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



 
 Conference Abstracts (1997 - Present) 

 
178. Hsiao KJ, Chiang SH.  Interlaboratory quality survey for maternal blood screening of Down syndrome in Taiwan.  2nd Asian Congress on Down Syndrome Screening, Taipei, 1997;36.   [ Abstract ]


179. Hsiao KJ.  Trends in diagnosing inherited metabolic disease.  J Paediatr Child Health, 1997;33 (Suppl.1):S14.   [ Abstract ]


180. Hsiao KJ, Chiang SH.  The organization of the neonatal screening program in Taiwan.  J Paediatr Child Health 1997;33(Suppl.1):S27.   [ Abstract ]


181. Liu TT, Lu SF, Hsiao KJ.  Genonic structure of the human 6-pyruvoyl-tetrahydropterin synthase gene.  12th Jonint Annual Conference of Biomedical Sciences , Taipei, 1997;260.   [ Abstract ]


182. Lee YR, Chen CH, Hsiao KJ.  Systematic search for variation in the human catechol-O-methyltransferase gene and Association study with schizophrenia.  12th Jonint Annual Conference of Biomedical Sciences, Taipei, 1997;261.   [ Abstract ]


183. Hsiao KJ, Liu TT, Lu SF, Wu SJ, Wu KF, Chiang SH.  Mutation characteriation of Chinese phenylketonuria caused by 6-pyruvoyl tetrahydropterin synthase deficiency.  7th Intl. Congreess of Inborn Errors of Metabolism, Vienna, 1997;45.   [ Abstract ]


184. Shiue HS, Chang CL, Chang PL, Wang SS, Lin AP, Wu JS, Hsiao KJ.  The pratical employment's experience in Internet for Chinese medical information.  Medical Informatics Symposium in Taiwan 1997;S2B-4. (in Chinese)   [ Abstract ]


185. Chen WY, Chen CH, Tsao T, Hsiao KJ.  Molecular Genetic Study of A Family with Nephrogenic Diabetes Insipidus.  13th Joint Annual Conference of Biomedical Sciences, Taipei, 1998;P48.   [ Abstract ]


186. Chiang PH, Hsiao KJ, Chuo YT, Liu DM.  Integration and Coordination of Biomedical Information: Implementation of Health Research Information Network (HINT).  Chin Med J(Taipei)1998;6(Suppl.):82. (in Chinese)   [ Abstract ]


187. Hsiao KJ, Liu TT, Chang YH, Chiou JY.  A gly170ser missense mutation and reduced RNA expression of dihydropteridine reductase gene detected in Chinese hyperphenylalaninemia.  5th European-Asian Workshop on Inborn Errors of metabolism, Warsaw, 1998;32.   [ Abstract ]


188. Hsiao KJ, Chiang SH, Wu SJ, Wu KF.  G6PD deficiency screening in Taiwan.  3rd Asia-Pacific Regional Meeting of the Intl Soc for Neonatal Screening, Chiangmai, 1998; 79.   [ Abstract ]


189. Wu SJ, Qiu DF, Hsiao KJ.  Application of electrospray tandem mass spectrometry in screening inherited disorders of amino acid metabolism.  14th Joint Annual Conference of Biomedical Sciences, Taipei, 1999; P35.   [ Abstract ]


190. Chang YS, Liu TT, Chiang SH, Wu KF, Hsiao KJ.  Identification of mutations causing 6-pyruvoyl-tetrahydropterin synthase deficiency in Chinese.  14th Joint Annual Conference of Biomedical Sciences, Taipei, 1999; P145.   [ Abstract ]


191. Hsiao KJ, Chang YH, Liu TT, Liu MY, Chiang SH, Wu KF.  Two novel mutations, 226C>TAND IVS3+1G>A, found in Chinese hyperphenylalaninemia caused by 6-pyruvoyl-tetrahydropterin synthase deficiency.  4th Meeting of the Intl Soc for Neonatal Screening, Stockholm, 1999;P31.   [ Abstract ]


