小児科のご紹介

業績集

2009年

英文原著

1) Abe T, Oguma E, Nozawa K, Sato Y, Arakawa A, Kikuchi A, Kishimoto H, Minami M : Malignant rhabdoid tumor of the liver: A case report with US and CT manifestation. Jpn J Radiol 27: 462-465, 2009

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

3) Akagi T, Ito T, Kato M, Jin Z, Cheng Y, Kan T, Yamamoto G, Olaru A, Kawamata N, Boult J, Soukiasian HJ, Miller CW, Ogawa S, Meltzer SJ, Koeffler HP: Chromosomal abnormalities and novel disease-related regions in progression from Barrett's esophagus to esophageal adenocarcinoma. Int J Cancer 15: 2349-2359, 2009

4) Akagi T, Shih LY, Kato M, Kawamata N, Yamamoto G, Sanada M, Okamoto R, Miller CW, Liang DC, Ogawa S, Koeffler HP: Hidden abnormalities and novel classification of t(15;17) acute promyelocytic leukemia (APL) based on genomic alterations. Blood 113: 1741-1748, 2009

5) Atsuta Y, Takita J (Collaborator 42), Japan Cord Blood Bank Network: Disease-specific analyses of unrelated cord blood transplantation compared with unrelated bone marrow transplantation in adult patients with acute leukemia. Blood 113:1631-1638, 2009

6) Fuji S, Kim SW, Yoshimura K, Akiyama H, Okamoto S, Sao H, Takita J, Kobayashi N, Mori S, Japan Marrow Donor Program: Possible association between obesity and posttransplantation complications including infectious diseases and acute graft-versus-host disease. Biol Blood Marrow Transplant 15: 73-82, 2009

7) Fukushi D, Watanabe N, Kasai F, Haruta M, Kikuchi A, Kikuta A, Kato K, Nakadate H, Tsunematsu Y, Kaneko Y: Centrosome amplification is correlated with ploidy divergence, but not with MYCN amplification, in neuroblastoma tumors. Cancer Genet Cytogenet 188: 32-41, 2009

8) Harita Y, Kurihara H, Kosako H, Tezuka T, Sekine T, Igarashi T, Ohsawa I, Ohta S, Hattori S: Phosphorylation of nephrin triggers Ca2+ signaling by recruitment and activation of phospholipase C-γ1. J Biol Chem 284: 8951-8962, 2009

9) Hasegawa D, Manabe A, Yagasaki H, Ohtsuka Y, Inoue M, Kikuchi A, Ohara A, Tsuchida M, Kojima S, Nakahata T, on behalf of Japanese Childhood MDS Study Group: Treatment of children with refractory anemia: the Japanese childhood MDS Study Group. Pediatr Blood Cancer 53: 1011-1015, 2009

10) Ide H, Yasunaga H, Koike S, Kodama T, Igarashi T, Imamura T: Shortage of pediatricians in Japan: a longitudinal analysis using physician's survey data. Pediatr Int 51: 645-649, 2009

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

12) Isojima T, Yokoya S, Ito J, Horikawa R, Tanaka T: Inconsistent determination of overweight by two anthrometric indices in girls with Turner syndrome. Acta Paediatrica 98: 513-518, 2009

13) Isojima T, Yokoya S, Ito J, Horikawa R, Tanaka T: New reference growth charts for Japanese girls with Turner syndrome. Pediatr Inter 51: 709-714, 2009

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

15) Kato M, Takita J, Takahashi K, Mimaki M, Chen Y, Koh K, Ida K, Oka A, Mizuguchi M, Ogawa S, Igarashi T: Hepatoblastoma in a patient with Sotos syndrome. J Pediatr 155: 937-939, 2009

16) Kato M, Sanada M, Kato I, Sato Y, Takita J, Tkeuchi 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: Frequent inactivation of A20 in B-cell lymphoma. Nature 459: 712-716, 2009

17) Khamrin P, Takanashi S, Chan-It W, Kobayashi M, Nishimura S, Katsumata N, Okitsu S, Maneekarn N, Nishio O, Ushijima H: Immunochromatography test for rapid detection of norovirus in fecal specimens. J Virol Methods 157: 219-222, 2009

18) Kikuchi A, Kigasawa H, Tsurusawa M, Kawa K, Kikuta A, Tsuchida M, Nagatoshi Y, Asami K, Horibe K, Makimoto A, Tsukimoto I: A study of rasburicase for the management of hyperuricemia in pediatric patients with newly diagnosed hematologic malignancies at high risk for tumor lysis syndrome. Int J Hematol 90: 492-500, 2009

19) Kitamura K, Itou Y, Yanazawa M, Ohsawa M, Suzuki-Migishima R, Umeki Y, Hohjoh H, Yanagawa Y, Shinba T, Itoh M, Nakamura K, Goto Y: Three human ARX mutations cause the lissencephaly-like and mental retardation with epilepsy-like pleiotropic phenotypes in mice. Hum Mol Genet 18: 3708-3724, 2009

