代表
電話045-711-2351

神奈川県立こども医療センター
電話番号0457112351
スライドメニューのアイコン
トップに戻る

2019年 発表論文2019 Papers Presented

2019年 発表論文

  1. Tamura S, Satake T, Muto M, Shibuya M, Narui K, Kobayashi S（形成外科）, Ishikawa T, Maegawa J. Immediate Breast Reconstruction with a Deep Inferior Epigastric Perforator Flap in the Lithotomy Position. Plast Reconstr Surg Glob Open. 2019 Dec 26;7(12):e2552.
  2. Kusakawa M, Sato T, Hosoda A, Araki E, Matsuzaki Y, Yamashita Y, Ishihara J, Inagaki Y（新生児科）, Uchida N, Ishii T, Hasegawa T. A neonatal case of HDR syndrome and a vascular ring with a novel GATA3 mutation. Hum Genome Var. 2019 Dec 23;6:55.
  3. Ikeda A, Yamamoto A, Ichikawa K, Tsuyusaki Y, Tsuji M, Iai M（神経内科）, Enomoto Y（臨床研究所）, Murakami H, Kurosawa K（遺伝科）, Miyatake S, Matsumoto N, Goto T（神経内科）. Epilepsy in Christianson syndrome: Two cases of Lennox-Gastaut syndrome and a review of literature. Epilepsy Behav Rep. 2019 Dec 5;13:100349.
  4. Keino D, Yokosuka T, Iwasaki F, Hamanoue S, Goto H（血液・腫瘍科）. Myelodysplastic syndrome following a Fontan procedure: A case report. Pediatr Int. 2019 Dec;61(12):1268-1270.
  5. Uchida K, Shimizu H, Nagafuchi H（救急・集中治療科）, Yamamoto A（神経内科）, Ono S（循環器内科）. Severe cardiac dysfunction induced by thiopental sodium. Pediatr Int. 2019 Dec;61(12):1270-1272.
  6. Shimizu A, Tanaka K, Takazawa S, Nishi A, Shimoyama S, Kobayashi T, Imagawa T(感染免疫科）, Hirato J, Yamada Y. A large superior mesenteric artery aneurysm and ileal obstruction: a rare presentation of polyarteritis nodosa in an infant. Oxf Med Case Reports. 2019 Sep 28;2019(9):omz092.
  7. Yasuhara J, Kuno T, Taki M, Toda K, Kumamoto T, Kojima T, Shimizu H（救急・集中治療科）, Yoshiba S, Kobayashi T, Sumitomo N. Predictors of Early Postoperative Supraventricular Tachyarrhythmias in Children After the Fontan Procedure. Int Heart J. 2019 Nov 30;60(6):1358-1365.
  8. Yamasaki K, Kiyotani C, Terashima K, Watanabe Y, Kanamori M, Koga Y, Hata N, Iwasaki F, Goto H（血液・腫瘍科）, Koh K, Kurihara J, Tokunaga S, Arakawa Y, Hasegawa D, Kosaka Y, Hara J. Clinical characteristics, treatment, and survival outcome in pediatric patients with atypical teratoid/rhabdoid tumors: a retrospective study by the Japan Children's Cancer Group. J Neurosurg Pediatr. 2019 Nov 15:1-10.
  9. Yokoi T（遺伝科）, Sei K（神経内科）, Enomoto Y（臨床研究所）, Naruto T, Kurosawa K（遺伝科）. Somatic mosaicism of a heterogeneous mutation of ACTA1 in nemaline myopathy. Pediatr Int. 2019 Nov;61(11):1169-1171.
  10. Miyamura T, Kudo K, Tabuchi K, Ishida H, Tomizawa D, Adachi S, Goto H（血液・腫瘍科）, Yoshida N, Inoue M, Koh K, Sasahara Y, Fujita N, Kakuda H, Noguchi M, Hiwatari M, Hashii Y, Kato K, Atsuta Y, Okamoto Y. Hematopoietic stem cell transplantation for pediatric acute myeloid leukemia patients with KMT2A rearrangement; A nationwide retrospective analysis in Japan. Leuk Res. 2019 Dec;87:106263.
  11. Tsurusaki Y（臨床研究所）, Kuroda Y（遺伝科）, Yamanouchi Y, Kondo E, Ouchi K, Kimura Y, Enomoto Y（臨床研究所）, Aida N（放射線科）, Masuno M, Kurosawa K（遺伝科）. Novel USP9X variants in two patients with X-linked intellectual disability. Hum Genome Var. 2019 Oct 21;6:49.
  12. Ohashi I（遺伝科）, Enomoto Y, Naruto T, Tsurusaki Y（臨床研究所）, Kuroda Y（遺伝科）, Ishikawa H（産婦人科）, Ohyama M（新生児科）, Aida N（放射線科）, Nishimura G, Kurosawa K（遺伝科）. A severe form of Ellis-van Creveld syndrome caused by novel mutations in EVC2. Hum Genome Var. 2019 Aug 26;6:40.
  13. Tominaga M（遺伝科）, Hamanoue S, Goto H（血液・腫瘍科）, Saito T, Nagai JI（新生児科）, Masuno M, Umeda Y, Kurosawa K（遺伝科）. Diamond-Blackfan anemia caused by chromosome 1p22 deletion encompassing RPL5. Hum Genome Var. 2019 Aug 8;6:36.
