国立研究開発法人国立成育医療研究センター 理事長

日本小児科学会 小児科専門医 日本腎臓学会 腎臓専門医

五十嵐 隆 いがらし たかし 先生

  • 東京都
  • 小児外科

基本情報

診療科

  • 小児外科

資格・所属学会

日本小児科学会 小児科専門医
日本腎臓学会 腎臓専門医

役職など

  • 日本小児科学会 前会長
  • 日本小児科学会 監事
  • 日本腎臓学会 評議員
  • 国立研究開発法人国立成育医療研究センター 理事長

所属病院

国立成育医療研究センター病院
国立成育医療研究センター病院
  • 内科 アレルギー科 血液内科 リウマチ科 外科 心療内科 精神科 神経内科 脳神経外科 腎臓内科 心臓血管外科 小児科 小児外科 整形外科 形成外科 皮膚科 泌尿器科 産婦人科 眼科 耳鼻咽喉科 リハビリテーション科 放射線科 歯科 矯正歯科 小児歯科 麻酔科 呼吸器内科 循環器内科 消化器内科
  • 東京都世田谷区大蔵2丁目10-1
  • 小田急線「成城学園前駅」 南口 バスの利用も可能(所要時間約10分 小田急バス/東急バス 国立成育医療センター前下車 徒歩1分) 車5分 東急田園都市線「用賀駅」 成城学園前駅行 国立成育医療センター前下車 徒歩1分 バス15分
所属病院について
1e4d968b77

医療記事

来歴等

略歴

1978年 東京大学医学部医学科 卒業
1978年 東京大学医学部附属病院小児科 研修医
1979年 静岡厚生連遠州総合病院小児科 医員
1982年 東京都立清瀬小児病院腎内科 医院
1989年 東京大学医学部附属病院小児科 助手
1985年 Harvard大学Boston小児病院 研究員
1988年 東京大学医学部附属病院小児科 助手
1989年 東京大学 医学博士
1991年 東京大学医学部附属病院分院小児科 講師
2000年 東京大学大学院医学系研究科小児医学講座小児科 教授
2003年 東京大学医学部附属病院 副院長
2011年 東京大学教育研究評議会 評議員
2012年 独立行政法人国立成育医療研究センター 理事長
2014年 東京大学 名誉教授

論文

  • Promotor-specific repression of hepatocyte nuclear factor (HNF)-β and HNF-1α transcriptional activity by an HNF-β missense mutant associated with type 5 maturity-onset diabetes of the young with hepatic and biliary manifestations.

    Kitanaka S, Miki Y, Hayashi Y, Igarashi T

  • Patients with Epstein-Fechtner syndrome owing to MYH9 R702 mutations develop progressive proteinuric renal disease. Kidney Int 78: 207-214, 2010

    Sekine T, Konno M, Sasaki S, Moritani S, Miura T, Wong WS, Nishio H, Nishiguchi T, Ohuchi MY, Tsuchiya S, Matsuyama T, Kanegane H, Ida K, Miura K, Harita Y, Hattori M, Horita S, Igarashi T, Saito H, Kunishima S

  • Defective membrane expression of the Na+-HCO3- cotransporter NBCe1 is associated with familial migraine. PNAS 107: 15963-15968, 2010

    Suzuki M, Paesschen WV, Stalmans I, Horita S, Yamada H, Bergmans BA, Legius E, Riant F, Jonghe PD, Li Y, Sekine T, Igarashi T, Fujimoto I, Mikoshiba K, Shimadzu M, Shohara M, Braverman N, Al-Gazali L, Fujita T, Seki J

  • Interstitial deletion of 13q14.13-q32.3 presenting with Arima syndrome and bilateral retinoblastoma. Brain & Develop 33: 353-356, 2010

    Takahashi K, Oka A, Mizuguchi M, Saitoh M, Takita J, Sato A, Mimaki M, Kato M, Ogawa S, Igarashi T

  • IDH1 and IDH2 mutations are rare in pediatric myeloid malignancies. Leukemia 25: 1-3, 2011

    Oki K, Takita J, Hiwatari M, NishimuraR, Sanada M, OkuboJ, Adachi M , Sotomatsu M, Kikuchi A, Igarashi T, HayashiY, Ogawa S

  • Increased Akt-mTOR signaling in lung epithelium is associated with respiratory distress syndrome in mice. Mol Cell Biol 31: 1054-1065, 2011

    Ikeda H, Shiojima I, Oka T, Yoshida M, Maemura K, Walsh K, Igarashi T, Komuro I

  • Congenital infection-like syndrome with intaracranial calcification. Brain & Develop 33: 530-533, 2011

    Mizuno Y, Takahashi K, Igarashi T, Saito M, Mizuguchi M

  • Aberrations of NEGR1 on 1p31 and MYEOV on 11q13 in neuroblastoma. Cancer Science 102 1645-1650, 2011

    Takita J, Chen Y, Sanada M, Adachi M, Ohki K, Nishimura R, Hanada R, Igarashi T, Hayashi Y, Ogawa S

  • Morphological and functional analyses of two infants with obstructive renal dysplasia. Clin Exp Nephrol 15: 602-606, 2011

    Miura K, Sekine T, Nishimura R, Kanamori Y, Yanagisawa A, Sakai K, Nagata M, Igarashi T

  • Tyrosine phosphorylation-dependent activation of TRPC6 regulated by PLC-γ1 and nephrin effect of mutations associated with focal segmental glomerulosclerosis. Mol Biol Cell. 22: 1824-35, 2011

    Kanda S, Harita Y, Shibagaki Y, Sekine T, Igarashi T, Inoue T, Hattori S

  • A synthetic prostacyclin agonist, ONO-1301, ameliorates ventricular remodeling after acute myocardial infarction via upregulation of HGF in rat. Biomedicine & Aging Pathology 1: 90–96, 2011

    Hirata Y, Soekia T, Yamadaa H, Shiotac A, Shimabukuroc M, Sakaid Y, Nakayamae M, Matsumotoe K, Igarashi T, Sataa M

  • Model combining hydrodynamics and fractal theory for analysis of in vivo peropheral pulmonary and systemic resistance of shunt cardiac defects. J Theoret Biology 287: 64-73, 2011

