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學術著作

 

Jia-Woei Hou, MD, PhD 侯家瑋 (A) PUBLISHED PAPERS:

  1. Hou JW, Lee CY (1984): Sudden infant death syndrome. Modern Medicine 11:883-885.(中文)
  2. Hou JW, Chen SH, Hsieh FJ, Sheh JM, Chen CL (1988): Congenital cystic adenomatoid malformation of the lung: report of a case. J Formosan Med Assoc (JFMA) 87:832-835.
  3. Wang PJ, Tzen QT, Hou JW, Lin MY, Wang TR, Shen YZ, Lee CY (1988): Metachromatic leukodystrophy: report of four cases. Acta Paediatr Sin 29:403-408.
  4. Hou JW, Chang MH, Wu MH, Lee CY (1989): Kawasaki disease complicated by gallbladder hydrops mimicking acute abdomen: a report of three cases.? Acta Paediatr Sin 30:52-60.
  5. Hou JW, Wang TR (1989): Mortality and survival in Down syndrome in Taiwan. Acta Paediatr Sin 30:172-179.
  6. Hou JW, Wang PJ, Lin MY, Shen YZ (1989): Complex partial status epilepticus: report of one case. Acta Paediatr Sin 30:254-260.
  7. Hou JW, Liu HC, Tso KI, Li YH (1989): Idiopathic spontaneous focal intestinal perforation in prematurity: report of three cases. Acta Paediatr Sin 30:326-332.
  8. Hou JW, Teng RZ, Lee CY (1989): Salmonella meningitis complicated with brain abscess and purpura fulminans: a case report.? Acta Paediatr Sin 30:408-413.
  9. Wang TR, Hou JW, Tsai HM (1990): Restriction fragment length polymorphisms of the ornithine transcarmylase locus in normal Chinese. Acta Paediatr Sin 31:221-225.
  10. Hou JW, Wang TR (1990): Isovaleric acidemia: report of a case. Acta Paediatr Sin 31:262-265.
  11. Wang TR, Hou JW, Tsai HM (1990): Restriction fragment length polymorphisms at the methylmalonyl-CoA mutase locus in Normal Chinese. Acta Paediatr Sin 31:275-279.
  12. Lin DT, Hou JW, Lin KH, et al (1990): Clinical observation of Wilms' tumor. Acta Paediatr Sin 31:299-305.
  13. Hou JW, Wang PJ (1990): Basal ganglia lesions after carbon monoxide intoxication. JFMA CME Series 2(4):502-507. (中文)
  14. Hou JW, Lee JS, Tsai WY (1990): The common endocrine disorders in children and management of the emergencies. JFMA CME Series 2(5):650-653. (中文)
  15. Hou JW, Wu MH (1990): Infective endocarditis complicated with systemic embolization and intracranial hemorrhage. JFMA CME Series 2(5):661-665. (中文)
  16. Lin SJ, Hou JW, Wang TR, et al (1991): Anthropometric study on Down syndrome in Taiwan. Acta Paediatr Sin 32:158-164. (中文)
  17. Hou JW, Lee ML, Wang TR (1992): Identification of sex chromosomal abnormalities by fluorescence in situ hybridization. Acta Paediatr Sin 33:332-340.
  18. Hou JW, Lin YJ, Wang PJ, Wang TR (1992): Symptomatic atlantoaxial subluxation and syringomyelia in Down syndrome: a case report. Acta Paediatr Sin 33:425-429.
  19. Hou JW, Wang TR, Lee ML (1992): Mosaic ring chromosome 13 analyzed by fluorescence in situ hybridization: report of a case. J Formosan Med Assoc 91:1108-1111.
  20. Hou JW, Wang TR, Lee ML (1993): Identification of marker chromosomes by fluorescence in situ hybridization and non-fluorescence enzymatic precipitation. J Genet Mol Biol 4:6-12.
  21. Hou JW, Tsai WY, Wang TR (1993): Cardiovascular disorders in Turner syndrome and its correlation to karyotype. J Formosan Med Assoc 92:188-189.
