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2020年 発表論文2020 Papers Presented

2020年 発表論文

  1. Mizutani A, Sabu Y, Naoi S, Ito S, Nakano S, Minowa K, Mizuochi T, Ito K, Abukawa D, Kaji S, Sasaki M, Muroya K（内分泌代謝科）, Azuma Y, Watanabe S, Oya Y, Inomata Y, Fukuda A, Kasahara M, Inui A, Takikawa H, Kusuhara H, Bessho K, Suzuki M, Togawa T, Hayashi H. Assessment of Adenosine Triphosphatase Phospholipid Transporting 8B1 (ATP8B1) Function in Patients With Cholestasis With ATP8B1 Deficiency by Using Peripheral Blood Monocyte-Derived Macrophages. Hepatol Commun. 2020 Sep 26;5(1):52-62.
  2. Murakami H（遺伝科）, Tamura N, Enomoto Y（臨床研究所）, Shimasaki K, Kurosawa K（遺伝科）, Hanada K. Intellectual disability-associated gain-of-function mutations in CERT1 that encodes the ceramide transport protein CERT. PLoS One. 2020 Dec 21;15(12):e0243980.
  3. Komazaki M（麻酔科）, Mihara T, Nakamura N, Ka K（麻酔科）, Goto T. Preventive effect of ramelteon on emergence agitation after general anaesthesia in paediatric patients undergoing tonsillectomy: a randomised, placebo-controlled clinical trial. Sci Rep. 2020 Dec 15;10(1):21996.
  4. Kobayashi S（形成外科）, Fukawa T, Yabuki Y, Satake T, Maegawa J. Le fort II distraction osteogenesis with a hybrid system for an Apert syndrome patient: A case report. JPRAS Open. 2020 Nov 26;27:34-39.
  5. Tsukamoto A, Kobayashi S, Yabuki Y, Yamada T（形成外科）, Itou S（脳神経外科）, Tanaka Y（病理診断科）, Maegawa J, Satake T. Intraoral Approach for a Congenital Teratoma in the Orbit Extending into the Pterygopalatine Fossa. Plast Reconstr Surg Glob Open. 2020 Nov 24;8(11):e3238.
  6. Honda S, Chatterjee A, Leichter AL, Miyagi H, Minato M, Fujiyoshi S, Ara M, Kitagawa N（外科）, Tanaka M, Tanaka Y（病理診断科）, Shinkai M（外科）, Hatanaka KC, Taketomi A, Eccles MR. A MicroRNA Cluster in the DLK1-DIO3 Imprinted Region on Chromosome 14q32.2 Is Dysregulated in Metastatic Hepatoblastomas. Front Oncol. 2020 Nov 12;10:513601.
  7. Riko M, Toyoshima K, Shimokaze T（新生児科）, Kumagai T, Suzuki H. Clinical Presentation of Preterm Infants with Ventricular Septal Defect. Tohoku J Exp Med. 2020 Dec;252(4):281-286.
  8. Enomura M, Murata S, Terado Y, Tanaka M, Kobayashi S（形成外科）, Oba T, Kagimoto S, Yabuki Y, Morita K, Uemura T, Maegawa J, Taniguchi H. Development of a Method for Scaffold-Free Elastic Cartilage Creation. Int J Mol Sci. 2020 Nov 11;21(22):8496.
  9. Shimokaze T（新生児科）, Yamamoto K, Miyamoto Y（麻酔科）, Toyoshima K, Katsumata K, Saito T（新生児科）. Acute respiratory effect of transpyloric feeding for respiratory exacerbation in preterm infants. J Perinat Med. 2020 Nov 11;49(3):383-387.
  10. Kashiki H, Li H, Miyamoto S, Ueno H, Tsurusaki Y, Ikeda C, Kurata H, Okada T, Shimazu T, Imamura H, Enomoto Y, Takanashi JI, Kurosawa K, Saitsu H, Inoue K（遺伝科）.[管理者4] POLR1C variants dysregulate splicing and cause hypomyelinating leukodystrophy. Neurol Genet. 2020 Oct 13;6(6):e524.
