| 1. |
Hsiao KJ, Li HC. Regulation of a
heart protein phosphatase
by ATP. Fed Proc 1975;34:618. |
|
|
| 2. |
Li HC, Hsiao KJ. Multiple forms of
protein phosphatase
from canine heart: isolation and properties of a Mg++/Mn++-dependent
casein
phosphatase and a Mn++-dependent histone phosphatase. Fed Proc
1976;35:1410. |
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|
| 3. |
Hsiao KJ, Li HC. The dissociation of
a nucleoside phosphate-stimulated histone phosphatase from canine
heart. Fed Proc 1977;36:778. |
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|
| 4. |
Li HC, Hsiao KJ. Purification of
protein phosphatases from canine heart. Fed Proc 1977;36:778. |
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|
| 5. |
Hsiao KJ, Chan WWS, Li HC. Evidence
for a protein
phosphatase of Mr=35,000 as a metalloenzyme. Advances in Cyclic
Nucleotide
Research 1978;9:750. |
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|
| 6. |
Hsiao KJ, Yang CF, Ting WK.
Determination of glycosylated
hemoglobin in Chinese by different micro-column methods. Proc
Annual Meeting
of Diabetes Assoc ROC 1981;13. (in Chinese) |
|
|
| 7. |
Yang CF, Hsiao KJ, Ting WK.
Evaluation of a new
resin adsorption method with references calibration for determination
of
glycosylated hemoglobin. Proc Annual Meeting of Taipei Medical
Technologist
Assoc 1981;13. (in Chinese) |
|
|
| 8. |
Hsiao KJ, Ou YC. Determination of
progesterone and
estrogen receptors in Chinese uterine tissues. Proc Annual
Meeting of Taipei
Medical Technologist Assoc 1981;12-3.(in Chinese) |
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|
| 9. |
Hsiao KJ,Yang CF, Ting WK. Study on
quantitation of glycosylated hemoglobin in Chinese by resin adsorption
and micro-column chromatography methods. J Formosan Med Assoc
1981;80:564-5. (in Chinese) |
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|
| 10. |
Lian JD, Liao HL, Ting WK, Hsiao KJ.
Serum gamma-glutamyl
transferase and its isoenzyme patterns in Chinese patients with liver
disease.
Chin Med J (Taipei) 1981;28:357. (in Chinese) |
|
|
| 11. |
Hsiao KJ, Yang CF, Ting WK.
Glycosylated hemoglobin levels in normal and diabetic Chinese. J
Clin Chem Clin Biochem 1981;19:704. |
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|
| 12. |
Lian JD, Liao HL, Ting WK, Hsiao KJ.
Isoenzyme patterns
of gamma-glutamyl transferase in Chinese patients with liver
diseases. Procf
III Intl Congress of Clin Enzymol, Salzburg, 1981;138. |
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|
| 13. |
Hsiao KJ, Wu SJ, Ting WK. Serum
glycylproline dipeptidyl
aminopeptidase activity in liver diseases. J Formosan Med Assoc
1981;80:1058.
(in Chinese) |
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|
| 14. |
Hsiao KJ, Chou P. Preliminary result
on mass screening
of 5000 cases for colorectal cancer in Taiwan. Bull Chinese Oncol
Soc 1981;2:33-4.
(in Chinese) |
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|
| 15. |
Ou YC, Hsiao KJ, Chou FF, Chen HF, Huang
MJ. Determination
of cytosol estrogen and progesterone receptors in Chinese uterine
tissue
and breast cancer. Proc Annual Meeting of Endocrine Soc ROC
1982;56-7. (in
Chinese) |
|
|
| 16. |
Hsiao KJ, Wu SJ, Ting WK.
Glycylproline dipeptidyl aminopeptidase activity in normal Chinese and
patient with liver diseases. Clin Chem 1982;28:1560-1. |
|
|
| 17. |
Hsiao KJ, Wu SJ, Ting WK. Study on
glycylproline dipeptidyl aminopeptidase activity in Chinese
serum. Proc ROC-Italy Seminar
on New Frontier in Biochemical Research, Taipei, 1982;19-21. |
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|
| 18. |
Ting M, Wu SJ, Hsiao KJ. Precision
and accuracy of micropipettes. J Tai Chung Med Tech 1982;6. (in
Chinese) |
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|
| 19. |
Wu SJ, Ting WK, Hsiao KJ.