  22. Wang TR, Hwu WL, Hou JW, et al (1993): Fragile-X mental retardation - a combination of cytogenetic and molecular approaches, with greater emphasis on DNA analysis. Acta Paediatr Sin 34:120-127.
  23. Wang TR, Hwu WL, Hou JW, et al (1993): Y-specific polymerase chain reaction for the interpretation of a chromosome marker. Acta Paediatr Sin 34:128-132.
  24. Hou JW, Wang PJ, Wang TR (1994): Tuberous sclerosis in children. Acta Paediatr Sin 35:347-353.
  25. Hou JW, Liu CH, Wang TR (1994): Molecular cytogenetic studies of children with marker chromosomes. J Formos Med Assoc 93:205-209.
  26. Hou JW, Wu MH, lin KH, Lue HC (1994): Prognostic significance of left ventricular diastolic indexes in β-thalassemia major. Arch Pediatr Adolesc Med (fomerly AJDC) 148:862-866.
  27. Hou JW, Wang TR (1994): Cytogenetic investigations in trisomy 21 with reciprocal 4/9 translocation. J Formos Med Assoc 93:958-960.
  28. Hou JW, Wang TR (1994) Pyridoxine-responsive homocystinuria with ruptured sinus of Valsalva in a Chinese boy. J Inher Metab Dis 17:759.
  29. Hou JW, Wang TR (1995): Transient tyrosinemia presenting as lactic acidosis in a term baby. Acta Paediatr Sin 36:217-220.
  30. Hou JW, Wang TR (1995): Molecular cytogenetic studies of duplication 9q32aq34.3 inserted into 9q13. Clin Genet 48:148-150.
  31. Hou JW, Wang TR (1995): Methylmalonic aciduria and urolithiasis in a Chinese boy with untreated phenylketonuria. J Inher Metab Dis 18:79-80.
  32. Lee T, Hou JW, Tsou Yau KI, Wang TR (1995): Trisomy 18 in a patient with CHARGE association. J Formos Med Assoc 94:60-62.
  33. Hou JW, Wang TR (1995): Idiopathic juvenile osteoporosis: five-year case follow-up. J Formos Med Assoc 94:277-80.
  34. Hou JW, Wang TR (1995): Microdeletion of chromosomal region 22q11 in DiGeorge syndrome: report of a case. J Formos Med Assoc 94:200-202.
  35. Hou JW, Wang TR (1995): Clinical variability in neonatal progeroid syndrome.? Am J Med Gent 58:195-196.
  36. Hou JW, Wang TR (1995): Galloway-Mowat syndrome in Taiwan. Am J Med Genet 58:245-248.
  37. Hou JW, Wang TR (1995): 3-Methylglutaconic aciduria presenting as Reye syndrome in a Chinese boy. J Inher Metab Dis 18: 645-646.
  38. Hou JW, Wang TR, Tunnessen WW (1995): Cleidocranial dysplasia: picture of the month. Arch Dis Child Adolesc 149:1391-1392.
  39. Hou JW, Wang TR, Tunnessen WW (1996): Glycogen storage disease, type Ia (von Gierke Disease) complicated by gouty arthritis and xanthomatosis: picture of the month. Arch Dis Child Adolesc 150:219-220.
  40. Hou JW, Wang TR (1996): Amino acid and DNA analyses in a family with ornithine transcarbamylase deficiency. J Formos Med Assoc 95(2):144-147.
  41. Hou JW, Wang TR (1996): Double aneuploidy with Down-Klinefelter syndrome. J Formos Med Assoc 95(4):350-352.
  42. Hou JW, Wang TR (1996): Prader-Willi syndrome: clinical and molecular cytogenetic investigations. J Formos Med Assoc 95(6): 474-479.
  43. Hou JW, Wang TR (1996): Chromosomal rearrangements detected by FISH and G-banding. J Formos Med Assoc 95(9): 686-691.
  44. Hou JW, Wang TR (1996): Amelia, dextrocardia, asplenia, and congenital short bowel in deleted ring chromosome 4. J Med Genet 33:879-881.
