| 1. |
Hsiao KJ, Li HC. Regulation of a heart protein
phosphatase by ATP. Fed Proc 1975;34:618. [ Abstract
] |
|
|
| 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.
[ Abstract ]
|
|
|
| 3. |
Hsiao KJ, Li HC. The dissociation of a nucleoside
phosphate-stimulated histone phosphatase from canine heart. Fed Proc
1977;36:778. [ Abstract
] |
|
|
| 4. |
Li HC, Hsiao KJ. Purification of protein phosphatases
from canine heart. Fed Proc 1977;36:778. [ Abstract
] |
|
|
| 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. [ Abstract
] |
|
|
| 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) [
Abstract ] |
|
|
| 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) [ Abstract
] |
|
|
| 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) [
Abstract ] |
|
|
| 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)
[ Abstract ]
|
|
|
| 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) [ Abstract
] |
|
|
| 11. |
Hsiao KJ, Yang CF, Ting WK. Glycosylated hemoglobin
levels in normal and diabetic Chinese. J Clin Chem Clin Biochem 1981;19:704.
[ Abstract ]
|
|
|
| 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. [
Abstract ] |
|
|
| 13. |
Hsiao KJ, Wu SJ, Ting WK. Serum glycylproline
dipeptidyl aminopeptidase activity in liver diseases. J Formosan Med
Assoc 1981;80:1058. (in Chinese) [ Abstract
] |
|
|
| 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) [ Abstract
] |
|
|
| 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) [ Abstract
] |
|
|
| 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. [ Abstract
] |
|
|
| 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.
[ Abstract ]
|
|
|
| 18. |
Ting M, Wu SJ, Hsiao KJ. Precision and accuracy
of micropipettes. J Tai Chung Med Tech 1982;6. (in Chinese) [
Abstract ] |
|
|
| 19. |
Wu SJ, Ting WK, Hsiao KJ. Determination of serum
glycylproline dipeptidyl aminopeptidase activity. J Tai Chung Med
Tech 1982;8. (in Chinese) [ Abstract
] |
|
|
| 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. [
Abstract ] |
|
|
| 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.
[ Abstract ]
|
|
|
| 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. [ Abstract
] |
|
|
| 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) [ Abstract
] |
|
|
| 24. |
Hsiao KJ, Wong YL, Ting WK. Serum total and unbound
bilirubin in Chinese neonates. Clin Chem 1983;29:1222. [
Abstract ] |
|
|
| 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.
[ Abstract ]
|
|
|
| 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. [
Abstract ] |
|
|
| 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) [
Abstract ] |
|
|
| 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) [ Abstract
] |
|
|
| 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. [ Abstract
] |
|
|
| 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. [
Abstract ] |
|
|
| 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) [ Abstract
] |
|
|
| 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. [ Abstract
] |
|
|
| 33. |
Hsiao KJ, Wuu KD, Chen CH, Ting WK. Phenylketonuria
in mentally retarded Chinese children in Taiwan. Rev Bras Anal Clin
1984;16:88. [ Abstract
] |
|
|
| 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.
[ Abstract ]
|
|
|
| 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) [ Abstract
] |
|
|
| 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) [ Abstract
] |
|
|
| 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). [ Abstract
] |
|
|
| 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) [ Abstract
] |
|
|
| 39. |
Lin E, Chi CS, Hsiao KJ. Propionic acidemia -
a case report. J Formosan Med Assoc 1984;83:S104. (in Chinese) [
Abstract ] |
|
|
| 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. [ Abstract
] |
|
|
| 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. [ Abstract
] |
|
|
| 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. [
Abstract ] |
|
|
| 43. |
Lin E, Chi CS, Hsiao KJ. Clinical observation
of congenital hypothyroidism. Chin Med J (Taipei) 1985;36:146. (in
Chinese) [ Abstract
] |
|
|
| 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. [
Abstract ] |
|
|
| 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. [ Abstract
] |
|
|
| 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)
[ Abstract ]
|
|
|
| 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. [ Abstract
] |
|
|
| 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. [ Abstract
] |
|
|
| 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) [ Abstract
] |
|
|
| 50. |
Lin E, Chiu PC, Hsiao KJ, Chi CS. Malignant phenylketonuria.