Determination of serum
glycylproline dipeptidyl aminopeptidase activity. J Tai Chung Med
Tech 1982;8.
(in Chinese) |
|
|
| 20. |
Hsiao KJ, Wu SJ, Chen PM, Ting WK.
Serum glycylproline dipeptidyl aminopeptidase activity in neoplastic
diseases. Proc 2nd Asian-Pacific
Congress of Clin Biochem, Singapore, 1982;119. |
|
|
| 21. |
Hsiao KJ, Ou YC, Chen HF, Huang MJ.
Determination of cytosol estrogen and progesterone receptors in uterine
tissues. Proc
2nd Asian-Pacific Congress of Clinical Biochem, Singapore, 1982;228. |
|
|
| 22. |
Hsiao KJ, Wong YL, Ting WK. Serum
bilirubin and
its binding parameters in Chinese neonates. Recent Advances in
Clin Biochem
(Post-APCCB Symp) Taipei, 1982;32-4. |
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|
| 23. |
Hsiao KJ, Wong YL, Ting WK.
Determination of unbound
bilirubin in the serum of Chinese newborns. Proc 92nd Natl
Seminar Pediatr
Assoc ROC 1982;29-30. (in Chinese) |
|
|
| 24. |
Hsiao KJ, Wong YL, Ting WK. Serum
total and unbound
bilirubin in Chinese neonates. Clin Chem 1983;29:1222. |
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|
| 25. |
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. Clin
Biochem 1983;16:A14-5. |
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|
| 26. |
Chen CH, Plettner C, Hsiao TSY, Ting WK, Hsiao
KJ. Screening for congenital hypothyroidism in mental
retarded children. Proc
Annual Meeting of Chinese Assoc for Clin Biochem 1983;19-20. |
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|
| 27. |
Hsiao KJ, Chaung HF, Shieh MG, Ting
WK. A colorimetric
method for determination of glycosylated hemoglobin. Proc Annual
Meeting
of Chinese Assoc for Clin Biochem 1983;24-5. (in Chinese) |
|
|
| 28. |
Hsiao KJ, Wu SJ, Ting WK. Study on
pseudocholinesterase activity by enzyme coupling method in Chinese
serum. J Formosan Med Assoc
1983;82:87-8. (in Chinese) |
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|
| 29. |
Hsiao KJ, Hsu NY, Chi CS, Wuu KD, Ting
WK. Laboratory
tests for screening, diagnosis and management of phenylketonuria.
Proc 1st
Conference of Asian & Oceanian Assoc of Child Neurology, Taipei,
1983;44. |
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|
| 30. |
Hsiao KJ, Chen CH, Hsiao TSY, Plettner IC,
Clemens PC, Ting WK. Screening for treatable inborn metabolic
diseases in mental
retarded Chinese children. Proc 1st Conference of Asian and
Oceanian Association
of Child Neurology, Taipei, 1983;89. |
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| 31. |
Yeh SL, Ma FC, Hsiao KJ, Shieh MJ, Wuu
KD. Study
on dietary therapy for phenylketonuric children in Taiwan. Proc
Annual Meeting
Chinese Nutrition Assoc 1984;25. (in Chinese) |
|
|
| 32. |
Hsiao KJ, Wuu KD, Sheen FM, Feng WC, Ting
WK. Congenital
hypothyroidism and phenylketonuria in mentally retarded Chinese
children.
Proc Symposium on Screening for Prevention of Mental Retardation and
Developmental
Disabilities, Taipei, 1984;11-2. |
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|
| 33. |
Hsiao KJ, Wuu KD, Chen CH, Ting WK.
Phenylketonuria in mentally retarded Chinese children in Taiwan.