192. Hsiao KJ, Wu SJ, Qiu DF.  Prenatal diagnosis of organic acid metabolic disorders with amniotic fluid by electrospray tandem mass spectrometry.  Clin Chem Lab Med 1999;37(suppl): S419.   [ Abstract ]


193. Hsiao KJ, Liu TT, Chang YH, Liu MY, Chiang SH, Wu KF.  Founder effect of 155A>G, 259C>T and 286G>A mutations in Chinese 6-pyruvoyl-tetrahydropterin synthase deficient hyperphenylalaninemia.  6th Asian-European Workshop on Inborn Errors of Metabolism, Korea, 1999;27-8.   [ Abstract ]


194. Lee SF, Liu TT, Wu SJ, Hsiao KJ.  Mutation analysis of mut gene in Chinese methylmalonic acidemia caused by methylmalonyl CoA mutase deficiency.  15th Joint Annual Conference of Biomedical Sciences, Taipei, 2000; P7.   [ Abstract ]


195. Liu MY, Chen CH, Wu SJ, Hsieh YT, Liu TT, Hsiao KJ.  Identification of three novel α-galactosidase a mutations (274G>T, 781G>A, and exon 2 deletion) in patients with fabry disease.  15th Joint Annual Conference of Biomedical Sciences, Taipei, 2000; P179.   [ Abstract ]


196. Liu HL, Liu TT, Wu SJ, Toung LC, Qu XB, Hsiao KJ.  Identification of a novel glucose-6-phosphate dehydrogenase (G6PD) 551C>T mutation in a Chinese family with G6PD deficiency.  15th Joint Annual Conference of Biomedical Sciences, Taipei, 2000; P180.   [ Abstract ]


197. Chen CY, Su JS, Chang HM, Chao KM, Hsiao KJ, Tsai SF.  The complete genome sequence of the human ADH gene family.  Human Genome Meeting 2000, Vancouver, 2000;85.   [ Abstract ]


198. Hsiao KJ, Chen CY, Chang HM, Wu KM, Chiang SH, Chung MY, Yang UC, Chou CK, Tsai SF.  Exploring chromosome 4q22-24 hepatocellular carcinoma tumor suppressor gene region by genome sequencing.  Human Genome Meeting 2000, Vancouver, 2000;87.   [ Abstract ]


199. Liu TT, Chang YH, Chiu YH, Chuang SH, Chen CY, Tsai SF, Hsiao KJ.  Isolation and the complete sequence of the human 6-pyruvoyl-tetrahydropterin synthase gene containing BAC clone 321H15.  Human Genome Meeting 2000, Vancouver, 2000;88.   [ Abstract ]


200. Tsai SF,Chang HM, Chen CY, Yeh SH, Lin CH, Yang UC, Chou CK, Hsiao KJ.  Exploring HCC tumor suppressor gene regions by genome sequencing.  Chinese Congress of Clinical Chemistry & Laboratory Medicine 2000, Hong Kong, 2000;45.   [ Abstract ]


201. Liu TT, Hsiao KJ.  Tetrahydrobiopterin deficient hyperphenylalaninemia in Chinese.  Chinese Congress of Clinical Chemistry & Laboratory Medicine 2000, Hong Kong, 2000;48.   [ Abstract ]


202. Okano Y, Asada M, Imamura T, Ohtake A, Murayama K, Choeh K, Hsiao KJ, Reichardt JKV, Yamano T.  Molecular characterization of galactokinase deficiency in Japanese.  J Inherit Metab Dis 2000;23(Suppl.1):159.   [ Abstract ]


203. Yu WM, Liu TT, Chang M, Zhou ZS, Shen M, Hsiao KJ.  The study of tetrahydrobiopterin deficiency in northern Chinese with hyperphenylalaninemia.  J Inherit Metab Dis 2000;23(Suppl.1):43.   [ Abstract ]


204. Chen CH, Tsai MT, Hung CC, Tsai CY, Liu MY, Chen YH, Hsiao KJ.  Systematic search of molecular variants of the human synapsin 3 gene and association study with schizophrenia.  Am J Hum Genet 2000;67(supp2):348.   [ Abstract ]