20) Masumura T, Yamamoto K, Shimizu N, Obi S, Ando J: Shear stress increases expression of the arterial endothelial marker ephrinB2 in murine ES cells via the VEGF-Notch signaling pathways. Arterioscler Thromb Vasc Biol 29: 2125-2131, 2009

21) Miura K, Sekine T, Iida A, Takahashi K, Igarashi T: Salt-losing nephrogenic diabetes insipidus caused by fetal exposure to angiotensin receptor blocker. Pediatr Nephrol 24: 1235-1238, 2009

22.Morita T, Ashida A, Fujieda A, Hayashi A, Meda A, Ohta K, Shimizu M, Sekine T, Igarashi T, Tamai H, Wakiguchi H: Four cases of postrenal renal failure induced by renal stone associated with rotavirus infection. Clin Nephrol 73: 398-402, 2009

23) Ogawa S, Matsubara A, Onizuka M, Kashiwase K, Sanada M, Kato M, Nannya Y, Akatsuka Y, Satake M, Takita J, Chiba S, Saji H, Maruya E, Inoko H, Morishima Y, Kodera Y, Takehiko S: Japan Marrow Donation Program (JMDP). Exploration of the genetic basis of GVHD by genetic association studies. Biol Blood Marrow Transplant 15(Suppl): 39-41, 2009

24) Oshima K, Kikuchi A, Mochizuki S, Toyama D, Uchisaka N, Yabe M and Hanada R: Fanconi anemia in infancy: report of hematopoietic stem cell transplantation to a 13-month-old patient. Int J Hematol 89: 722-723, 2009

25) Oshima K, Kikuchi A, Mochizuki S, Yamane M, Date H and Hanada R: Living-donor single lobe lung transplantation for bronchiolitis obliterans from mother to child following previous allogeneic hematopoietic stem cell transplantation from the same donor. Int J Hematol 90: 540-542, 2009

26) Saito H, Takahashi S, Nagata M, Tsuchiya T, Mugishima H, Yan K, Kondo Y, Matsuyama T, Sekine T, Igarashi T: Reevaluation of glomerular charge selective protein-sieving function. Pediatr Nephrol 24: 609-612, 2009

27) Saito T, Fukumoto S, Ito N, Suzuki H, Igarashi T, Fujita T: A novel mutation in the GAT3 gene of a Japanese patient with PTH-deficient hypoparathyroidsm. J Bone Miner Metab 27: 386-389, 2009

28) Saito T, Nishii Y, Yasuda T, Ito N, Suzuki H, Igarashi T, Fukumoto S, Fujita T: Familial hypophosphatemic rickets caused by a large deletion in PHEX gene. Eur J Endocrinol 161: 647-651, 2009

29) Sanada M, Suzuki T, Shih LY, Otsu M, Kato M, Yamazaki S, Tamura A, Honda H, Sakata-Yanagimoto M, Kumano K, Oda H, Yamagata T, Takita J, Gotoh N, Nakazaki K, Kawamata N, Onodera M, Nobuyoshi M, Hayashi Y, Harada H, Kurokawa M, Chiba S, Mori H, Ozawa K, Omine M, Hirai H, Nakauchi H, Koeffler HP, Ogawa S: Gain-of-unction of mutated C-CBL tumour suppressor in myeloid neoplasms. Nature 460: 904-908, 2009

30) Sato A, Mizuguchi M, Mimaki M, Takahashi K, Jimi H, Oka A, Igarashi T: Cortical gray matter lesions in acute encephalopathy with febrile convulsive status epilepticus. Brain Dev 31: 622-624, 2009

31) Sekine T, Miura K, Takahashi K, Igarashi T: Children's toxicology from bench to bed--Drug-induced renal injury (1): The toxic effects of ARB/ACEI on fetal kidney development. J Toxicol Sci 34: 245-250, 2009

32) Sekine T, Endou H: Children's toxicology from bench to bed--Drug-induced renal injury (3): Drug transporters and toxic nephropathy in childhood. J Toxicol Sci 34: 259-265, 2009

33) Shinozaki Y, Osawa M, Sakuma H, Komaki H, Nakagawa E, Sugai K, Sasaki M, Goto Y: Expansion of the first polyalanine tract of the ARX gene in a boy presenting with generalized dystonia in the absence of infantile spasms. Brain Dev 31: 469-472, 2009

34) Takanashi S, Oishi Y, Ito N, Nanba Y, Tsukamoto K, Nakamura T, Ito Y, Hayashi S, Sago H, Kuroda T, Honna T: Evaluating mortality and disease severity in congenital diaphragmatic hernia using the McGoon and pulmonary artery indices. J Pediatr Surg 44: 2101-2106, 2009

35) Takanashi S, Hashira S, Matsunaga T, Yoshida A, Shiota T, Tung PG, Khamrin P, Okitsu S, Mizuguchi M, Igarashi T, Ushijima H: Detection, genetic characterization and quantification of norovirus RNA from sera of children with gastroenteritis. J Clin Virol 44: 161-163, 2009