Rev Bras Anal Clin 1984;16:88. |
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|
| 34. |
Hsiao KJ, Wuu KD, Sheen FM, Feng WC, Ting
WK. Congenital
metabolic diseases in mentally retarded Chinese children: screening for
congenital
hypothyroidism, phenylketonuria, galactosemia, maple syrup urine
disease
and homocystinuria. Chin Med J (Taipei) 1984;34:31-2. |
|
|
| 35. |
Hsiao KJ, Sun KH, Huang CS.
Semiquantitative screening
test for glucose-6-phosphate dehydrogenase. Proc Joint Annual
Meeting of
Chinese Biochem Soc and Chinese Assoc for Clin Biochem 1984. (in
Chinese) |
|
|
| 36. |
Hung SH, Yeh F, Hsiao KJ.
Identification of Abnormal
urinary organic acids in phenylketonuria by gas chromatography/mass
spectroscopy.
Proc Joint Annual Meeting of Chinese Biochem Soc and Chinese Assoc Clin
Biochem,
1984. (in Chinese) |
|
|
| 37. |
Hsiao KJ, Liu YA. Interfacing
microcomputer and
spectrophotometer and its application in clinical biochemistry. J
Formosan
Med Assoc 1984;83:S20-1. (in Chinese). |
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|
| 38. |
Hsiao KJ, Wuu KD. Neonatal screening
for congenital metabolic disease in Taiwan: newborn delivered in
hospital. J Formosan Med
Assoc 1984;83:S91-2. (in Chinese) |
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|
| 39. |
Lin E, Chi CS, Hsiao KJ. Propionic
acidemia - a
case report. J Formosan Med Assoc 1984;83:S104. (in Chinese) |
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|
| 40. |
Hsiao KJ, Lin E, Chiu PC, Lo ZJ, Wuu
KD. Screening for congenital hypothyroidism in Chinese neonates
by TSH enzymeimmunoassay. Proc Annual Meeting of Endocrine
Society ROC 1985;19-20. |
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|
| 41. |
Wang PSG, Sheu WJ, Hsiao KJ, Ho LT.
The preparation of antibody to human thyrotropin-beta subunit.
Proc Annual Meeting of Endocrine
Society ROC 1985;37. |
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|
| 42. |
Hsiao KJ. Quality control in
clinical biochemistry in developing countries: gaps between theory and
practice. Proc Symp on
Quality Assurance in Clinical Laboratory, Taipei, 1985;32-4. |
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|
| 43. |
Lin E, Chi CS, Hsiao KJ. Clinical
observation of
congenital hypothyroidism. Chin Med J (Taipei) 1985;36:146. (in
Chinese) |
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|
| 44. |
Hsiao KJ, Chiu PC, Cheng WH, Chao
SL. Atypical phenylketonuria
with mild mental retardation caused by tetrahydrobiopterin deficiency
in
a Chinese family. 23rd Annual Symp of Society for the Study of
Inborn Errors
of Metabolism, Liverpool, 1985;78. |
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|
| 45. |
Liu TT, Wu SJ, Hsiao KJ.
Determination of urinary
pterins by high performance liquid chromatography for differential
diagnosis
of variant forms of phenylketonuria. Proc 3rd Asian-Pacific
Congress of
Clin Biochem, Bali,1985;109. |
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|
| 46. |
Hsiao KJ, Wu SJ. Determination of
dihydropteridine reductase on dried blood spot and its application in
differential diagnosis of atypical phenylketonuria. Proc Joint
Annual Meeting of Chinese Assoc
Clin Biochem and Chinese Biochem Soc, Taipei, 1985;50. (in Chinese) |
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|
| 47. |
Hsiao KJ, Wuu KD. A pilot program
for an integrated nationwide system for neonatal screening of
congenital metabolic diseases in Taiwan. Proc 1st Pan-Pacific
Congress of the Screening of Inborn Errors
of Metabolism, Kanazawa, 1985;F-5. |
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|
| 48. |
Lin CY, Hwang B, Hsiao KJ. Pomp's
disease in Chinese
and the prenatal diagnosis by determination of glucosidase
activity. Proc
1st Pan-Pacific Congress of the Screening of Inborn Errors of
Metabolism, Kanazawa, 1985;F-17. |
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|
| 49. |
Hsiao KJ, Chen CH, Chiu PC, Wuu KD.