205. Qi Y, Liu TT, Chiang SH, Pan H, Zhang Y, Wang CX, Lu JJ, Bao XH, Wei YH, Hsiao KJ, Wu XR.  Five de novo polymorphisms found in Chinese mitochondrial genome.  1st Symposium of the Both Side of Taiwan Strait on Mitochondrial Medicine, Beijing, 2000;23-26.   [ Abstract ]


206. Lin CH, Liu MY, Chiang SH, Hsiao KJ.  Common 1034>A mutation of galactose-1-phosphate uridyl transferase (GALT) in Chinese GALT deficiency patients.  16th Joint Annual Conference of Biomedical Sciences, Taipei, 2001; P417.   [ Abstract ]


207. Yen PF, Liu MY, Liu TT, Hsiao KJ.  The complete genomic sequence of human DHPR gene and the mutation 697A>C detected in Chinese hyperphenylalaninemia (HPA).  16th Joint Annual Conference of Biomedical Sciences, Taipei, 2001; P417.   [ Abstract ]


208. Chiu YH, Liu TT, Liu MY, Hsiao KJ.  Molecular characterization of F40L mutation in Chinese 6-pyruvoyl-tetrahydropterin synthase deficient hyperphenylalaninemia.  16th Joint Annual Conference of Biomedical Sciences, Taipei, 2001; P417.   [ Abstract ]


209. Chiang SH, Wu KF, Hsiao KJ.  Quality Assurance Program for Neonatal Screening of G6PD Deficiency.  4th Asia Pacific Regional Meeting of the International Society for Neonatal Screening, Manila, 2001; PL-32.   [ Abstract ]


210. Liu TT, Chiang SH, Wu SJ, Hsiao KJ.  Screening differential diagnosis and prenatal disgnosis of hyperphenylalaninemia.  17th Joint Annual Conference of Biomedical Sciences, Taipei, 2002; S15.   [ Abstract ]


211. Liu YN, Liu TT, Wu SJ, Hsiao KJ.  Mutation analysis of PCCB gene in Chinese patients with propionic acidemia.  17th Joint Annual Conference of Biomedical Sciences, Taipei, 2002; P366.   [ Abstract ]


212. Lin CH, Liu TT, Hsiao KJ.  Assessment of electronic data collection from PubMed for the establishment of Chinese Gene Variation Database (CGVdb).  HGM2002, Shanghai, 2002;320.   [ Abstract ]

 
213. Liu TT, Yen PF, Lin CH, Chiang SH, Chen CY, Tsai SF, Hsiao KJ.  Isolation and the complete sequence of the human BAC clone 395N09: The complete genomic sequence of dihydropteridine reductase gene and its mutation in Chinese hyperphenylalaninemia.  HGM2002, Shanghai, 2002;321.   [ Abstract ]

 
214. Liu MY, Chen CH, Wu SJ, Hsieh YT, Liu TT, Hsiao KJ.  Identification and characterization of alpha-galactosidase a mutations in Chinese patients with Fabry disease.  J. Inherit Metab Dis 2002;25(Suppl.1):115.   [ Abstract ]


215. Liu TT, Lin CH, Liu MY, Chern SR, Chiang SH, Hsiao KJ.  Two novel mutations, 1034C>A and IVS9+1G>T, of galactose-1-phosphate uridyltransferase (GALT) gene identified in Chinese galactosemia.  8th Annual Asia-European Workshop of Inborn Error of Metabolism (AEWIEM), Vilnius.  Laboratorine Medicina 2002;(Suppl):S62.   [ Abstract ]


216. Kobayashi K, Okano Y, Nishi I, Lu YB, Choeh K, Hsiao KJ, Hwu WL, Yang YL, Saheki T.  Frequency of heterozygote with the mutated SLC25A13 gene in East Asia.  45th annual meeting of Japanese Inherited Metabolic Diseases Society and the 2nd annual symposium of Asian Inherited Metabolic Diseases Society, Kobe, 2002.   [ Abstract ]


