Publications 1998

  • Tamai S, Sato S, Kamimaki T, Ishi T, Sasaki G, Shimamura Y, Tsubota Y, Watanabe H, Matsuo N.: Linear growth in an adolescent girl of family dysfunction: Emotional deprivation and anorexia nervosa. Clin Pediatr Endocrinol (1998) 7:121-123
  • Kitanaka S, Takeyama K, Murayama A, Sato T, Okumura K, Nogami M, Hasegawa Y, Niimi T, Yanagisawa J, Tanaka T, Katoh S.: Inactivating mutations in the 25-hydroxyvitamin D (beta)3 1-hydroxylase gene in patients with pseudovitamin D deficiency ricket. New Engl J Med (1998) 340:653-660
  • Watanabe H: Child psychiatry training for pediatricians: Japanese perspectives in infant psychiatry. Psychiatry and Clinical Neurosciences 52 (1998) (Supplement): S285-S287
  • Anzai H, Kikuchi A, Kinoshita A, Nishikawa T: Recurrent annular erythema in juvenile chronic myelogenous leukaemia Brit J Dermatol (1998) 138:1058-1060
  • Burwinkel B, Amat L, Gray RG, Matsuo N, Muroya K, Narisawa K, Sokol RJ, Vilaseca MA, Kilimann MW.: Variability of biochemical and clinical phenotype in X-linked liver glycogenosis with mutations in the phosphorylase kinase PHKA2 gene. Hum Genet (1998) 102:423-9
  • Caviness VS Jr, Takahashi T.: La cytogenese neocorticale: le gradient proliferatif de l’epithelium pseudostratifie ventriculaire(PVE) et histogenese du cortex cerebral. Percentiel (1998) 3:5-10
  • Enosawa S, Suzuki S, Li XK, Okuyama T, Fujino M, Amemiya H: Higher efficiency of retrovirus transduction in the late stage of primary culture of hepatocytes from nontreated than from partially hepatectomized rat. Cell Transplant (1998) 7:413-416
  • Goseki-Sone, M., Orimo, H., Iimura, T., Takagi, Y., Watanabe, H., Taketa, K., Sato, S., Mayanagi, H., Shimada, T., Oida, S.: Hypophosphatasia: identification of five novel missense mutations (G507A, G705A, A748G, T1155C, G1320A) in the tissue-nonspecific alkaline phosphatase gene among Japanese patients. Hum Mutat Suppl (1998) 1:S263-267
  • Guioli S, Schmitt K, Critcher R, Bouzyk M, Spurr N K, Ogata T, Hoo J J, Pinsky L, Gimelli G, Pasztor L, Goodfellow PN.: Molecular analysis of 9p deletions associated with XY sex reversal: refining the localization of a sex-determining gene to the tip of the chromosome. Am J Hum Genet (1998) 63:905-908
  • Hasegawa T, Hasegawa Y, Rosenfeld RG, Cohen P: Insulin-like growth factor binding protein-4 accumulation is negatively correlated with growth rate in TM-3 cells. Growth Horm IGF Res (1998) 8:277-282
  • Hasegawa T, Hasegawa Y, Takada M, Ishii T, Sato S, Matsuo N: Free form of insulin-like growth factor-I in circulation is normal in children with simple obesity. Horm Res 49 Suppl (1998) 1:51
  • Hasegawa T, Hasegawa Y, Takada M, Kurimoto F, Tsuchiya Y: Insulin-like growth factors – insulin-like growth factor binding protein axis and diabetic control in insulin-dependent diabetes mellitus. Endocr J 45 (1998) Suppl:S129-131
  • Hirai K, Seki T, Takuma Y: Cerebrospinal fluid somatostatin in West syndrome: changes in response to combined treatment with high-dose pyridoxal phosphate and low-dose corticotropin. Neuropeptides (1998) 32:581-586
  • Honda K, Nagao T, Hanabusa H, et al.: Prospective matched control study concerning the treatment and quality of life of hemophiliacs with inhibitors. Rinsho Ketsueki (1998) 39:416-421
