Publication List of Kwang-Jen Hsiao, Ph.D.  (蕭 廣 仁 教 授)

 Scientific Publications (1977 - 1996) 

1. Li HC, Hsiao KJ.  Isolation and properties of a Mn++- activated phosphohistone phosphatase from canine heart. Arch Biochem Biophys 1977;179:147-56.      [ Abstract ]   [ PDF ]

2. Hsiao KJ, Chan WWS, Li HC.  Dissociation of phosphohistone phosphatases from canine heart.  Biochem Biophys Acta 1977;483:337-47.   [ PDF ]

3. Li HC, Hsiao KJ.  Effects of nucleoside phosphates and salts on the activity of a heart phosphoprotein phosphatase and its catalytic subunit.  Eur J Biochem 1977;77:383-91.      [ Abstract ]   [ PDF ]

4. Li HC, Hsiao KJ, Chan WWS.  Purification and properties of phosphoprotein phosphatases with different substrate and divalent cation specificities from canine heart.  Eur J Biochem 1978;84:215-25.   [ Abstract ]      [ PDF ]

5. Hsiao KJ, Sandberg AR, Li HC.  The role of ATP and divalent cations in the regulation of a cardiac phosphorylase phosphatase (phosphoprotein phosphatase) of Mr=35,000.  J Biol Chem 1978;253:6901-7.   [ PDF ]

6. Li HC, Hsiao KJ, Sampathkumar S.  Characterization of a novel alkaline phosphatase activity which co-purifies with a phosphorylase (phosphoprotein) phosphatase of Mr=35,000 from cardiac muscle.  J Biol Chem 1979;254:3368-74.      [ Abstract ]   [ PDF ]

7. Ou YC, Hsiao KJ, Chou FF, Huang MJ.  Study on cytosol estrogen and progesterone receptors in Chinese breast cancer tissue.  Chang Gung Med J 1983;6:270-6.      [ Abstract ]   [ PDF ]

8. Hsiao KJ, Wu SJ, Kasahara Y, Ting WK.  Determination of pseudocholinesterase activity by an enzyme coupling method in the serum of patients with liver disease. In: Werner M, Goldberg DM, eds.  Selected Topics in Clinical Enzymology, Vol 2. Berlin: Walter de Gruyter 1984;79-88.      [ Abstract ]   [ PDF ]

9. Yeh SL, Ma FC, Shieh MJ, Wuu KD, Hsiao KJ.  Dietary therapy for phenylketonuric patients in Taiwan.  J Formosan Med Assoc 1985;84:546-61. (in Chinese)      [ Abstract ]   [ PDF ]

10. Hsiao KJ, Hung SH, Wu SJ, Yeh SF.  Gas chromatographic analysis of abnormal urinary organic acids in phenylketonuria.  J Formosan Med Assoc 1985;84:1240-50.      [ Abstract ]   [ PDF ]

11. Lin E, Chi CS, Hsiao KJ.  Propionic acidemia - a case report.  Chin Med J (Taipei) 1986;37:159-64. (in Chinese)      [ Abstract ]   [ PDF ]

12. Hsiao KJ, Chiu PC, Cheng WH, Chao SL.  Atypical phenylketonuria with mild mental retardation caused by tetrahydrobiopterin deficiency in a Chinese family.  J Inher Metab Dis 1986;9(suppl.2):240-3.       [ Abstract ]   [ PDF ]

13. Hsiao KJ, Chen CH, Chiu PC, Huang SC, Wuu KD.  A Chinese family with phenylketonuria and maternal phenylketonuria detected by family screening.  Eur J Pediatr 1986;145:409-12.   [ PDF ]

14. Hsiao KJ, ChungHF, Ting WK.  Evaluation of chemical colorimetric method for determination of glycated hemoglobin.  J Formosan Med Assoc 1986;85:755-65. (in Chinese)      [ Abstract ]   [ PDF ]

15. Yeh SF, Hsiao KJ, Hung SH, Chang KT.  Identification of abnormal urinary organic acids in inherited metabolic diseases by gas chromatography - mass spectrometry.  J Chin Chem Soc 1986;33:251-6.      [ Abstract ]   [ PDF ]

16. Lin CY, Hwang B, Hsiao KJ, Jin YR.  Study of a-D-glucosidase activity in patients with Pompe's disease.  J Formosan Med Assoc 1986;85:766-70.      [ Abstract ]   [ PDF ]

17. Chen CW, Wu JK, Hsiao KJ.  Fabry's disease - ocular findings and enzymatic assay in a female carrier.  Trans Ophth Soc R.O.C. 1986;25:734-9. (in Chinese)      [ Abstract ]   [ PDF ]