217. Touma EH, Romstad A, Khneisser I, Hsiao KJ, Loiselet J, Dhondt JL.  Epidemiology of hyperphenylalaninemia (HPA) in Lebanon.  5th Meeting of the International Society for Neonatal Screening, Genova, 2002.   [ Abstract ]


218.
Hsiao KJ, Liu TT.  Gene diagnosis and therapy of neonatal inherited metabolic diseases.  Clin Chem Lab Med 2002;40(Suppl):S25.   [ Abstract ]

 
219.
Teng YT, Wu SJ, Lam WF, Liu TT, Hsiao KJ.  Identification of three methylmalonyl CoA mutase gene mutations (1106G>A, 1741C>T, IVS9-1G>A) in Chinese patients with methylmalonic acidemia.  18th Joint Annual Conference of Biomedical Sciences, Taipei, 2003;P440.


220.
Hsiao KJ, Lin CH, Fan JW, Tu CH, Chiang SH, Liu TT.  Development of the Chinese Gene Variation Database (CGVdb).  Japanese Journal of Inherited Metabolic Diseases 2003;19:249.   [ Abstract ]
   
221.
Liu TT, Chiu YH, Chang YC, Chiang SH, Wu SJ, Yu WM, Yang YL, Ye J, Okano Y, Lee DH, Choeh K, Hsiao KJ.  PTS Gene Mutations in Chinese 6-Pyruvoyl-tetrahydropterin Synthase Deficient Hyperphenylalaninemia and The Founder Effect of 155A>G, 259C>T, 286G>A Mutations in Chinese, Japanese and Korean populations.  Japanese Journal of Inherited Metabolic Diseases 2003;19:220.   [ Abstract ]

 
222. Hsiao KJ, Chiang SH. Developments of neonatal screening in Taiwan. Annual Meeting of Chinese Medical Association, Taipei, 2004.   [ Abstract ]
   
223. Hsiao KJ. Neonatal screening of glucose-6-phosphate dehydrogenase deficiency. 5th Asia Pacific Regional Meeting of International Society for Neonatal Screening, Shanghai, 2004;50-1.   [ Abstract ]
   
224. Liu TT, Chiu YH, Chang YC, Chiang SH, Wu SJ, Yu WM, Yang YL, Ye J, Okano Y, Lee DH, Choeh KC, Hsiao KJ. Tetrahydrobiopterin synthesis deficient hyperphenylalaninemia in Oriental. 5th Asia Pacific Regional Meeting of International Society for Neonatal Screening, Shanghai, 2004;84-5.   [ Abstract ]
   
225. Liu TT, Chiang SH, Wu SJ, Yen PF, Chang YH2, Chiou JY, Hsiao KJ. Dihydropteridine reductase deficient hyperphenylalaninemia in Chinese. 5th Asia Pacific Regional Meeting of International Society for Neonatal Screening, Shanghai, 2004;86.   [ Abstract ]
   
226. Liu TT, Teng YT, Lee SF, Lam WF, Liu MY, Wu SJ, Yang YL, Hsiao KJ. Screening, diagnosis and molecular genetics of methylmalonic acidemia in Chinese. 5th Asia Pacific Regional Meeting of International Society for Neonatal Screening, Shanghai, 2004;108.   [ Abstract ]
   
227. Chiang SH, Fan CH, Wu KF, Hsiao KJ. Quality assurance program for neonatal screening of glucose-6-phosphate dehydrogenase deficiency. 5th Asia Pacific Regional Meeting of International Society for Neonatal Screening, Shanghai, 2004;134.   [ Abstract ]
   
228. Yang YL, Qi Y, Zhao XT, Hsiao KJ, Shi CY, Qin J, Wu XR. Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. 5th Asia Pacific Regional Meeting of International Society for Neonatal Screening, Shanghai, 2004;81.   [ Abstract ]
   