  14. Ichikawa K, Tsuyusaki Y（神経内科）, Shimbo H（臨床研究所）, Goto T（神経内科）. Late-onset Leigh syndrome with m.9176T>C mutation in the mitochondrial ATPase 6 gene. Pediatr Int. 2019 Oct;61(10):1055-1056.
  15. Hijiya N, Maschan A, Rizzari C, Shimada H, Dufour C, Goto H（血液・腫瘍科）, Kang HJ, Guinipero T, Karakas Z, Bautista F, Ducassou S, Yoo KH, Zwaan CM, Millot F, Aimone P, Allepuz A, Quenet S, Hourcade-Potelleret F, Hertle S, Sosothikul D. Phase 2 study of nilotinib in pediatric patients with Philadelphia chromosome- positive chronic myeloid leukemia. Blood. 2019 Dec 5;134(23):2036-2045.
  16. Sugisawa C, Takamizawa T, Abe K, Hasegawa T, Shiga K, Sugawara H, Ohsugi K, Muroya K, Asakura Y, Adachi M（内分泌代謝科）, Daitsu T, Numakura C, Koike A, Tsubaki J, Kitsuda K, Matsuura N, Taniyama M, Ishii S, Satoh T, Yamada M, Narumi S. Genetics of Congenital Isolated TSH Deficiency: Mutation Screening of the Known Causative Genes and a Literature Review. J Clin Endocrinol Metab. 2019 Dec 1;104(12):6229-6237.
  17. Onakatomi Y, Asou T, Takeda Y（心臓血管外科）, Ueda H（循環器内科）, Goda M, Masuda M. Aortic erosion occurring in over 5 years after Amplatzer septal Occluder implantation for secundum atrial septal defect: a case report. J Cardiothorac Surg. 2019 Sep 6;14(1):159.
  18. Kondo E, Ikeda T, Goto H（血液・腫瘍科）, Nishikori M, Maeda N, Matsumoto K, Kitagawa H, Noda N, Sugimoto S, Hara J. Pharmacokinetics of thiotepa in high-dose regimens for autologous hematopoietic stem cell transplant in Japanese patients with pediatric tumors or adult lymphoma. Cancer Chemother Pharmacol. 2019 Oct;84(4):849-860.
  19. Hiraide T, Kaba Yasui H（神経内科）, Kato M, Nakashima M, Saitsu H. A de novo variant in RAC3 causes severe global developmental delay and a middle interhemispheric variant of holoprosencephaly. J Hum Genet. 2019 Nov;64(11):1127-1132.
  20. Kawaguchi A, Kunimoto K, Inaba Y, Mikita N, Kaminaka C, Kanazawa N, Yamamoto Y, Kakimoto N, Suenaga T, Takeuchi T, Suzuki H, Baba N（皮膚科）, Jinnin M. Distribution analysis of infantile hemangioma or capillary malformation on the head and face in Japanese patients. J Dermatol. 2019 Oct;46(10):849-852.
  21. Miyoshi T, Maeno Y, Hamasaki T, Inamura N, Yasukochi S, Kawataki M, Horigome H, Yoda H, Taketazu M, Nii M, Hagiwara A（内科）, Kato H, Shimizu W, Shiraishi I, Sakaguchi H, Ueda K, Katsuragi S, Yamamoto H, Sago H, Ikeda T; Japan Fetal Arrhythmia Group. Antenatal Therapy for Fetal Supraventricular Tachyarrhythmias: Multicenter Trial. J Am Coll Cardiol. 2019 Aug 20;74(7):874-885.
  22. Kitagawa Y, Kim KS（循環器内科）, Kawataki M（新生児科）, Ono S, Yanagi S, Ueda H（循環器内科）. Fetal case of right atrial isomerism with infracardiac total anomalous pulmonary venous connection and agenesis of the ductus venosus. J Obstet Gynaecol Res. 2019 Nov;45(11):2275-2279.
  23. Hyakuna N, Hashii Y, Ishida H, Umeda K, Takahashi Y, Nagasawa M, Yabe H, Nakazawa Y, Koh K, Goto H（血液・腫瘍科）, Fujisaki H, Matsumoto K, Kakuda H, Yano M, Tawa A, Tomizawa D, Taga T, Adachi S, Kato K. Retrospective analysis of children with high-risk acute myeloid leukemia who underwent allogeneic hematopoietic stem cell transplantation following complete remission with initial induction chemotherapy in the AML-05 clinical trial. Pediatr Blood Cancer. 2019 Oct;66(10):e27875.
