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2021年 発表論文2021 Papers Presented

2021年 発表論文

  1. Tomomasa D, Isoda T, Mitsuiki N, Yamashita M, Morishita A, Tomoda T, Okano T, Endo A, Kamiya T, Yanagimachi M（血液・腫瘍科）, Imai K, Kanegane H, Takagi M, Morio T. Successful ruxolitinib administration for a patient with steroid-refractory idiopathic pneumonia syndrome following hematopoietic stem cell transplantation: A case report and literature review. Clin Case Rep. 2021 Dec 22;9(12):e05242.
  2. Nakachi T, Kato S, Saito N（検査科）, Fukui K, Iwasawa T, Endo T, Kosuge M, Utsunomiya D, Kimura K, Tamura K. Non-Invasive Evaluation of Patients Undergoing Percutaneous Coronary Intervention for Chronic Total Occlusion. J Clin Med. 2021 Oct 14;10(20):4712.
  3. Ono S, Yanagi S, Wakamiya T, Ichikawa Y, Kawai S, Kim KS, Ueda H（循環器内科）. Correlation of exercise-induced peripheral venous hypertension with exercise intolerance in patients with Fontan circulation. Cardiol Young. 2021 Oct 22:1-5.
  4. Somazu S, Tanaka Y, Tamai M, Watanabe A, Kagami K, Abe M, Harama D, Shinohara T, Akahane K, Goi K, Sugita K, Moriyama T, Yang J, Goto H（血液・腫瘍科）, Minegishi M, Iwamoto S, Takita J, Inukai T. NUDT15 polymorphism and NT5C2 and PRPS1 mutations influence thiopurine sensitivity in acute lymphoblastic leukaemia cells. J Cell Mol Med. 2021 Nov;25(22):10521-10533.
  5. Nagae G, Yamamoto S, Fujita M, Fujita T, Nonaka A, Umeda T, Fukuda S, Tatsuno K, Maejima K, Hayashi A, Kurihara S, Kojima M, Hishiki T, Watanabe K, Ida K, Yano M, Hiyama Y, Tanaka Y（病理診断科）, Inoue T, Ueda H, Nakagawa H, Aburatani H, Hiyama E. Genetic and epigenetic basis of hepatoblastoma diversity. Nat Commun. 2021 Sep 20;12(1):5423.
  6. Yamamoto S, Kato M, Watanabe K, Ishimaru S, Hasegawa D, Noguchi M, Hama A, Sato M, Koike T, Iwasaki F（血液・腫瘍科）, Yagasaki H, Takahashi Y, Kosaka Y, Hashii Y, Morimoto A, Atsuta Y, Hasegawa D, Yoshida N. Prognostic value of the revised International Prognostic Scoring System five-group cytogenetic abnormality classification for the outcome prediction of hematopoietic stem cell transplantation in pediatric myelodysplastic syndrome. Bone Marrow Transplant. 2021 Dec;56(12):3016-3023.
  7. Yanagimachi M（血液・腫瘍科）, Fukuda S, Tanaka F, Iwamoto M, Takao C, Oba K, Suzuki N, Kiyohara K, Kuranobu D, Tada N, Nagashima A, Ishii T, Ino Y, Kimura Y, Nawa N, Fujiwara T, Naruto T, Morio T, Doi S, Mori M. Leucine-rich alpha-2-glycoprotein 1 and angiotensinogen as diagnostic biomarkers for Kawasaki disease. PLoS One. 2021 Sep 9;16(9):e0257138.
  8. Terui K, Furukawa T, Nagata K, Hayakawa M, Okuyama H, Amari S, Yokoi A, Masumoto K, Yamoto M, Okazaki T, Inamura N, Toyoshima K（新生児科）, Uchida K, Okawada M, Sato Y, Usui N. Best pre-ductal PaO2 prior to extracorporeal membrane oxygenation as predictor of mortality in patients with congenital diaphragmatic hernia: a retrospective analysis of a Japanese database. Pediatr Surg Int. 2021 Dec;37(12):1667-1673.