  11. Ikeda S, Akamatsu C, Ijuin A, Nagashima A, Sasaki M, Mochizuki A, Nagase H（産婦人科）, Enomoto Y（臨床研究所）, Kuroda Y, Kurosawa K（遺伝科）, Ishikawa H（産婦人科）. Prenatal diagnosis of Fraser syndrome caused by novel variants of FREM2. Hum Genome Var. 2020 Oct 2;7:32.
  12. Nishimura N, Kumaki T, Murakami H（遺伝科）, Enomoto Y（臨床研究所）, Katsumata K, Toyoshima K（新生児科）, Kurosawa K（遺伝科）. Arthrogryposis multiplex congenita with polymicrogyria and infantile encephalopathy caused by a novel GRIN1 variant. Hum Genome Var. 2020 Sep 25;7:29.
  13. Inoue M（耳鼻いんこう科）, Hirama M, Kobayashi S（形成外科）, Ogahara N, Takahashi M, Oridate N. Long- term outcomes in children with and without cleft palate treated with tympanostomy for otitis media with effusion before the age of 2 years. Acta Otolaryngol. 2020 Dec;140(12):982-989.
  14. Kumano Y, Hayashi C, Gohbara A, Yamazaki Y（泌尿器科）. A simple screening tool for an unfavorable bladder in children with myelomeningocele: Is the height to width ratio of the cystogram useful to predict high-pressure bladder? J Pediatr Urol. 2020 Dec;16(6):839.e1-839.e5.
  15. 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 of STAG2 result in distinct congenital anomalies. Hum Genome Var. 2020 Sep 18;7:26.
  16. Shinohara T, Urayama KY, Watanabe A, Akahane K, Goi K, Huang M, Kagami K, Abe M, Sugita K, Okada Y, Goto H（血液・腫瘍科）, Minegishi M, Iwamoto S, Inukai T. Inherited genetic variants associated with glucocorticoid sensitivity in leukaemia cells. J Cell Mol Med. 2020 Nov;24(22):12920-12932.
  17. Kubota Y, Seki M, Kawai T, Isobe T, Yoshida M（病理診断科）, Sekiguchi M, Kimura S, Watanabe K, Sato-Otsubo A, Yoshida K, Suzuki H, Kataoka K, Fujii Y, Shiraishi Y, Chiba K, Tanaka H, Hiwatari M, Oka A, Hayashi Y, Miyano S, Ogawa S, Hata K, Tanaka Y（病理診断科）, Takita J. Comprehensive genetic analysis of pediatric germ cell tumors identifies potential drug targets. Commun Biol. 2020 Sep 30;3(1):544.
  18. Akiyama T, Hyodo Y, Hasegawa K, Oboshi T, Imai K, Ishihara N, Dowa Y, Koike T, Yamamoto T, Shibasaki J（新生児科）, Shimbo H（臨床研究所）, Fukuyama T, Takano K, Shiraku H, Takeshita S, Okanishi T, Baba S, Kubota M, Hamano SI, Kobayashi K. Pyridoxal in the Cerebrospinal Fluid May Be a Better Indicator of Vitamin B6-dependent Epilepsy Than Pyridoxal 5'-Phosphate. Pediatr Neurol. 2020 Dec;113:33-41.
  19. Okamoto Y, Nakazawa Y, Inoue M, Watanabe K, Goto H（血液・腫瘍科）, Yoshida N, Noguchi M, Kikuta A, Kato K, Hashii Y, Atsuta Y, Kato M. Hematopoietic stem cell transplantation in children and adolescents with nonremission acute lymphoblastic leukemia. Pediatr Blood Cancer. 2020 Dec;67(12):e28732.
  20. Yokoi T（遺伝科）, Enomoto Y（臨床研究所）, Tsurusaki Y, Naruto T（臨床研究所）, Kurosawa K（遺伝科）. Cantú syndrome with novel pathogenic variant in nucleotide-binding domain 1 of ABCC9. Pediatr Int. 2020 Oct;62(10):1206-1208.