229. Wang L, Yu WM, He C, Shen S, Liu TT, Hsiao KJ. Long-term outcome of 30 patients with 6-pyruvoyl-tetrahydropterin synthase deficiency. 5th Asia Pacific Regional Meeting of International Society for Neonatal Screening, Shanghai, 2004;87.   [ Abstract ]
   
230. Yang YL, QI Y, Shi CY, Liu TT, Hsiao KJ, Gu Q, Song JQ, Sun F, Qian N, Zhang ZX, Lin Q, Qin J, Wu XR. Clinical and biochemical study for the diagnosis, treatment and prenatal diagnosis of tetrahydrobiopterin deficiency due to 6-pyruvoyl tetrahydropterin synthase deficiency. 5th Asia Pacific Regional Meeting of International Society for Neonatal Screening, Shanghai, 2004;178-9.   [ Abstract ]
   
231. Hsiao KJ, Chiang SH, Liu TT. Developments of neonatal screening in Taiwan. Bratisl Lek Listy 2004;105:325-6.   [ Abstract ]
   
232. Kobayashi K, Lu YB, Ushikai M, Li MX, Hsiao KJ, Yang Y, Lee DH, Saheki T. Population analysis in East Asia of twelve SLC25A13 mutations found in Japanese patients with Citrin deficiency (CTLN2 and NICCD). Bratisl Lek Listy 2004;105:328.   [ Abstract ]
   
233. Liu MY, Liu YN, Wu SJ, Liu TT, Hsiao KJ. Identification of the PCCA and PCCB gene mutations in Chinese propionic acidemia patients. Bratisl Lek Listy 2004;105:331.   [ Abstract ]
   
234. Liu TT, Teng YT, Lee SF, Lam WF, Liu MY, Wu SJ, Hsiao KJ. Methylmalonyl CoA mutase gene mutations in Chinese methylmalonic acidemia. Bratisl Lek Listy 2004;105:331.   [ Abstract ]
   
235. Hsiao KJ, Chiang SH. Developments of Neonatal Screening in Taiwan. International Conference on Genetic Medicine and Promoting Healthcare for Rare Disorder, Taipei, 2005;255-8.   [ Abstract ]
   
236. Liu MY, Chiang SH, Yang YL, Hsiao KJ, Liu TT. Identification of MMACHC gene mutations in northern Chinese cblC patients with combined methylmalonic acidemia and homocystinuria. J Inherit Metab Dis 2006;29(Suppl 1):103.   [ Abstract ]
   
237. Wang L, Yu WM, He C, Li XW, Chang M, Shen M, Shen S, Liu TT, Hsiao KJ. The difference of seizure between patients with tetrahydropterin (BH4) deficiency and phenylketonuria (PKU). J Inherit Metab Dis 2006;29(Suppl 1):91.   [ Abstract ]
   
238. He C, Yu WM, Wang L, Li XW, Chang M, Shen M, Shen S, Liu TT, Hsiao KJ. The incidence of tetrahydropterin synthase deficiency in northern Chinese population and outcome of late-treated patients. J Inherit Metab Dis 2006;29(Suppl 1):92.   [ Abstract ]
   
239. Liu TT, Hsiao KJ, Chang YC, Chiang SH, Wu SJ, Niu DM, Yu WM, Yang YL, Ye J, Jiang JH. Hyperphenylalaninemia caused by 6-pyruvoyltetrahydropterin synthase deficiency in Chinese population. Tetrahydrobiopterin and Alternative Treatment in PKU, Cardiovascular Diseases, and Diabetes, Sendai, Japan, 2006.   [ Abstract ]
   
240. Niu DM, Liu KM, Lee NC, Liu TT, Cheng LY, Huang JY, Hsiao KJ. Long-term follow-up of Taiwan Chinese patients who received early treatment for 6-pyruvoyl-tetrahydropterin synthase deficiency. Tetrahydrobiopterin and Alternative Treatment in PKU, Cardiovascular Diseases, and Diabetes, Sendai, Japan, 2006.   [ Abstract ]
   
241. Hsiao KJ. Neonatal Screening of Glucose-6-Phosphate Dehydrogenase Deficiency. 2nd Congress of Asian Society for Pediatric Research, Yokohama, 2006:74. [ Abstract ]
   