  9. Masutani S, Isayama T, Kobayashi T, Pak K, Mikami M, Tomotaki S, Iwami H, Yokoyama T, Toyoshima K（新生児科）; PLASE (Patent ductus arteriosus and Left Atrial Size Evaluation in preterm infants) study group investigators. Ductus diameter and left pulmonary artery end-diastolic velocity at 3 days of age predict the future need for surgical closure of patent ductus arteriosus in preterm infants: A post-hoc analysis of a prospective multicenter study. J Cardiol. 2021 Dec;78(6):487-492.
  10. Miyamoto S, Umeda K, Kurata M, Nishimura A, Yanagimachi M（血液・腫瘍科）, Ishimura M, Sato M, Shigemura T, Kato M, Sasahara Y, Iguchi A, Koike T, Takahashi Y, Kajiwara M, Inoue M, Hashii Y, Yabe H, Kato K, Atsuta Y, Imai K, Morio T. Hematopoietic Cell Transplantation for Severe Combined Immunodeficiency Patients: a Japanese Retrospective Study. J Clin Immunol. 2021 Nov;41(8):1865-1877.
  11. Takeyoshi D, Cao Y, Ikarashi J, Asai H, Tachibana T（心臓血管外科）. [Modified Carpentier Technique is Useful Method for Tricuspid Regurgitation in Hypoplastic Left Heart Syndrome]. Kyobu Geka. 2021 Sep;74(9):647-651. Japanese.
  12. Shibasaki J（新生児科）, Niwa T, Piedvache A, Tomiyasu M（放射線科）, Morisaki N, Fujii Y（放射線科）, Toyoshima K（新生児科）, Aida N（放射線科）. Comparison of Predictive Values of Magnetic Resonance Biomarkers Based on Scan Timing in Neonatal Encephalopathy Following Therapeutic Hypothermia. J Pediatr. 2021 Dec;239:101-109.e4.
  13. Inoue M（耳鼻いんこう科）, Yamamoto K, Hirama M, Ogahara N, Takahashi M, Oridate N. Prognostic factors of early-onset otitis media with effusion in children treated using tympanostomy. Acta Otolaryngol. 2021 Aug;141(8):742-748.
  14. Kanamori M, Takami H, Suzuki T, Tominaga T, Kurihara J, Tanaka S, Hatazaki S, Nagane M, Matsuda M, Yoshino A, Natsumeda M, Yamaoka M, Kagawa N, Akiyama Y, Fukai J, Negoto T, Shibahara I, Tanaka K, Inoue A, Mase M, Tomita T, Kuga D, Kijima N, Fukami T, Nakahara Y, Natsume A, Yoshimoto K, Keino D（血液・腫瘍科）, Tokuyama T, Asano K, Ujifuku K, Abe H, Nakada M, Matsuda KI, Arakawa Y, Ikeda N, Narita Y, Shinojima N, Kambe A, Nonaka M, Izumoto S, Kawanishi Y, Kanaya K, Nomura S, Nakajima K, Yamamoto S, Terashima K, Ichimura K, Nishikawa R. Necessity for craniospinal irradiation of germinoma with positive cytology without spinal lesion on MR imaging-A controversy. Neurooncol Adv. 2021 Jun 25;3(1):vdab086.
  15. Sakamoto M, Sasaki K, Sugie A, Nitta Y, Kimura T, Gürsoy S, Cinleti T, Iai M（神経内科）, Sengoku T, Ogata K, Suzuki A, Okamoto N, Iwama K, Tsuchida N, Uchiyama Y, Koshimizu E, Fujita A, Hamanaka K, Miyatake S, Mizuguchi T, Taguri M, Ito S, Takahashi H, Miyake N, Matsumoto N. De novo ARF3 variants cause neurodevelopmental disorder with brain abnormality. Hum Mol Genet. 2021 Dec 17;31(1):69-81. doi: 10.1093/hmg/ddab224.