  21. Hasegawa D, Tawa A, Tomizawa D, Watanabe T, Saito AM, Kudo K, Taga T, Iwamoto S, Shimada A, Terui K, Moritake H, Kinoshita A, Takahashi H, Nakayama H, Koh K, Goto H（血液・腫瘍科）, Kosaka Y, Miyachi H, Horibe K, Nakahata T, Adachi S. Attempts to optimize postinduction treatment in childhood acute myeloid leukemia without core-binding factors: A report from the Japanese Pediatric Leukemia/Lymphoma Study Group (JPLSG). Pediatr Blood Cancer. 2020 Dec;67(12):e28692.
  22. Kawashima S, Yagi H, Hirano Y, Toki M, Izumi K, Dateki S, Namba N, Kamimaki T, Muroya K（内分泌代謝科）, Tanaka T, Fukami M, Kagami M; Japanese SHOX study group. Screening for imprinting disorders in 58 patients with clinically diagnosed idiopathic short stature. J Pediatr Endocrinol Metab. 2020 Aug 31;33(10):1335-1339.
  23. Yanagimachi M（血液・腫瘍科）, Kato K, Iguchi A, Sasaki K, Kiyotani C, Koh K, Koike T, Sano H, Shigemura T, Muramatsu H, Okada K, Inoue M, Tabuchi K, Nishimura T, Mizukami T, Nunoi H, Imai K, Kobayashi M, Morio T. Hematopoietic Cell Transplantation for Chronic Granulomatous Disease in Japan. Front Immunol. 2020 Jul 29;11:1617.
  24. Iwahashi-Odano M, Nagasaki K, Fukami M, Nishioka J, Yatsuga S, Asakura Y, Adachi M, Muroya K（内分泌代謝科）, Hasegawa T, Narumi S. Congenital Hypothyroidism Due to Truncating PAX8 Mutations: A Case Series and Molecular Function Studies. J Clin Endocrinol Metab. 2020 Nov 1;105(11):dgaa584.
  25. Murakami H（遺伝科）, Tsurusaki Y（臨床研究所）, Enomoto K, Kuroda Y, Yokoi T, Furuya N, Yoshihashi H, Minatogawa M, Abe-Hatano C, Ohashi I, Nishimura N, Kumaki T（遺伝科）, Enomoto Y, Naruto T（臨床研究所）, Iwasaki F（血液・腫瘍科）, Harada N（検査科）, Ishikawa A, Kawame H, Sameshima K, Yamaguchi Y, Kobayashi M, Tominaga M, Ishikiriyama S, Tanaka T, Suzumura H, Ninomiya S, Kondo A, Kaname T, Kosaki K, Masuno M, Kuroki Y, Kurosawa K（遺伝科）. Update of the genotype and phenotype of KMT2D and KDM6A by genetic screening of 100 patients with clinically suspected Kabuki syndrome. Am J Med Genet A. 2020 Oct;182(10):2333-2344.
  26. Yokoi T（遺伝科）, Enomoto Y（臨床研究所）, Uehara T, Kosaki K, Kurosawa K（遺伝科）. A Japanese girl with mild xeroderma pigmentosum group D neurological disease diagnosed using whole- exome sequencing. Hum Genome Var. 2020 Aug 7;7:22.
  27. Keino D, Yokosuka T, Hirose A, Sakurai Y, Nakamura W, Fujita S, Hayashi A, Miyagawa N, Iwasaki F, Hamanoue S, Yanagimachi M, Shiomi M, Goto S（血液・腫瘍科）, Kitagawa N（外科）, Tanaka M（病理診断科）, Nozawa K（放射線科）, Tanaka Y（病理診断科）, Goto H（血液・腫瘍科）. Pilot study of the combination of sorafenib and fractionated irinotecan in pediatric relapse/refractory hepatic cancer (FINEX pilot study). Pediatr Blood Cancer. 2020 Nov;67(11):e28655.
  28. Kumamoto T, Goto H（血液・腫瘍科）, Ogawa C, Hori T, Deguchi T, Araki T, Saito AM, Manabe A, Horibe K, Toyoda H. FLEND (nelarabine, fludarabine, and etoposide) for relapsed T-cell acute lymphoblastic leukemia in children: a report from Japan Children's Cancer Group. Int J Hematol. 2020 Nov;112(5):720-724.