18. Tsao D, Hsiao KJ, Wu JC, Chou CK, Lee SD.  Two-site enzyme immunoassay for alpha-fetoprotein in dried blood samples collected on filter paper.  Clin Chem 1986;32:2079-82.   [ PDF ]

19. Lin CY, Hwang B, Hsiao KJ, Jin YR.  Pompe's disease in Chinese and the prenatal diagnosis by determination of a-glucosidase activity.  J Inher Metab Dis 1987;10:11-7.   [ PDF ]

20. Lee FY, Won JGS, Hsiao KJ, Ching KN.  Acute intermittent porphyria: report of a case.  J Formosan Med Assoc 1987;86:442-7.      [ Abstract ]   [ PDF ]

21. Hsiao KJ, Lee FY, Wu SJ, Chang WJ.  Determination of erythrocyte prophobilinogen deaminase activity using porphobilinogen as substrate.  Clin Chim Acta 1987;168:257-8.   [ PDF ]

22. Lin E, Chen KH,Chi CS, Lee SH, Ho WL, Hsiao KJ.  Late-onset type cystinosis: report of a case.  J Formosan Med Assoc 1987;86:1307-11.      [ Abstract ]   [ PDF ]

23. Chu YK, Chao T, Hsiao KJ, Liu RS, Yeh SH.  Thyroid ectopia associated with congenital hypothyroidism: diagnostic role of pertechnetate scintiscanning.  Ann Nucl Med 1988;1:91-6. (in Chinese)      [ Abstract ]   [ PDF ]

24. Wuu KD,Hsiao KJ, Chen CH, Hsiao TSY SY, Chang CY, Chu YK.  Screening for inherited metabolic diseases and congenital hypothyroidism in 4,477 mentally retarded school children in Taiwan. Jpn J Human Genet 1988;33:33-40.      [ Abstract ]   [ PDF ]

25. Wu JC, Lee SD, Hsiao KJ, Wang SS, Chou P, Tsao D, Tsai YT, Lui WY, Chiang JH, Lo KJ.  Mass screening of primary hepatocellular carcinoma by alpha-fetoprotein in a rural area of Taiwan a dried blood spot method.  Liver 1988;8:100-4.   [ PDF ]

26. Lee FY, Hsiao KJ, Tsai YT, Lee SD, Wu SJ, Jen HS.  Erythrocyte hydroxymethylbilane synthase activity in a Chinese family with acute intermittent porphyria.  Ann Clin Biochem 1988;25:706-7.   [ PDF ]

27. Chou P, Jih LY, Hsiao KJ, Tsao D, Wu JC, Lee SD.  Screening for liver cancer in Luh-Guu township.  J Formosan Med Assoc 1988;87:1021-4. (in Chinese)      [ Abstract ]   [ PDF ]

28. Lee FY, Hsiao KJ, Tsai YT, Lee SD, Wu SJ, Jen HS.  Determination of erythrocyte hydroxymethylbilane synthase activity and its application for study of acute intermittent porphyria.  J Formosan Med Assoc 1988;87:1029-35.      [ Abstract ]   [ PDF ]

29. Chen SH, Hsiao KJ, Lin LH, Liu TT, Tang RB, Su TS.  Study of restriction fragment length polymorphisms at human phenylalanine hydroxylase locus and evaluation of its potential application in prenatal diagnosis of phenylketonuria in Chinese.  Hum Genet 1989;81:226-30.   [ PDF ]

30. Hsiao KJ, Wu JC, Lee SD, Chou P.  Mass screening of liver cancer by determination of alpha-fetoprotein in dried blood spots on filter paper. In: Ting SW, Chen JS, Schwartz MK, eds.  Human Tumor Markers. Amsterdam: Elsevier 1989;199-210.   [ PDF ]

31. Hsiao KJ, Chen CH, Liu TT, Wu SJ, Plettner C, Clemens P.  Screening of congenital hypothyroidism, phenylketonuria, galactosemia, homocystinuria, and maple syrup urine disease in moderate to severe mentally retarded Chinese children.  J Formosan Med Assoc 1989;88:18-22.   [ PDF ]

32. Hsiao KJ, Wuu KD.  Neonatal screening for inborn metabolic diseases: the experience in Taiwan. In: Lin HJ, Swaminathan R, Robertshaw AM, eds.  Proc 4th Asian-Pacific Congress of Clin Biochem. Hong Kong: Gardiner-Caldwell 1989;214-8.    [ PDF ]

33. Chen CH, Hsiao KJ.  A Chinese classic phenylketonuria manifested as autism.  Brit J Psychiat 1989;155:251-3.   [ PDF ]

34. Shiue JW, Lee FY, Hsiao KJ, Tsai YT, Lee SD, Wu SJ.  Abnormal thyroid function and hypercholesterolemia in a case of acute intermittent porphyria.  J Formosan Med Assoc 1989;88:729-31.   [ PDF ]