  • Honda M, Shishido S.: Recent developements in the management of infants with end-stage renal disease Clin Exp Nephrol (1998) 2:1-11
  • Hoshiya M, Awazu M: Trapidil inhibits platelet-derived growth factor-stimulated mitogen-activated protein kinase cascade. Hypertension (1998) 31:665-671
  • Ikegawa S, Nishimura G, Nagai T, Hasegawa T, Ohashi H, Nakamura Y.: Mutation of the typeX collagen gene (COL10A1) causes spondylometaphyseal dysplasia. Am J Hum Genet (1998) 63:1659-1662
  • Inukai T, Sugita K, Iijima K, Goi K, Tezuka T, Kojika S, Kagami K, Mori T, Kinoshita A, Suzuki T, Koyama T, Nakazawa S: Leukemic cells with 11q23 translocations express granulocyte colony-stimulating factor(G-CSF) receptor and their proliferation is stimulated with G-CSF Leukemia (1998) 12:382-389
  • Kakinuma Y, Hama H, Sugiyama F, Yagami K, Goto K, Murakami K, Fukamizu A.: Impaired blood-brain barrier function in angiotensinogen-deficient mice. Nature Med (1998) 4:1078-1080
  • Kakinuma Y, Miyauchi T, Sakai S, Kobayashi T, Yuki K, Goto K.: Gene expression of endothelin (ET)-2 is altered reciprocally to that of ET-1 in the rat heart. Jp J Pharmacol (1998) 76(Suppl.I):148
  • Katagiri M, Tatsuna K, Imaoka S, Funae Y, Honma K, Matsuo N, Yokoi H, Ishimura K, Itabashi F, Kagawa N.: Evidence that immature rat liver is capable of participating in steroidgenesis by expressing 17 alpha hydorxylase/17,20-lyase P450c17.F. Steroid Biochemistry and Molecular Biology 64 (1998) (1/2):121-128
  • Kato S, Nishimura H, Sako M, Kato K, Azuma E, Kawano Y, Kawa K, Kinoshita A, Sugita K, Okimoto Y, Inamitsu T: Cord blood transplantation from sibling donors in Japan report of the national survey Int J Hematol (1998) 67:389-396
  • Kikuchi H, Takata A, Akasaka Y, Fukuzawa R, Yoneyama H, Kurosawa Y, Honda M, Kamiyama Y, Hata J.: Do intronic mutations affecting splicing of WT1 exon 9 cause Frasier syndrome? J Med Genet (1998) 35:45-48
  • Kiyokawa N, Taguchi T, Mori T, Uchida H, Sato N, Takeda T, Fujimoto J: Induction of Apoptosis in Normal Human Renal Tubular Epithelial Cells by Escherichia coli Shiga Toxin (Stx)1 and Stx2. J Infec Dis (1998) 178:178-184
  • Kobayashi Y, Honda M, Yoshikawa N, Ito H: Immunohistological study in sixteen children with acute tubulointerstitial nephritis. Clin Nephrol (1998) 50:14-20
  • Kosaki K, Casey B: Genetics of human left-right axis malformations. Semin Cell Dev Biol (1998) 9:89-99
  • Li XK, Okuyama T, Tamura A, Enosawa S, Kaneda Y, Takahara S, Funashima N, Yamada M, Amemiya H, Suzuki S: Prolonged survival of rat liver allografts transfected with Fas ligand-expressing plasmid. Transplantation (1998) 66:1416-1423
  • Li XK, Okuyama T, Tamura A, Fujino M, Funeshima N, Kaneda Y, Kita Y, Enosawa S, Amemiya H, Suzuki S: Prolonged survival of recipient rats with Fas-ligand-transfected liver allografts by using HVJ-liposome Transplantation Proceedings (1998) 30:943
  • Maki S, Miyauchi T, Kakinuma Y, Sakai S, Kobayashi T, Sugiyama F, Fukamizu A, Goto K, Yamaguchi I, Sugishita Y.: Endothelin receptor antagonist ameliorates the hypertensive phenotypes of the transgenic hypertensive mice with renin-angiotensin genes and discloses roles of organ specific activation of endothelin system in the transgenic mice. Circulation (1998) 98: I-204
