| 小児科学 | |||||||
| Pediatrics | |||||||
| 整理番号 | 論文の種類 | 著者名 | 論文タイトル | 誌名・書名等 | 巻号ページ | 年 | doi |
| 2144001 | 症例報告 | Ikeuchi M, Kiyota K, Itonaga T, Kawano-Matsuda F, Ohata Y, Fujiwara M, Kubota T,Ozono K, Ihara K. |
A case of HDR syndrome coexisting with tetralogy of Fallot, with a novel GATA3 mutation, which manifested as a renal abscess. | CEN Case Rep | 10(2):241-243. | 2021 | 10.1007/s13730-020-00551-0 |
| 2144002 | 症例報告 | Oyake M, Itonaga T, Hirano N, Suenobu S, Ihara K. |
Hydrocortisone improved dexamethasone-induced neuropsychological adverse effects. | Pediatr Int | 63(3):339-342. | 2021 | 10.1111/ped.14413 |
| 2144003 | 症例報告 | Kawano-Matsuda F, Maeda T, Kaname T, Yanagi K, Ihara K. |
X-linked mental retardation and severe short stature with a novel mutation of the KDM5C gene. | Clin Pediatr Endocrinol | 30:61-64. | 2021 | https://doi.org/10.1297/cpe.30.61 |
| 2144004 | 症例報告 | Kawano N, Itonaga T, Tojigamori M, Daa T, Ihara K. | A Japanese infant presenting with hypocalcemic seizures resulting from hypovitaminosis D induced by non-celiac gluten sensitivity. | Clin Pediatr Endocrinol | 30(2):105-110. | 2021 | 10.1297/cpe.30.105 |
| 2144005 | 原著 | Miyahara H, Natsumeda M, Kanemura Y, Yamasaki K, Riku Y, Akagi A, Oohashi W, Shofuda T, Yoshioka E, Sato Y, Taga T, Naruke Y, Ando R, Hasegawa D, Yoshida M, Sakaida T, Okada N., Watanabe H, Ozeki M, Arakawa Y, Yoshimura J, Fujii Y, Suenobu S, Ihara K, Hara J, Kakita A, Yoshida M, Iwasaki Y. |
Topoisomerase IIβ immunoreactivity (IR) co-localizes with neuronal marker-IR but not glial fibrillary acidic protein-IR in GLI3-positive medulloblastomas: an immunohistochemical analysis of 124 medulloblastomas from the Japan Children's Cancer Group. | Brain Tumor Pathol | 38(2):109-12. | 2021 | 10.1007/s10014-021-00396-0. |
| 2144006 | 症例報告 | Sakamoto A, Ishiguro A, Fukuda A, Sakamoto S, Suenobu S, Matsumoto T, Nogami K, Ohga S, Kasahara M. | Liver transplantation for congenital protein C deficiency with initial poor graft function: a case report with literature review. | Int J Hematol | 114(1):141-145. | 2021 | 10.1007/s12185-021-03103-z. |
| 2144007 | 症例報告 | Tanaka K, Anan M, Tsubouchi Y, Iwasaki T, Kawano M, Itonaga I,
Ikeda S, Kataoka M, Suenobu S, Tsumura H. |
Gait analysis of a patient who underwent complete resection of the patella and quadriceps femoris for soft tissue sarcoma. | Eur J Phys Rehabil Med | 57(2):298-302. | 2021 | 10.23736/S1973-9087.21.06395-4. |
| 2144008 | 症例報告 | Hirano N, Houbara R, Korematsu S, Hatano Y, Ihara K. | Psoriasis with short stature improved by adalimumab. | Pediatr Dermatol | 38(5):1379-1381. | 2021 | 10.1111/pde.14784. |
| 2144009 | 症例報告 | Okawa Y, Okanari K, Hirano N, Kawano T, Nishio S, Usami S,
Maeda T, Ihara K. |
Unilateral Sensorineural Hearing Loss in Children Associated With Sjögren's Syndrome. | Cureus | 17;13(10):e18832. | 2021 | 10.7759/cureus.18832. |