  16. Yoshino A（内分泌代謝科）, Kawamoto S, Abe T, Hidaka Y, Muroya K,[管理者2] Tokumoto T, Takeda T. A case of hypoparathyroidism, sensorineural deafness, and renal dysplasia syndrome with kidney failure and recurrent pancreatitis: Answers. Pediatr Nephrol. 2021 Dec;36(12):4071-4075. doi: 10.1007/s00467-021-05190-w. Epub 2021 Jul 29.
  17. Yoshino A, Kawamoto S, Abe T, Hidaka Y, Muroya K（内分泌代謝科）, Tokumoto T, Takeda T. A case of hypoparathyroidism, sensorineural deafness, and renal dysplasia syndrome with kidney failure and recurrent pancreatitis: Questions. Pediatr Nephrol. 2021 Dec;36(12):4067-4069.
  18. 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, Patterson B, Samis J, Aimone P, Allepuz A, Titorenko K, Sosothikul D. A phase 2 study of nilotinib in pediatric patients with CML: long-term update on growth retardation and safety. Blood Adv. 2021 Jul 27;5(14):2925-2934.
  19. Goto H, Yoshino Y, Ito M（血液・腫瘍科）, Nagai J（検査科）, Kumamoto T, Inukai T, Sakurai Y, Miyagawa N, Keino D, Yokosuka T, Iwasaki F, Hamanoue S, Shiomi M, Goto S（血液・腫瘍科）. Correction to: Aurora B kinase as a therapeutic target in acute lymphoblastic leukemia. Cancer Chemother Pharmacol. 2021 Dec;88(6):1055-1056.
  20. Ito N, Kubota T, Kitanaka S, Fujiwara I, Adachi M（内分泌代謝科）, Takeuchi Y, Yamagami H, Kimura T, Shinoda T, Minagawa M, Okazaki R, Ozono K, Seino Y, Fukumoto S. Clinical performance of a novel chemiluminescent enzyme immunoassay for FGF23. J Bone Miner Metab. 2021 Nov;39(6):1066-1075.
  21. Ono S, Takeshita K, Kiridoshi Y, Kato M, Kamiya T, Hoshino A, Yanagimachi M（血液・腫瘍科）, Arai K, Takeuchi I, Toita N, Imamura T, Sasahara Y, Sugita J, Hamamoto K, Takeuchi M, Saito S, Onuma M, Tsujimoto H, Yasui M, Taga T, Arakawa Y, Mitani Y, Yamamoto N, Imai K, Suda W, Hattori M, Ohara O, Morio T, Honda K, Kanegane H. Hematopoietic Cell Transplantation Rescues Inflammatory Bowel Disease and Dysbiosis of Gut Microbiota in XIAP Deficiency. J Allergy Clin Immunol Pract. 2021 Oct;9(10):3767-3780.
  22. Takizaki N, Hanakawa J, Iwano R, Hirano Y, Muroya K（内分泌代謝科）. Very long-chain acyl- CoA dehydrogenase deficiency: No developmental delay after cardiopulmonary arrest. Pediatr Int. 2021 Aug;63(8):992-994.
  23. Kawanishi Y, Endo M, Fujii M, Masuda T, 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, Taguchi T, Okuyama H. Optimal timing of delivery for pregnancies with prenatally diagnosed congenital diaphragmatic hernia: a propensity-score analysis using the inverse probability of treatment weighting. J Perinatol. 2021 Aug;41(8):1893-1900.
  24. Kobayashi S, Yasumura K（形成外科）, Mizuno Y, Suzuki M（言語聴覚科）, Hirakawa T, Satake T, Yabuki Y, Maegawa J. A procedure combining double opposing Z-plasty with buccal flap and skin graft for a cleft palate patient with short palate. JPRAS Open. 2021 Apr 24;29:55-59.
  25. Chang Y, Min J, Jarusiewicz JA, Actis M, Yu-Chen Bradford S, Mayasundari A, Yang L, Chepyala D, Alcock LJ, Roberts KG, Nithianantham S, Maxwell D, Rowland L, Larsen R, Seth A, Goto H（血液・腫瘍科）, Imamura T, Akahane K, Hansen BS, Pruett-Miller SM, Paietta EM, Litzow MR, Qu C, Yang JJ, Fischer M, Rankovic Z, Mullighan CG. Degradation of Janus kinases in CRLF2-rearranged acute lymphoblastic leukemia. Blood. 2021 Dec 9;138(23):2313-2326.