J Formosan Med Assoc 1985;84:S124. (in Chinese) [ Abstract
] |
|
|
| 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. [ Abstract
] |
|
|
| 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)
[ Abstract ]
|
|
|
| 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. [ Abstract
] |
|
|
| 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. [ Abstract
] |
|
|
| 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. [
Abstract ] |
|
|
| 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. [ Abstract
] |
|
|
| 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. [
Abstract ] |
|
|
| 58. |
Chiu PC, Hsiao KJ. Neonatal screening of congenital
hypothyroidism. Acta Paediatr Sinica 1986;35-6. (in Chinese) [
Abstract ] |
|
|
| 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) [ Abstract
] |
|
|
| 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. [
Abstract ] |
|
|
| 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. [ Abstract
] |
|
|
| 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. [ Abstract
] |
|
|
| 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) [ Abstract
] |
|
|
| 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) [ Abstract
] |
|
|
| 65. |
Hsiao KJ, Wuu KD. Galactosemia detected by neonatal
screening in Taiwan. J Formosan Med Assoc 1986;85:S112-3. (in Chinese)
[ Abstract ]
|
|
|
| 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. [
Abstract ] |
|
|
| 67. |
Hung CT, Hsiao KJ, Chou P. Preliminary report
of diabetes epidemiological study in pescador. Proc Annual Meeting
of Endocrine Society ROC 1987;79. [ Abstract
] |
|
|
| 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.
[ Abstract ]
|
|
|
| 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. [ Abstract
] |
|
|
| 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. [
Abstract ] |
|
|
| 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. [ Abstract
] |
|
|
| 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) [ Abstract
] |
|
|
| 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) [ Abstract
] |
|
|
| 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. [
Abstract ] |
|
|
| 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. [ Abstract
] |
|
|
| 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. [ Abstract
] |
|
|
| 77. |
Hung CT, Hsiao KJ, Chou P. Preliminary report
of diabetes epidemiological study in pescador. Diabet Res Clin Practice
1987;3(Suppl 1):S7. [ Abstract
] |
|
|
| 78. |
Chao T, Hwang B, Hsiao KJ. Transient
Hypothyroidism. J Formosan Med Assoc 1987;86(Suppl 2):S118. (in Chiness)
[ Abstract ]
|
|
|
| 79. |
Hsiao KJ. Phenylketonuria and its variants in
Taiwan area. J Formosan Med Assoc 1987;86(Suppl 2):S168-9. (in Chinese)
[ Abstract ]
|
|
|
| 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) [ Abstract
] |
|
|
| 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. [
Abstract ] |
|
|
| 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. [ Abstract
] |
|
|
| 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. [ Abstract
] |
|
|
| 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) [ Abstract
] |
|
|
| 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.
[ Abstract ]
|
|
|
| 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. [
Abstract ] |
|
|
| 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. [ Abstract
] |
|
|
| 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. [
Abstract ] |
|
|
| 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. [ Abstract
] |
|
|
| 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. [ Abstract
] |
|
|
| 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. [ Abstract
] |
|
|
| 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) [ Abstract
] |
|
|
| 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. [
Abstract ] |
|
|
| 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. [ Abstract
] |
|
|
| 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. [ Abstract
] |
|
|
| 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) [ Abstract
] |
|
|
| 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) [ Abstract
] |
|
|
| 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) [ Abstract
] |
|
|
| 99. |
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. [ Abstract
] |
|
|
| 100. |
Hsiao KJ. National screening for congenital hypothyroidism
in Taiwan. Chin Med J (Taipei) 1989;43:412. [ Abstract
] |
|
|
| 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. [
Abstract ] |
|
|
| 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. [ Abstract
] |
|
|
| 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)
[ Abstract ]
|
|
|
| 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. [ Abstract
] |
|
|
| 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. [ Abstract
] |
|
|
| 106. |
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. [ Abstract
] |
|
|
| 107. |
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. [ Abstract
] |
|
|
| 108. |
Hsiao KJ, Wuu KD. Neonatal screening for inborn
metabolic diseases in Taiwan. Colloquium on Inborn Errors of Metabolism
(Medical Research Council, South Africa and National Science Council, R.O.C.),
1989;11-2. [ Abstract
] |
|
|
| 109. |
Hsiao KJ, Su TS, Wuu KD. Classical and tetrahydrobiopterin
deficient phenylketonuria in Taiwan. Colloquium on Inborn Errors of
Metabolism (Medical Research Council, South Africa and National Science
Council, R.O.C.), 1989;20-1. [ Abstract
] |
|
|
| 110. |
Hsiao KJ, Chiang SH, Wu SJ, Liu TT, Chiu PC.