  45. Hou JW, Chou SP, Wang TR (1996): Metabolic function and liver histopathology in Reye-like illnesses. Acta Paediatrica 85:1053-1057.
  46. Gau SF, Soong WT, Liu HM, Hou JW, et al (1996): Kleine-Levin syndrome in a boy with Prader-Willi syndrome. Sleep 19:13-17.
  47. 侯家瑋 (1996): 先天畸形兒知多少? 健康世界 121:111-117. (中文)
  48. Lu CY, Hou JW, Wang PJ, Chiu HH, Wang TR (1996): Homocystinuria presenting as fatal common carotid artery occlusion. Pediatr Neurol 15:159-162.
  49. Chuang SC, Hwu WL, Wu CC, Hou JW, Wang TR (1996): Diagnosis of mucopolysaccharidosis type IIIB. Acta Paediatr Sin 37:320-323.
  50. Hou JW (1997): 人類染色體區域15q11-q13之遺傳變異及其基因型-表現型關聯 (國立臺灣大學博士論文)(民國86年7月通過)
  51. Hou JW, Wang TR (1997): Primed in situ (PRINS) labeling for rapid detection of numerical and structural chromosome anomalies. J Formos Med Assoc 96(1): 46-50.
  52. Hou JW, Wang JK, Wang TR (1997): Microdeletion of chromosomal region 7q11.23 in Williams syndrome. J Formos Med Assoc 96(2): 137-140.
  53. Hou JW, Wang PJ, Wang TR (1997): Angelman syndrome assessed by neurological and molecular cytogenetic investigations. Pediatr Neurol 16(1):17-22.
  54. Lu FL, *Hou JW, Tsai WS, Teng RJ, Tsou Yau KI, Wang TR (1997): Tricho-rhino-phalangeal syndrome type II associated with epiglottic aplasia and congenital nephrotic syndrome. J Formos Med Assoc 96(3): 217-221(corresponding author).
  55. Hou JW, Wang TR (1997): Differentiation of Fanconi anemia from aplastic anemia by chromosomal breakage test. Acta Paediatr Sin 38:121-126.
  56. Jeng SF, Liao HF, Lai JS, Hou JW (1997): Optimization of walking in children. Med Sci Sports Exerc 29:370-376.
  57. Hou JW, Wang JK, Tsai WY, Chou CC, Wang TR (1997): CATCH 22: deletion of locus 22q11 in velocardiofacial syndrome, DiGeorge anomaly, and nonsyndromic conotruncal defects. J Formos Med Assoc 96(6):419-423.
  58. Hsu HL, Hsiao PH, *Hou JW, Tsai WY, Wang TR (1997): Partial DiGeorge anomaly associated with 10p deletion. J Formos Med Assoc 96(12):996-999 (corresponding author)
  59. Hou JW, Wang TR (1998): Unusual features in children with inv dup(15) supernumerary marker: a study of genotype-phenotype correlation in Taiwan. J Eur Pediatr 157:122-127.
  60. Lin JH, *Hou JW, Lin KH, Wang TR (1998): Jacobsen syndrome with myelodysplastic changes of hemopoietic cells in distal 11q. Am J Med Genet 75:341-344 (corresponding author).
  61. Hou JW, Wang TR, Chuang SM (1998): An epidemiological and etiological study of children with intellectual disability in Taiwan. J Intell Disabil Research 42:137-143.
  62. Lu CY, Teng RJ, Hou JW, Cheng TJ (1998): Bifid tongue associated with midline cleft palate, mandible, cervical vertebral and linea alba. Eur J Pediatr 157:86.
  63. 侯家瑋(1998):親子鑑定之原理及應用。台北市醫師公會會刊。42(10):25-28.(中文)
  64. Hou JW, Wang JK, Wang TR (1998): FISH analysis in both classical and atypical cases of Williams-Beuren syndrome. Acta Paediatr Sin 39:398-403.
  65. Hou JW, Wang TR(1999):Extreme Poland anomaly associated with congenital diaphragmatic pernia. Eur J Pediatr 158: 433-434.