  26. Baba S, Okanishi T, Homma Y, Yoshida T, Goto T（神経内科）, Fukasawa T, Kobayashi S, Kamei A, Fujii Y, Hino-Fukuyo N, Yamada K, Daida A, Kawawaki H, Hoshino H, Sejima H, Ishida Y, Okazaki T, Inui T, Kanai S, Motoi H, Itamura S, Nishimura M, Enoki H, Fujimoto A. Efficacy of long-term adrenocorticotropic hormone therapy for West syndrome: A retrospective multicenter case series. Epilepsia Open. 2021 May 28;6(2):402-412.
  27. Asai H（心臓血管外科）, Shingu Y, Ikarashi J, Cao Y, Takeyoshi D（心臓血管外科）, Arai Y, Ebuoka N, Tachibana T（心臓血管外科）. Apex rotation as a risk factor for total anomalous pulmonary connection repair in single ventricle. J Card Surg. 2021 Sep;36(9):3078-3084.
  28. Keino D（血液・腫瘍科）, Kinoshita A, Sudo A, Ohyama R, Mori T. Suspected chronic myeloid leukemia-like BCR-ABL1-positive acute lymphoblastic leukemia. Pediatr Int. 2021 Jun;63(6):728-729.
  29. Hara-Isono K, Matsubara K, Hamada R, Shimada S, Yamaguchi T, Wakui K, Miyazaki O, Muroya K（内分泌代謝科）, Kurosawa K（遺伝科）, Fukami M, Ogata T, Kosho T, Kagami M. A patient with Silver-Russell syndrome with multilocus imprinting disturbance, and Schimke immuno-osseous dysplasia unmasked by uniparental isodisomy of chromosome 2. J Hum Genet. 2021 Nov;66(11):1121-1126.
  30. Hara J, Kosaka Y, Koh K, Matsumoto K, Kumamoto T, Fujisaki H, Ishida Y, Suzuki R, Mochizuki S, Goto H（血液・腫瘍科）, Yuza Y, Koga Y. Phase III study of palonosetron for prevention of chemotherapy-induced nausea and vomiting in pediatric patients. Jpn J Clin Oncol. 2021 Aug 1;51(8):1204-1211.
  31. Enomoto Y, Tsurusaki Y（臨床研究所）, Tominaga M（遺伝科）, Kobayashi S（形成外科）, Inoue M（耳鼻いんこう科）, Fujita K（放射線科）, Kumaki T, Murakami H, Kurosawa K（遺伝科）. A Recurrent Variant in POLR1B, c.3007C>T; p.Arg1003Cys, Associated with Atresia of the External Canal and Microtia in Treacher Collins Syndrome Type 4. Mol Syndromol. 2021 Apr;12(2):127-132.
  32. Kobayashi S, Fukawa T（形成外科）, Satake T, Maegawa J. Considering the view from the inside of the maxillary sinus in Le Fort II osteotomy. J Plast Reconstr Aesthet Surg. 2021 Aug;74(8):1931-1971.
  33. Minami S（救急・集中治療科）, Doi T, Abe T, Takeuchi I. Neutrophil gelatinase-associated lipocalin as a biomarker for short-term outcomes among trauma patients: A single-center observational study. PLoS One. 2021 May 10;16(5):e0251319.
  34. Miyamoto S, Kato M, Hiraide T, Shiohama T, Goto T（神経内科）, Hojo A, Ebata A, Suzuki M, Kobayashi K, Chong PF, Kira R, Matsushita HB, Ikeda H, Hoshino K, Matsufuji M, Moriyama N, Furuyama M, Yamamoto T, Nakashima M, Saitsu H. Comprehensive genetic analysis confers high diagnostic yield in 16 Japanese patients with corpus callosum anomalies. J Hum Genet. 2021 Nov;66(11):1061-1068.
