平成30（2018）年度
論文・著書など
論文（欧文）
- Cardiomyopathy in children with mitochondrial disease: Prognosis and genetic background
Imai-Okazaki A, Kishita Y, Kohda M, Mizuno Y, Fushimi T, Matsunaga A, Yatsuka Y, Hirata T, Harashima H, Takeda A, Nakaya A, Sakata Y, Kogaki S, Ohtake A, Murayama K, Okazaki Y.
Int J Cardiol. 2019 Jan 5. - The detection of retrograde flow from the left anterior descending artery into the main pulmonary artery by 4D-flow cardiac magnetic resonance in a patient with Bland-White-Garland syndrome.
Tsuneta S, Oyama-Manabe N, Takeda A, Taniguchi K, Manabe O.
Eur Heart J Cardiovasc Imaging. 2019 Jan 9 - Progressive left ventricular dysfunction and myocardial fibrosis in Duchenne and Becker muscular dystrophy: a longitudinal cardiovascular magnetic resonance study.
Aikawa T, Takeda A, Oyama-Manabe N, Naya M, Yamazawa H, Koyanagawa K, Ito YM, Anzai T.
Pediatr Cardiol. 2018 Dec 18. - Attenuation of Pulse Pressure Amplification in Patients with Complete Transposition of the Great Arteries After an Arterial Switch Operation in Children.
Murakami T, Shiraishi M, Murakami T, Takeda A.
Pediatr Cardiol. 2018 Jun 19. - Role of BRCA1-associated protein (BRAP) variant in childhood pulmonary arterial hypertension.
Chida-Nagai A, Shintani M, Sato H,Nakayama T, Nii M, Akagawa H, et al.
PLoS ONE 2019;14(1): e0211450. - CD44-Positive Glomerular Parietal Epithelial Cells in a Mouse Model of Calcineurin Inhibitors-Induced Nephrotoxicity.
Asako Hayashi, Takayuki Okamoto, Takeshi Yamazaki, Yasuyuki Sato,Toshiyuki Takahashi, Tadashi Ariga
Nephron. 2019 Feb 20:1-11. doi: 10.1159/000497325. [Epub ahead of print] - Persistent systemic rotavirus vaccine infection in a child with X-linked severe combined immunodeficiency.
Yoshikawa T, Ihira M, Higashimoto Y, Hattori F, Miura H, Sugata K, Komoto S, Taniguchi K, Iguchi A, Yamada M, Ariga T.
J Med Virol. 2019 Jan 27. doi: 10.1002/jmv.25410. [Epub ahead of print] - Myositis-specific autoantibodies in Japanese patients with juvenile idiopathic inflammatory myopathies.
Ueki M, Kobayashi I, Takezaki S, Tozawa Y, Okura Y, Yamada M, Kuwana M, Ariga T
Mod Rheumatol. 2018 Mar 13:1-16. doi: 10.1080/14397595.2018.1452353. [Epub ahead of print] - Evaluation of systemic activity of pediatric primary Sjogren’s syndrome by EULAR Sjogren’s syndrome disease activity index (ESSDAI).
Kobayashi I, Okura Y, Ueki M, Tozawa Y, Takezaki S, Yamada M, Ariga T.
Mod Rheumatol. 2018 Mar 13:1-12. doi: 10.1080/14397595.2018.1452174. [Epub ahead of print] - Genetic basis for childhood interstitial lung disease among Japanese infants and children.
Hayasaka I, Cho K, Akimoto T, Ikeda M, Uzuki Y, Yamada M, Nakata K, Furuta I, Ariga T, Minakami H.
Pediatr Res. 2018 Feb;83(2):477-483. doi: 10.1038/pr.2017.217. Epub 2017 Nov 1. - Two siblings with congenital central hypothyroidism caused by a novel mutation in the IGSF1 gene
Makiko Oguma1, Mizuki Kobayashi1, Masayo Yamazaki1, Koji Yokoyama1, Shuntaro Morikawa2,Takeshi Yamaguchi2, Takanori Yamagata1, and Toshihiro Tajima1
1 Department of Pediatrics, Jichi Medical University, Tochigi, Japan
2 Department of Pediatrics, Hokkaido University School of Medicine, Hokkaido, Japan
Clin Pediatr Endocrinol 2018; 27(2), 95–100 - Four Japanese Patients with Congenital Nephrogenic Diabetes Insipidus due to the AVPR2 Mutations
Noriko Namatame-Ohta, Shuntaro Morikawa, Akie Nakamura, Kumihiro Matsuo, Masahide Nakajima, Kazuhiro Tomizawa, Yusuke Tanahashi, and Toshihiro Tajima
Case Reports in Pediatrics Volume 2018, Article ID 6561952 - Hypoglycemia in type 1A diabetes can develop before insulin therapy: a retrospective cohort study.
Yamaguchi T, Hachiya R, Watanabe-Yamamoto S, Sawano K, Morikawa S, Nakamura A, Hasegawa Y.
Diabetes Res Clin Pract. 2018 Nov 24. pii: S0168-8227(18)31036-2. doi: 10.1016/j.diabres.2018.11.011. [Epub ahead of print] - Povidone-iodine lowers incidence of catheter-associated bloodstream infections.
Sugiyama M, Iguchi A, Terashita Y, Ohshima J, Cho Y.
Pediatr Int. 2018 Dec 20. Doi: 10.1111/ped.13759. [Epub ahead of print]