  66. Lin SC, Hu FR, Hou JW, et al. (1999): Corneal opacity and congenital glaucoma associated with massive heparan sulfaturia. Acta Paediatr Sin 40:49-52.
  67. Hou JW, Tsai WY, Wang TR (1999): Detection of KAL-1 gene deletion with fluorescence in situ hybridization. J Formos Med Assoc 98: 448-451.
  68. Hsieh YC, *Hou JW (1999): Oral-facial-digital syndrome with Y-shaped fourth metacarpals and endocardial cushion defect. Am J Med Genet 86; 278-281. (corresponding author).
  69. 侯家瑋(1999): 黏寶寶--談黏多醣症的成因, 症狀與治療. 新聞深度分析簡訊 66: 1-8.(中文)
  70. Hou JW, Wang TR (1999): Study of human Y chromosome polymorphism in Taiwan. Acta Paediatr Tw 40: 302-304.
  71. Hou JW (1999): Developmental biology: frontiers for clinical genetics. Acta Paediatr Tw 40: 367-368.
  72. Hou JW, Tunnessen WW (2000): Costello syndrome: picture of the month. Arch Dis Child Adolesc. 154:631-632.
  73. Su PH, Hou JW, Hwu WL, et al. (2000): Congenital contractural arachnodactyly (Beals syndrome). Acta Paediatr Tw 41:59-62.
  74. Chang PF, Huang SF, Hou JW, et al.(2000): Metabolic disorders mimicking Reye's syndrome. J Formos Med Assoc 99:295-299.
  75. 侯家瑋(2000): 迎接21世紀- 基因治療時代的來臨. 長庚醫訊 21:29-32.
  76. 侯家瑋(2000): 普拉德 - 威利二氏症之臨床表現及基因診斷. 臺灣醫界 43:13-16
  77. .Hou JW(2000): Your Diagnosis: A newborn with diffuse skin rashes and an occipital mass: Klippel-Trenaunay-Weber syndrome. Acta Paediatr Tw 41:237-238.
  78. Chang KW, Hou JW, Lin SJ, et al.(2000): Alstrom syndrome with hepatic dysfunction: report of one case. Acta Paediatr Tw 41:270-272.
  79. Chang P, Tsau YK, Tasi WY, Tsai WS, Hou JW, et al.(2000): Renal malformation in children with Turner's syndrome. J Formos Med Assoc 99:796-798.
  80. Chang P, Tsai WY, Hou JW, et al. (2000): Autoimmune thyroiditis in children with Turner syndrome. J Formos Med Assoc 99: 823-826.
  81. Hou JW (2001): Your Diagnosis: An infant with multiple joint contractures: Freeman-Sheldon syndrome. Acta Paediatr Tw 42:67-68.
  82. 侯家瑋,王作仁(2001): X染色體脆折症之臨床及分子生物學研究. 臺灣醫界 44(11):8-12.
  83. Hou JW (2002): Double partial monosomies (10p- and Xp-) in a female with choanal atresia. Chang Gung Med J 25:260-265.
  84. Hou JW (2002): Primary systemic carnitine deficiency presenting with recurrent Reye-like syndrome and dilated cardiomyopathy. Chang Gung Med J 25: 832- 837.
  85. Chen MH, Chen KS, Hou JW, et al (2002): Coexistence of autosomal dominant polycystic kidney disease and neurofibromatosis: report of a family. Am J Nephrol 22:376-380.
  86. Hou JW, Lee TH (2002): Genetic factors in young patients with stroke in Taiwan. Am J Hum Genet 71 (suppl): 475.
  87. Hou JW (2002): Your Diagnosis: A boy with long-lasting fever and poor hair growth: Ectodermal dysplasia. Acta Paediatr Tw 43:181-182.
  88. Hou JW (2003): Smith-Magenis syndrome: report of one case. Acta Paediatr Tw 44:161-164.
  89. Hou JW, Mai CF (2003): Restrictive dermopathy in two sisters. Chang Gung Med J. 26:510-514.
  90. Hou JW (2003): Hallermann-Streiff syndrome associated with small cerebellum, endocrinopathy and increased chromosomal breakage. Acta Paediatr. 92 (7):869-871.
