| 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
] |
|
|
|
|
( 臨床生化研究室 )