    Nakamura Y, Awa S, Kato H, Ito YM, Kamiya A, Igarashi T

  • V2 vasopressin receptor (V2R) mutations in partial nephrogenic diabetes insipidus highlights protean agonism of V2R antagosists. J Biol Chem 287: 2099-2106, 2012

    Takahashi K, Makita N, Manaka K, Hisano M, Akioka Y, Miura K, Takubo N, Iida A, Ueda N, Hashimoto M, Fujita T, Igarashi T, Sekine T, Iiri T

  • Clinical characteristics of obstructive uropthy associated with rotavirus gastroenteritis in Japan. Clin Nephrol 77: 49-54, 2012

    Ashida A, Fujieda M, Ohta K, Nakakura H, Matsumura H, Morita T, Igarashi T, Tamai H

  • Early occurrence of nephrotic syndrome associated with cord blood stem cell transplantation. Clin Exp Nephrol 16: 180-182, 2012

    Miura K, Sekine T, Takamizawa M, Terashima H, Furuya A, Koh K, Takita J, Ida K, Igarashi T

  • SIRPα interacts with nephrin at the podocyte slit diaphragm. FEBS J 279: 3010-3021, 2012

    Kajiho Y, Harita Y, Kurihara H, Horita S, Matsunaga A, Tsurumi H, Kanda S, Sugawara N, Miura K, Sekine T, Hattori S, Hattori M, Igarashi T

  • Association of vitamin D-related gene polymorphisms with manifestation of vitamin D deficiency inchildren. Endocrine J 59: 1007-1014, 2012

    Kitanaka S, Isojima T, Takaki M, Numakura C, Hayasaka K, Igarashi T

  • The long-term use of enalapril and hydrochlorothaiazide in two novel mutations patients with Dent’s disease. J Bras Nefrol 34: 78-81, 2012

    Vaisbich MH, Henriques Ldos S, Igarashi T, Sekine T, Seki G, Koch VH

  • Aberrant activation of ALK kinase by a novel truncated form ALK protein in neuroblastoma. Oncogene 31: 4667-4676, 2012

    Okubo J, Takita J, Chen Y, Oki K, Nishimura R, Kato M, Sanada M, Hiwatari M, Hayashi Y, Igarashi T, Ogawa S

  • Endothelin regulates neural crest development and fate to form great vessels through Dlx5/Dlx6-independent mechanism. Mech Dev 130:553-66, 2013

    Kim KS, Arima Y, Kitazawa T, Nishiyama K, Asai R, Uchijima Y, Sato T, Levi G, Kitanaka S, Igarashi T, Kurihara Y, Kurihara H

  • Neonatal herpes encephalitis confirmed acyclovir-resistant herpes simplex virus 1 strain. J Clin Microbio 51: 356-359, 2013

    Kakiuchi S, Nonoyama S, Wakamatssu H, Kogawa K, Wang L, Kinoshita-Yamaguchi H, Takayama-Ito M, Lim CK, Mizuguchi M, Igarashi T, Saijo M

  • Japanese Dent disease has a wider clinical spectrum than Dent disease in Europe/USA genetic and clinical studies of 86 unrelated patients with low-molecular-weight proteinuria. Nephrol Dial Transplant 29:376-384, 2014

    Sekine T, Komoda F, Miura K, Takita J, Shimadzu M, Matsuyama T, Ashida A, Igarashi T

  • Decreased glomerular filtration as the primary factor of elevated circulating suPAR levels in focal segmental glomerulosclerosis. Pediatr Nephrol 29: 1553-1560, 2014

    Harita Y, Ishizuka K, Tanego A, Sugawara N, Chikamoto H, Akioka Y, Tsurumi H, Miura K, Gotoh Y, Tsujita M, Yamamoto T, Horike K, Takeda A, Oka A, Igarashi T, Hattori M

  • Epithelial protein lost in neoplasm modulates platelet-derived growth factor-mediated adhesion and motility of mesangial cells. Kidney Int 86: 548-557, 2014

    Tsurumi H., Harita Y, Kurihara H, Kosako H, Hayashi K, Matsunaga A, Kajiho Y, Kanda S, Miura K, Sekine T, Oka A, Ishizuka K, Horita S, Hattori M, Hattori S, Igarashi T

  • Multifocal kaposiform hemangioendothelioma in multiple visceral organs: an autopsy of 9-day-old female baby. Human Patho 45: 1773-1777, 2014

    Nakaya T, Morita K, Kurata A, Ushiku T, Igarashi T, Kuroda M, Fukayama M

  • Molecular effect of a novel missense mutation, L266V, on function of ClC-5 protein in a Japanese patient with Dent’s disease. Clin Nephrol 82: 58-61, 2014

    Ashida A, Yamamoto D, Nakakura H, Shirasu A, Matsumura H, Sekine T, Igarashi T, Tamai H

  • Bialleic DICER1 mutations in sporadic pleuropulmonary blastoma. Cancer Res 74: 2742-2749, 2014

    Seki M, Yoshida K, Shiraishi Y, Shimamura T, Sato Y, Nishimura R, Okuno Y, Chiba K, Tanaka H, Kato K, Kato M, Hanada R, Nomura Y, Oark Myong-Ja, Ishida T, Oka A, Igarashi T, Miyano S, Hayashi Y, Ogawa S, Takita J

  • Study group for establishing guidelines for the diagnosis and therapy of hemolytic uremic syndrome Guidelines for the management and investigation of hemolytic uremic syndrome. Clin Exp Nephrol 18: 525-557, 2014

    Igarashi T, Ito S, Sako M, Saitoh M, Hataya S, Mizuguchi M, Morishima T, Ohnishi K, Kawamura N, Kitayama H, Ashida A, Kaname S, Taneichi H, Tang J, Ohnishi M

  • for the Japanese Study Group of Kidney Disease in Children: A multicenter randomized trial indicates initial prednisolone treatment for childhood nephrotic syndrome for two months is not inferior to six-month treatment, Kidney Int 87: 225-232, 2015