  24. Watanabe A, Inukai T, Kagami K, Abe M, Takagi M, Fukushima T, Fukushima H, Nanmoku T, Terui K, Ito T, Toki T, Ito E, Fujimura J, Goto H（血液・腫瘍科）, Endo M, Look T, Kamps M, Minegishi M, Takita J, Inaba T, Takahashi H, Ohara A, Harama D, Shinohara T, Somazu S, Oshiro H, Akahane K, Goi K, Sugita K. Resistance of t(17;19)-acute lymphoblastic leukemia cell lines to multiagents in induction therapy. Cancer Med. 2019 Sep;8(11):5274-5288.
  25. Hori D, Kobayashi R, Fujita N, Suzumiya J, Suzuki R, Kato K, Kawata T, Fukuda T, Inoue M, Goto H（血液・腫瘍科）, Hama A, Iwato K, Okumura H, Eto T, Hashii Y, AtsutaY, Mitsui T. The effectiveness of busulfan-based conditioning regimens for stem cell transplantation against lymphomas in children, adolescents, and young adults in Japan. Pediatr Blood Cancer. 2019 Oct;66(10):e27918.
  26. Okumura Y, Adachi Y, Shirahase T, Nagashima Y, Tanaka Y（病理診断科）, Taki Y, Watanabe J, Uegaki M, Sakatani T, Ikehara S. Malignant rhabdoid tumour in an adult kidney: A case report. Mol Clin Oncol. 2019 Jul;11(1):55-58.
  27. Tomotaki S, Toyoshima K, Shimokaze T（新生児科）, Kawai M. Reliability of real-time continuous glucose monitoring in infants. Pediatr Int. 2019 Oct;61(10):1001-1006.
  28. Taguchi I, Yamada T, Akaishi R, Imoto I, Kurosawa K（遺伝科）, Nakatani K, Nomura F, Hamanoue H, Hyodo M, Murakami H, Yoshihashi H, Yotsumoto J, Kosugi S. Attitudes of clinical geneticists and certified genetic counselors to genome editing and its clinical applications: A nation-wide questionnaire survey in Japan. J Hum Genet. 2019 Sep;64(9):945-954.
  29. Kobayashi S（形成外科）, Hirakawa T, Sasaki Y（歯科）, Fukawa T, Maegawa J. Orthodontic premaxillary setback versus premaxillary osteotomy with gingivoperiosteoplasty for Bilateral cleft lip and palate patients: 4-year observation outcomes. J Plast Reconstr Aesthet Surg. 2019 Nov;72(11):1813-1818.
  30. Toyoshima K（新生児科）, Isayama T, Kobayashi T, Su C, Mikami M, Yokoyama T, Iwami H, Nagasawa H, Kawasaki H, Amari S, Nakayama A, Ikeda T, Okada N, Yamamoto Y, Masutani S; Patent ductus arteriosus, Left Atrial Size Evaluation in preterm infants (PLASE) study group investigators. What echocardiographic indices are predictive of patent ductus arteriosus surgical closure in early preterm infants? A prospective multicenter cohort study. J Cardiol. 2019 Dec;74(6):512-518.
  31. Miyamoto S, Nakashima M, Ohashi T, Hiraide T, Kurosawa K（遺伝科）, Yamamoto T, Takanashi J, Osaka H, Inoue K, Miyazaki T, Wada Y, Okamoto N, Saitsu H. A case of de novo splice site variant in SLC35A2 showing developmental delays, spastic paraplegia, and delayed myelination. Mol Genet Genomic Med. 2019 Aug;7(8):e814.
  32. Ogushi K, Muroya K（内分泌代謝科）, Shima H, Jinno T, Miyado M, Fukami M. SHOX far- downstream copy-number variations involving cis-regulatory nucleotide variants in two sisters with Leri-Weill dyschondrosteosis. Am J Med Genet A. 2019 Sep;179(9):1778-1782.
  33. Fujita A, Higashijima T, Shirozu H, Masuda H, Sonoda M, Tohyama J, Kato M, Nakashima M, Tsurusaki Y, Mitsuhashi S, Mizuguchi T, Takata A, Miyatake S, Miyake N, Fukuda M, Kameyama S, Saitsu H, Matsumoto N. Pathogenic variants of DYNC2H1, KIAA0556, and PTPN11 associated with hypothalamic hamartoma. Neurology. 2019 Jul 16;93(3):e237-e251.
  34. Mikami T, Koyama A, Hashimoto K, Maegawa J, Yabuki Y, Kagimoto S, Kitayama S, Kaneta T, Yasumura K（形成外科）, Matsubara S, Iwai T. Pathological changes in the lymphatic system of patients with secondary upper limb lymphoedema. Sci Rep. 2019 Jun 11;9(1):8499.