  35. Wakabayashi T, Fukumura S, Takahashi S, Kurosawa K, Miyamoto S, Tsuchida K, Kato S, Tsugawa T, Sakai Y, Kawasaki Y（遺伝科）. Stereotyped Upper Limb Movement in MECP2 Duplication Syndrome. Neurology. 2021 Jul 13;97(2):92-94.
  36. Kitano T, Aoki H（新生児科）. The incremental burden of invasive pneumococcal disease associated with a decline in childhood vaccination using a dynamic transmission model in Japan: A secondary impact of COVID-19. Comput Biol Med. 2021 Jun;133:104429.
  37. Saito J, Kojima T, Tanifuji S, Kato Y, Oka S, Ichikawa Y, Miyagi E, Tachibana T, Asou T（心臓血管外科）, Yokoyama U. Transcriptome Analysis Reveals Differential Gene Expression between the Closing Ductus Arteriosus and the Patent Ductus Arteriosus in Humans. J Cardiovasc Dev Dis. 2021 Apr 16;8(4):45.
  38. Saito Y, Urashima M, Takahashi Y, Ogawa A, Kiyotani C, Yuza Y, Koh K, Watanabe K, Kosaka Y, Goto H（血液・腫瘍科）, Kikuta A, Okada K, Koga Y, Fujimura J, Inoue M, Sato A, Atsuta Y, Matsumoto K. Effect of high-dose chemotherapy plus stem cell rescue on the survival of patients with neuroblastoma modified by MYCN gene gain/amplification and remission status: a nationwide registration study in Japan. Bone Marrow Transplant. 2021 Sep;56(9):2173-2182.
  39. Haruta M, Arai Y, Okita H, Tanaka Y（病理診断科）, Takimoto T, Kamijo T, Oue T, Souzaki R, Taguchi T, Kuwahara Y, Chin M, Nakadate H, Hiyama E, Ishida Y, Koshinaga T, Kaneko Y. Frequent breakpoints of focal deletion and uniparental disomy in 22q11.1 or 11.2 segmental duplication region reveal distinct tumorigenesis in rhabdoid tumor of the kidney. Genes Chromosomes Cancer. 2021 Aug;60(8):546-558.
  40. Okawada M, Ohfuji S, Yamoto M, Urushihara N, Terui K, Nagata K, Taguchi T, Hayakawa M, Amari S, Masumoto K, Okazaki T, Inamura N, Toyoshima K（新生児科）, Inoue M, Furukawa T, Yokoi A, Kanamori Y, Usui N, Tazuke Y, Saka R, Okuyama H; Japanese Congenital Diaphragmatic Hernia Study Group. Thoracoscopic repair of congenital diaphragmatic hernia in neonates: findings of a multicenter study in Japan. Surg Today. 2021 Oct;51(10):1694-1702.
  41. Takae S, Furuta S, Keino D（血液・腫瘍科）, Shiraishi E, Iwahata Y, Oyama K, Iwahata H, Nishiya Y, Kawaguchi K, Obayashi J, Tanaka K, Sawada S, Suzuki Y, Sugishita Y, Deura I, Horage Y, Nagae H, Kondo H, Sakamoto M, Mori T, Kitagawa H, Suzuki N. Surgical management of unilateral oophorectomy for ovarian tissue cryopreservation in high-risk children and adolescents with varied backgrounds. Pediatr Surg Int. 2021 Aug;37(8):1021-1029.
  42. Ito M, Terui K, Nagata K, Yamoto M, Shiraishi M, Okuyama H, Yoshida H, Urushihara N, Toyoshima K（新生児科）, Hayakawa M, Taguchi T, Usui N; Japanese Congenital Diaphragmatic Hernia Study Group. Clinical guidelines for the treatment of congenital diaphragmatic hernia. Pediatr Int. 2021 Apr;63(4):371-390.
  43. Morita Y, Aida N（放射線科）. [Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes(MELAS)]. No Shinkei Geka. 2021 Mar;49(2):349-355. Japanese.