  91. Hou JW, Wang TR (2003): A 20-year follow-up of a male patient with type Ia glycogen storage disease. Chang Gung Med J. 26:283-287.
  92. Hou JW (2003): Del (9p) syndrome: report of four cases. Acta Paediatr Tw 44:50-53.
  93. Yu MC, Hou JW (2003): Pseudohypoaldosteronism presenting as acute gastroenteritis: report of one case. Acta Paediatr Tw 44:44-46. (corresponding author)
  94. Su CW, Lin KL, Hou JW, et al (2003): Spontaneous recovery from a medulloblastoma by a female with Gorlin-Goltz syndrome. Pediatr Neurol 28:231-234.
  95. Hou JW (2003): Supernumerary chromosome marker der(22)t(11;22) resulting from a maternal balanced translocation. Chang Gung Med J. 26:48-52.
  96. Hou JW (2003): A boy with hepatomegaly, muscle hypertrophy and absence of adipose tissue. Berardinelli-Seip syndrome. Acta Paediatr Tw 44:189-190.
  97. Hou JW (2003): Wolf-Hirschhorn syndrome: clinical and molecular cytogenetic studies in Taiwan. Am J Hum Genet 73 (suppl): 273.
  98. Hou JW (2003): Chromosomal 10q26 trisomy resulting from paternal t(9;10)(pter;q26.1). J Formos Med Assoc 102:887-892.
  99. Hou JW (2004): Biotin-responsive multiple carboxylase deficiency presenting as diabetic ketoacidosis. Chang Gung Med J. 27:129-133.
  100. Hou JW (2004): Variable expressivity in a family with Kabuki make-up (Niikawa-Kuroki) syndrome. Chang Gung Med J. 27:307-311.
  101. Hou JW (2004): Your Diagnosis: A female infant with hypotonia and cardiomegaly: Pompe disease. Acta Paediatr Tw 45:1-3.
  102. Hou JW (2004): Mosaic ring chromosome 14 and monosomy 14 presenting with growth retardation, epilepsy, and blepharophimosis. Chang Gung Med J. 27:373-378.
  103. Teng YT, Su WJ, Hou JW, Huang SF (2004): Infantile-onset glycogen storage disease type II: report of a case with genetic diagnosis and pathological findings. Chang Gung Med J 27:379-384.
  104. Hou JW (2004): Partial chromosomal 11q trisomy as an unbalanced result of t(11;13)(q23.1;q34)mat in two sisters. J Formos Med Assoc 103:239-243.
  105. Hou JW (2004): 49, XXXXY syndrome. Chang Gung Med J 27:551-554.
  106. Hou JW (2004): Congenital arhinia with de novo reciprocal translocation, t(3;12)(q13.2;p11.2). Am J Med Genet 130A(2):200-203.
  107. Hou JW (2004): Bardet-Biedl syndrome initially presenting as McKusick-Kaufman syndrome. J Formos Med Assoc 103(8):629-632.
  108. Hou JW (2004): Fetal warfarin syndrome: case report. Chang Gung Med J. 27:691-695.
  109. Hou JW (2004): Inherited tandem duplication of the X chromosome: dup(X)(q13.2-q21.2) in a family. Chang Gung Med J 27:685-690.
  110. Hou JW (2004): Long-term follow-up of Marshall-Smith syndrome: report of one case. Acta Paediatr Tw 45:232-235.
  111. Hou JW (2004): Cholelithiasis and pseudocholelithiasis in childhood.
    Acta Paediatr Tw 45:264.
  112. Wang PJ, Hou JW, Sue WC, Lee WT (2005): Electroclinical characteristics of seizures-comparing Prader-Willi syndrome with Angelman syndrome. Brain Dev 27:101-107.
  113. Hou JW, Huang SF (2005): Recurrent panniculitis associated with generalized lipodystrophy and growth hormone deficiency. J Formos Med Assoc 104: 518-521.