  • Matsuoka R, Kimura M, Scambler J. P, Morrow E. B, Imamura S, Minoshita S, Shimizu N, Yamagishi H, Joh K, Watanabe S, Oyama K, Saji T, Ando M, Takao A, Momma K: Molecular and clinical study of 183 patients with conotruncal anomaly face syndrome Human Genet (1998) 103:70-80
  • Miura T, Takayama S, Taki M, Shimotohno K: Mother-to-child transmission of hepatitis G virus. Pediatrics (1998) 102:1222-1223
  • Nakajima C, Kijimoto C, Yokoyama Y, Miyakawa T, Tsuchiya Y, Kuroda T, Nakano M, Saeki M: Longitudinal follow up of pulmonary function after lobectomy in childhood. Pediatr Surg Int (1998) 13:341-345
  • Nishimura G, Hasegawa T, Sugii K, Tsuyama K, Matsuo N: Joint laxity, vitreoretinal degeneration, facial abnormalities, and generalized skeletal alterations: a new syndrome? J Hum Genet (1998) 43:191-194
  • Nishimura H, Ohnuma K, Ikuta K, Isoyama K, Kinoshita A, Toyoda Y, Ohira M, Okumura J, Nakajima F.: Unrelated umbilical cord-blood stem cell transplantation: a report from Kanagawa Cord Blood Bank, Japan. Int J Hemat (1998) 68:193-202
  • Niwa T, Yabusaki Y, Honma K, Matsuo N, Tatsuta K, Ishibashi F, Katagiri M.: Contribution of human hepatic cytochrome P450 isoforms to region selective hydroxylation of steroid hormones. Xenobiotica (1998) 28:539-547
  • Ogata T, Hasegawa T, Tamai S, Sato S, Hasegawa Y, Matsuo N: Hypergonadotropic hypogonadism in a 3-year-old girl with blepharophimosis, ptosis, and epicanthus inversus syndrome. Horm Res (1998) 50:190-192
  • Ogata T, Muroya K, Tsukahara M: Noonan syndrome: genotype analysis of the Noonan syndrome critical region at chromosome 12q in a three-generation family. Am J Med Genet (1998) 79:153-154
  • Ogata T, Wakui K, Muroya K, Ohashi H, Matsuo N, Brown DM, Ishii T, Fukushima Y: Microphthalmia with linear skin defects syndrome in a mosaic female infant with monosomy for the Xp22 region: molecular analysis of the Xp22 breakpoint and the X-inactivation pattern. Hum Genet (1998) 103:51-56
  • Ohro Y, Suzuki Y, Tsutsumi Y, Ogata T.: Female external genitalia, absent uterus, and probable agonadism in a 46,XY infant with bilateral upper amelia. Clin Genet (1998) 54:52-55
  • Ohyama K, Tanaka T, Tachibana K, Niimi H, Fujieda K, Matsuo N, Satoh M, Hibi I.: Timing for discontinuation of treatment with a long-acting gonadotropin-releasing hormone analog in girls with central precocious puberty. TAP- 144SR CPP Study Group. Endocrine J (1998) 45:351-356
  • Okuyama T, Fujino M, Li XK, Funeshima N, Kosuga M, Saito I, Suzuki S, Yamada M: Efficient Fas-ligand gene expression in rodent liver after intravenous injection of a recombinant adenovirus by the use of a Cre-mediated switching system. Gene Ther (1998) 5:1047-1053
  • Okuyama T, Kosuga M, Takahashi S, Sasaki K, Yamada M.: Hepatocyte-specific gene expression by a recombinant adeno-associated virus vector carrying apolipoprotein E enhancer and a1-antitrypsin promoter. Gene Ther Mol Biol (1998) 3:67-74
  • Okuyama T, Li XK, Funeshima N, Fujino M, Sasaki K, Kita Y, Kosuga M, Takahashi M, Saito H, Suzuki S, Yamada M: Fas-mediated apoptosis is involved in the elimination of gene-transduced hepatocytes with E1/E3-deleted adenoviral vectors. J Gastroenterol Hepatol 13 (1998) Suppl:S113-118