  35. Nagashima K, Hiro T, Fukamachi D, Okumura Y, Watanabe I, Hirayama A, Tanaka M, Tanaka T, Takamisawa I, Taguchi I, Sato A, Aonuma K, Fukamizu S, Nakada A, Watanabe A, Amioka N, Suzuki Y, Matsumoto N, Koizumi J, Kumagai K, Naya M, Higuchi Y, Naito Y, Masuyama T, Kawamura M, Tsunoda R, Suzuki S, Ishii H, Murohara T, Shimizu T, Takeishi Y, Shiina K, Yamashita J, Imamura T, Sumitomo N, Noguchi T, Aso T（心臓血管外科）, Furukawa K, Takata A, Nakashima M, Saitsu H, Mizuguchi T, Mitsuhashi S, Takahashi Y, Okamoto N, Osaka H, Nakamura K, Tohyama J, Haginoya K, Takeshita S, Kuki I, Okanishi T, Goto T, Sasaki M, Sakai Y, Miyake N, Miyatake S, Tsuchida N, Iwama K, Minase G, Sekiguchi F, Fujita A, Imagawa E, Koshimizu E, Uchiyama Y, Hamanaka K, Ohba C, Itai T, Aoi H, Saida K, Sakaguchi T, Den K, Takahashi R, Ikeda H, Yamaguchi T, Tsukamoto K, Yoshitomi S, Oboshi T, Imai K, Kimizu T, Kobayashi Y, Kubota M, Kashii H, Baba S, Iai M（神経内科）, Kira R, Hara M, Ohta M, Miyata Y, Miyata R, Takanashi JI, Matsui J, Yokochi K, Shimono M, Amamoto M, Takayama R, Hirabayashi S, Aiba K, Matsumoto H, Nabatame S, Shiihara T, Kato M, Matsumoto N. Comprehensive analysis of coding variants highlights genetic complexity in developmental and epileptic encephalopathy. Nat Commun. 2019 Jun 7;10(1):2506.
  36. Sugiyama M, Hamanoue S（血液・腫瘍科）, Nagai JI（検査科）, Tsurusaki Y（臨床研究所）, Kurosawa K（遺伝科）, Tanaka M, Tanaka Y（病理診断科）, Goto H（血液・腫瘍科）. Hemoglobin beta Kanagawa [c.443A>C; p.(Ter148Serext*21)]: A novel β-globin gene mutation causing dominantly inherited β-thalassemia. Pediatr Blood Cancer. 2019 Sep;66(9):e27871.
  37. Kamikado Y, Mihara T, Ka K（麻酔科）. Anesthetic management of a pediatric patient with Loeys-Dietz syndrome: A case report. Paediatr Anaesth. 2019 Aug;29(8):875-877.
  38. Imel EA, Glorieux FH, Whyte MP, Munns CF, Ward LM, Nilsson O, Simmons JH, Padidela R, Namba N, Cheong HI, Pitukcheewanont P, Sochett E, Högler W, Muroya K（内分泌代謝科）, Tanaka H, Gottesman GS, Biggin A, Perwad F, Mao M, Chen CY, Skrinar A, San Martin J, Portale AA. Burosumab versus conventional therapy in children with X-linked hypophosphataemia: a randomised, active-controlled, open-label, phase 3 trial. Lancet. 2019 Jun 15;393(10189):2416-2427.
  39. Nagahara N, Tanaka M, Tanaka Y（病理診断科）, Ito T. Novel Characterization of Antioxidant Enzyme, 3-Mercaptopyruvate Sulfurtransferase-Knockout Mice: Overexpression of the Evolutionarily-Related Enzyme Rhodanese. Antioxidants (Basel). 2019 May 1;8(5):116.
  40. Murakami H（遺伝科）, Kimura Y, Enomoto Y, Tsurusaki （臨床研究所）, Akahira-Azuma M, Kuroda Y（遺伝科）, Tsuji M, Goto T（神経内科）, Kurosawa K（遺伝科）. Discordant phenotype caused by CASK mutation in siblings with NF1. Hum Genome Var. 2019 Apr 26;6:20.
  41. Hara R, Umebayashi H, Takei S, Okamoto N, Iwata N, Yamasaki Y, Nakagishi Y, Kizawa T, Kobayashi I, Imagawa T（感染免疫科）, Kinjo N, Amano N, Takahashi Y, Mori M, Itoh Y, Yokota S. Intravenous abatacept in Japanese patients with polyarticular-course juvenile idiopathic arthritis: results from a phase III open-label study. Pediatr Rheumatol Online J. 2019 Apr 30;17(1):17.
  42. Kubota M, Osuga Y, Kato K, Ishikura K, Kaneko K, Akazawa K, Yonekura T, Tazuke Y, Ieiri S, Fujino A, Ueno S, Hayashi Y, Yoshino K, Yanai T, Iwai J, Yamaguchi T, Amae S, Yamazaki Y（泌尿器科）, Sugita Y, Kohno M, Kanamori Y, Bitoh Y, Shinkai M（外科）, Ohno Y, Kinoshita Y. Treatment guidelines for persistent cloaca, cloacal exstrophy, and Mayer-Rokitansky-Küster-Häuser syndrome for the appropriate transitional care of patients. Surg Today. 2019 Dec;49(12):985-1002.