    Yoshikawa N, Nakanishi K, Sako M, Oba MS, Mori R, Ota E, Ishikura K, Hataya H, Honda M, Ito S, Shima Y, Kaito H, Nozu K, Nakamura H, Igarashi T, Ohashi Y and Iijima I

  • End-stage renal disease in Japanese children: a nationwide survey during 2005-2011. Clin Exp Nephrol 2014

    Hattori M, Sako M, Kaneko T, Ashida A, Matsunaga A, Igarashi T, Itami N, Ohta T, Gotoh Y, Satomura K, Honda M, Igarashi T

  • Post-traumatic stress disorder in children following natural disasters a systematic review of the long-term follow-up studies. Int J Child Youth Family Studies 6: 111-133, 2015

    Terasaka A, Tachibana Y, Okuyama M, Igarashi T

  • Fanconi syndrome, pp1039-1068, Pediatric Nephrology six edition, vol 1, Edited by Avner ED, Harmon WE, Niaudet P, Yoshikawa N, Springer-Verlag, Berlin, Heidelberg, 2009

    Igarashi T

  • Pedatric Nephrology around the world, Japan, pp1951-1954, Pediatric Nephrology, vol 2, Edited by Avner ED, Harmon WE, Niaudet P, Yoshikawa N, Springer-Verlag, Berlin, Heidelberg, 2009

    Igarashi T

  • Renal Fanconi syndrome, Dent’s disease and Bartter’s syndrome. pp 553-568, Genetics of Bone Biology and Skeletal Disease. Edited by Thakker RV, Whyte MP, Eisman JA, Igarashi T, Elsevier, Amsterdam, 2013

    Devuyst O, Igarashi T

  • Red cell adenylate kinase deficiency associated with hereditary nonspherocytic anemia: Clinical and biological studies. Am J Hematol 14:325-333, 1983

    Miwa S, Fujii H, Tani K, Takahashi K, Takizawa T, Igarashi T

  • Familial cases of congenital nephrogenic diabetes insipidus type II: Remarkable increment of urinary adenosine 3', 5' monophosphate in response to antidiuretic hormone. J Pediatr 104:593-595, 1984

    Ohzeki T, Igarashi T, Okamoto A

  • Activation of platelet function in Fabry's disease. Am J Hematol 22:63-67, 1986

    Igarashi T, Sakuraba H, Suzuki Y

  • Cardiovascular manifestations in Fabry's disease. Clin Genet 29:276-283, 1986

    Sakuraba H, Yanagawa Y, Igarashi T, Suzuki Y

  • Effect of vitamin E and ticlopidine on platelet aggregation in Fabry's disease. Clin Genet 31:349-354, 1987

    Sakuraba H, Igarashi T, Suzuki Y

  • Congenital nephrotic syndrome with focal segmental glomerular sclerosis, renal insufficiency and tubular dysfunction. Acta Paediatr Jpn 29:614-618, 1987

    Igarashi T, Shibata T, Iwata T, Kamoshita S

  • Molecular basis for the deficiency of complement 1 inhibitor in type I hereditary angioneurotic edema. J Clin Invest 79:698-702, 1987

    Cicardi M, Igarashi T, Rosen FS, Davis III AE

  • Restriction fragment polymorphism of the C1 inhibitor gene in hereditary angioneurotic edema. J Clin Invest 80:1640-1644, 1987

    Cicardi M, Igarashi T, Kim M, Frangi D, Agostomi A, Davis III AE

  • Molecular analysis of hypoxanthine-guanine phosphoribosyltransferase mutations in five unrelated Japanese patients. Acta Paediatr Jpn 31:303-313, 1989

    Igarashi T, Minami M, Nishida Y

  • Congenital anterior urethral diverticulum and urinary tract infection. Acta Paediatr Jpn 31:493-495, 1989

    Igarashi T, Higashihara E

  • Type I C1 inhibitor deficiency with a small messenger RNA resulting from deletion of one exon. J Clin Invest 83:1883-1893, 1989

    Ariga T, Igarashi T, Ramesh N, Parad R, Cicardi M, Davis III AE

  • Carrier detection of partial hypoxanthine-guanine phosphoribosyltransferase deficiency by analysis with Bam HI restriction fragment length polymorphisms and oligonucleotide probes. Pediatr Res 27:417-421, 1990

    Igarashi T, Kamoshita S

  • Carrier detection of partial hypoxanthine-guanine phosphoribosyltransferase deficiency by analysis with Bam HI restriction fragment length polymorphisms and oligonucleotide probes. Pediatr Res 27:417-421, 1990

    Igarashi T, Kamoshita S

  • Bam HI restriction fragment length polymorphisms for hypoxanthine-guanine phosphoribosyltransferase (HPRT) gene of carriers and controls of HPRT deficiency in Japan. Acta Paediat Jpn 32:12-15, 1990

    Igarashi T, Ikegami H, Yamazaki H, Minami M

  • Reversible low-molecular-weight proteinuria in patients with distal renal tubular acidosis. Pediatr Nephrol 4:593-596, 1990

    Igarashi T, Kawato H, Kamoshita S

  • Renal cyst formation as a complication of primary distal renal tubular acidosis. Nephron 59:75-79, 1990

    Igarashi T, Shibuya K, Kamoshita S, Higashihara E, Kawato H, Hagishima K, Kosugi T

  • Two unknown renal complications in primary distal renal tubular acidosis. Contrib Nephrol 95:178-184, 1991

    Igarashi T, Kawato H, Kamoshita S, Kosugi T, Hagishima K

  • Transient neonatal distal renal tubular acidosis with secondary hyperparathyroidism. Pediatr Nephrol 6:267-269, 1992

    Igarashi T, Sekine Y, Kamoshita S, Kawato H, Saigusa Y

  • Uchimura H, Ohkubo A: An uncommon peptide band detected in urine of premature babies and newborns. Progress in Clin Biochem 3: 883-885, 1992

    Mashige F, Igarashi T, Watanabe H, Yamada A

  • Acute tubulointerstitial nephritis with uveitis syndrome presenting as multiple tubular dysfunction including Fanconi's syndrome. Pediatr Nephrol 6:547-549, 1992