242. Chiang SH, Hsiao KJ. Quality assurance program for neonatal screening of G6PD deficiency. 6th Asia Pacific Regional Meeting of International Society for Neonatal Screening, Singapore. Paediatr Child Adolesc Health 2007;47(Suppl.1):27.   [ Abstract ]
   
243. Niu DM, Liu KM, Cheng LY, Lee NC, Liu TT, Hsiao KJ, Liou PC. Long-term followup of Taiwan Chinese patients who received early treatment for 6-pyruvoyl-tetrahydrobiopterin synthase deficiency. J Inhert Metab Dis 2007;30(Suppl.1):18.   [ Abstract ]
   
244. Liu TT, Hsiao KJ, Chiang SH, Fang YL, Chang YC, Niu DM. Short/branched-chain acyl-CoA dehydrogenase deficiency in a Taiwanese infant identified by MS/MS newborn screening. J Inhert Metab Dis 2007;30(Suppl.1):43.   [ Abstract ]
   
245. Liu TT, Liu MY, Fang YL, Chang YC, Chiang SH, Niu DM, Hsiao KJ. Mutation identification for Taiwanese patients with isolated methylmalonic acidemia. J Inherit Metab Dis 2008;31(Suppl 1): 22.   [ Abstract ]
   
246. Liu TT, Hsiao KJ. Tetrahydrobiopterin deficient phenylketonuria in Chinese. Shanghai International Pediatric Elites Forum 2008, Branch Forum on Pediatric Endocrinology and Genetic Metabolism. Shanghai, 2008; 36-7 [ Abstract ]
   
247. Liu MY, Chang YC, Chiang SH, Lin SP, Jong YJ, Hsiao KJ, Liu TT. Mutation analysis of genes responsible for B12-responsive methylmalonic aciduria in Taiwanese patients. 24th Joint Annual Conference of Biomedical Sciences, Taipei, 2009; P114.   [ Abstract ]
   
248. Liu TT, Chang YC, Fang YL, Chiang SH, Hsiao KJ. Tetrahydrobiopterin Synthesis Deficient Hyperphenylalaninemia in Oriental. Japanese J Inherit Metab Dis 2010; 26(Suppl):80. [ Abstract ]
   
249. Hsiao KJ. Quality assurance program for neonatal screening of glucose-6-phosphate dehydrogenase deficiency. 7th Asia Pacific Regional Meeting of International Society for Neonatal Screening, Bali. Paediatrica Indonesiana 2010;50(Suppl 5):28. [ Abstract ]
   
250. Liu TT, Chang YC, Fang YL, Chiang SH, Hsiao KJ. Tetrahydrobiopterin synthesis deficient hyperphenylalaninemia in East Asian Populations. 9th Asia Pacific Conference on Human Genetics, Hong Kong, 2010; 40-1. [ Abstract ]
   
251. Chiu YH, Liu TT, Chang YC, Fang YL, Chiang SH, Hsiao KJ. Tetrahydrobiopterin synthesis deficient hyperphenylalaninemia in Chinese. 10th Chinese Laboratory Medicine Conference, Taipei, 2011; 50. [ Abstract ]
   
252. Hsiao KJ. Mutation profile of methylmalonic aciduria in Chinese populations. 2nd Asian Congress for Inherited Metabolic Diseases, Seoul, 2012; 54. [ Abstract ]
   
253. Chiang SH, Fan ML, Shiau YS, Hsiao KJ. Quality Assurance Program for Neonatal Screening of glucose-6-phosphate dehydrogenase deficiency. 2nd Asian Congress for Inherited Metabolic Diseases, Seoul, 2012; 95. [ Abstract ]
   
254. Chiu YH, Chang YC, Hsiao KJ, Liu TT. Pathogenetic mechanisms of PTS mutations associated with mild clinical phenotype. 2nd Asian Congress for Inherited Metabolic Diseases, Seoul, 2012; 106. [ Abstract ]
   