35. Tsai TF, Hsiao KJ, Su TS.  Phenylketonuria mutation in Chinese haplotype 44 identical with haplotype 2 mutation in northern-European Caucasians.  Hum Genet 1990;84:409-11.   [ PDF ]

36. Yeh SL, Wu SJ, Shieh MJ, Hsiao KJ.  Erythrocyte glutathione peroxidase activity in normal Chinese and in patients with inherited metabolic diseases.  J Biomed Lab Sci 1990;1:23-31.   [ Abstract ]      [ PDF ]

37. Hsiao KJ, Chiang SH, Liu TT, Chiu PC, Wuu KT.  Tetrahydrobiopterin deficient phenylketonuria detected by neonatal screening in Taiwan. In: Curtius HC, Ghisla S, Blau N, eds.  Chemistry and Biology of Pteridines 1989. Berlin: Walter de Gruyter 1990;402-7.    [ PDF ]

38. Shintaku H, Fujioka M, Sawada Y, Isshiki G, Yamaoka S, Oura T, Hsiao KJ, Liu TT, Chen RG.  Prenatal diagnosis of 6-pyruvoyl tetrahydropterin synthase deficiency in East Asia. In: Curtius, HC, Ghisla S, Blau N, eds.  Chemistry and Biology of Pteridines 1989. Berlin: Walter de Gruyter 1990;408-13.    [ PDF ]

39. Yeh SL, Wu SJ, Shieh MJ, Hsiao KJ.  Determination of erythrocyte glutathione peroxidase activity and its reference range in Chinese adults.  J Formosan Med Assoc 1990;89:519-25.   [ PDF ]

40. Hsu WC, Lin SP, Huang FY, Wang PA, Hsiao KJ.  Propionic Acidemia: report of a case that is successfully managed by peritoneal dialysis and sodium benzoate therapy.  Chin Med J (Taipei) 1990;46:306-10. (in Chinese)   [ PDF ]

41. Soong BW, Tsai TF, Su CH, Kao KP, Hsiao KJ, Su TS.  DNA polymorphisms and deletion analysis of the Duchenne-Becker muscular dystrophy gene in the Chinese.  Am J Med Genet 1991;38:593-600.   [ PDF ]

42. Hsiao KJ, Lee SY, Chuang HC, Yang ML, Hsu HJ, Liu CC, Liao H, Chen HT, He SC.  Antenatal screening of maternal alpha-fetoprotein with dried-blood spot sample on filter paper.  J Formosan Med Assoc 1991;90:598-604. (in Chinese) [ PDF ]

43. Wuu KD,Chiu PC, Li SY, Chen JY, Chao MC, Ko FJ, Wang TR, Hsiao KJ.  Chromosomal and biochemical screening on mentally retarded school children in Taiwan.  Jpn J Human Genet 1991;36:267-74.   [ PDF ]

44. Horng CJ, Hsiao KJ, Chen CH, Tsai SR, Sim CB.  Urinary neopterin and biopterin levels in Patients with depression.  Chinese Psychiatry 1991;5:20-7.   [ Abstract ]    [ PDF ]

45. Hsiao KJ, Chiang SH, Chang TT, Liew DG, Chao Yu YM.  Experience of neonatal G6PD deficiency screening in Taiwan. In: Wilcken B, Webster D, eds.  Neonatal Screening in the Nineties. New South Wales: Kelvin Press 1991;217-8. [ PDF ]

46. Hsiao KJ, Chiang SH, Wu HY, Chen Mc, Huang TM, Liew DG, Chao Yu YM.  Inter-laboratory quality assurance program for determination of glucose-6-phosphate dehydrogenase activity in Taiwan. In: Wilcken B, Webster D, eds.  Neonatal Screening in the Nineties. New South Wales: Kelvin Press 1991;274-6. [ PDF ]

47. Chou P, Chen HH, Hsiao KJ.  Community-based epidemiological study on diabetes in Pu-Li, Taiwan.  Diabetes Care 1992;15:81-9.   [ PDF ]

48. Chou P, Hsiao KJ, Lin JWH, Chen ST.  Community-based survey on blood pressure, blood biochemistry and dietary habits in Pu-Li, Taiwan.  Chin Med J (Taipei) 1992;50:279-87. [ PDF ]

49. Hsiao, KJ.  Genetic disorders and neonatal screening. In: Miyai K, Kanno T, Ishikawa E, eds.  Progress in Clinical Biochemistry. Amsterdam: Elsevier 1992;289-92. [ PDF ]

50. Lin CH, Hsiao KJ, Tsai TF, Chao HK, Su TS.  Identification of a missense phenylketonuria mutation at codon 408 in the Chinese.  Hum Genet 1992;89:593-6.   [ PDF ]