    Igarashi T, Kawato H, Kamoshita S, Nosaka K, Seiya K, Hayakawa H

  • Normal serum uric acid concentration for age and sex and incidence of renal hypouricemia in Japanese school children. Pediatr Nephrol 7:239-240, 1993

    Igarashi T

  • Sekine T, Sugimura H, Hayakawa H, Arayama T: Acute renal failure after exercise in a child with renal hypouricemia. Pediatr Nephrol 7:292-293, 1993

    Igarashi T

  • High prevalence of serum antibodies to verotoxin-1 and verotoxin-2 among healthy adults in Japan. J Infection 27:211-213, 1993

    Takeda T, Nakao H, Yamanaka T, Igarashi T, Terada Y, Kobayashi N

  • Impairment by verotoxin of tubular function contributes to the renal damage seen in haemolytic uraemic syndrome. J Infection 27: 339-341, 1993

    Takeda T, Dohi S, Igarashi T, Yamanaka T, Yoshiya K, Kobayashi N

  • Persistent isolated proximal renal tubular acidosis-a systemic disease with a distinct clinical entity. Pediatr Nephrol 8: 70-71, 1994

    Igarashi T, Ishii T, Watanabe K, Hayakawa H, Horio K, Sone Y, Ohga K

  • The incidence of renal cyst formation in patients with primary distal renal tubular acidosis. Nephron 66: 474, 1994

    Igarashi T, Kosugi T

  • Weber Christian disease with benign cytophagic histiocytes in the skin lesion. Acta Pediatr Jpn 37: 105-107, 1995

    Inatomi J, Watanabe K, Igarashi T, Hayakawa H

  • Hypercalciuria and nephrocalcinosis in patients with idiopathic low molecular weight proteinuria in Japan: Is the disease identical to Dent's disease in United Kingdom? Nephron 69: 242-247, 1995

    Igarashi T, Hayakawa H, Shiraga H, Kawato H, Yan K, Kawaguchi H, Yamanaka T, Tsuchida S, Akagi K

  • A case of juvenile nephronophthisis presenting severe short stature. Clin Pediatr Endocrinol 4 (Supple 6): 95-98, 1995

    Yoshizawa A, Yokoya S, Igarashi T

  • How does the early start of gammaglobulin therapy influence the prognosis of Kawasaki syndrome? Kawasaki Disease, ed. Kato H, et al. pp310-314, Elsevier Science N.Y., 1995

    Kohsaka T, Noma S, Takeuchi N, Simizu S, Sekiya T, Igarashi T, Kamoshita S, Kobayashi N

  • Neuronal and vascular pathology produced by verocytotoxin 2 in the rabbit central nervous system. Acta Neuropathol 91: 254-262, 1996

    Mizuguchi M, Tanaka S, Fujii I, Tanizawa H, Suzuki Y, Igarashi T, Yamanaka T, Takeda T, Miwa M

  • Studies on the latex agglutination inhibition method for assay of plasma theophylline concentration. Jpn J Hosp Pharm 22: 330-341, 1996

    Kizu J, Watanabe S, Ono H, Inatomi J, Sasaki K, Watanabe K, Igarashi T, Iwata T, Hayakawa H, Imai K

  • Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to mutations of the renal chloride channel (CLCN5). J Clin Invest 99:561-568, 1997

    Lloyd SE, Pearce SHS, Günther W, Kawaguchi H, Igarashi T, Jentsch TJ, Thakker RV

  • Mutations of CLCN5 in Japanese children with idiopathic low molecular weight proteinuria, hypercalciuria and nephrocalcinosis. Kidney Int 52: 911-916, 1997

    Akuta N, Lloyd SE, Igarashi T, Shiraga H, Matsuyama T, Yokoro S, Cox JPD, Thakker RV

  • Cloning, functional characterization and localization of a rat renal Na+-dicarboxylate transporter. Am J Physiol 275 (Renal Physiol. 44): F298-F305, 1998

    Sekine T, Cha SH, Hosoyamada M, Kanai Y, Watanabe N, Huruta Y, Hukuda K, Igarashi T, Endou H

  • Functional characterization of renal chloride channel, CLCN5, mutations associated with Dent’s Japan disease. Kidney Int 54: 1850-1856, 1998

    Igarashi T, Günter W, Sekine T, Inatomi J, Shiraga H, Takahashi S, Suzuki J, Tsuru N, Yanagihara T, Shimazu M, Jentsch TJ, Thakker RV

  • Mutations in SLC4A4 cause permanent isolated proximal renal tubular acidosis with ocular abnormalities. Nature Genet 23:264-266, 1999

    Igarashi T, Inatomi J, Sekine T, Cha SH, Kanai Y, Kunimi M, Tsukamoto K, Satoh H, Shimadzu M, Tozawa F, Mori T, Shiobara M, Seki G, Endou H

  • Failure of pre-diarrheal antibiotics to prevent hemolytic uremic syndrome in serologically-proven Escherichia coli 0157:H7 gastrointestinal infection. J Pediatr 135: 768-769, 1999

    Igarashi T, Inatomi J, Wake A, Takamizawa M, Katayama H, Iwata T

  • Clinical and genetic studies of CLCN5 mutations in Japanese families with Dent’s disease. Kidney Int 58: 520-527, 2000

    Igarashi T, Inatomi J, Ohara T, Kuwahara T, Shimadzu M, Thakker RV

  • Disorders in the immune responses of T- and B-cells in mice administered intravenous Verotoxin 2. Life Sci 67: 1059-1072, 2000

    Sugatani J, Igarashi T, Shimura M, Yamanaka T, Takeda T, Miwa M

  • Activation of coagulation in C57BL/6 mice given verotoxin 2 (VT2) and the effect of co-administration of LPS with VT2. Thromb Res 100: 61-72, 2000

    Sugatani J, Igarashi T, Munakata M, Komiyama Y, Takahashi H, Komiyama N, Maeda T, Takeda T, Miwa M

  • Genetic and long-term data on a patient with permanent isolated proximal renal tubular acidosis. Eur J Pediatr 159: 892-894, 2000

    Shiohara M, Igarashi T, Mori T, Komiyama A

  • Identification of two novel mutations in the CLCN5 gene in Japanese patients with familial low molecular weight proteinuria (Japanese Dent’s disease). Am J Kidney Dis 37: 138-143, 2001