  44. Ohashi I, Kuroda Y（遺伝科）, Enomoto Y（臨床研究所）, Murakami H（遺伝科）, Masuno M, Kurosawa K（遺伝科）. 6p21.33 Deletion encompassing CSNK2B is associated with relative macrocephaly, facial dysmorphism, and mild intellectual disability. Clin Dysmorphol. 2021 Jul 1;30(3):139-141.
  45. Morio T, Gotoh K, Imagawa T（感染免疫科）, Morita K, Ohnishi H, Yasui K, Hofmann J, Lawo JP, Shebl A, Rojavin MA. Safety and tolerability of IgPro10 in Japanese primary immunodeficiency patients: a registrational study. Int J Hematol. 2021 Jun;113(6):921-929.
  46. Sakaguchi H, Miyamura T, Tomizawa D, Taga T, Ishida H, Okamoto Y, Koh K, Yokosuka T（血液・腫瘍科）, Yoshida N, Sato M, Noguchi M, Okada K, Hori T, Takeuchi M, Kosaka Y, Inoue M, Hashii Y, Atsuta Y. Effect of extramedullary disease on allogeneic hematopoietic cell transplantation for pediatric acute myeloid leukemia: a nationwide retrospective study. Bone Marrow Transplant. 2021 Aug;56(8):1859-1865.
  47. Yamato G, Deguchi T, Terui K, Toki T, Watanabe T, Imaizumi T, Hama A, Iwamoto S, Hasegawa D, Ueda T, Yokosuka T（血液・腫瘍科）, Tanaka S, Yanagisawa R, Koh K, Saito AM, Horibe K, Hayashi Y, Adachi S, Mizutani S, Taga T, Ito E, Watanabe K, Muramatsu H. Predictive factors for the development of leukemia in patients with transient abnormal myelopoiesis and Down syndrome. Leukemia. 2021 May;35(5):1480-1484.
  48. Ikeda A（神経内科）, Ueda H（循環器内科）, Matsui K（総合診療科）, Iai M, Goto T（神経内科）. Recurrent pulmonary hemorrhage in juvenile patients with KCNT1 mutation. Pediatr Int. 2021 Mar;63(3):352-354.
  49. Ichikawa K（神経内科）. Reply to the letter: "Is the variant m.9176T>C in MT-ATP6 truly responsibly for Leigh syndrome?". Pediatr Int. 2021 Feb;63(2):240.
  50. Ueda H（循環器内科）. Transcatheter Closure of an Atrial Septal Defect. Intern Med. 2022 Jan 1;61(1):1-2. doi: 10.2169/internalmedicine.6946-20. Epub 2021 Feb 15.
  51. Nagase H（産婦人科）, Ohyama M（新生児科）, Yamamoto M, Akamatsu C, Miyake Y, Nagashima A, Sasaki M, Ishikawa H（産婦人科）. Prenatal ultrasonographic findings and fetal/neonatal outcomes of body stalk anomaly. Congenit Anom (Kyoto). 2021 Jul;61(4):118-126.
  52. Sasakawa Y, Nakamura Y, Saitoh I, Nakajima T, Tsukuno S, Hozawa M, Sotome T, Nogami Y, Kurosawa M（歯科）, Iwase Y, Hayashi T, Hayasaki H. Lip-closing pressure during food intake from a spoon in normal children. J Oral Rehabil. 2021 Jun;48(6):711-719.
  53. Shimokaze T, Toyoshima K, Noguchi T, Aoki H, Saito T（新生児科）. Acute effect of hydrocortisone for respiratory deterioration in preterm infants: Oxygenation, ventilation, vital signs, and electrolytes. Early Hum Dev. 2021 Mar;154:105320.