Maternal phenylketonuria
in a Chinese phenylketonuria family. J Formosan Med Assoc
1985;84:S106-7.
(in Chinese) |
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|
| 50. |
Lin E, Chiu PC, Hsiao KJ, Chi CS.
Malignant phenylketonuria.
J Formosan Med Assoc 1985;84:S124. (in Chinese) |
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|
| 51. |
Wuu KD, Hsiao KJ. Screening for
inherited metabolic
diseases and congenital hypothyroidism in 4,744 mentally retarded
school
children in Taiwan. Am J Hum Genet 1985;37:A228. |
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|
| 52. |
Chou P, Hsiao KJ, Tsao D, Wu JC, Wang SS,
Lee SD, Yang IJ, Liao S. Determination of alpha-fetoprotein on
dry blood spot for
mass screening of hepatoma. J Chinese Oncol Soc 1986;2:72. (in
Chinese) |
|
|
| 53. |
Hsiao KJ, Lo ZJ, Yang YM. Familial
neonatal transient
hypothyroidism born by a mother with autoimmune hypothyroidism.
Proc Annual
Meeting of Endocrine Society ROC 1986:24-5. |
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|
| 54. |
Hsiao KJ, Wu SJ, Chen CW, Wu JK.
Determination of
plasma a -galactosidase and its application
to
diagnosis of Fabry's disease in Chinese. Proc 1st Joint Annual
Conference
of Biome Sci, Taipei, 1986;74. |
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|
| 55. |
Tsao D, Hsiao KJ, Chou HR. Two-site
enzyme immunoassay
for alpha-fetoprotein in dried blood samples collected on filter
paper.
Proc 1st Joint Annual Conference of Biomed Sci, Taipei, 1986;111. |
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|
| 56. |
Hsiao KJ, Liu TT, Sheen FM, Chen CC.
Effect of
trichloroacetic acid concentration in standard solution for
fluorometric determination
of plasma phenylalanine. Proc 1st Joint Annual Conference of
Biomed Sci,Taipei,
1986;146. |
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|
| 57. |
Hsiao KJ, Tan YY. Determination of
propionyl CoA
carboxylase and its application on prenatal diagnosis of propionic
acidemia.
Proc 1st Joint Annual Conference of Biomed Sci, Taipei, 1986;147. |
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|
| 58. |
Chiu PC, Hsiao KJ. Neonatal
screening of congenital hypothyroidism. Acta Paediatr Sinica
1986;35-6. (in Chinese) |
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|
| 59. |
Wu JC, Lee SD, Wang SS, Hsiao KJ, Tsao D,
Chou P, et al. Early detection of hepatocellular carcinoma in a
community by screening
of alpha-fetoprotein on dry blood spot. Chinese J Gastroenterol
1986;3:25.
(in Chinese) |
|
|
| 60. |
Hsiao KJ, Liu TT, Wu SJ.
Determination of urinary
pterins by high performance liquid chromatography for detection of
heterozygotes
of atypical phenylketonuria caused by biopterin synthetase
deficiency. Proc
Intl Chromatography Symp, Tamsui, Taiwan, 1986;37-8. |
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|
| 61. |
Hsiao KJ, Liu TT, Yang ZL. Analysis
of pterins in
aminotic fluid for prenatal diagnosis of atypical phenyletonuria caused
by
tetrahydrobiopterin synthesis deficiency. Proc 7th Intl Congress
of Human
Genetics, Berlin,1986;336. |
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|
| 62. |
Hsiao KJ. Two site enzyme
immunoassay for AFP in
dried blood spot on filter paper. Meeting of Alphafetoprotein in
Diagnosis
and Screening, Berlin, 1986. |
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|
| 63. |
Yu MH, Wuu KD, Hsiao KJ, Chen GJ.
An epidemiological study of G-6-PD deficient neonates. Proc.
Annual Meeting of the National Public Health Assoc, ROC, 1986;47-8. (in
Chinese) |
|
|
| 64. |
Hsiao KJ, Chen MS, Chang WC, Huang CS,
Shih MC. Comparison between dried-blood spot method and
cord-blood quantitative method
for neonatal screening of glucose-6-dehydrogenase deficiency.