    Takemura T, Hino S, Ikeda M, Okada M, Igarashi T, Inatomi J, Yoshioka K

  • A new approach to mRNA in proximal tubule cells of patients with CLCN5 channelopathy. Pediatr Nephrol 16: 110-112, 2001

    Morimoto T, Chiba A, Kondo Y, Takahashi S, Igarashi T, Inoue CN, Iinuma K

  • Unraveling the molecular basis of hereditary renal tubular acidosis. Clin Exp Nephrol 5: 8-12, 2001

    Igarashi T, Inatomi J, Sekine T, Seki G

  • Novel nonsense mutation in the Na+/HCO3- cotransporter gene (SLC4A4) in a patient with permanent isolated proximal renal tubular acidosis and bilateral glaucoma. J Am Soc Nephrol 12: 713-718, 2001

    Igarashi T, Inatomi J, Sekine T, Seki G, Shimadzu M, Tozawa F, Takeshima Y, Takumi T, Takahashi T, Yoshikawa N, Nakamura H, Endou H

  • Molecular basis of ocular abnormalities associated with proximal renal tubular acidosis. J Clin Invest 108: 107-115, 2001

    Usui T, Hara M, Satoh H, Moriyama N, Kagaya H, Amano S, Oshika T, Ishii Y, Ibaraki N, Hara C, Kunimi M, Noiri E, Tsukamoto K, Inatomi J, Kawakami H, Endou H, Igarashi T, Goto A, Fujita T, Araie M, Seki G

  • Three families with autosomal dominant nephrogenic diabetes insipidus caused by aquaporin-2 mutations in the C-terminus. Am J Human Genetics 69: 738-748, 2001

    Kuwahara M, Iwai K, Ooeda T, Igarashi T, Ogawa E, Katsushima Y, Shinbo I, Uchida S, Terada Y, Fujiwara TM, Arthus MF, Lonergan M, Bicher DG, Marumo F

  • Pediatrician in Nepal. Indian Pediatrics 38: 685-686, 2001

    Basnet NB, Igarashi T

  • Enhanced expression of a-series gangaliosides in fibroblasts of patients with peroxisome biogenesis disorders. Bioche Biophys Acta 1535: 285-293, 2001

    Tatsumi K, Saito M, Lin B, Iwamori M, Ichiseki H, Shimozawa N, Kamoshita, Igarashi T

  • Urinary megalin deficiency implicates abnormal tubular endocytic receptor trafficking in the Fanconi syndrome. J Am Soc Nephrol 13: 125-133, 2002

    Norden AGW, Lapsley M, Christensen EI, Igarashi T, Matsuyama T, Shiraga H, Kelleher CL, Lee P, Scheinman SJ, Thakker RV, Unwin RJ, Verroust P, Wrong O, Moestrup S

  • Prothrombotic coagulation abnormalities preceding the hemolytic uremic syndrome. New Eng J Med 246: 23-32, 2002

    Chandler WL, Jelacic S, Boster D, Ciol M, Watkins S, Igarashi T, Tarr PI

  • Molecular identification of a renal/urate/anion exchanger that regulates blood urate levels. Nature 417: 447-452, 2002

    Enomoto A, Kimura H, Chairoungdua A, Shigeta Y, Jutabha P, Cha SH, Hosoyamada M, Takeda M, Sekine T, Igarashi T, Matsuo H, Kikuchi Y, Oda T, Ichida K, Hosoya T, Shimokata K, Niwa T, Kanai Y, Endou H

  • Detection of ATM gene mutation in human glioma cell line M059J by a rapid frameshift/stop codon assay in yeast. Radiat Res 158: 195-201, 2002

    Tsuchida R, Yamada T, Takagi M, Sjimada A, Ishioka C, Katsuki Y, Igarashi T, Chessa L, Delia D, Teraoka H, Mizutani S

  • Urinary concentrating defect in rats given Shiga toxin: elevation in urinary AQP2 level associated with polyuria. Life Science 71: 171-189, 2002

    Sugatani J, Komiyama N, Mochizuki T, Hoshino M, Miyamoto D, Igarashi T, Hoshi S, Miwa M

  • Molecular pathogenesis of proximal renal tubular acidosis. J Nephrol 15 (Suppl 5): S135 – S141, 2002

    Igarashi T, Sekine T, Watanabe H

  • Activation markers of human basophils: CD69 expression is strongly and preferentially induced by IL-3. J Allergy Clin Immunol 109: 817-823, 2002

    Yoshimura C, Yamaguchi M, Iikura M, Izumi S, Kudo K, Nagase H, Ishii A, Walls AF, Ra C, Iwata T, Igarashi T, Yamamoto K, Hirai K

  • Preventive effect of TAK-751S on complications of hemorrhagic colitis (results of clinical study of TAK-751S). Jpn J Antibiot 55: 203-227, 2002

    Ito H, Takeda T, Honda M, Igarashi T, Joh K, Hashizume T, Yamaoka K

  • Unrabelling the molecular pathogenesis of isolated proximal renal tubular acidosis. J Am Soc Nephrol 13:2171-2177, 2002

    Igarashi T, Sekine T, Inatomi J, Seki G

  • Molecular cloning of Chinese hamster ceremide glucosyltransferase and its enhanced expression in peroxisome-defective mutant Z65 cells. Arch Biochem Biophys 403:171-178, 2002

    Saito M, Fukushima Y, Tatsumi K, Bei L, Fujiki Y, Iwamori M, Igarashi T

  • Efficacy and safety of immunization for pre- and post-liver transplantation. Transplantation 74: 543-550, 2002

    Kano H, Mizuta K, Kato H, Miki Y, Shibuya N, Saito M, Narita M, Kawarasaki H, Igarashi T, Hashizume K, Iwata T

  • New therapeutic approaches for patients with Fabry’s disease. Inter Med 41: 913-914, 2002

    Igarashi T

  • Localization of Na+/HCO3- cotransporter (pNBC-1) variants in rat and human pancreas. Am J Physiol Cell Physiol 284: C729-C737, 2003