  114. Hou JW (2005): Rubinstein-Taybi syndrome: clinical and molecular cytogenetics studies. Acta Paediatr Tw 46: 143-148.
  115. Hou JW (2005): Detection of gene deletions in children with chondrodysplasia punctata, ichthyosis, Kallmann syndrome, and ocular albinism by FISH studies. Chang Gung Med J 28: 463-450.
  116. Hou JW (2005): Trisomy chromosome (22)(q13.1-qter) as a result of paternal inversion (22)(p11q13.1) proved using region-specific FISH probes. Chang Gung Med J 28: 657-661.
  117. Hou JW (2005): Hyperammonemia in neonates: a transient phenomenon or an early sign of inborn errors of metabolism? Acta Paediatr Tw 46:59-60.
  118. Miyake N, Shimokawa O, Harada N, Sosonkina N, Okubo A, Kawara H, Okamoto N, Ohashi H, Kurosawa K, Naritomi K, Kaname T, Nagai T, Shotelersuk V, Hou JW, Fukushima Y, Kondoh T, Matsumoto T, Shinoki T, Kato M, Tonoki H, Nomura M, Yoshiura KI, Kishino T, Ohta T, Niikawa N, Matsumoto N (2006): No detectable genomic aberrations by BAC array CGH in Kabuki make-up syndrome patients. Am J Med Genet A 140:291-293.
  119. Hou JW (2006): Progressive osseous heteroplasia controlled by intravenous administration of pamidronate. Am J Med Genet A 140(8):910-913.
  120. Jaing TH, Hou JW, Chen SH, Huang IA, Wang CJ, Lee WI.(2006): Successful unrelated mismatched cord blood transplantation in a child with malignant infantile osteopetrosis. Pediatr Transplant 10:629-631.
  121. Wang SM, Hou JW, Lin JL (2006): A retrospective epidemiologic and etiological study of metabolic disorders in children with cardiomyopathies. Acta Paediatr Tw 47: 83-87. (Corresponding author)
  122. Hou JW (2006): Chromosome 10q24.3-qter deletion associated with left-sided first branchial arch defect, diaphragmatic eventration, and duplicated renal pelvis. Am J Med Genet 140A:2241-2244.
  123. Hou JW (2006): Double aneuploidy: trisomy 18 and XXY in a boy. Chang Gung Med J 29 (4 Suppl): 6-12.
  124. Hou JW (2006): Atlantoaxial subluxation with recurrent consciousness disturbance in a boy of Lesch-Nyhan syndrome. Acta Paediatr 95:1500-1504.
  125. Chen RL, Hou JW, Chang PY, et al. (2007): Matched unrelated bone marrow transplantation without splenectomy for a child with Gaucher disease caused by homozygosity of the L444P mutation, who also suffered from schizencephaly. J Pediatr Hematolo/Oncol 29(1): 57-59.
  126. Sato D, Shimokawa O, Harada N, Olsen OE, Hou JW, et al. (2007): Congenital arhinia: Molecular-genetic analysis of five patients. Am J Med Genet 143A(6):546-552.
  127. 侯家瑋(2007): 生長激素於兒科疾病治療之新應用。台北市醫師公會會刊 (Journal of Taipei Medical Association)。51(6):42-46.(中文)
  128. Hsu HF, Hou JW (2007): Variable expressivity in Patau syndrome in not all related to trisomy 13 mosaicism. Am J Med Genet (Corresponding author) 143A(15):1739-1748.
  129. Huang JJ, Hou JW, TanYC, Chen KT, Lo LJ, Chen YR (2007): Van der Woude syndrome: Clinical presentation in 64 patients. Cleft Plate-Craniofac J 44(6): 649-652.
  130. Shaw SW, Chen CP, Cheng PJ, Wang TH, Hou JW, Lin CT, Chang SD, Hwa HL, Lin JL, Chao AS, Soong YK, Hsieh FJ (2008): Gene dosage change of TPTE and BAGE2 and breakpoint analysis in Robertsonian Down syndrome. J Hum Genet 53(2):136-143.