51. Yu MW, Hsiao KJ, Wuu KD, Chen CJ.  Association between glucose-6-phosphate dehydrogenase deficiency and neonatal jaundice: interaction with multiple risk factors.  Intl J Epidemiol 1992;21:947-52. [ PDF ]

52. Shintaku H, Nakajima T, Sawada Y, Hase Y, Fujioka M, Nishimura A, Isshiki G, Oura T, Hsiao KJ, Chen RG.  Prenatal diagnosis of tetrahydrobiopterin (BH4) synthase deficiency.  Pteridines 1992;3:17-8. [ PDF ]

53. Hsiao KJ, Chiang SH.  Neonatal screening strategy for congenital metabolic diseases.  WARTA HKKI 1992;3:23-30. [ PDF ]

54. Wu SJ, Chiang SH, Hsiao KJ.  A microplate method for determination of glucose in plasma.  J Biomed Lab Sci 1993;5:16-9.      [ Abstract ]   [ PDF ]

55. Chou P, Liao MJ, Kuo HS, Wu GS, Hsiao KJ, Jap TS, Chiang H, Chang MS.  Program description and preliminary health survey data in Kin-Hu, Kinmen.  Chin Med J (Taipei) 1993;52:241-8.   [ PDF ]

56. Yeung CY, Lin SP, Kao HA,Shen EY, Lee HC, Lin CH, Hsiao KJ.  Maple syrup urine disease: report of two cases.  J Formos Med Assoc 1993; 92:765-8. [ PDF ]

57. Pai JT, Tsai SF, Horng CJ, Chou PC, Cheng MY, Hsiao KJ, Wuu KD.  Absence of FMR-1 gene expression can be detected with RNA extracted from dried blood specimens.  Hum Genet 1994;93:488-93.   [ PDF ]

58. Shintaku H, Hsiao KJ, Liu TT, Imamura T, Hase Y, Chen RG, Isshiki G, Oura T.  Prenatal diagnosis of 6-pyruvoyl tetrahydropterin synthase deficiency in seven subjects.  J Inher Metab Dis 1994;17:163-6.   [ PDF ]

59. Sheu SS, Chan LP, Liao SC, Hsiao KJ, Shu KH, Lu YS, Cheng CH, Lian JD.  Fabry's disease: Clinical, pathologic and biochemical manifestations in two Chinese males.  Chin Med J (Taipei) 1994;54:368-72. [ PDF ]

60. Chou P, Liao MJ, Kuo HS, Hsiao KJ, Tsai ST.  A population survey on the prevalence of diabetes in Kin-Hu, Kinmen.  Diabetes Care 1994;17:1055-8.   [ PDF ]

61. Chang HS, Ro LS, Cheng ST, Tang LM, Hsiao KJ.  Fabry's disease: Report of a case.  J Formos Med Assoc 1995;94:346-50.   [ PDF ]

62. Hsiao KJ, Chiang SH.  Interlaboratory quality assurance program for determination of blood glucose-6-phosphate dehydrogenase activity: Experience in Taiwan. In: Ohba Y, Kanno T, Okabe H, et al. eds.  Quality Control in the Clinical Laboratory 95. Tokyo: Excerpta Medica 1995;241-6.   [ PDF ]

63. Wu SJ, Hsiao KJ.  Determination of plasma a-galactosidase A activity in patients with Fabry's disease and its normal reference rang in Chinese.  J Biomed Lab Sci 1995;7:141-6.       [ Abstract ]   [ PDF ]

64. Niu DM, Hsiao KJ, Wang NH, Chin LS, Chen CH.  Chinese achondroplasia is also defined by recurrent G380R mutations of fibroblast growth factor receptor-3 gene.  Hum Genet 1996;98:65-7.     [ PDF ]

65. Liu TT, Hsiao KJ.  Identification of a common 6-pyruvoyl-tetrahydropterin synthase mutation at codon 87 in Chinese phenylketonuria caused by tetrahydrobiopterin synthesis deficiency.  Hum Genet 1996;8:313-6.   [ PDF ]

66. Chen CH, Lee YR, Liu MY, Wei FC, Koong FJ, Hwu HG, Hsiao KJ.  Identification of a Bgl I polymorphism of catechol-O-methyltransferase (COMT) gene and association study with schizophrenia.  Am J Med Genet 1996;67:556-9.   [ PDF ]

 Scientific Publications  1977 - 1996  1997 - Present
 Conference Abstracts     1975 - 1996  1997 - Present
 Other Publications

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Preventive Medicine Foundation, Taipei   (預防醫學基金會)

Updated Mar. 17, 2014 by K.-J.Hsiao 蕭 廣 仁 教 授   ( 臨床生化研究室