Bull Assoc
Lab Med 1986;1:42. (in Chinese) |
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|
| 65. |
Hsiao KJ, Wuu KD. Galactosemia
detected by neonatal
screening in Taiwan. J Formosan Med Assoc 1986;85:S112-3. (in
Chinese) |
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| 66. |
Lee SD, Wu JC, Hsiao KJ, et al.
Mass screening of
primary hepatocellular carcinoma by alpha-fetoprotein in a rural area
of
Taiwan --- a dried blood spot method. Proc. 1st Intl Symp on
Viral Hepatitis
and Hepatocellular Carcinoma, Taipei, 1986;138. |
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| 67. |
Hung CT, Hsiao KJ, Chou P.
Preliminary report of
diabetes epidemiological study in pescador. Proc Annual Meeting
of Endocrine
Society ROC 1987;79. |
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|
| 68. |
Hsiao KJ, Chiang SH, Huang KS.
Determination of
galactose and galactose-1-phosphate in dried blood spot by enzymatic
method.
Proc 2nd Joint Annual Conference of Biomed Sci, Taipei, 1987;93. |
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|
| 69. |
Chen MS, Hsiao KJ. Determination of
galactose-1-phosphate uridyltransferase in human erythrocytes for
diagnosis and heterozygote detection
of galactosemia. Proc 2nd Joint Annual Conference of Biomed Sci,
Taipei,
1987;95. |
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| 70. |
Hsiao KJ, Liu TT, Wu SJ, Yang ZL, Yang
ML. Determination
of pterins in amniotic fluid by HPLC and it's application for prenatal
diagnosis
of atypical phenylketonuria caused by tetrahydrobiopterin
deficiency. Proc
2nd Joint Annual Conference of Biomed Sci, Taipei, 1987;125. |
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|
| 71. |
Hsiao KJ, Lee FY, Chang WJ, Wu SJ.
Determination of prophobilinogen deaminase activity in erythrocyte for
the diagnosis of
acute intermittent porphyria. Proc 2nd Joint Annual Conference of
Biomed
Sci, Taipei, 1987;125. |
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|
| 72. |
Lee FY, Hsiao KJ, Tsai YT. Jeng HS.
A clinical and
biochemical study in a Chinese family with acute intermittent
prophyria. Chinese J Gastroenterol 1987;4:37-8. (in Chinese) |
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|
| 73. |
Chou P, Jih LY, Hsiao KJ, Tsao D, Wu JC,
Lee SD. Comparison of community-based and non-community-based
liver cancer screening. J Formosan Med Assoc 1987;86:S34-5. (in
Chinese) |
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| 74. |
Hsiao KJ, Liu TT, Wu SJ. Atypical
phenylketonuria caused by tetrahydrobiopterin synthesis deficiency:
neonatal screening, diagnosis,
heterozygote detection and prenatal diagnosis. Proc 4th Intl
Congress of
Inborn Errors of Metabolism, Sendai, 1987;45. |
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|
| 75. |
Hsiao KJ, Wu JC, Lee SD, et al.
Determination of
alpha-fetoprotein in dried-blood spot by enzyme immunoassay for mass
screening
of hepatocellular carcinoma. Ann Clin Biochem 1987;24 (Suppl
2):59. |
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| 76. |
Hsiao KJ. Neonatal screening of
glucose-6-phosphate dehydrogenase deficiency. Proc 15th Annual
Conference of Screening of Inborn
Errors of Metabolism, Osaka, 1987;24-5. |
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| 77. |
Hung CT, Hsiao KJ, Chou P.
Preliminary report of
diabetes epidemiological study in pescador. Diabet Res Clin
Practice 1987;3(Suppl
1):S7. |
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| 78. |
Chao T, Hwang B, Hsiao KJ.
Transient Hypothyroidism. J Formosan Med Assoc 1987;86(Suppl
2):S118. (in Chiness) |
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| 79. |
Hsiao KJ. Phenylketonuria and its
variants in Taiwan
area. J Formosan Med Assoc 1987;86(Suppl 2):S168-9. (in Chinese) |
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|
| 80. |
Shih KC, Wu SJ, Shieh MJ, Hsiao KJ.