  43. Hangai M, Urayama KY, Tanaka J, Kato K, Nishiwaki S, Koh K, Noguchi M, Kato K, Yoshida N, Sato M, Goto H（血液・腫瘍科）, Yuza Y, Hashii Y, Atsuta Y, Mizuta S, Kato M. Allogeneic Stem Cell Transplantation for Acute Lymphoblastic Leukemia in Adolescents and Young Adults. Biol Blood Marrow Transplant. 2019 Aug;25(8):1597-1602.
  44. Adachi M（内分泌代謝科）, Takamasu T, Inuo C（アレルギー科）. Hyponatremia secondary to severe atopic dermatitis in early infancy. Pediatr Int. 2019 Jun;61(6):544-550.
  45. Hongo Y, Kaneko J, Suga H, Ishima D, Kitamura E, Akutsu T, Onozawa Y, Kanazawa N, Goto T（神経内科）, Nishiyama K, Iizuka T. Correction to: A cluster of disseminated small cortical lesions in MELAS: its distinctive clinical and neuroimaging features. J Neurol. 2019 Jun;266(6):1473.
  46. Iwasawa S, Yanagi K, Kikuchi A, Kobayashi Y, Haginoya K, Matsumoto H, Kurosawa K（遺伝科）, Ochiai M, Sakai Y, Fujita A, Miyake N, Niihori T, Shirota M, Funayama R, Nonoyama S, Ohga S, Kawame H, Nakayama K, Aoki Y, Matsumoto N, Kaname T, Matsubara Y, Shoji W, Kure S. Recurrent de novo MAPK8IP3 variants cause neurological phenotypes. Ann Neurol. 2019 Jun;85(6):927-933.
  47. Takenaka S, Kuroda Y（遺伝科）, Ohta S, Mizuno Y, Hiwatari M, Miyatake S, Matsumoto N, Oka A. A Japanese patient with RAD51-associated Fanconi anemia. Am J Med Genet A. 2019 Jun;179(6):900-902.
  48. Inuo C（アレルギー科）, Tanaka K, Nakajima Y, Yamawaki K, Matsubara T, Iwamoto H, Tsuge I, Urisu A, Kondo Y. Tolerability of partially and extensively hydrolysed milk formulas in children with cow's milk allergy. Asia Pac J Clin Nutr. 2019;28(1):49-56.
  49. Hongo Y, Kaneko J, Suga H, Ishima D, Kitamura E, Akutsu T, Onozawa Y, Kanazawa N, Goto T（神経内科）, Nishiyama K, Iizuka T. A cluster of disseminated small cortical lesions in MELAS: its distinctive clinical and neuroimaging features. J Neurol. 2019 Jun;266(6):1459-1472.
  50. Kondo A, Akada S, Akiyama K, Arakawa M, Ichi S, Inamoto Y, Ishida T, Ishikawa H（産婦人科）, Itoh T, Izumi A, Kimura F, Kondo AS, Matsuoka R, Miyauchi A, Mochizuki J, Momohara Y, Morikawa S, Morioka M, Morota N, Nakabe K, Obayashi S, Oku M, Samura O, Sasahara J, Sase M, Shimamoto K, Shimamura K, Sumigama S, Tada K, Takahashi H, Tani A, Wada S, Wada-HIraike O, Watanabe T, Yamaguchi M, Yasui T, Yokomine M. Real prevalence of neural tube defects in Japan: How many of such pregnancies have been terminated? Congenit Anom (Kyoto). 2019 Jul;59(4):118-124.
  51. Kuroda Y, Murakami H（遺伝科）, Enomoto Y, Tsurusaki Y（臨床研究所）, Takahashi K, Mitsuzuka K, Ishimoto H, Nishimura G, Kurosawa K（遺伝科）. A novel gene (FAM20B encoding glycosaminoglycan xylosylkinase) for neonatal short limb dysplasia resembling Desbuquois dysplasia. Clin Genet. 2019 Jun;95(6):713-717.
  52. Nakamura N（整形外科）, Inaba Y, Aota Y, Machida J, Saito T（新生児科）. Characteristic Reconstitution of the Spinal Langerhans Cell Histiocytosis in Young Children. J Pediatr Orthop. 2019 Apr;39(4):e308-e311.
  53. Nagafuchi H（救急・集中治療科）, Eguchi Y, Ikeda T. Impact of Antithrombin Supplementation and Concomitant Anticoagulation Therapy in Pediatric Patients With Disseminated Intravascular Coagulation. Clin Appl Thromb Hemost. 2019 Jan- Dec;25:1076029619834350.
  54. Matsubara K, Itoh M, Shimizu K, Saito S, Enomoto K, Nakabayashi K, Hata K, Kurosawa K（遺伝科）, Ogata T, Fukami M, Kagami M. Exploring the unique function of imprinting control centers in the PWS/AS-responsible region: finding from array-based methylation analysis in cases with variously sized microdeletions. Clin Epigenetics. 2019 Feb 28;11(1):36.