    Satoh H, Moriyama N, Hara C, Yamada H, Horita S, Kunimi M, Tsukamoto K, Iso-O N, Inatomi J, Kawakami H, Kudo A, Endou H, Igarashi T, Goto A, Fujita T, Seki G

  • The kinesin superfamily protein RabKIFL is not involved in the pathophysiology of Charcot-Marie-Tooth disease type 4C. Int J Mol Med 11: 45-47, 2003

    Nagura M, Nagao Y, Takita J, Igarashi T, LeGuren E, Hayashi Y

  • A family of episodic ataxia type 2: No evidence of genetic linkage to the CACNA1A gene. Int J Mol Med 11: 187-189, 2003

    Hirose H, Arayama T, Takita J, Igarashi T, Hayashi Y, Nagao Y

  • Renal function in patients with Menkes disease. Eur J Pediatr 162: 51-52, 2003

    Ozawa H, Kodama H, Kawaguchi H, Mochizuki T, Kobayashi M, Igarashi T

  • Comparative effects of basophil-directed growth factors. Biochem Biophys Res Comm 302: 201-206, 2003

    Yoshimura-Uchiyama C, Yamaguchi M, Nagase H, Fujisawa T, Ra C, Matsushima K, Iwata T, Igarashi T, Yamamoto K, Hirai K

  • Altered polarity and expression of H+-ATPase without ultrastructural changes in kidney of Dent’s disease patients. Kidney Int 63: 1285-1295, 2003

    Moulin P, Igarashi T, Van der Smissen P, Cosyns JP, Verroust P, Thakker RV, Scheinman SJ, Courtoy PJ, Devuyst O

  • Comparative ontogeny, processing, and segmental distribution of the renal chloride channel, ClC-5. Kidney Int 65: 198-208, 2004

    Jouret F, Igarashi T, Gafflot F, Wilson PD, Karet FE, Thakker R, Devuyst O

  • Alterations of fatty acid metabolism and membrane fluidity in peroxisome-defective mutant ZP102 cells. Lipids 39: 43-50, 2004

    Nagura M, Saito M, Iwamori M, Igarashi T

  • Newspaper reporting on child raising in Japan. J Pediatr Nursing 19: 113-120, 2004

    Basnet NB, Kato H, Nakamura Y, Watanabe H, Igarashi T

  • Molecular and clinical studies of Dent’s disease in Japan: biochemical examination and renal ultrasonography do not predict carrier state. Clin Nephrol 61: 231-237, 2004

    Matsuyama T, Awazu M, Oikawa T, Inatomi J, Sekine T, Igarashi T

  • Exercise-induced acute renal failure associated with renal hypouricemia: results of a questionnaire-based survey in Japan. Nephrol Dial Transplant 19: 1447-1453, 2004

    Ohta T, Sakano T, Igarashi T, Itami N, Ogawa T

  • The W258X mutation in SLC22A is the predominant cause of Japanese renal hypouricemia. Pediatr Nephrol 19:728-733, 2004

    Komoda F, Sekine T, Inatomi J, Enomoto A, Endou H, Ota T, Matsuyama T, Ogata T, Ikeda M, Awadzu M, Muroya K, Kamimaki I, Igarashi T

  • Mutational and functional analysis of SLC4A4 in a patient with proximal renal tubular acidosis. Pfluger Arch – Eur J Physiol 448: 438-444, 2004

    Inatomi J, Horita S, Braverman N, Sekine T, Yamada H, Suzuki Y, Kawahara K, Moriyama N, Kudo A, Kawakami H, Shimadzu M, Endou H, Fujita T, Seki G, Igarashi T

  • Neonatal intensive care unit hospitalization of very low birth weight Japanese infants with congenital heart disease. J Nepal Med Asso 43: 28-30, 2004

    Basnet NB, Noma S, Basnet SB, Igarashi T

  • A family of generalized epilepsy with febrile seizures plus type 2-a new missense mutation of SCN1A found in the pedigree of several patients with complex febrile seizures. Epilepsy Res 63: 151-156, 2005

    Nagao Y, Mazaki-Miyazaki E, Okamura N, Takagi M, Igarashi T

  • Functional characterization of LMX1B mutations associated with nail-patella syndrome. Pediatr Res 57: 783-788, 2005

    Sato U, Kitanaka S, Sekine T, Takahashi S, Ashida A, Igarashi T

  • Mutational analysis of idiopathic renal hypouricemia in Korea. Pediatr Nephrol 20:886-890, 2005

    Cheong HI, Kang JH, Lee JH, Ha IS, Kim S, Komoda F, Sekine T, Igarashi T, Choi Y

  • Functional analysis of NBC1 mutants associated with proximal tubular acidosis and ocular abnormalities. J Am Soc Nephrol 16:2270-2278, 2005

    Horita S, Yamada H, Inatomi J, Moriyama N, Sekine T, Igarashi T, Endo Y, Dasouki M, Ekim M, Al-Gazali L, Shimada M, Seki G, Fujita T

  • Aberration of the CHK2 gene are rare in pediatric solid tumors. Int J Mol Med 16: 85-91, 2005

    Chen YY, Takita J, Tanaka K, Ida K, Koh K, Igarashi T, Hanada R, Kikuchi A, Tanaka Y, Toyoda Y, Hayashi Y

  • Intrapulmonary solitary fibrous tumor in an eight-year-old male. Pediatr Pulmonol 40:261-264, 2005

    Kanamori Y, Hashizume K, Sugiyama M, Motoi T, Fukuyama M, Ida K, Igarashi T

  • A familial case of muticystic dysplastic kidney. Pediatr Nephrol 20: 1245-1248, 2005

    Sekine T, Namai Y, Yanagisawa A, Shirahama H, Tashiro Y, Terahara M, Nagata M, Harita Y, Fukuoka U, Inatomi J, Igarashi T

  • Distal renal tubular acidosis associated with large ventricular aqueduct and sensorineural hearing loss. Acta Oto-Laryngo 125: 667-670, 2005

    Shinjo Y, Kaga K, Igarashi T

  • A novel mutation in fibroblast growth factor (FGF) 23 gene as a cause of tumor calcinosis. J Clin Endocrinol Metab 90: 5523- 5527, 2005