| 2144010 | 原著 | Inoue M, Miyahara H, Shiraishi H, Shimizu N, Tsumori M, Kiyota K, Maeda M, Umeda R, Ishitani T, Hanada R, Ihara K, Hanada T. | Leucyl-tRNA synthetase deficiency systemically induces excessive autophagy in zebrafish. | Sci Rep | Apr 16;11(1):8392. | 2021 | 10.1038/s41598-021-87879-4. |
| 2144011 | 原著 | Sekiguchi K, Miyahara H, Inoue M, Maeda T, Kiyota K, Sakai K,
Hanada T, Ihara K. |
Metabolome Characteristics of Liver Autophagy Deficiency under Starvation Conditions in Infancy. | Nutrients | 29;13(9):3026. | 2021 | 10.3390/nu13093026. |
| 2144012 | 症例報告 | Itonaga T, Akiba K, Hasegawa Y. | Therapeutic needs from early childhood in four patients with 21-hydroxylase deficiency harboring the P30L mutation on one allele. | Clin Pediatr Endocrinol | 30(4):187-193. | 2021 | 10.1297/cpe.30.187. |
| 2144013 | 原著 | Maeda T, Kobayashi O, Ihara K, Bos AF |
Fidgety Movements Assessment Accuracy Survey in Japan. | Int J Environ Res Public Health | 20;18(24):13428. | 2021 | 10.3390/ijerph182413428. |
| 2144014 | 原著 | 東矢俊一郎、古賀友紀、 岡本康裕、 野村優子、中山秀樹、大園秀一、 本田裕子、 興梠雅彦、西 眞範、 右田昌宏、 興梠健作、 舩越康智、 末延聡一、齋藤祐介、新小田雄一、 比嘉 猛、百名伸之、唐川修平、 武 淳吉、大賀正一. |
COVID19パンデミック下における小児がん診療の現状 〜九州・沖縄ブロック小児がん連携病院における調査〜 | 日本小児血液・がん学会雑誌 | 58(2): 132-137. | 2021 | |
| 2144015 | 原著 | Egami N, Ochiai M, Ichiyama M, Inoue H, Sonoda M, Ishimura M, Suenobu S, Nishikubo T, Ishiguro A, Hotta T, Uchiumi T, Kang D, Ohga S. |
Clinical Impact of Heritable Thrombophilia on Neonatal-Onset Thromboembolism: A Nationwide Study in Japan. | J Pediatr | 238:259-267.e2. | 2021 | 10.1016/j.jpeds.2021.07.001. |
| 2144016 | 原著 | Moriya K, Imamura T, Katayama S, Kaino A, Okamoto K, Yokoyama N,
Uemura S, Kitazawa H, Sekimizu M, Hiramatsu H, Usami I, Ishida H, Hasegawa D,
Hama A, Moriya-Saito A, Sato A, Sasahara Y, Suenobu S, Horibe K, Hara J. |
The incidence of symptomatic osteonecrosis is similar between Japanese children and children in Western countries with acute lymphoblastic leukaemia treated with a Berlin-Frankfurt-Münster (BFM)95-based protocol. | Br J Haematol | 196(5):1257-1261. | 2021 | 10.1111/bjh.17988. |
| 2144017 | 原著 | Nishigaki S, Itonaga T, Hasegawa Y, Kawai K. | Starting age of oestrogen-progestin therapy is negatively associated with bone mineral density in young adults with Turner syndrome independent of age and body mass index. | Clin Endocrinol | 95(1):84-91. | 2021 | 10.1111/cen.14484. |
| 2144018 | その他 | 井原健二 | 早老症って何？ | 小児科診療Up-to-Date. | 50:42-45. | 2021 | |
| 2144019 | 総説 | 井原健二 | ハッチンソン・ギルフォード早老症候群 | 日本老年医学会雑誌 | 58(3), 409-412. | 2021 | |
| 2144020 | その他 | 末延聡一 | III. 疾患別ガイド 1. 急性リンパ性白血病（ALL) | 小児がん治療後の長期フォローアップガイド | 124-131. | 2021 | |
| 2144021 | その他 | 末延聡一 | III. 疾患別ガイド 8. ランゲルハンス細胞組織球症（LCH) | 小児がん治療後の長期フォローアップガイド | 169-174. | 2021 | |
| 2144022 | その他 | 末延聡一 | III. 疾患別ガイド 9. 神経芽腫（NB) | 小児がん治療後の長期フォローアップガイド | 175-185. | 2021 | |