  55. Kuroda Y, Murakami H, Yokoi T（遺伝科）, Kumaki T（神経内科）, Enomoto Y, Tsurusaki Y（臨床研究所）, Kurosawa K（遺伝科）. Two unrelated girls with intellectual disability associated with a truncating mutation in the PPM1D penultimate exon. Brain Dev. 2019 Jun;41(6):538-541.
  56. Koshinaga T, Takimoto T, Okita H, Tanaka Y（病理診断科）, Inoue E, Oue T, Nozaki M, Tsuchiya K, Haruta M, Kaneko Y, Fukuzawa M. Blastemal predominant type Wilms tumor in Japan: Japan Children's Cancer Group. Pediatr Int. 2019 Apr;61(4):351-357.
  57. Matsumura N（眼科）, Suzuki T, Goto S, Fujita T（眼科）, Yamane S, Maruyama-Inoue M, Kadonosono K. Transcanalicular endoscopic primary dacryoplasty for congenital nasolacrimal duct obstruction. Eye (Lond). 2019 Jun;33(6):1008-1013.
  58. Aoi H, Lei M, Mizuguchi T, Nishioka N, Goto T（神経内科）, Miyama S, Suzuki T, Iwama K, Uchiyama Y, Mitsuhashi S, Itakura A, Takeda S, Matsumoto N. Nonsense variants in STAG2 result in distinct sex-dependent phenotypes. J Hum Genet. 2019 May;64(5):487-492.
  59. Kuwajima M, Goto M, Kurane K, Shimbo H（臨床研究所）, Omika N, Jimbo EF, Muramatsu K, Tajika M, Shimura M, Murayama K, Kurosawa K（遺伝科）, Yamagata T, Osaka H. MELAS syndrome with m.4450 G > A mutation in mitochondrial tRNAMet gene. Brain Dev. 2019 May;41(5):465-469.
  60. Okamoto Y, Kudo K, Tabuchi K, Tomizawa D, Taga T, Goto H（血液・腫瘍科）, Yabe H, Nakazawa Y, Koh K, Ikegame K, Yoshida N, Uchida N, Watanabe K, Koga Y, Inoue M, Kato K, Atsuta Y, Ishida H. Hematopoietic stem-cell transplantation in children with refractory acute myeloid leukemia. Bone Marrow Transplant. 2019 Sep;54(9):1489-1498.
  61. Numakura C, Tamiya G, Ueki M, Okada T, Maisawa SI, Kojima-Ishii K, Murakami J, Horikawa R, Tokuhara D, Ito K, Adachi M（内分泌代謝科）, Abiko T, Mitsui T, Hayasaka K. Growth impairment in individuals with citrin deficiency. J Inherit Metab Dis. 2019 May;42(3):501-508.
  62. Fujita N, Kobayashi R, Atsuta Y, Iwasaki F（血液・腫瘍科）, Suzumiya J, Sasahara Y, Inoue M, Koh K, Hori T, Goto H（血液・腫瘍科）, Ichinohe T, Hashii Y, Kato K, Suzuki R, Mitsui T. Hematopoietic stem cell transplantation in children and adolescents with relapsed or refractory B-cell non-Hodgkin lymphoma. Int J Hematol. 2019 Apr;109(4):483-490.
  63. Adachi M（内分泌代謝科）, Fukami M, Kagami M, Sho N（児童思春期精神科）, Yamazaki Y（泌尿器科）, Tanaka Y（病理診断科）, Asakura Y, Hanakawa J, Muroya K（内分泌代謝科）. Severe in utero under-virilization in a 46,XY patient with Silver-Russell syndrome with 11p15 loss of methylation. J Pediatr Endocrinol Metab. 2019 Feb 25;32(2):191-196.
  64. Aizawa Y, Shoji T, Ito K, Kasai M, Sakurai H, Toyofuku E（感染免疫科）, Minami K, Hoshino T, Horikoshi Y. Multidrug-resistant Gram-negative Bacterial Bloodstream Infections in Children's Hospitals in Japan, 2010-2017. Pediatr Infect Dis J. 2019 Jul;38(7):653-659.
  65. Handa A, Nozaki T, Makidono A, Okabe T, Morita Y, Fujita K（放射線科）, Matsusako M, Kono T, Kurihara Y, Hasegawa D, Kumamoto T, Ogawa C, Yuza Y, Manabe A. Pediatric oncologic emergencies: Clinical and imaging review for pediatricians. Pediatr Int. 2019 Feb;61(2):122-139.
  66. Haruta M, Arai Y, Okita H, Tanaka Y（病理診断科）, Takimoto T, Sugino RP, Yamada Y, Kamijo T, Oue T, Fukuzawa M, Koshinaga T, Kaneko Y. Combined Genetic and Chromosomal Characterization of Wilms Tumors Identifies Chromosome 12 Gain as a Potential New Marker Predicting a Favorable Outcome. Neoplasia. 2019 Jan;21(1):117-131.