  131. Hou JW (2008): Rapidly progressive scoliosis after successful treatment for osteopenia in Costello syndrome. Am J Med Genet 2008; 146A(3):393-396.
  132. Jaing TH, Hsia SH, Chiu CH, Hou JW, Wang CJ, Chow R (2008): Successful unrelated cord blood transplantation in a girl with malignant infantile osteopetrosis. Chin Med J (Engl) 121(13):1245-1246.
  133. Chiang MC, Huang SF, Hsueh C, Lai MW, Hou JW (2008): Restrictive dermopathy: report of one case and the metabolic and post-mortem findings. Turk J Pediatr 50:492-494. (Corresponding author)
  134. Fang CY, Lee CH, Wu CC, Chang YT, Yu SL, Chou SP, Huang PT, Chen CL, Hou JW, Chen JY (2009): Recurrent chemical reactivation of EBV promotes genome instability and enhances tumor progression of nasopharyngeal carcinoma cells. J Cancer 124:2016-2025.
  135. Hou JW (2009): Natural course of neonatal progeroid syndrome. Pediatr Neonatol 50(3):102-109.
  136. Hou JW (2009): Changing demography and variable expressivity in autosomal trisomy syndromes. Pediatr Neonatol 50(4):133-134.
  137. Hou JW (2009): Amelioration of hypophosphatemic rickets and osteoporosis with pamidronate and growth hormone in Lowe syndrome. J Formos Med Assoc 108(9): 730-735.
  138. Chen CM, Chen CL, Hou JW, et al (2010): Developmental profiles and mentality in preschool children with Prader-Willi syndrome: a preliminary study. Chang Gung Med J 33(4):436-442.
  139. Feng WK, Hung KL, Hou JW (2010): Clinical analysis of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome. Fu-Jen J Med 8(2):115-122.
  140. Tsai MH, Hou JW, Yang CP, Yang PH, Chu SM, Hsu JF, Chiang MC, Huang HR (2011): Transient myeloproliferative disorder and GATA1 mutation in neonates with and without Down syndrome.Indian J Pediatr Feb 2. [Epub ahead of print]
  141. Hannibal MC, Buckingham KJ, Ng SB, Ming JE, Hou JW, et al (2011): Spectrum of MLL2 (ALR) mutations in 110 cases of Kabuki syndrome. Am J Med Genet Jun 10 [Epub ahead of print]

 

INTERNATIONAL CONFERENCE PAPERS:

  • Hou JW, Wu MH, Lue HC (1990): Left ventricular function in beta-thalassemia major by echocardiography. 5th International Symposium of the International College of Pediatrics, April 1-5, 1990. Taipei, Taiwan.
  • Hou JW, Wang TR, Tsai MH (1990): Study of the gene locus of human ornithine transcarbamylase by restriction fragment length polymorphism in normal Chinese. 5th International Symposium of the International College of Pediatrics, April 1-5, 1990, Taipei, Taiwan.
  • Lin SJ, Hu SC, Hsu SF, Hou JW, Chio PC, Chao MC, Wang TR (1990): Growth study in Chinese children with Down syndrome in Taiwan: 1 month to 18 years of age. 41st Annual Meeting of the American Society of Human Genetics, October 16-20, 1990, Cincinnati, USA.
  • Hyland KM, Wydner KL, Hou JW (1991): Use of in situ hybridization in determining the origin of a fragment in a Turner mosaic. 8th International Congress of Human genetics, October 6-11, 1991, Washington D.C., U.S.A.
  • Wang TR, Hwu WL, Hou JW (1992): Current status of detecting fragile-X syndrome using molecular biology techniques at the National Taiwan University Hospital. In: 1992 San Diego Conference on Nucleic acids: Genetic Recognition.
  • Hou JW (2001): Clinical and genetic criteria in Taiwan. 2nd Organizational Meeting for International Genetic Epidemiology of Oral Clefts, April 9&10, 2001, Singapore. (Invited Speaker)
  • Hou JW (2001): Neonatal progeroid disorders: more than one disease. 10th International Congress of Human Genetics, May 14-19, 2001, Vienna, Austria.