255. Liu MY, Chang YC, Fan YL, Chao MC, Hsiao KJ, Liu TT. A large genomic deletion detected by SNP array in one methylmalonic aciduria family. 2nd Asian Congress for Inherited Metabolic Diseases, Seoul, 2012; 116. [ Abstract ]
   
256. Liu TT, Fan YL, Chiu YH, Chang YC, Hsiao KJ. Determination of propionyl-CoA carboxylase activity in human lymphocytes by high performance liquid chromatography. 2nd Asian Congress for Inherited Metabolic Diseases, Seoul, 2012;117. [ Abstract ]
   
257. Hsiao KJ. Neonatal Screening of Glucose-6-Phosphate Dehydrogenase Deficiency in Asia. 10th Newborn Screening Convention, Moving on: Expanded Newborn Screening for Filipino Newborns, Manila, 2012; 34. [ Abstract ]
   
258. Hsiao KJ. Developmental Strategy and Results of Regional Newborn Hearing Screening Program in Taipei. 2012 IALP Taiwan Composium, Taichung, 2012; 279-80. (in Chinese) [ Abstract ]
   
259. Hsiao KJ. Mutation Profile of Methylmalonic Aciduria in Chinese Populations. 5th National Newborn Screening Conference, Changsha, 2012; 31-4. (in Chinese) [ Abstract ]
   
260. Chiang SH, Shiau YS, Lai JY, Hsiao KJ. Developmental Strategy and Results of Newborn Hearing Screening Program in Taipei Area. 5th National Newborn Screening Conference, Changsha, 2012; 54-6. (in Chinese) [ Abstract ]
   
261. Fan ML, Chiang SH, Hsiao KJ. Quality Assurance Program for Neonatal G6PD Screening. 5th National Newborn Screening Conference, Changsha, 2012;57-9. (in Chinese) [ Abstract ]
   
262. Hsiao KJ. Prevention and Policy Development of Genetic and Rare Diseases in Taiwan. 2nd Capital (International) Forum on Clinical Translational Medicine in Genetic Diseases, Beijing, 2013. (in Chinese) [ PDF ]
   
263. Hsiao KJ. The Development of Newborn Screening for Critical Congenital Heart Disease in Taipei. 6th National Newborn Screening Conference, HuangShan, 2014;33-4. (in Chinese) [ Abstract ]
   
264. Chiu YH, Liu YN, Fan YL, Liu TT, Hsiao KJ. A Practical Enzymatic Assay for Determination of Propionyl-CoA Carboxylase Activity Using High-Performance Liquid Chromatography. J Inherit Metab Dis 2014;37(Suppl 1):S47-8.   [ Abstract ] [ Poster ]
   
265. Fan ML, Shiau YS, Chiang SH, Hsiao KJ. Quality Assurance Program for Neonatal Screening of Glucose-6-Phosphate Dehydrogenase Deficiency. EQALM Symposium 2014, Toulouse, 2014:30-1.   [ Abstract ] [ Poster ]
   
266. Chiu YH, Liu MY, Liu YN, Hsiao KJ, Liu TT. The Advantage of Cultured Lymphocytes in Activity Assays for Propionyl-CoA Carboxylase and Methylmalonyl-CoA Mutase. 4th Asian Congress for Inherited Metabolic Diseases, Taipei, 2015;PI-03.   [ Abstract ] [ Poster ]
   
267. Fan ML, Chiang SH, Jomento CM, Padilla CD, Hsiao KJ. External Quality Assurance Program for Neonatal Screening of Glucose-6-Phosphate Dehydrogenase Deficiency. 4th Asian Congress for Inherited Metabolic Diseases, Taipei, 2015;PL-03.   [ Abstract ] [ Poster ]
   
268. Chiu YH, Liu YN, Chang YC, Liu TT, Hsiao KJ. Identification of G6PD Common Mutations Using a Multiplex Primer Extension-Based Method. J Inherit Metab Dis 2015;38(Suppl 1):S79-80. [ Abstract ] [ Poster ]
   