  54. Nihira H, Izawa K, Ito M, Umebayashi H, Okano T, Kajikawa S, Nanishi E, Keino D（血液・腫瘍科）, Murakami K, Isa-Nishitani M, Shiba T, Honda Y, Hijikata A, Yasu T, Kubota T, Hasegawa Y, Kawashima Y, Nakano N, Takada H, Ohga S, Heike T, Takita J, Ohara O, Takei S, Takahashi M, Kanegane H, Morio T, Iwaki-Egawa S, Sasahara Y, Nishikomori R, Yasumi T. Detailed analysis of Japanese patients with adenosine deaminase 2 deficiency reveals characteristic elevation of type II interferon signature and STAT1 hyperactivation. J Allergy Clin Immunol. 2021 Aug;148(2):550-562.
  55. Takeguchi R, Takahashi S, Akaba Y, Tanaka R, Nabatame S, Kurosawa K（遺伝科）, Matsuishi T, Itoh M. Early diagnosis of MECP2 duplication syndrome: Insights from a nationwide survey in Japan. J Neurol Sci. 2021 Mar 15;422:117321.
  56. Shima H, Ishikawa T, Ito J, Emoto K, Kurosawa T, Keino D（血液・腫瘍科）, Yamazaki F, Goto H（血液・腫瘍科）, Shimada H. Severe bloody diarrhea due to cytokine release syndrome after chimeric antigen receptor T cell therapy for refractory acute lymphoblastic leukemia. Blood Cell Ther. 2021 Jan 28;5(1):31-34.
  57. Tamai M, Huang M, Kagami K, Abe M, Somazu S, Shinohara T, Harama D, Watanabe A, Akahane K, Goi K, Sugita K, Goto H（血液・腫瘍科）, Minegishi M, Iwamoto S, Inukai T. Association of relapse-linked ARID5B single nucleotide polymorphisms with drug resistance in B-cell precursor acute lymphoblastic leukemia cell lines. Cancer Cell Int. 2020 Sep 4;20(1):434.
  58. Mori S, Tanoue K（総合診療科）, Shimizu H, Nagafuchi H（救急・集中治療科）, Kim KS（循環器内科）, Murakami H, Kurosawa K（遺伝科）, Matsui K（総合診療科）. Lung disease due to FLNA mutation improved after shunt closure for congenital heart disease. Pediatr Pulmonol. 2021 May;56(5):1280-1282.
  59. 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. Correction to: 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. 2021 Feb;113(2):308-309.
  60. Padidela R, Whyte MP, Glorieux FH, Munns CF, Ward LM, Nilsson O, Portale AA, Simmons JH, 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, Williams A, Nixon A, Sun W, Chen A, Skrinar A, Imel EA. Patient-Reported Outcomes from a Randomized, Active-Controlled, Open-Label, Phase 3 Trial of Burosumab Versus Conventional Therapy in Children with X-Linked Hypophosphatemia. Calcif Tissue Int. 2021 May;108(5):622-633.
  61. Mochizuki K（外科）, Yokoi A, Urushihara N, Yabe K, Nakashima H, Kitagawa N（外科）, Maeda K, Fukumoto K, Shinkai M（外科）. Characteristics and treatment of congenital esophageal stenosis: A retrospective collaborative study from three Japanese children's hospitals. J Pediatr Surg. 2021 Oct;56(10):1771-1775.
  62. Kobayashi Y, Tohyama J, Takahashi Y, Goto T（神経内科）, Haginoya K, Inoue T, Kubota M, Fujita H, Honda R, Ito M, Kishimoto K, Nakamura K, Sakai Y, Takanashi JI, Tanaka M, Tanda K, Tominaga K, Yoshioka S, Kato M, Nakashima M, Saitsu H, Matsumoto N. Clinical manifestations and epilepsy treatment in Japanese patients with pathogenic CDKL5 variants. Brain Dev. 2021 Apr;43(4):505-514.
  63. Ushijima K, Ogawa Y, Terao M, Asakura Y, Muroya K（内分泌代謝科）, Hayashi M, Ishii T, Hasegawa T, Sekido R, Fukami M, Takada S, Narumi S. Identification of the first promoter-specific gain-of-function SOX9 missense variant (p.E50K) in a patient with 46,XX ovotesticular disorder of sex development. Am J Med Genet A. 2021 Apr;185(4):1067-1075.
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