Dihydropteridine reductase deficient phenylketonuria detected by neonatal
screening in Taiwan. Proc 5th Joint Annual Conference of Biomed Sci,
Taipei, 1990;172. [ Abstract
] |
|
|
| 111. |
Hsiao KJ, Sheu SH, Wu SJ, Chen MS, Chiang SH, Chang
TT, Chung YC, Lin CH. Amino acid analysis and urinary abnormal organic
acids in patients with maple syrup urine disease. Proc 5th Joint Annual
Conference of Biomed Sci, Taipei, 1990;173. [ Abstract
] |
|
|
| 112. |
Hsiao KJ, Chen MS, Wu KF, Wu SJ, Huang MR, Yang ML.
Prenatal diagnosis of propionic acidemia with amniocytes. Proc 5th
Joint Annual Conference of Biomed Sci, Taipei, 1990;173. [ Abstract
] |
|
|
| 113. |
Yeh SL, Wu SJ, Shieh MJ, Hsiao KJ. Determination
of erythrocyte glutathione peroxidase activity and its reference range in
Chinese adults. Proc 5th Joint Annual Conference of Biomed Sci, Taipei,
1990;174. [ Abstract
] |
|
|
| 114. |
Lin SS, Chian SH, Chung MC, Hsiao KJ. Enzymeimmunoassay
of 17-hydroxyprogesterone in dried blood spot for screening of congenital
adrenal hyperplasia. Proc 5th Intl Congress of IEM, Monterey, 1990;P90.
[ Abstract ]
|
|
|
| 115. |
Hsiao KJ, Su TS, Liu TT, Tsai TF, Yang ML. Prenatal
diagnosis of different forms of phenylketonuria (PKU). Proc 5th Intl
Congress of IEM, Monterey, 1990;W4.2. [ Abstract
] |
|
|
| 116. |
Chen MS, Wu KF, Wu SJ, Huang MR, Yang ML, Hsiao KJ.
Prenatal diagnosis of propionic acidemia and methylmalonic acidemia with
amniocytes. Proc 5th Intl congress of IEM, Monterey, 1990;W8.6. [
Abstract ] |
|
|
| 117. |
Chen CY, Wu KF, Lou IF, May BH, Hsiao KJ. b
-Thalassemia carrier screening in Hsiulin district of Hualien county.
Proc 6th Joint Annual Conference of Biomed Sci, Taipei, 1991;190. [
Abstract ] |
|
|
| 118. |
Lin SS, Chiang SH, Liu TT, Hsiao KJ. Study of
serum steroids by high performance liquid chromatography. Proc 6th
Joint Annual Conference of Biomed Sci, Taipei, 1991;271. [ Abstract
] |
|
|
| 119. |
Horng C, Wu SJ, Liu TT, Sim CB, Hsiao KJ. Determination
of human placenta methylmalonyl-CoA mutase activity by high performance
liquid chromatography. Proc 6th Joint Annual Conference of Biomed
Sci, Taipei, 1991;272. [ Abstract
] |
|
|
| 120. |
Chen YC, Liu TT, Hsiao KJ. Determination of sepiapterin
reductase activity in erythrocyte by high performance liquid chromatography.
Proc 6th Joint Annual Conference of Biomed Sci, Taipei, 1991;272. [
Abstract ] |
|
|
| 121. |
Hsiao KJ. Genetic disorders and neonatal screening.
Proc 5th Asian-Pacific Congress of Clin Biochem, Kobe, 1991;50. [
Abstract ] |
|
|
| 122. |
Horng CJ, Hsiao KJ, Chen CH, Tsai SR, Sim CB.
Urinary neopterin and biopterin levels in patients with depression.
