F
Fukiko Ichida
Researcher at University of Toyama
Publications - 190
Citations - 6689
Fukiko Ichida is an academic researcher from University of Toyama. The author has contributed to research in topics: Left ventricular noncompaction & Cardiomyopathy. The author has an hindex of 34, co-authored 183 publications receiving 5772 citations. Previous affiliations of Fukiko Ichida include International University of Health and Welfare.
Papers
More filters
Journal ArticleDOI
Role of TBX1 in human del22q11.2 syndrome
Hisato Yagi,Yoshiyuki Furutani,Hiromichi Hamada,Takashi Sasaki,Shuichi Asakawa,Shinsei Minoshima,Fukiko Ichida,Kunitaka Joo,Misa Kimura,Shin Ichiro Imamura,Naoyuki Kamatani,Kazuo Momma,Atsuyoshi Takao,Makoto Nakazawa,Nobuyoshi Shimizu,Rumiko Matsuoka +15 more
TL;DR: The results suggest that the TBX1 mutation is responsible for five major phenotypes in del22q11.2 syndrome, and conclude thatTBX1 is a major genetic determinant of the del22Q11.
Journal ArticleDOI
Clinical Features of Isolated Noncompaction of the Ventricular Myocardium Long-term Clinical Course, Hemodynamic Properties, and Genetic Background
Fukiko Ichida,Yuji Hamamichi,Toshio Miyawaki,Yasuo Ono,Tetsuro Kamiya,Teiji Akagi,Hiromichi Hamada,Osamu Hirose,Takeshi Isobe,Katsuhiko Yamada,Shunji Kurotobi,Hiroshi Mito,Toshiharu Miyake,Yasuo Murakami,Takeshi Nishi,Makoto Shinohara,Masashi Seguchi,Shinjiro Tashiro,Hirofumi Tomimatsu +18 more
TL;DR: In Japanese children, INVM can be found by screening examinations at asymptomatic stage, and it might have a longer dinical course with gradually depressed left ventricular function and restrictive hemodynamics, implying that INVM is a distinctive clinical entity with a heterogeneous genetic background.
Journal ArticleDOI
Novel Gene Mutations in Patients With Left Ventricular Noncompaction or Barth Syndrome
Fukiko Ichida,Shinichi Tsubata,Karla R. Bowles,Noriyuki Haneda,Keiichiro Uese,Toshio Miyawaki,W. Jeffrey Dreyer,John Messina,Hua Li,Neil E. Bowles,Jeffrey A. Towbin +10 more
TL;DR: These data demonstrate genetic heterogeneity in LVNC, with mutation of a novel gene, &agr;-dystrobrevin, identified in LV NC associated with CHD, and confirm that mutations in G4.5 result in a wide phenotypic spectrum of cardiomyopathies.
Journal ArticleDOI
Efficacy of immunoglobulin plus prednisolone for prevention of coronary artery abnormalities in severe Kawasaki disease (RAISE study): a randomised, open-label, blinded-endpoints trial
Tohru Kobayashi,Tsutomu Saji,Tetsuya Otani,Kazuo Takeuchi,Tetsuya Nakamura,Hirokazu Arakawa,Taichi Kato,Toshiro Hara,Kenji Hamaoka,Shunichi Ogawa,Masaru Miura,Yuichi Nomura,Shigeto Fuse,Fukiko Ichida,Mitsuru Seki,Ryuji Fukazawa,Chitose Ogawa,Kenji Furuno,Hirohide Tokunaga,Shinichi Takatsuki,Shinya Hara,Akihiro Morikawa +21 more
TL;DR: Addition of prednisolone to the standard regimen of intravenous immunoglobulin improves coronary artery outcomes in patients with severe Kawasaki disease in Japan.
Journal ArticleDOI
Neurodevelopmental outcomes after cardiac surgery in infancy.
J. William Gaynor,Christian Stopp,David Wypij,Dean B. Andropoulos,Joseph Atallah,Andrew M. Atz,John Beca,Mary T. Donofrio,Kim F. Duncan,Nancy S. Ghanayem,Caren S. Goldberg,Hedwig H. Hövels-Gürich,Fukiko Ichida,Jeffrey P. Jacobs,Robert N. Justo,Beatrice Latal,Jennifer S. Li,William T. Mahle,Patrick S. McQuillen,Shaji C. Menon,Victoria L. Pemberton,Nancy A. Pike,Christian Pizarro,Lara S. Shekerdemian,Anne Synnes,Ismee A. Williams,David C. Bellinger,Jane W. Newburger +27 more
TL;DR: Early neurodevelopmental outcomes for survivors of cardiac surgery in infancy have improved modestly over time, but only after adjustment for innate patient risk factors.