  29. Kimura S, Toyoshima K, Shimokaze T, Hoshino R（新生児科）. Using airway resistance measurement to determine when to switch ventilator modes in congenital diaphragmatic hernia: a case report. BMC Pediatr. 2020 Aug 3;20(1):365.
  30. Nakaminami H, Ozawa K, Sasai N, Ikeda M, Nemoto O, Baba N（皮膚科）, Matsuzaki Y, Sawamura D, Shimoe F, Inaba Y, Kobayashi Y, Kawasaki S, Ueki T, Funatsu S, Shirahama S, Noguchi N. Current status of Panton-Valentine leukocidin-positive methicillin-resistant Staphylococcus aureus isolated from patients with skin and soft tissue infections in Japan. J Dermatol. 2020 Nov;47(11):1280-1286.
  31. Usui H, Shinkai M, Kitagawa N, Mochizuki K, Kawakita I, Tsuzuki Y, Shinohara S, Yagi Y（外科）, Masuda M. Lymphatic malformations compromising the upper airway in children: ultrasound-guided intralesional focal sclerotherapy with bleomycin targeting culprit lesions. Pediatr Surg Int. 2020 Sep;36(9):1047-1054.
  32. Tsuchiya M, Yamada T, Akaishi R, Hamanoue H, Hirasawa A, Hyodo M, Imoto I, Kosho T, Kurosawa K（遺伝科）, Murakami H, Nakatani K, Nomura F, Sasaki A, Shimizu K, Tamai M, Umemura H, Watanabe A, Yoshida A, Yoshihashi H, Yotsumoto J, Kosugi S. Attitudes toward and current status of disclosure of secondary findings from next-generation sequencing: a nation-wide survey of clinical genetics professionals in Japan. J Hum Genet. 2020 Dec;65(12):1045-1053.
  33. Sekiguchi M, Seki M, Kawai T, Yoshida K, Yoshida M, Isobe T, Hoshino N, Shirai R, Tanaka M（病理診断科）, Souzaki R, Watanabe K, Arakawa Y, Nannya Y, Suzuki H, Fujii Y, Kataoka K, Shiraishi Y, Chiba K, Tanaka H, Shimamura T, Sato Y, Sato-Otsubo A, Kimura S, Kubota Y, Hiwatari M, Koh K, Hayashi Y, Kanamori Y, Kasahara M, Kohashi K, Kato M, Yoshioka T, Matsumoto K, Oka A, Taguchi T, Sanada M, Tanaka Y（病理診断科）, Miyano S, Hata K, Ogawa S, Takita J. Integrated multiomics analysis of hepatoblastoma unravels its heterogeneity and provides novel druggable targets. NPJ Precis Oncol. 2020 Jul 7;4:20.
  34. Ito S, Yokoyama U, Nakakoji T, Cooley MA, Sasaki T, Hatano S, Kato Y, Saito J, Nicho N, Iwasaki S, Umemura M, Fujita T, Masuda M, Asou T（心臓血管外科）, Ishikawa Y. Fibulin-1 Integrates Subendothelial Extracellular Matrices and Contributes to Anatomical Closure of the Ductus Arteriosus. Arterioscler Thromb Vasc Biol. 2020 Sep;40(9):2212-2226.
  35. Kinjo K, Nagasaki K, Muroya K（内分泌代謝科）, Suzuki E, Ishiwata K, Nakabayashi K, Hattori A, Nagao K, Nozawa RS, Obuse C, Miyado K, Ogata T, Fukami M, Miyado M. Rare variant of the epigenetic regulator SMCHD1 in a patient with pituitary hormone deficiency. Sci Rep. 2020 Jul 3;10(1):10985.