Proc 5th Asian-Pacific Congress of Clin Biochem, Kobe, 1991;130. [
Abstract ] |
|
|
| 123. |
Horng CJ, Wu SJ, Liu TT, Sim CB, Hsiao KJ. Determination
of methylmalonyl-CoA mutase activity in human placenta by high performance
liquid chromatography. Am J Hum Genet 1991;49(Suppl):115. [
Abstract ] |
|
|
| 124. |
Yang ML, Lin HH, Chen CY, Chen CH, Lin CK, Hsiao KJ,
Ng HT. Carrier screening and prenatal diagnosis of alpha-thalassemia
by dual restriction enzyme analysis. Am J Hum Genet 1991;49(Suppl):208.
[ Abstract ]
|
|
|
| 125. |
Hsiao KJ, Lee SY, Chiang SH, Low EF, Huang CH, Huang
MF, Chen HT, Chen IK. A pilot study of maternal alpha-fetoprotein
screening with dried-blood spot samples collected on filter paper.
Am J Hum Genet 1991;49(Suppl):219. [ Abstract
] |
|
|
| 126. |
Wuu K, Li S, Chao M, Hsiao KJ, Wang T. Chromosomal
and metabolic screening on mentally retarded school children in Taiwan.
Am J Hum Genet 1991;49(Suppl):331. [ Abstract
] |
|
|
| 127. |
Hsiao KJ, Chiang SH, Wu HY, Huang TM, Liew DG, Chao
Yu YM, Chen MC. Interlaboratory quality assurance program for determination
of glucose-6-phosphate dehydrogenase activity in Taiwan. Professor
Arthur M.O. Veal Memorial Meeting, Auckland, 1991;17. [ Abstract
] |
|
|
| 128. |
Hsiao KJ, Chiang SH, Chang TT, Liew DG, Chao Yu YM.
Experience of neonatal G6PD deficiency screening program in Taiwan.
Proc 8th Intl Neonatal Screening Symp, Australia, 1991;O57. [
Abstract ] |
|
|
| 129. |
Hsiao KJ, Chen CY, Wu SJ, Yang ML. Screening
for b -thalassemia carrier using dried blood
spots collected on filter paper. Proc 8th Intl Neonatal Screening
Symp, Australia, 1991;P79. [ Abstract
] |
|
|
| 130. |
Horng CJ, Hsiao KJ, Sim CB. Association between
schizophrenia and HindIII polymorphism probed with MCM26b. Proc 30th
Ann conference of the Soc of Psychiatry, Taiwan, 1991;71-2. (in Chinese)
[ Abstract ]
|
|
|
| 131. |
Yang ML, Hsiao KJ, Wu KF, Chen MS, Wang SY, Wu SJ.
Prenatal diagnosis of organic acidemia - propionic acidemia. J Perinat
Med 1991;19(Suppl 2):65. [ Abstract
] |
|
|
| 132. |
Hong YM, Wu SJ, Liu TT, Hsiao KJ. Analysis of
restrction fragment length polymorphism in Chinese dihydropteridine reductase
gene locus. Proc 7th Joint Annual Conference of Biomed Sci, Taipei,
1992;92. [ Abstract
] |
|
|
| 133. |
Wu SJ, Wu KF, Hsiao KJ. Determination of dihydropteridine
reductase (DHPR) activity in amniotic fluid cells and its application for
prenatal diagnosis of DHPR deficiency. Proc 7th Joint Annual Conference
of Biomed Sci, Taipei, 1992;92. [ Abstract
] |
|
|
| 134. |
Shih MS, Wu SJ, Yeh CT, Chiang SH, Hsiao KJ.
A microplate method for determination of glucose in plasma. Proc 7th
Joint Annual Conference of Biomed Sci, Taipei, 1992;97. [ Abstract
] |
|
|
| 135. |
Chang TT, Chiang SH, Hsiao KJ. A microplate method
for determination of glucose and galactose-1-phosphate in dried blood spots
for neonatal screening of galactosemia. Proc 7th Joint Annual Conference
of Biomed Sci, Taipei, 1992;98. [ Abstract
] |
|
|
| 136. |
Hsiao KJ. Neonatal screening strategy for congenital
metabolic disease. Proc Joint Meeting of the 3rd Combined Conference
of Singapore Society of Pathology and Malaysian Society of Pathologists
and 1992 Scientific Meeting of the Singapore Association of Clinical Biochemists,
Singapore, 1992;27. [ Abstract
] |
|
|
| 137. |
Hsiao KJ. Neonatal screening strategy for congenital
metabolic diseases. Proc National Congress of Indonesia Association
of Clinical Chemistry, Indonesia, 1992;21. [ Abstract
] |
|
|
| 138. |
Hsiao KJ, Su TS, Liu TT, Hung YM, Wu SJ, Lin CH, Tsai
TF, Chao HK, Yang ML. Prenatal diagnosis of different forms of phenylketonuria.