  • Sakaguchi M, Nakayama T, Inouye S: Cases of systemic immediate-type urticaria associated with acellular diphtheria-tetanus-pertussis vaccination. Vaccine (1998) 16:1138-1140
  • Sasaki G, Ogata T, Sato S, Hasegawa Y, Matsuo N.: Normally sustained growth in a boy with panhypopituitarism: A case report. Clin Pediatr Endocrinol (1998) 7:87-92
  • Sasaki Y, Iseki M, Yamaguchi S, Kurosawa Y, Yamamoto T, Moriwaki Y, Kenri T, Sasaki T, Yamashita R: Direct evidence of autosomal recessive inheritance of Arg24 to termination codon in purine nucleoside phosphorylase gene in a family with a severe combined immunodeficiency patient Hum Genet (1998) 103:81-85
  • Taguchi T, Uchida H, Kiyokawa N, Sato H, Mori T, Horie H, Takeda T, Fujimoto J: Verotoxins induce apoptosis in human renal tubular epithelium derived cells. Kid Int (1998) 53:1681-1688
  • Takami T, Kawashima H, Takei Y, Miyajima T, Mori T, Nakayama T, Hoshika A: Usefulness of nested PCR and sequence analysis in a nosocomial outbreak of neonatal enterovirus infection. J Clin Virol (1998) 11:67-75
  • Takiyama N, Matsumoto K: Age-and sex-related differences of serum carnitine in a Japanese population. J Am Coll Nutr (1998) 17:71-74
  • Takiyama N, Mohney T, Swaney W, Bahnson A, Rice E, Beeler M, Scheirer-Fochler S, Ball E, Barranger J.: Comparison of methods for retroviral mediated transfer of glucocerebrosidase gene to CD34+ hematopoietic progenitor cells. Eur J Haematol (1998) 61:1-6
  • Takuma Y: ACTH therapy for infantile spasms: A combination therpy with high-dose pyridoxal phosphate and low-dose ACTH Epilepsia (1998) 39:42-45
  • Taniguchi K, Sugiyama F, Kakinuma Y, Uehara S, Nishijo A, Tanimoto K, Murakami K, Fukamizu A, Yagami K.: Pathologic characterization of hypotensive C57BL/6J-agt: Angiotensiongen-deficient C57BL/6J mice. Int J Mol Med (1998) 1:583-587
  • Thomas T, Kurihara H, Yamagishi H, Kurihara Y, Yazaki Y, Olson EN, Srivastava D: A signaling cascade involving endothelin-1, dHAND and msxl regulaters development of neural-crest-derived branchial arch mesenchyme Development (1998) 125:3005-3014
  • Thomas T, Yamagishi H, Overbeek PA, Olson EN, Srivastava D: The bHLH factors, dHAND and eHAND, specify pulmonary and systemic cardiac ventricles independent of left-right sidedness. Dev Biol (1998) 196:228-236
  • Tokieda K, Morikawa Y, Natori M, Hayashida S, Mori K, Ikeda K: Intrauterine growth acceleration in the case of a severe form of mucopolysaccharidosis type VII. J Perinat Med (1998) 26:235-239
  • Yamada M, Hasegawa T, Hasegawa Y: Increase in free insulin-like growth factor-I levels in precocious and normal puberty. Endocr J (1998) 45:407-412
  • Yamagishi H, Furutani M, Kamisago M, Morikawa Y, Kojima Y, Hino Y, Furutani Y, Kimura M, Imamura S, Takao A, Momma K, Matsuoka R: A de novo missense mutation (R1623Q) of the SCN5A gene in a Japanese girl with sporadic long QT sydrome. Mutations in brief no. 140. Online. Hum Mutat (1998) 11:481
  • Yamagishi H, Ishii C, Maeda J, Kojima Y, Matsuoka R, Kimura M, Takao A, Momma K, Matsuo N: Phenotypic discordance in monozygotic twins with 22q11.2 deletion. Am J Med Genet (1998) 78:319-321
  • Yoshikawa T, Morooka M, Suga S, Niinomi Y, Kaneko T, Shinoda K, Muraki Y, Takahashi K, Sugaya N, Asano Y: Five cases of thrombocytopenia induced by primary human herpesvirus 6 infection. Acta Paediatr Jpn (1998) 40:278-81