  36. Yasuda T, Sanada M, Nishijima D, Kanamori T, Iijima Y, Hattori H, Saito A, Miyoshi H, Ishikawa Y, Asou N, Usuki K, Hirabayashi S, Kato M, Ri M, Handa H, Ishida T, Shibayama H, Abe M, Iriyama C, Karube K, Nishikori M, Ohshima K, Kataoka K, Yoshida K, Shiraishi Y, Goto H（血液・腫瘍科）, Adachi S, Kobayashi R, Kiyoi H, Miyazaki Y, Ogawa S, Kurahashi H, Yokoyama H, Manabe A, Iida S, Tomita A, Horibe K. Clinical utility of target capture-based panel sequencing in hematological malignancies: A multicenter feasibility study. Cancer Sci. 2020 Sep;111(9):3367-3378.
  37. Ikemoto S, Hamano SI, Kikuchi K, Koichihara R, Hirata Y, Matsuura R, Hiraide T, Nakashima M, Inoue K, Kurosawa K（遺伝科）, Saitsu H. A recurrent TMEM106B mutation in hypomyelinating leukodystrophy: A rapid diagnostic assay. Brain Dev. 2020 Sep;42(8):603-606.
  38. Yamada M, Shiraishi Y, Uehara T, Suzuki H, Takenouchi T, Abe-Hatano C, Kurosawa K（遺伝科）, Kosaki K. Diagnostic utility of integrated analysis of exome and transcriptome: Successful diagnosis of Au-Kline syndrome in a patient with submucous cleft palate, scaphocephaly, and intellectual disabilities. Mol Genet Genomic Med. 2020 Sep;8(9):e1364.
  39. Norioka R, Kumada S, Tobisawa S, Tsuyusaki Y（神経内科）, Isozaki E. Clinical characteristics of children and adults with anti-N-methyl-D-aspartate receptor encephalitis. Clin Neurol Neurosurg. 2020 Sep;196:106015.
  40. Watanabe A, Miyake K, Nordlund J, Syvänen AC, van der Weyden L, Honda H, Yamasaki N, Nagamachi A, Inaba T, Ikawa T, Urayama KY, Kiyokawa N, Ohara A, Kimura S, Kubota Y, Takita J, Goto H（血液・腫瘍科）, Sakaguchi K, Minegishi M, Iwamoto S, Shinohara T, Kagami K, Abe M, Akahane K, Goi K, Sugita K, Inukai T. Association of aberrant ASNS imprinting with asparaginase sensitivity and chromosomal abnormality in childhood BCP-ALL. Blood. 2020 Nov 12;136(20):2319-2333.
  41. Omi Y, Yamamoto T, Nagashima Y, Abe K, Karasawa K, Tanaka Y（病理診断科）, Okamoto T. Parathyroid carcinoma in a 13-year-old girl with a long-term survival. Surg Case Rep. 2020 Jun 22;6(1):145.
  42. Nishimura N, Kumaki T, Murakami H（遺伝科）, Enomoto Y, Tsurusaki Y（臨床研究所）, Tsuji M, Tsuyusaki Y, Goto T（神経内科）, Aida N（放射線科）, Kurosawa K（遺伝科）. Expanding the phenotype of COL4A1-related disorders-Four novel variants. Brain Dev. 2020 Oct;42(9):639-645.
  43. Horibe K, Morris JD, Tuglus CA, Dos Santos C, Kalabus J, Anderson A, Goto H（血液・腫瘍科）, Ogawa C. A phase 1b study of blinatumomab in Japanese children with relapsed/refractory B-cell precursor acute lymphoblastic leukemia. Int J Hematol. 2020 Aug;112(2):223-233.
  44. 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. Retraction Note to: Nonsense variants in STAG2 result in distinct sex-dependent phenotypes. J Hum Genet. 2020 Sep;65(9):811.
  45. Akahane K, Yasuda T, Tsuzuki S, Hayakawa F, Kiyokawa N, Somazu S, Watanabe A, Kagami K, Abe M, Harama D, Goi K, Kawazu M, Kojima S, Imamura T, Goto H（血液・腫瘍科）, Iwamoto S, Minegishi M, Abe M, Hojo H, Inaba T, Mano H, Sugita K, Inukai T. High prevalence of MEF2D fusion in human B-cell precursor acute lymphoblastic leukemia cell lines. Hematol Oncol. 2020 Oct;38(4):614-617.