Proc 2nd Intl Symp on Genet, Health and Dis 1993;43. [ Abstract
] |
|
|
| 139. |
Tzeng CL, Liu TT, Hsiao KJ. Determination of
GTP cyclohydrolase I activity in stimulated leukocyte by high performance
liquid chromatorgraphy. J Biomed Lab Sci 1993;5:S24. [
Abstract ] |
|
|
| 140. |
Chen MS, Yang CC, Chiang SH, Wu SJ, Hsiao KJ.
Globin chain analysis by HPLC and restriction fragments analysis of polymerase
chain reaction (PCR) amplified DNA for detection of HbE mutation.
J Biomed Lab Sci 1993;5:S8. [ Abstract
] |
|
|
| 141. |
Hung YM, Yang CC, Chiang SH, Wu SJ, Tang TK, Hsiao KJ.
Analysis of common glucose-6-phosphate dehydrogenase mutations in Chinese
by polymerase chain reaction using dried blood spots collected on filter
paper. J Biomed Lab Sci 1993;5:S10. [ Abstract
] |
|
|
| 142. |
Chen JY, Yang CC, Tsai MT, Chiang SH, Hsiao KJ.
Application of dried blood spots collected on filter paper for screening
of maternal b -thalassemia carrier. J Biomed
Lab Sci 1993;5:S11. [ Abstract
] |
|
|
| 143. |
Liu TT, Chiang MH, Chen YC, Hsiao KJ. Analysis
of pterins in dried urine spots collected on filter paper for detecting
patients with tetrahydrobiopterin synthesis deficiency. J Biomed Lab
Sci 1993;5:S12. [ Abstract
] |
|
|
| 144. |
Yang CC, Chiang SH, Wu SJ, Hsiao KJ. Non-radioactive
detection of common b -thalassemia mutations
in Chinese by polymerase chain reaction (PCR) using dried blood spot specimens.
J Biomed Lab Sci 1993;5:S9. [ Abstract
] |
|
|
| 145. |
Liu TT,Hung YM, Yang CC, Chiang SH, Wu SJ, Tang TK, Hsiao
KJ. Analysis of common glucose-6-phosphate dehydrogenase mutations
in Chinese by polymerase chain reaction using dried blood spots collected
on filter paper. Proc Mutations in Human Genome, Italy, 1993;57. [
Abstract ] |
|
|
| 146. |
Hung YM, Yang CC, Chiang SH, Wu SJ, Hsiao KJ.
Detection of common glucose-6-phosphate dehydrogenase mutations in southern
Chinese by polymerase chain reaction (PCR) using dried blood spot specimens.
Proc 1st Asian Pacific Regional Meeting of International Society for Neonatal
Screening, Sapporo, 1993:41. New Trends in Neonatal Screening 1994;87. [
Abstract ] |
|
|
| 147. |
Hsiao KJ, Yang CC, Chen MS, Wu SJ Chiang SH, Tsai MT.
Material screening of b -thalassemia carrier
using dried blood samples collected on filter paper. Clin Biochem
Rev 1993;14:281(PS347). [ Abstract
] |
|
|
| 148. |
Yang CC, Hung YM, Tan IK, Chio LF, Wu SJ, Chiang SH, Hsiao
KJ. Study of the common southern Chinese glucose-6-phosphate dehydrogenase
mutations in Singapore and Taiwan. Clin Biochem Rev 1993;14:281(PS348).
[ Abstract ]
|
|
|
| 149. |
Liu TT, Hsiao KJ. Isolation of human 6-pyruvoyl
tetrahydropterin synthase cDNA. J Biomed Lab Sci 1994;6:A22. [
Abstract ] |
|
|
| 150. |
Hsiao KJ, Yang CC, Wu SJ, Chiang SH, Tan IK, Lam S.
