression due to epidural extraosseous tumour spread. J Clin
Pathol 1994; 47: 669-671
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Lam
CW, Jain K, ChanKY, Silva DK, Chan YW, Wong LJC. Diagnosis of mitochondrial
encephalomyopathy, lactic acidosis, and stroke-like episodes in a Chinese
family by PCR/restriction enzyme analysis. J Clin Path Mol Pathol 1995;
48: M285-288
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Kong
TK, Lam CW, Lee KC, Au KL. Clinicopathological conference: amyloidosis and
light chain myeloma in a 68-year-old man. J HK Geriatr Soc 1995; 6: 29-36
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Lam
CW. Normocalcaemic primary hyperparathyroidism and renal stone formers. J
HK Geriatr Soc 1996; 7: 44
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Lam
CW, Lau CH, Williams JC, Chan YW, Wong LJC. Mitochondrial myopathy,
encephalopathy, lactic acidosis and stroke-like episodes (MELAS) triggered by
valproate therapy. Eur J Ped 1997; 156: 562-564
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Yuen
WF, Lam CW, TC Chow, MC Chiu. A characteristic dissection microscopy appearance
of a renal biopsy of a Fabry heterozygote. Nephron 1997; 77: 354-356
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Wong
LJC, Lam CW. Alternative, non-invasive tissues for quantitative screening of
mutant mitochondrial DNA. Clin Chem 1997; 43: 1241-1243
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Pang
CP, Law LK, Mak YT, Shek CC, Cheung KL, Mak TWL, Lam CW, AYW Chan, Fok TF.
Biochemical Investigation of young hospitalised Chinese children: results over
a seven-year period. Am J Med Genet 1997; 72: 417-421
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Lam
CW, Lai CK, Chan YW. Simultaneous fluorescence detection of fecal urobilins and
porphyrins by reversed-phase high-performance thin-layer chromatography. Clin
Chem 1998; 44: 345-346
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Lam
CW, But WM, Shek CC, Tong SF, Chan YS, Choy KW, Tse WY, Pang CP,HjelmNM.
Glucose-6-phosphatase gene (727G®T) splicing mutation is prevalent in Hong Kong
Chinese patients with glycogen storage disease type 1a. Clin Genet 1998;
53: 184-190
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Lam
CW, Liang MH, Pang CP, Tong SF, Wong LJC. A novel DraI polymorphism in the 3¢
untranslated region of human glucose-6-phosphatase gene: useful for carrier
detection and prenatal diagnosis of glycogen storage disease type 1a. Clin
Genet 1998; 53: 502-503
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Lam
CW. A mathematical relationship between the number of isomers of alkenes and
alkynes: a result established from the enumeration of isomers of alkenes from
alkyl biradicals. J Math Chem 1998; 23: 421-428
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Xie
J, Murone M, Luoh SM, Ryan A, Gu Q, Zhang C, Bonifas JM, Lam CW, Hynes M,
Goddard A, Rosenthal A, Epstein EH Jr, de Sauvage FJ. Activating Smoothened
mutations in sporadic basal-cell carcinoma. Nature 1998; 391: 90-92
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Wong
LJC, Liang MH, Hwu WL, Lam CW. Linkage disequilibrium and linkage analysis of
glucose-6-phosphatase gene. Hum Genet 1998; 103: 199-203
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Lam
CW, Xie J, To KF, Ng HK, Lee KC, Yuen NWF, Lim PL, Chan YS, Tong SF, McCormick
F. A frequent activated smoothened mutation in sporadic basal cell carcinomas.
Oncogene 1999; 18: 833-836
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Lam
CW, Chan BY, Tong SF. Definition of the correct sequence in the donor splice
site of intron 2 in the human glucose-6-phosphate translocase gene. FEBS Lett
1999; 445: 449-450
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Galli
L, Orrico A, Marcolongo P, Fulceri R, Burchell A, Melis D, Parini R, Gatti R,
Lam CW, Benedetti A, Sorrentino V. Mutations in the glucose-6-phosphate
transporter (G6PT) gene in patients with glycogen storage diseases type 1b and
1c. FEBS Lett 1999; 459: 255-258
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Lam
CW, Tong SF, Lam YY, Chan BY, Ma CH, Lim PL. Identification of a novel missense
mutation (G149E) in glucose-6-phosphate translocase gene in a Chinese family
with glycogen storage disease 1b. Hum Mut 1999; 13: 507
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Law
WK, Choy KW, Lam CW. Novel single nucleotide polymorphism (9678G®A) for linkage
analysis of acute intermittent porphyria. Clin Chem 1999; 45: 308-309