    Araya K, Fukumoto S, Backenroth R, Takeuchi Y, Kanayama K, Ito N, Yoshii N, Yamazaki Y, Yamashita T, Silver J, Igarashi T, Fujita T

  • Functional characterization of rat organic anion transporter 5 (SLC22A19) at the apical membrane of renal proximal tubules. J Pharmacol Exp Ther 315: 534-544, 2005

    Anzai N, Jutabha P, Enomoto A, Yokoyama H, Nonoguchi H, Hirata T, Shiraya K, He X, Cha SH, Takeda M, Miyazaki H, Sakata T, Tomita K, Igarashi T, Kanai Y, Endou H

  • Altered expression of junctional adhesion molecule 4 (JAM4) in injured podocytes. Am J Physiol Renal Physiol 290:F335-F344,2005

    Harita Y, Miyauchi N, Karasawa T, Suzuki K, Han GD, Koike H, Igarashi T, Shimizu F, Kawachi H

  • A case of intrapericardial diaphragmatic hernia with a massive pericardial effusion: fetal diagnosis and therapy. J Pediatr Surg 40: e43-45, 2005

    Kanamori Y, Hashizume K, Sugiyama M, Tomonaga T, Goishi K, Yokoyama Y, Igarashi T, Kikuchi A, Kawana Y, Kozuma S, Taketani Y

  • A compound heterozygous mutation in the BSND gene detected in Bartter syndrome type IV. Pediatr Nephrol 21: 190-193, 2006

    Kitanaka S, Sato U, Maruyama K, Igarashi T

  • A novel compound heterozygous mutation in the thyroglobulin gene resulting in congenital goitrous hypothyroidism with high serum triiodothyronine levels. J Hum Genet 51: 379-382, 2006

    Kitanaka S, Takeda A, Sato U, Miki Y, Hishimura A, Ieiri T, Igarashi T

  • Mutations of the PTPN11 and RAS genes in rhabdomyosarcoma and pediatric hematological malignancies. Genes, Chrom & Cancer 45: 583-591, 2006

    Chen Y, Takita J, Hiwatari M, Igarashi T, Hanada R, Kikuchi A, Hongo T, Taki T, Ogasawara M, Shimada A, Hayashi Y

  • A case of panayiotopolos syndrome showing an atypical course. Seizure 15: 643-648, 2006

    Saitoh M, Kubota M, Kimura I, Mizuguchi M, Igarashi T

  • OCRL1 mutations in patients with Dent phenotype in Japan. Pediatr Nephrol 22: 975-980, 2007

    Sekine T, Nozu K, Iyengar R, Fu XJ, Matsuo M, Tanaka R, Iijima K, Matsui E, Harita Y, Inatomi J, Igarashi T

  • A case of primary erythermalgia, wintry hypothermia and encephalopthy. Neuropediatr 38: 157-159, 2007

    Takahashi K, Saitoh M, Hoshino H, Mimaki M, Takamizawa M, Mizuguchi M, Lin Z-M, Yang Y, Igarashi T

  • Alterations in the molecular species of plasmalogen phospholipids and glycolipids due to peroxisomal dysfunction in Chinese hamster ovary-mutant Z65 cells by FABMS method. J Chromato B 852: 367-373, 2007

    Saito M, Horikawa M, Iwamori Y, Mizuguchi M, Igarashi T, Fujiki Y, Iwamori M

  • Functional analysis of a novel missense NBC1 mutation and of other mutations causing proximal renal tubular acidosis. Pflugers Arch-Eur J Physiol 455: 583-593, 2008

    Suzuki M, Vaisbich MH, Yamada H, Horita S, Li Y, Sekine T, Moriyama N, Igarashi T, Endo Y, Cardoso TP, de Sa LC, Koch VH, Seki G, Fujita T

  • Molecular analysis of digenic inheritance in Bartter syndrome with sensorineural deafness. J Med Genet 45: 182-186, 2008

    Nozu K, Inagaki T, Fu XJ, Nozu Y, Kanda K, Sekine T, Igarashi T, Nakanishi N, Yoshikawa N, Iijima K, Matsuo M

  • Ischemic colitis as a complication in a patient with steroid-dependent nephrotic syndrome. Pediatr Nephrol 23:655-657, 2008

    Yanagisawa A, Namai Y, Sekine T, Igarashi T

  • A case of cerebral salt-wasing syndrome associated with aseptic meningitis in an 8-year-old girl. Pediatr Nephrol 23:659-662, 2008

    Inatomi J, Yokoyama Y, Sekine T, Igarashi T

  • Cyclic strain induces mouse embryonic stem cell differentiation into vascular smooth muscle cells by activating PDGF receptor β. J Appl Physiol 104:766-772, 2008

    Shimizu N, Yamamoto K, Obi S, Kumagaya S, Masumura T, Shimano Y, Naruse K, Yamashita JK, Igarashi T, Ando J

  • Development of a rapid immunochromtographic test for noroviruses genogroups I and II. J Viral Methods 148:1-8, 2008

    Takanashi S, Okame M, Shiota T, Takagi M, Yagyu F, Tung PG, Nishimura S, Katsumata N, Igarashi T, Okitsu S, Ushijima H

  • Activation and inactivation of Na-H-HCO3 cotransporter NBC1. J Epithel Pharm 1 35-39, 2008

    Seki G, Yamada H, Horita S, Suzuki M, Sekine T, Igarashi T, Fujita T

  • Differential gene responses in endothelial cells exposed to a combination of shear stress and cyclic stretch. J Biotechnol 133: 239-244, 2008

    Toda M, Yamamoto K, Shimizu N, Obi S, Kumagaya S, Igarashi T, Kamiya A, Ando J

  • Imaging findings of upper abdominal involvement by acute megakaryoblastic leukemia. Pediatr Radiol 38 : 457-461, 200

    Amemiya S, Akahane M, Takita J, Igarashi T, Ohtomo K

  • Juvenile pustular psoriasis associated with steroid withdrawal syndrome due to topical corticosteroid. J Dermatol 35: 601-603, 2008

    Saeki H, Watanabe A, Tada Y, Kakinuma T, Komine M, IHN H, Asahina A, Etoh T, Ktanaka S, Sato U, Kano H, Igarashi T, Tamaki K