  46. Miura M, Ishiyama A, Nakagawa E, Sasaki M, Kurosawa K（遺伝科）, Inoue K, Goto YI. 13q13.3 microdeletion associated with apparently balanced translocation of 46,XX,t(7;13) suggests NBEA involvement. Brain Dev. 2020 Sep;42(8):581-586.
  47. Yasuhara J, Kuno T, Kumamoto T, Kojima T, Shimizu H（救急・集中治療科）, Yoshiba S, Kobayashi T, Sumitomo N. Comparison of transcatheter patent ductus arteriosus closure between children and adults. Heart Vessels. 2020 Nov;35(11):1605-1613.
  48. Kobayashi S（形成外科）, Ohashi Y, Fukushima R（言語聴覚科）, Hirakawa T, Fukawa T, Satake T, Maegawa J. Treatment of congenital short palate using bilateral buccal musculomucosal flaps. Case Reports Plast Surg Hand Surg. 2020 May 6;7(1):57-62.
  49. Katayama K, Ishikawa D,（医療情報管理室）,Miyagi Y, Takemiya S, Okamoto N, Ogawa A. Qualitative analysis of cancer telephone consultations: Differences in the counseling needs of Japanese men and women. Patient Educ Couns. 2020 May 16:S0738-3991(20)30278-0.
  50. Arora V, Leon E, Diaz J, Hove HB, Carvalho DR, Kurosawa K, Nishimura N（遺伝科）, Nishimura G, Saxena R, Ferreira C, Puri RD, Verma IC. Unique skeletal manifestations in patients with Primrose syndrome. Eur J Med Genet. 2020 Aug;63(8):103967.
  51. Nogimori Y, Seo H, Ueda H（循環器内科）. A three-dimensional computer graphics tool for congenital heart diseases. Pediatr Int. 2020 Jun;62(6):738-740.
  52. Asou T（心臓血管外科）, Kawataki M（新生児科）, Takeda Y, Asai H, Tachibana T（心臓血管外科）, Toyoshima K（新生児科）, Kim KS, Ueda H（循環器内科）. Rapid two-stage Starnes approach in high-risk neonates with Ebstein anomaly. Eur J Cardiothorac Surg. 2020 Nov 1;58(5):957-963.
  53. Miyagi H, Ishii D, Hirasawa M, Yasuda S, Toriumi N, Sarashina T, Tanino M, Tanaka M, Tanaka Y（病理診断科）, Miyamoto K. Spontaneous pneumothorax caused by an inflammatory myofibroblastic tumor-like lesion in a 14-year-old girl: a case report. Surg Case Rep. 2020 May 24;6(1):109.
  54. Yoshida N, Takahashi Y, Yabe H, Kobayashi R, Watanabe K, Kudo K, Yabe M, Miyamura T, Koh K, Kawaguchi H, Goto H（血液・腫瘍科）, Fujita N, Okada K, Okamoto Y, Kato K, Inoue M, Suzuki R, Atsuta Y, Kojima S; Pediatric Aplastic Anemia Working Group of the Japan Society for Hematopoietic Cell Transplantation. Conditioning regimen for allogeneic bone marrow transplantation in children with acquired bone marrow failure: fludarabine/melphalan vs. fludarabine/cyclophosphamide. Bone Marrow Transplant. 2020 Jul;55(7):1272-1281.
  55. Yokoi T（遺伝科）, Enomoto Y（臨床研究所）, Naruto T, Kurosawa K（遺伝科）, Higurashi N. Tatton-Brown-Rahman syndrome with a novel DNMT3A mutation presented severe intellectual disability and autism spectrum disorder. Hum Genome Var. 2020 May 18;7:15.
  56. Kobayashi S, Inui A, Tsunoda T, Umetsu S, Sogo T, Mori M, Shinkai M（外科）, Fujisawa T. Liver cirrhosis in a child associated with Castleman's disease: A case report. World J Clin Cases. 2020 May 6;8(9):1656-1665.