36) Takita J, Motomura A, Koh K, Ida K, Taki T, Hayashi Y, Igarashi T: Acute megakaryoblastic leukemia in a child with the MLL-AF4 fusion gene. Eur J Haematol 83: 149-153, 2009

37) Tomizawa D, Koh K, Hirayama M, Miyamura T, Hatanaka M, Saikawa Y, Ishii E: Outcome of recurrent or refractory acute lymphoblastic leukemia in infants with MLL gene rearrangements: A report from the Japan infant leukemia study group. Pediatr Blood Cancer 52:808-813, 2009

38) Uchisaka N, Takahashi N, Sato M, Kikuchi A, Mochizuki S, Imai K, Nonoyama S, Ohara O, Watanabe F, Mizutani S, Hanada R, Morio T: Two brothers with ataxia-telangiectasia-like disorder with lung adenocarcinoma. J Pediatr 155: 435-438, 2009

39) Yin D, Ogawa S, Kawamata N, Tunici P, Finocchiaro G, Eoli M, Ruckert C, Huynh T, Liu G, Kato M, Sanada M, Jauch A, Dugas M, Black KL, Koeffler HP. High-resolution genomic copy number profiling of glioblastoma multiforme by single nucleotide polymorphism DNA microarray. Mol Cancer Res 7: 665-677, 2009

40) Yoshida N, Yagasaki H, Yoshimi A, Takahashi Y, Xu Y, Hama A, Nishio N, Muramatsu H, Watanabe N, Matsumoto K, Kato K, Ueyama J, Inada H, Goto H, Yabe M, Mimaya J, Kikuchi A, Manabe A, Kojima S: Clinical features and prognostic impact of GM-CSF signaling pathway-related genes in juvenile myelomonocytic leukemia. Pediatr Res 65: 334-340, 2009

和文原著

1) 青木良則, 康勝好, 滝田順子, 堀江豪, 関正史, 古屋彩夏, 井田孔明, 五十嵐隆:最近当科で経験した1歳以上の神経芽腫stage 4の10例.小児がん 46: 184-189, 2009

2) 安藤亜希,小林さより,仁後綾子,浦田純,絹巻暁子,黒澤照喜,小高学,柳原知子,和気彰子,榊原裕史,松岡典子,小鍛冶雅之,寺川敏郎,横路征太郎:診断確定時に血清CRP値が1.0mg/dl未満であった重症細菌感染症の3例―当院の髄膜炎症例における血清CRP値と他の指標の比較―.小児科臨床 62: 1893-1900, 2009

3) 伊藤淳, 五石圭司, 松岡貴子, 石黒秋生, 西村力, 亀井良政, 五十嵐隆:塩酸イソプロテレノールの粉砕内服にて完全房室ブロックの心拍数管理を試みた新生児ループス症候群の1例. 小児科臨床 62: 2249-2255, 2009

4) 大嶋宏一, 菊地陽, 望月慎史, 花田良二:小児血液・腫瘍患者におけるインフルエンザワクチンの抗体反応. 日本小児科学会雑誌113: 533-538, 2009

5) 菊地陽:Down症候群のTransient Abnormal Myelopoiesis (TAM)について. 日本小児血液学会雑誌23:8-61, 2009

6) 五石圭司:感染対策-MRSA対策.小児科診療 72 : 1801-1805, 2009

7) 塩崎純子, 康勝好, 佐藤詩子, 三浦健一郎, 関根孝司, 五十嵐隆:初発時に著明な高カルシウム血症を認めた急性リンパ性白血病の1例. 日本小児体液研究会誌, 1: 17-19, 2009

8) 塩澤亮輔, 井田孔明, 三浦健一郎, 本村あい, 康勝好, 滝田順子, 佐藤詩子, 関根孝司, 五十嵐隆:大量MTX療法後に低Ca血漿を呈した急性リンパ性白血病の1例. 日本小児体液研究会誌 1: 20-22, 2009

9) 田村美沙, 滝田順子, 古屋彩夏, 康勝好, 井田孔明, 滝智彦, 大西宏明, 別所文雄, 五十嵐隆:治療関連白血病(二次性白血病)の3例. 日本小児血液学会雑誌23: 199-203, 2009

10) 松山健, 清水マリ子, 五月女友美子, 田中百合子, 浦清, 山内邦昭, 北川照男, 伊藤雄平, 五十嵐隆:学校検尿システムにおける潜血反応のカットオフ値の検討. 小児科臨床62: 1085-1089, 2009

11) 三浦健一郎, 関根孝司, 西村力, 金森豊, 長田道夫, 五十嵐隆:生直後に多発性嚢胞および著明な水尿管を呈し, 1ヶ月後には嚢胞の消退傾向をみたobstructive renal dysplasiaと考えられる1例. 発達腎研究会誌17: 13-15, 2009

12) 山本将平, 菊地陽, 望月慎史, 大嶋宏一, 加藤元博, 新井心, 花田良二:小児血液悪性疾患の治療初期に発症した腫瘍崩壊症候群(TLS)に対する血液浄化療法の検討. 日本小児血液学会雑誌23: 345-349, 2009

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