  • Oncogenic mutations of ALK kinase in neuroblastoma. Nature 455: 971-975, 2008

    Chen Y, Takita J, Choi YM, Kato M, Ohira M, Sanada M, Wang L, Soda M, Kikuchi A, Igarashi T, Nakagawara A, Hayashi Y, Mano H, Ogawa S

  • Neph 1, a component of the kidney slit diaphragm, is tyrosine-phosphorylated by the Src family tyrosine kinase and modulates intracellular signaling by binding to Grbs. J Biol Chem 283: 9177-9186, 2008

    Harita Y, Kurihara H, Kosako H, Tezuka T, Sekine T, Igarashi T, Hattori S

  • Reevaluation of glomerular charge selective protein-sieving function. Pediatr Nephrol 24: 609-612, 2008

    Saito H, Takahashi S, Nagata M, Tsuchiya T, Mugishima H, Yan K, Kondo Y, Matsuyama T, Sekine T, Igarashi T

  • Survival in a neonate with complete urorectal malformtion sequence after fetal vesico-amniotic shunting for a prominently dilated cloacae. Fetal Diagn Ther 24: 458-461, 2008

    Kanamori Y, Iwanaka T, Nakahara S, Kawashima H, Komura M, Sugiyama M, Kamei Y, Hyodo H, Yamaguchi SI, Kohzuma S, Taketani Y, Goishi K, Ishiguro S, Takamizawa M, Igarashi T

  • Antenatally diagnosed giant multicystic dysplastic kidney resected during the neonatal period. J Pediatr Surg 43: 2118-2120, 2008

    Komura M, Kanamori Y, Sugiyama M, Nakahara S, Kawashima H, Hatanaka A, Takazawa Y, Goishi K, Igarashi T, Iwanaka T

  • Cortical gray matter lesions in acute encephalopathy with febrile convulsive status epilepticus. Brain Dev 31: 622-624, 2009

    Sato A, Mizuguchi M, Mimaki M, Takahashi K, Jimi H, Oka A, Igarashi T

  • A novel mutation in the GAT3 gene of a Japanese patient with PTH-deficient hypoparathyroidsm. J Bone Miner Metab 27: 386-389, 2009

    Saito T, Fukumoto S, Ito N, Suzuki H, Igarashi T, Fujita T

  • Detection, genetic characterization and quantification of norovirus RNA from sera of children with gastroenteritis. J Clin Virol 44: 161-163, 2009

    Takanashi S, Hashira S, Matsunaga T, Yoshida A, Shiota T, Tung PG, Khamrin P, Okitsu S, Mizuguchi M, Igarashi T, Ushijima H

  • Age-associated difference in gene expression of paediatric acute myelomonocytic leukaemia (FAB M4 and M5 subtypes) and its correlation with prognosis. Br J Haematol 144: 917-929, 2009

    Jo A, Tsukimoto I, Ishii E, Asou N, Mitani S, Shimada A, Igarashi T, Hayashi Y, Ichikawa H

  • Phosphorylation of nephrin triggers Ca2+ signaling by recruitment and activation of phospholipase C-γ1. J Biol Chem 284: 8951-8962, 2009

    Harita Y, Kurihara H, Kosako H, Tezuka T, Sekine T, Igarashi T, Hattori S

  • Frequent inactivation of A20 in B-cell lymphoma. Nature 459: 712-716, 2009

    Kato M, Sanada M, Kato I, Sato Y, Takita J, Takeuchi K, Miwa A, Cehn Y, Nakazaki K, Nomoto J, Asakura Y, Muto S, Tamura A, Iio M, Akatsuka Y, Hayashi Y, Mori H, Igarashi T, Kurokawa M, Chiba S, Mori S, Ishikawa Y, Okamaoto K, Tobinai K, Nakagawa H, Nakahra T, Yoshino T, Kobayashi Y, Ogawa S

  • Acute megakaryoblastic leukemia in a child with the MLL-AF4 fusion gene. Eur J Haematol 83: 149-153, 2009

    Takita J, Motomura A, Koh K, Ida K, Taki T, Hayashi Y, Igarashi T

  • Shortage of pediatricians in Japan: a longitudinal analysis using physician’s survey data. Pediatr Int 51: 645-649, 2009

    Ide H, Yasunaga H, Koike S, Kodama T, Igarashi T, Imamura T

  • Skin and subcutaneous blood flows of very low birth weight infants during the first 3 postnatal days. J: Matern Fetal Neonatal Med 11: 1-7, 2009

    Ishiguro A, Sekine T, Kakiuchi S, Nishimura R, Goishi K, Tsuchida S, Ohtsu H, Igarashi T

  • YA4, deleted in a case with middle interhemispheric variant of holoprosencephaly, interacts with SIX3 both physically and functionally. Hum Mutat 30: E946-955, 2009

    Abe Y, Oka A, Mizuguchi M, Igarashi T, Ishikawa S, Aburatani H, Yokoyama S, Asahara,H, Nagao K, Yamada M, Miyashita T

  • Hepatoblastoma in a patient with Sotos syndrome. J Pediatr 155: 937-939, 2009

    Kato M, Takita J, Takahashi K, Mimaki M, Chen Y, Koh K, Ida K, Oka A, Mizuguchi M, Ogawa S, Igarashi T

  • Salt-losing nephrogenic diabetes insipidus caused by fetal exposure to angiotensin receptor blocker. Pediatr Nephrol 24: 1235-1238, 2009

    Miura K, Sekine T, Iida A, Takahashi K, Igarashi T

  • Four cases of postrenal renal failure induced by renal stone associated with rotavirus infection. Clin Nephrol 73: 398-402, 2010

    Morita T, Ashida A, Fujieda A, Hayashi A, Meda A, Ohta K, Shimizu M, Sekine T, Igarashi T, Tamai H, Wakiguchi H

  • Prenatal intervention for severe anterior urethral valve. Pediatr Inter 52: e92-e95, 2010

    Mizuno Y, Tsuchida S, Kakiuchi S, Ishiguro A, Goishi K, Kamei Y, Kanamori Y, Yamazaki Y, Sekine T, Igarashi T

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