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Author/Creator Togawa, Takao

1. A combination of genetic and biochemical analyses for the diagnosis of PI3K-AKT-mTOR pathway-associated megalencephaly. Issue 1 (December 2017)

Authors:
Negishi, Yutaka; Miya, Fuyuki; Hattori, Ayako; Johmura, Yoshikazu; Nakagawa, Motoo; Ando, Naoki; Hori, Ikumi; Togawa, Takao; Aoyama, Kohei; Ohashi, Kei; Fukumura, Shinobu; Mizuno, Seiji; Umemura, Ayako; Kishimoto, Yoko; Okamoto, Nobuhiko; Kato, Mitsuhiro; Tsunoda, Tatsuhiko; Yamasaki, Mami; Kanem...
Journal:
BMC medical genetics
Issue:
Volume 18:Issue 1(2017)
Page Start:
1
Record Type:
Journal Article
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2. Assessment of Adenosine Triphosphatase Phospholipid Transporting 8B1 (ATP8B1) Function in Patients With Cholestasis With ATP8B1 Deficiency by Using Peripheral Blood Monocyte‐Derived Macrophages. Issue 1 (26th September 2020)

Authors:
Mizutani, Ayumu; Sabu, Yusuke; Naoi, Sotaro; Ito, Shogo; Nakano, Satoshi; Minowa, Kei; Mizuochi, Tatsuki; Ito, Koichi; Abukawa, Daiki; Kaji, Shunsaku; Sasaki, Mika; Muroya, Koji; Azuma, Yoshihiro; Watanabe, Satoshi; Oya, Yuki; Inomata, Yukihiro; Fukuda, Akinari; Kasahara, Mureo; Inui, Ayano; Taki...
Journal:
Hepatology communications
Issue:
Volume 5:Issue 1(2021)
Page Start:
52
Record Type:
Journal Article
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3. Combined genetic analyses can achieve efficient diagnostic yields for subjects with Alagille syndrome and incomplete Alagille syndrome. (2nd August 2017)

Authors:
Ohashi, Kei; Togawa, Takao; Sugiura, Tokio; Ito, Koichi; Endo, Takeshi; Aoyama, Kohei; Negishi, Yutaka; Kudo, Toyoichiro; Ito, Reiko; Saitoh, Shinji
Journal:
Acta pædiatrica
Issue:
Volume 106:Number 11(2017)
Page Start:
1817
Record Type:
Journal Article
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4. Effects of 4‐phenylbutyrate therapy in a preterm infant with cholestasis and liver fibrosis. Issue 6 (4th February 2016)

Authors:
Ito, Shogo; Hayashi, Hisamitsu; Sugiura, Tokio; Ito, Koichi; Ueda, Hiroko; Togawa, Takao; Endo, Takeshi; Tanikawa, Ken; Kage, Masayoshi; Kusuhara, Hiroyuki; Saitoh, Shinji
Journal:
Pediatrics international
Issue:
Volume 58:Issue 6(2016)
Page Start:
506
Record Type:
Journal Article
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5. Single nucleotide polymorphisms in AGTR1, TFAP2B, and TRAF1 are not associated with the incidence of patent ductus arteriosus in Japanese preterm infants. Issue 6 (3rd February 2016)

Authors:
Kawase, Koya; Sugiura, Tokio; Nagaya, Yoshiaki; Yamada, Takaharu; Sugimoto, Mari; Ito, Koichi; Togawa, Takao; Nagasaki, Rika; Kato, Takenori; Kouwaki, Masanori; Koyama, Norihisa; Saitoh, Shinji
Journal:
Pediatrics international
Issue:
Volume 58:Issue 6(2016)
Page Start:
461
Record Type:
Journal Article
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