  • Hou JW, Lee TH (2002): Genetic factors in young patients with stroke in Taiwan. American Society of Human Genetics, 52nd Annual Meeting, Oct 15-19, 2002, Baltimore, USA. [Am J Hum Genet 71 (suppl): 475.]
  • Wang SM, Hou JW, Lin J (2002): Treatment experience of neonatal hyperammonemia. American Society of Human Genetics, 52nd Annual Meeting, Oct 15-19, 2002, Baltimore, USA. [Am J Hum Genet 71 (suppl): 412.]
  • Lin J, Wang S, Hou JW (2002): Evaluating clinical efficacy and safety of palmidronate in patients with osteogenesis imperfecta. American Society of Human Genetics, 52nd Annual Meeting, Oct 15-19, 2002, Baltimore, USA. [Am J Hum Genet 71 (suppl): 255.]
  • Hou JW (2003): No evidence of HESX1 mutation in five cases of septo-optic dysplasia with variable phenotype, including metabolic cardiomyopathy and further brain anomalies. European Human Genetics Conference 2003, May 3-6 Birmingham, England.
  • Hou JW (2003): Wolf-Hirschhorn syndrome: clinical and molecular cytogenetic studies in Taiwan. American Society of Human Genetics, 53rd Annual Meeting, Nov. 14-8, 2003, Los Angeles, USA. [Am J Hum Genet 73 (suppl): 273.]
  • Hou JW (2004): Growth hormone deficiency associated with chronic diseases. 15th Symposium on Growth Hormone and Endocrinology, Apr. 1-3, 2004, Malta.
  • Hou JW (2004): Issues and management of GHD in Taiwan. North Asia Paediatric Endocrinology Workshop, July 10-11, Guilin, China. (Invited Speaker)
  • Hou JW (2004): Effects of coenzyme Q10 and growth hormone on psychomotor in children with Prader-Willi syndrome. The 3rd Biennial Scientific Meeting Asia Pacific Paediatric Endocrine Society, Sept 24-26, Kobe, Japan
  • Hou JW (2004): American Society of Human Genetics, 54th Annual Meeting, Dec. 26-30, 2004, Toronto, Canada. [Am J Hum Genet 74 (suppl):]
  • Hou JW (2005): Long-term follow-up of patients with Kabuki syndrome in Taiwan. European Human Genetics Conference, May 7-10, 2005, Prague, Czech Republic.
  • Hou JW (2006): Clinical Approach to Carnitine Deficiency Disorders. 4th International Huaxia Congress of Endocrinology, Dec 15-18, 2006, Hong Kong. (Invited Speaker)
  • Hou JW (2007): MPS diseases. 10th Annual Asia LSD Symposium, Dec 9-12, 2007, Kuala Lumpur, Malaysia. (Invited Speaker)
  • Tato L, Chatelain P, Duk-Hee K, Bashnina E, Sultanova L, Hou JW, Olivier C, Saunders H, Clayton P, and the PREDICT investigators (2008): Baseline auxological and biochemical characteristics of prepubertal growth hormone deficient (GHD) versus Turner syndrome (TS) children in the PREDICT study. The Endocrine Society’s 90th Annual Meeting, June 15-18, 2008, San Francisco, USA.
  • Hou JW (2010): Maple syrup urine disease and infantile epilepsy. International Symposium on Epilepsy in Neurometabolic Diseases. The 13th Annual Meeting of Infantile Seizure Society. Mar 26-28, Taipei, Taiwan (Invited Speaker)
  • Feng WK, Hung KL, Hou JW (2010): Epilesies in MELAS syndrome. International Symposium on Epilepsy in Neurometabolic Diseases. The 13th Annual Meeting of Infantile Seizure Society. Mar 26-28, Taipei
  • Hou JW (2010): Identification and carrier-frequency detection of maple syrup urine disease in the aboriginal tribes of north Taiwan: different gene preference from Asian Society for Pediatric Research. Apr 15-18, Taipei

 


更新時間:2020/3/3