A pilot neonatal
mass- screening study for biotinidase deficiency using dried-blood
samples.
Bull Assoc Lab Med 1987;2:26. (in Chinese) |
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|
| 81. |
Lin H, Tan YY, Hsiao KJ. In vivo
14C-propionate incorporation for detection of defects in propionate
metabolism. Proc 3rd
Joint Annual Conference of Biomedical Sciences, Taipei, 1988;158. |
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| 82. |
Hsiao KJ, Liu TT, Wu SJ.
Heterozygote detection of classical phenylketonuria by determination of
phenylalanine and tyrosine in fasting plasma. Proc 3rd Joint
Annual Conference of Biomed Sci, Taipei,
1988;159. |
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| 83. |
Chen SH, Hsiao KJ, Lin LH, Liu TT, Tang
RB, Su TS. Study of restriction fragment length polymorphisms at
the human phenylalanine hydroxylase locus and evaluation of its
potential application in prenatal diagnosis of phenylketonuria in
Chinese. Proc 3rd Joint Annual Conference of Biomed Sci, Taipei,
1988;159. |
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| 84. |
Lee YJ, Huang FY, Kao HA, Hsu CH, Hung HY, Shen
EY, Shih SL, Wang CH, Hsiao KJ. Congenital
hypothyroidism-emphasizing the
importance of newborn thyroid screening. J Formosan Med Assoc
1988;87(Suppl
1):S29. (in Chinese) |
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| 85. |
Hsiao KJ, Shieh MJ, Chiang SH, Su
FY. Autoimmunity in congenital hypothyroidism detected by
neonatal screening. Research in
Congenital Hypothyroidism (NATO Advanced Res Workshop), Brussels,
1988;Abstr13. |
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| 86. |
Hsiao KJ, Chen MH, Chiang SH.
Neonatal Screening for glucose-6-phosphate dehydrogenase (G6PD)
deficiency in Taiwan. Proc
6th Natl Neonatal Screening Symp, Portland, 1988;24. |
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| 87. |
Hsiao KJ. Neonatal screening for
inborn metabolic disease: the experience in Taiwan. Proc 4th
Asian-Pacific Congress of Clin
Biochem, Hong Kong, 1988;51. |
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| 88. |
Liu TT, Hsiao KJ. Analysis of
biopterin and neopterin
in amniotic fluid by high performance liquid chromatography. Proc
4th Aisan-Pacific
Congress of Clin Biochem, Hong Kong, 1988;135. |
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| 89. |
Shieh MJ, Chiang SH, Hsiao KJ.
Enzyme immunoassay of 17- hydroxyprogesterone in dried blood spots for
neonatal screening of
congenital adrenal hyperplasia. Proc 4th Aisan-Pacific Congress
of Clin
Biochem, Hong Kong, 1988;135. |
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| 90. |
Chen WC, Wu SJ, Hsiao KJ.
Determination of glucose
in dried blood spots collected on filter paper by glucose dehydrogenase
method.
Proc 4th Aisan-Pacific Congress of Clin Biochem, Hong Kong, 1988;153. |
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| 91. |
Chen MS, Chiang SH, Hsiao KJ.
Bacteriophage assay
for galactose and galactose-1- phosphate in neonatal screening for
galactosemia
in Taiwan. Proc 4th Aisan-Pacific Congress of Clin Biochem, Hong
Kong, 1988:218. |
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| 92. |
Lin SP, Shen EY, Huang FY, Kao HA, Ho MY, Chen
MR, Hung HY, Lee HC, Wang TR, Hsiao KJ. Neonatal
hyperammonemia. Acta Paediatr
Sinica, 1988. (in Chinese) |
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| 93. |
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. J Biomed Lab Sci
1988;1(Suppl1):S22. |
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| 94. |
Shieh MJ, Chiang SH, Hsiao KJ.