The comparison of the incidence of common southern Chinese glucose-6-phosphate
dehydrogenase mutations in Singapore, Hong Kong and Taiwan. J Biomed
Lab Sci 1994;6:A21. [ Abstract
] |
|
|
| 151. |
Hsiao KJ, Yang CC, Wu SJ, Chiang SH, Tan IK, Chio LF,
Lam STS, Yuen MLM. The comparison of the incidence of southern Chinese
glucose-6-phosphate dehydrogenase mutations in Singapore, Hong Kong and
Taiwan. Proc 6th Intl Congress of Inborn Errors of Metabolism, Milano,
1994;68(W5.4). [ Abstract
] |
|
|
| 152. |
Hsiao KJ, Chiang SH, Liu TT, Niu DM, Chao T, Chiu PC.
Neonatal screening of phenylketonuria in Taiwan. Proc 6th Intl Congress
of Inborn Errors of Metabolism, Milano, 1994;104(W12.6). [ Abstract
] |
|
|
| 153. |
Hsiao KJ, Yang CC, Wu SJ, Chiang SH, Lam STS, Yuen
MLM. The incidence of southern Chinese glucose-6-phosphate dehydrogenase
mutations in Hong Kong and Taiwan. Proc 21st World Congress of Medical
Technology, Hong Kong, 1994;82. [ Abstract
] |
|
|
| 154. |
Tan IK, Chio LF, Chan MK, Hsiao KJ. Common southern
Chinese glucose-6-phosphate dehydrogenase mutations in Singapore and Taiwan.
28th Singapore-Malaysia Congress of Medicine, Singapore, 1994. [
Abstract ] |
|
|
| 155. |
Hsiao KJ, Lin CC, Chiang SH. A pilot study on
neonatal screening of congenital adrenal hyperplasia in Taiwan. Advances
in Obstetrics and Perinatology 1994;2:37. [ Abstract
] |
|
|
| 156. |
Chiang SH, Chen MH, Wu SJ, Hsiao KJ. External
quality assurance program for determination of erythrocyte glucose-6-phosphate
dehydrogenase activity in Taiwan. J Biomed Lab Sci 1995;7:A16. [
Abstract ] |
|
|
| 157. |
Chiou JY, Liu TT, Hsiao KJ. Study of restriction
fragment length polymorphisms at the human dihydropteridine reductase locus
and its application in prenatal diagnosis of dihydropteridine reductase
deficient phenylketonuria in Chinese. J Biomed Lab Sci 1995;7:A23.
[ Abstract ]
|
|
|
| 158. |
Wang SS, Liu TT, Hsiao KJ. Purification of sepiapterin
reductase from rat erythrocytes. J Biomed Lab Sci 1995;7:A24. [
Abstract ] |
|
|
| 159. |
Chen CH, Wu SJ, Hsiao KJ. A high frequency PAH
missense mutation M276V in Kyushu Japanese phenylketonuric patients is not
found among Chinese phenylketonuric patients. J Biomed Lab Sci 1995;7:A38.
[ Abstract ]
|
|
|
| 160. |
Hsiao KJ, Chiang SH, Wang HF, Liew DG, Chao Yu YM.
Interlaboratory quality assurance program for determination of blood glucose-6-phosphate
dehydrogenase activity in Taiwan. Abstracts of The 8th Intl Symp on
Quality Control, Kobe, 1995;76. [ Abstract
] |
|
|
| 161. |
Hsiao KJ, Wu KF, Wu SJ. Prenatal diagnosis of
methylmalonic aciduria and propionic acidemia. Abstracts of 7th Asian-Pacific
Congress of Clin Biochem, Bangkok, 1995;68. [ Abstract
] |
|
|
| 162. |
Chen CH, Shyu PW, Wu SJ, Sheu SS, Hsiao KJ. A
novel point mutation in galactosidase A gene causing Fabry disease in Chinese.
Am J Hum Genet 1995;57(suppl):A177(1013). [ Abstract
] |
|
|
| 163. |
Niu DM, Chen CH, Wang NH, Chin LS, Hsiao KJ.
Chinese achondroplasia is also defined by recurrent G380R mutations of FGFR3.