269. Hsiao KJ. G6PD Deficiency Screening: External Quality Assurance Program Issue. 9th Asia-Pacific Regional Meeting of the International Society for Neonatal Screening, Penang, 2015;37-8. [ Abstract ]
   
270. Chiang SH, Shiau YS, Ho HC, Liu YL, Chung YF, Tsao PC, Hwang B, Hsiao KJ. Development of Newborn Screening for Critical Congenital Heart Diseases in Taipei. 9th Asia-Pacific Regional Meeting of the International Society for Neonatal Screening, Penang, 2015;P08. [ Abstract ] [ Poster ]
   
271. Fan ML, Shiau YS, Chiang SH, Hsiao KJ. Internal Quality Control Program for Neonatal Screening of Glucose-6-Phosphate Dehydrogenase Deficiency. 9th Asia-Pacific Regional Meeting of the International Society for Neonatal Screening, Penang, 2015;P09. [ Abstract ] [ Poster ]
   
272. Hsiao KJ, Yeh HL, Shiau YS, Tsao PC, Chiang SH, Chiang PH. Long-Term Outcome of Newborn G6pd Screening Program in Taiwan. ISNS 9th International Symposium, Hague. Int J Neonatal Screen 2016; 2: 5, 20-1. DOI:10.3390/ijns2030005 [ Abstract ]
   
273. Chiang SH, Shiau YS, Shen Y, Yu Y, Ho HC, Liu L, Wu YR, Chen S, Xiao-Qing Liu XQ, Hsiao KJ. Newborn Screening for Critical Congenital Heart Diseases (CCHD) in a Remote County of Shanghai, China. ISNS 9th International Symposium, Hague. Int J Neonatal Screen 2016; 2: 5, 55. DOI:10.3390/ijns2030005 [ Abstract ] [ Poster ]
   
274. Fan ML, Shiau YS, Jomento C, Chiang SH, Padilla C, Hsiao KJ. External Quality Assurance Program for Neonatal Screening of Glucose-6-Phosphate Dehydrogenase Deficiency. ISNS 9th International Symposium, Hague. Int J Neonatal Screen 2016; 2: 5, 70-1. DOI:10.3390/ijns2030005 [ Abstract ] [ Poster ]
   
275. Hsiao KJ. Newborn Screening for Lysosomal Storage Diseases - Taiwan Experience. 7th National Newborn Screening Conference, Taiyuan, 2016;69-70. (in Chinese) [ Abstract ]
   
276. Hsiao KJ, Tsao PC, Chiang PH. Long-Term Outcome of Newborn Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency Screening Program in Taiwan. 14th Asia-Pacific Federation for Clinical Biochemistry and Laboratory Medicine, Taipei, 2016; S16-1. [ Abstract ]
   
277. Hsiao KJ. Pompe Disease: Screening, Diagnosis and Treatment. 8th National Newborn Screening Conference, Shenzhen, 2018; 40-43. (in Chinese) [ Abstract ]
   
278. Chiang SH, Chiang PH, Tsao PC, Shiau YS, Hsiao KJ. Health Impacts on the Universal Newborn G6PD Screening in Taiwan. 8th National Newborn Screening Conference, Shenzhen, 2018; 77. (in Chinese) [ Abstract ]
   
279. Hsiao KJ, Yeh SL, Shiau YS, Tsao PC, Chiang SH, Chiang PH, Wang YW. Outcome of Newborn Glucose-6-Phosphate Dehydrogenase (G6PD) Screening Program in Taiwan. 26th International Conference on Health Promoting Hospitals & Health Services, Bologna. Clinical Health Promotion 2018;8(Suppl 1):207-8. [ Abstract ] [ Poster ]
   
280. Hsiao KJ. Prenatal Diagnosis of Inherited Metabolic Diseases. 5th Asian Congress of Inherited Metabolic Diseases, Wuhan, 2018; Symp. 5. [ Poster ]
   

 
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Updated Dec. 24, 2018 by K.-J.Hsiao 蕭 廣 仁 教 授   ( 臨床生化研究室