  57. Hiyama E, Hishiki T, Watanabe K, Ida K, Ueda Y, Kurihara S, Yano M, Hoshino K, Yokoi A, Takama Y, Nogami Y, Taguchi T, Mori M, Kihira K, Miyazaki O, Fuji H, Honda S, Iehara T, Kazama T, Fujimura J, Tanaka Y（病理診断科）, Inoue T, Tajiri T, Kondo S, Oue T, Yoshimura K. Outcome and Late Complications of Hepatoblastomas Treated Using the Japanese Study Group for Pediatric Liver Tumor 2 Protocol. J Clin Oncol. 2020 Aug 1;38(22):2488-2498.
  58. Haeberle B, Rangaswami A, Krailo M, Czauderna P, Hiyama E, Maibach R, Lopez-Terrada D, Aronson DC, Alaggio R, Ansari M, Malogolowkin MH, Perilongo G, O'Neill AF, Trobaugh-Lotrario AD, Watanabe K, Schmid I, von Schweinitz D, Ranganathan S, Yoshimura K, Hishiki T, Tanaka Y（病理診断科）, Piao J, Feng Y, Rinaldi E, Saraceno D, Derosa M, Meyers RL. The importance of age as prognostic factor for the outcome of patients with hepatoblastoma: Analysis from the Children's Hepatic tumors International Collaboration (CHIC) database. Pediatr Blood Cancer. 2020 Aug;67(8):e28350.
  59. Kasai M, Shibata A, Hoshino A, Maegaki Y, Yamanouchi H, Takanashi JI, Yamagata T, Sakuma H, Okumura A, Nagase H, Ishii A, Goto T（神経内科）, Oka A, Mizuguchi M. Epidemiological changes of acute encephalopathy in Japan based on national surveillance for 2014-2017. Brain Dev. 2020 Aug;42(7):508-514.
  60. Adachi M（内分泌代謝科）, Tajima T, Muroya K（内分泌代謝科）. Correction to: Dietary potassium restriction attenuates urinary sodium wasting in the generalized form of pseudohypoaldosteronism type 1. CEN Case Rep. 2020 Aug;9(3):294.
  61. Masahata K, Usui N, Nagata K, Terui K, Hayakawa M, Amari S, Masumoto K, Okazaki T, Inamura N, Urushihara N, Toyoshima K（新生児科）, Uchida K, Furukawa T, Okawada M, Yokoi A, Okuyama H, Taguchi T. Risk factors for pneumothorax associated with isolated congenital diaphragmatic hernia: results of a Japanese multicenter study. Pediatr Surg Int. 2020 Jun;36(6):669-677.
  62. Kato N, Tachibana T（心臓血管外科）, Asai H, Ebuoka N, Shingu Y, Ooka T, Kato H, Wakasa S. Persistent Fifth Aortic Arch With Left Ventricular Dysfunction and Left Bronchial Obstruction. Ann Thorac Surg. 2020 Nov;110(5):e361-e363.
  63. Miyoshi Y, Yorifuji T, Shimizu C, Nagasaki K, Kawai M, Ishiguro H, Okada S, Kanno J, Takubo N, Muroya K（内分泌代謝科）, Ito J, Horikawa R, Yokoya S, Ozono K. A nationwide questionnaire survey targeting Japanese pediatric endocrinologists regarding transitional care in childhood, adolescent, and young adult cancer survivors. Clin Pediatr Endocrinol. 2020;29(2):55-62.
  64. Nishimura N, Murakami H（遺伝科）, Hayashi T, Sato H（脳神経外科）, Kurosawa K（遺伝科）. Multiple craniosynostosis and facial dysmorphisms with homozygous IL11RA variant caused by maternal uniparental isodisomy of chromosome 9. Congenit Anom (Kyoto). 2020 Sep;60(5):153-155.
  65. Kanda J, Umeda K, Kato K, Murata M, Sugita J, Adachi S, Koh K, Noguchi M, Goto H（血液・腫瘍科）, Yoshida N, Sato M, Koga Y, Hori T, Cho Y, Ogawa A, Inoue M, Hashii Y, Atsuta Y, Teshima T; JSHCT GVHD Working Group. Effect of graft-versus-host disease on outcomes after pediatric single cord blood transplantation. Bone Marrow Transplant. 2020 Jul;55(7):1430-1437.
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