  67. Nozawa K（放射線科）, Niwa T, Aida N. Imaging of Cystic Lung Lesions in Infants Using Pointwise Encoding Time Reduction with Radial Acquisition (PETRA). Magn Reson Med Sci. 2019 Oct 15;18(4):299-300.
  68. Murase N, Hinoki A, Shirota C, Tomita H, Shimojima N, Sasaki H, Nio M, Tahara K, Kanamori Y, Shinkai M（外科）, Yamamoto H, Sugawara Y, Hibi T, Ishimaru T, Kawashima H, Koga H, Yamataka A, Uchida H. Multicenter, retrospective, comparative study of laparoscopic and open Kasai portoenterostomy in children with biliary atresia from Japanese high-volume centers. J Hepatobiliary Pancreat Sci. 2019 Jan;26(1):43-50.
  69. Chino K, Sasaki Y, Miyagawa N（血液・腫瘍科）, Meredith B, Delaney KM, Goto H（血液・腫瘍科）, Rosario F. Pediatric cancer care can be complicated by language barriers: A case involving parents with limited Japanese proficiency. Pediatr Blood Cancer. 2019 Apr;66(4):e27563.
  70. Hamanaka K, Miyatake S, Koshimizu E, Tsurusaki Y（臨床研究所）, Mitsuhashi S, Iwama K, Alkanaq AN, Fujita A, Imagawa E, Uchiyama Y, Tawara N, Ando Y, Misumi Y, Okubo M, Nakashima M, Mizuguchi T, Takata A, Miyake N, Saitsu H, Iida A, Nishino I, Matsumoto N. RNA sequencing solved the most common but unrecognized NEB pathogenic variant in Japanese nemaline myopathy. Genet Med. 2019 Jul;21(7):1629-1638.
  71. Ikeda A, Watanabe Y, Kaba H（神経内科）, Kaneko K, Takahashi T, Takeshita S. MRI findings in pediatric neuromyelitis optica spectrum disorder with MOG antibody: Four cases and review of the literature. Brain Dev. 2019 Apr;41(4):367-372.
  72. Kobayashi, Fukawa T, Yasumura K, Yabuki Y（形成外科）, Satake T, Maegawa J. Overcorrected Midface Advancement to Improve Airway Problems in Severe Pfeiffer Syndrome Types II and III. J Craniofac Surg. 2019 Jan;30(1):53-56.
  73. Kobayashi S, Fukawa T, Yasumura K（形成外科）, Satake T, Maegawa J. Perinasal Osteotomy With Distraction Osteogenesis for a Mild Syndromic Craniosynostosis. J Craniofac Surg. 2019 Jan;30(1):50-52.
  74. Umeki I, Niihori T, Abe T, Kanno SI, Okamoto N, Mizuno S, Kurosawa K（遺伝科）, Nagasaki K, Yoshida M, Ohashi H, Inoue SI, Matsubara Y, Fujiwara I, Kure S, Aoki Y. Delineation of LZTR1 mutation-positive patients with Noonan syndrome and identification of LZTR1 binding to RAF1-PPP1CB complexes. Hum Genet. 2019 Jan;138(1):21-35.
  75. Sakaguchi H, Muramatsu H, Hasegawa D, Kudo K, Ishida H, Yoshida N, Koh K, Noguchi M, Shiba N, Tokimasa S, Fukuda T, Goto H（血液・腫瘍科）, Miyamura T, Nakazawa Y, Hashii Y, Inoue M, Atsuta Y; Pediatric AML Working Group of the Japan Society for Hematopoietic Cell Transplantation. Comparison of conditioning regimens for autologous stem cell transplantation in children with acute myeloid leukemia: A nationwide retrospective study in Japan. Pediatr Blood Cancer. 2019 Jan;66(1):e27459.
  76. Tsuda K, Iwata S, Mukai T, Shibasaki J（新生児科）, Takeuchi A, Ioroi T, Sano H, Yutaka N, Takahashi A, Takenouchi T, Osaga S, Tokuhisa T, Takashima S, Sobajima H, Tamura M, Hosono S, Nabetani M, Iwata O; Baby Cooling Registry of Japan Collaboration Team. Body Temperature, Heart Rate, and Short-Term Outcome of Cooled Infants. Ther Hypothermia Temp Manag. 2019 Mar;9(1):76-85.
  77. Tulyeu J, Tamaura M（神経内科）, Jimbo E, Shimbo H（臨床研究所）, Takano K, Iai M, Yamashita S, Goto T（神経内科）, Aida N（放射線科）, Tokuhiro E, Yamagata T, Osaka H. Aggregate formation analysis of GFAP R416W found in one case of Alexander disease. Brain Dev. 2019 Feb;41(2):195-200.