Am J Hum Genet 1995;57(suppl):A183(1041). [ Abstract
] |
|
|
| 164. |
Hsiao KJ, Chiang SH. The experience of neonatal
screening in Taiwan. J Biomed Lab Sci 1995;7(suppl):A107-8. (in Chinese)
[ Abstract ]
|
|
|
| 165. |
Hsiao KJ. Neonatal screening of glucose-6-phosphate
dehydrogenase deficiency in Taiwan. 2nd Asian Pacific Regional Meeting
of Intl Soc for Neonatal Screening, Hong Kong, 1995;L13. [ Abstract
] |
|
|
| 166. |
Tang DJ, Ma XQ, Song CY, Lin BH, Wu SJ, Chiang SH, Hsiao
KJ. Glucose-6-phosphate dehydrogenase mutations among Cantonese
revealed by polymerase chain reaction using dried blood spots. 2nd
Asian Pacific Regional Meeting of Intl Soc for Neonatal Screening, Hong
Kong, 1995;L15. [ Abstract
] |
|
|
| 167. |
Chen CH, Wu SJ, Hsiao KJ. Frequencies of different
glucose-6-phosphate dehydrogenase mutations in southern Chinese populations.
3rd Intl Symp on Genet Health Disease, Amritsar, 1995;41-2. [
Abstract ] |
|
|
168.
|
Shyu PW, Liu MY, Chen ML, Lee YL, Hong CJ, Hsiao KJ,
Chen CH. Screening of fragile mutations at FRAXE and FRAXE loci in
mentally retarded males using a non-radioactive PCR method. J Biomed
Lab Sci 1996;8:A11. [ Abstract
] |
|
|
169.
|
Hsiao KJ. Interlaboratory QA on determination
of blood G6PD activity. Symposium on Quality Management of Clinical
Laboratory. Chang Hua,Taiwan, 1996;19-20.(in Chinese) [ Abstract
] |
|
|
170.
|
Hsiao KJ, Liu TT. Identification of a common
6-pyruvoyl-tetrahydropterin synthase mutation at codon 87 in Chinese phenylketonuria
caused by tetrahydrobiopterin synthesis deficiency. J Biomed Lab Sci
1996;8:A12. [ Abstract
] |
|
|
171.
|
Hsiao KJ, Chiang SH. The Experience of neonatal
screening in Taiwan. 4th Asian-European Workshop on Inborn Errors
of Metabolism, Munich, 1996;27. [ Abstract
] |
|
|
172.
|
Liu XQ, Liu TT, Hsiao KJ, Zhang M, Ye J, Chen RG.
Mutations detected in the 6-pyruvoyl-tetrahydropterin synthase gene from
Chinese phenylketonuria patients. 4th Asian-European Workshop on Inborn
Errors of Metabolism, Munich, 1996;35. [ Abstract
] |
|
|
173.
|
Zhang M, Gu XF, Hsiao KJ, Su TS, Chao HK, Zhang YF,
Ye J, Huang XD, Shwn YN, Shen RG. Mutations in exon 7 phenylalanine
hydroxylase gene of PKU from southern China. 4th Asian-European Workshop
on Inborn Errors of Metabolism, Munich, 1996;56. [ Abstract
] |
|
|
174.
|
Lee YR, Chen CH, Liu MY, Wei FC, Hwu HG, Hsiao KJ.
Allelic association study of Nla III and MspI polymorphisms of catechol-O-methyltransferase
gene and schizophrenia. Am J Hum Genet 1996;59(suppl):A384. [
Abstract ] |
|
|
175.
|
Chen CH, Hong CJ, Shyu PW, Liu MY, Wang-Wuu S, Wuu KD, Hsiao
KJ. Identification of FRAXA and FRAXE syndromes by using a non-radioactive
duplex PCR and Southern blot analysis in Chinese mentally retarded males
from Taiwan. Am J Hum Genet 1996;59(suppl):A394. [ Abstract
]
|
|
|
176.
|
Tang DJ, Ma XQ, Song CY, Lin BH, Wu SJ, Chiang SH, Hsiao
KJ. Glucose-6-phosphate dehydrogenase mutations among Cantonese revealed
by polymerase chain reaction using dried blood spots. 3rd Meeting of the
Intl Soc for Neonatal Screening, Boston, 1996;P56. [ Abstract
]
|
|
|
177.
|
Hsiao KJ, Liu TT, Wu SJ, Wu KF, Chiang SH. The
mutations found in 6-pyruvoyl-tetrahydropterin synthase deficient phenylketonuria.
Proc 3rd Meeting of the Intl Soc for Neonatal Screening, Boston, 1996;28-9.
[ Abstract ]
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( 臨床生化研究室 )