Determination of
17-hydroxyprogesterone in dried blood spot by enzymeimmunoassay and its
application
to neonatal screening of congenital adrenal hyperplasia. J Biomed
Lab Sci
1989;2:121. |
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| 95. |
Hsiao KJ, Chuang HJ, Yang ML, Ho SC, Lie
CC, Liao S. Determination of alpha-fetoprotein in dried-blood
spot on filter paper
for maternal screening. J Biomed Lab Sci 1989;2:122. |
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| 96. |
Yu YS, Chou PC, Hsiao KJ. A case
report of homocystinuria.
Symp on Diagnosis and Treatment of Inherited Diseases,Taipei, 1989;8.
(in
Chinese) |
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| 97. |
Huang MJ, Chiang SH, Hsiao KJ.
Follow-up, diagnosis
and treatment of phenylketonuria and congenital hypothyroidism detected
by
neonatal screening. Symp on Diagnosis and Treatment of Inherited
Diseases,
Taipei, 1989;21. (in Chinese) |
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| 98. |
Hsiao KJ, Chuang HC, Yang ML, Ho SC, Liu
CC, Liao S. Determination of alpha-fetoprotein in dried-blood
spot collected on filter
paper for maternal screening. Symp on Diagnosis and Treatment of
Inherited
Diseases, Taipei, 1989;23. (in Chinese) |
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Hsiao KJ, Chiang SH, Liu TT, Chiu PC, Wuu
KD. High
incidence of tetrahydrobiopterin deficient phenylketonuria in the
Chinese
population of Taiwan. Proc 1989 Annual Meeting of the Society for
Inherited
Metabolic Disorders, Florida, 1989;16. |
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Hsiao KJ. National screening for
congenital hypothyroidism
in Taiwan. Chin Med J (Taipei) 1989;43:412. |
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| 101. |
Su TS, Chen SH, Tsai TF, Lin LH, Liu TT, Tang RB,
Hsiao KJ. Study of restriction fragment length
polymorphisms at the human
phenylalanine hydroxylase locus and evaluation of its potential
application in prenatal diagnosis of phenylketonuria in Chinese.
Proc Symp on Molecular
Approaches to Genetic Disorders, Taipei, 1989;23. |
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| 102. |
Hsiao KJ, Wuu KD. Neonatal screening
for inborn metabolic diseases in Taiwan. Proc Symp on Molecular
Approaches to Genetic
Disorders, Taipei, 1989;16-8. |
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| 103. |
Yeh SL, Wu SJ, Shieh MJ, Hsiao KJ.
Erythrocyte glutathione
peroxidase activity and its application in assessing selenium status of
patients
with inherited metabolic disorder. 14th Society Conference
Program of the
Chinese Nutrition Soc, Taipei, 1989;72. (in Chinese) |
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| 104. |
Hsiao KJ, Chiang SH, Liu TT, Chiu PC, Wuu
KD. Tetrahydrobiopterin
deficient phenylketonuria detected by neonatal screening in
Taiwan. Proc
9th Intl Symp on Pteridines and Folic Acid Derivatives, Zurich, 1989;61. |
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| 105. |
Shintaku H, Fujioka M, Isshiki G, Sawaka Y, Ohura
T, Yamaoka S, Ueda T, Hatanaka K, Suzuki M, Murata R, Matsumoto M, Hsiao
KJ, Liu
TT, Chen RG. Prenatal diagnosis of 6-pyruvoyl tetrahydropterin
synthetase
deficiency in East Asia. Proc 9th Intl Symp on Pteridines and
Folic Acid
Derivatives, Zurich, 1989;61. |
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Chiu PC, Hsiao KJ. Phenylketonuria
caused by tetrahydrobiopterin
synthesis deficiency in Taiwan. Proc 27th Annual Symp of the
Society for
the Study of Inborn Errors of Metabolism, Munich, 1989;P029. |
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Hsiao KJ, Lin SS, Shieh MJ, Chiang
SH. The effect
of extraction precedure on the enzymeimmunoassay of
17-hydroxyprogesterone in dried blood spot. Bull Assoc Lab Med
1989;4:30. |
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Hsiao KJ, Wuu KD. Neonatal screening
for inborn metabolic diseases in Taiwan. Colloquium on Inborn
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