  78. Ohuchi H, Inai K, Nakamura M, Park IS, Watanabe M, Hiroshi O, Kim KS（循環器内科）, Sakazaki H, Waki K, Yamagishi H, Yamamura K, Kuraishi K, Miura M, Nakai M, Nishimura K, Niwa K; JSACHD Fontan Investigators. Mode of death and predictors of mortality in adult Fontan survivors: A Japanese multicenter observational study. Int J Cardiol. 2019 Feb 1;276:74-80.
  79. Yakushijin K, Ikezoe T, Ohwada C, Kudo K, Okamura H, Goto H（血液・腫瘍科）, Yabe H, Yasumoto A, Kuwabara H, Fujii S, Kagawa K, Ogata M, Onishi Y, Kohno A, Watamoto K, Uoshima N, Nakamura D, Ota S, Ueda Y, Oyake T, Koike K, Mizuno I, Iida H, Katayama Y, Ago H, Kato K, Okamura A, Kikuta A, Fukuda T. Clinical effects of recombinant thrombomodulin and defibrotide on sinusoidal obstruction syndrome after allogeneic hematopoietic stem cell transplantation. Bone Marrow Transplant. 2019 May;54(5):674-680.
  80. Tomizawa D, Yoshida M, Kondo T, Miyamura T, Taga T, Adachi S, Koh K, Noguchi M, Kakuda H, Watanabe K, Cho Y, Fukuda T, Kato M, Shiba N, Goto H（血液・腫瘍科）, Okada K, Inoue M, Hashii Y, Atsuta Y, Ishida H. Allogeneic hematopoietic stem cell transplantation for children and adolescents with high-risk cytogenetic AML: distinctly poor outcomes of FUS-ERG-positive cases. Bone Marrow Transplant. 2019 Mar;54(3):393-401.
  81. Yokoi T（遺伝科）, Saito T, Nagai JI（新生児科）, Kurosawa K（遺伝科）. 17q21.32-q22 Deletion in a girl with osteogenesis imperfecta, tricho-dento-osseous syndrome, and intellectual disability. Congenit Anom (Kyoto). 2019 Mar;59(2):51-52.
  82. Kato M, Kurata M, Kanda J, Kato K, Tomizawa D, Kudo K, Yoshida N, Watanabe K, Shimada H, Inagaki J, Koh K, Goto H（血液・腫瘍科）, Kato K, Cho Y, Yuza Y, Ogawa A（歯科）, Okada K, Inoue M, Hashii Y, Teshima T, Murata M, Atsuta Y. Impact of graft-versus-host disease on relapse and survival after allogeneic stem cell transplantation for pediatric leukemia. Bone Marrow Transplant. 2019 Jan;54(1):68-75.
  83. Okano T, Imai K, Tsujita Y, Mitsuiki N, Yoshida K, Kamae C, Honma K, Mitsui-Sekinaka K, Sekinaka Y, Kato T, Hanabusa K, Endo E, Takashima T, Hiroki H, Yeh TW, Tanaka K, Nagahori M, Tsuge I, Bando Y, Iwasaki F, Shikama Y（感染免疫科）, Inoue M, Kimoto T, Moriguchi N, Yuza Y, Kaneko T, Suzuki K, Matsubara T, Maruo Y, Kunitsu T, Waragai T, Sano H, Hashimoto Y, Tasaki K, Suzuki O, Shirakawa T, Kato M, Uchiyama T, Ishimura M, Tauchi T, Yagasaki H, Jou ST, Yu HH, Kanegane H, Kracker S, Durandy A, Kojima D, Muramatsu H, Wada T, Inoue Y, Takada H, Kojima S, Ogawa S, Ohara O, Nonoyama S, Morio T. Hematopoietic stem cell transplantation for progressive combined immunodeficiency and lymphoproliferation in patients with activated phosphatidylinositol-3-OH kinase δ syndrome type 1. J Allergy Clin Immunol. 2019 Jan;143(1):266-275.
  84. Ichikawa K, Tsuji M, Tsuyusaki Y（神経内科）, Tomiyasu M, Aida N（放射線科）, Goto T（神経内科）. Serial Magnetic Resonance Imaging and 1H-Magnetic Resonance Spectroscopy in GABA Transaminase Deficiency: A Case Report. JIMD Rep. 2019;43:7-12.
診療科

総合医療部門

内科系専門医療部門

外科系専門医療部門

こころの医療部門

周産期医療部門

医療技術部門

局・その他

緩和ケア普及室

医療安全推進室

スキンケア・褥瘡相談室

感染制御室

地域連携・家族支援局

遺伝カウンセリングセンター

⼩児がんセンター

メディカルゲノムセンター

総合周産期医療センター

成⼈移⾏期⽀援センター

アレルギーセンター

こどものこころの
ケアネットワーク事業

看護局

スペシャリストチーム等

専門医資格

入所施設

医療型障害児入所施設

臨床研究所

臨床研究所

ご来院される方へFor those visiting the hospital

受診のご案内

地域医療連携室

当センターの診療は、医療機関等からの紹介予約制になっています。

  • 診療受付時間08:30～15:00
  • 休診日土曜・日曜・祝日

診療時間は各診療科によって異なります。
詳しくは外来担当医週間一覧表をご確認ください。

アクセス

詳しく見る

〒232-8555　
神奈川県横浜市南区六ツ川 2-138-4

公共交通機関でお越しの方
お車・タクシーでお越しの方

関連サイト