Mak CM - Search Results

1

Determination of cerebrospinal fluid adenosine deaminase activity cut-off for the diagnosis of tuberculous meningitis in Hong Kong.

Chan TCH, Chen SPL, Mak CM, Ching CK, Luk KS, Tsang YM, Leung DCW. Chan TCH, et al. Among authors: mak cm. J Clin Pathol. 2020 Dec;73(12):800-802. doi: 10.1136/jclinpath-2019-206397. Epub 2020 May 18. J Clin Pathol. 2020. PMID: 32423993

2

Hereditary spastic paraplegias.

Lau KK, Ching CK, Mak CM, Chan YW. Lau KK, et al. Among authors: mak cm. Hong Kong Med J. 2009 Jun;15(3):217-20. Hong Kong Med J. 2009. PMID: 19494379 Free article.

3

Hereditary spastic paraplegia: identification of an SPG3A gene mutation in a Chinese family.

Chan KY, Ching CK, Mak CM, Lam CW, Chan AY. Chan KY, et al. Among authors: mak cm. Hong Kong Med J. 2009 Aug;15(4):304-7. Hong Kong Med J. 2009. PMID: 19652243 Free article.

4

Circulatory collapse in a patient with gastrinoma after metoclopramide administration.

Lau KK, Chan KW, Lok CM, Lam AW, Lee HH, Luk WF, Mak CM, Ching CK, Lo J, Li SM, Chan AY. Lau KK, et al. Among authors: mak cm. Hong Kong Med J. 2009 Dec;15(6):478-81. Hong Kong Med J. 2009. PMID: 19966355 Free article.

5

Application of pharmacogenetics: UGT1A1*28 and nilotinib-induced unconjugated hyperbilirubinaemia in a patient with chronic myeloid leukaemia.

Chen SP, Poon WT, Mak CM, Lam CW, Kwong YL, Chan AY, Tam S. Chen SP, et al. Among authors: mak cm. Pathology. 2011 Apr;43(3):273-4. doi: 10.1097/PAT.0b013e328343f0b4. Pathology. 2011. PMID: 21436639 No abstract available.

6

Analysis of inborn errors of metabolism: disease spectrum for expanded newborn screening in Hong Kong.

Lee HC, Mak CM, Lam CW, Yuen YP, Chan AO, Shek CC, Siu TS, Lai CK, Ching CK, Siu WK, Chen SP, Law CY, Tai HL, Tam S, Chan AY. Lee HC, et al. Among authors: mak cm. Chin Med J (Engl). 2011 Apr;124(7):983-9. Chin Med J (Engl). 2011. PMID: 21542954

7

Phenylketonuria in Hong Kong Chinese: a call for hyperphenylalaninemia newborn screening in the Special Administrative Region, China.

Mak CM, Ko CH, Lam CW, Lau WL, Siu WK, Chen SP, Law CY, Lai CK, Yu CM, Chan AY. Mak CM, et al. Chin Med J (Engl). 2011 Aug;124(16):2556-8. Chin Med J (Engl). 2011. PMID: 21933604

8

Electronic chemical pathology consultation service and dried blood spot metabolic screening in hospital patients.

Mak CM, Siu WK, Law CY, Wong CK, Lee HK, Yeung S, Sham CO, Tse K, Lee HH, Chen SP, Ching CK, Au CK, Poon WT, Lam CW, Kwong NS, Chan AY. Mak CM, et al. J Clin Pathol. 2012 Dec;65(12):1141-5. doi: 10.1136/jclinpath-2012-200837. Epub 2012 Aug 10. J Clin Pathol. 2012. PMID: 22888119

9

Arginase deficiency with new phenotype and a novel mutation: contemporary summary.

Tsang JP, Poon WL, Luk HM, Fung CW, Ching CK, Mak CM, Lam CW, Siu TS, Tam S, Wong VC. Tsang JP, et al. Among authors: mak cm. Pediatr Neurol. 2012 Oct;47(4):263-9. doi: 10.1016/j.pediatrneurol.2012.06.012. Pediatr Neurol. 2012. PMID: 22964440

10

Biochemical and molecular diagnosis of tyrosinemia type I with two novel FAH mutations in a Hong Kong chinese patient: recommendation for expanded newborn screening in Hong Kong.

Mak CM, Lam CW, Chim S, Siu TS, Ng KF, Tam S. Mak CM, et al. Clin Biochem. 2013 Jan;46(1-2):155-9. doi: 10.1016/j.clinbiochem.2012.09.010. Epub 2012 Sep 18. Clin Biochem. 2013. PMID: 23000314

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