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Differing clinical features between Japanese siblings with cerebrotendinous xanthomatosis with a novel compound heterozygous CYP27A1 mutation: a case report.
Published in:
2022
By:
- Koyama, Shingo;
- Okabe, Yuma;
- Suzuki, Yuya;
- Igari, Ryosuke;
- Sato, Hiroyasu;
- Iseki, Chifumi;
- Tanji, Kazuyo;
- Suzuki, Kyoko;
- Ohta, Yasuyuki
Publication type:
journal article
Anti-IgLON5 Disease Showing an Improvement in Dysautonomia, Including Vocal Cord Palsy, via Combined Immunotherapy.
Published in:
Internal Medicine, 2024, v. 63, n. 15, p. 2187, doi. 10.2169/internalmedicine.2865-23
By:
- Daisuke Sato;
- Hiroyasu Sato;
- Toshiyuki Kondo;
- Ryosuke Igari;
- Chifumi Iseki;
- Hikaru Kawahara;
- Shintaro Amano;
- Yoya Ono;
- Akio Kimura;
- Takayoshi Shimohata;
- Yasuyuki Ohta
Publication type:
Article
Paraneoplastic Cerebellar Degeneration Accompanied by Seropositivity for Anti-GAD65, Anti-SOX-1 and Anti-VGCC Antibodies Due to Small-cell Lung Cancer.
Published in:
Internal Medicine, 2024, v. 63, n. 6, p. 857, doi. 10.2169/internalmedicine.0738-22
By:
- Naomi Takahashi;
- Ryosuke Igari;
- Chifumi Iseki;
- Hikaru Kawahara;
- Daisuke Suzuki;
- Yuya Suzuki;
- Hiroyasu Sato;
- Shingo Koyama;
- Maki Kobayashi;
- Yasuyuki Ohta
Publication type:
Article
A Case with Anti-ganglioside Antibodies Showing Multiple Cranial Nerve Palsies Detected on Gadolinium-enhanced Magnetic Resonance Imaging.
Published in:
Internal Medicine, 2023, v. 62, n. 23, p. 3541, doi. 10.2169/internalmedicine.1389-22
By:
- Daisuke Suzuki;
- Shingo Koyama;
- Naomi Takahashi;
- Yuya Suzuki;
- Ryosuke Igari;
- Chifumi Iseki;
- Hiroyasu Sato;
- Toshitada Hiraka;
- Masafumi Kanoto;
- Yasuyuki Ohta
Publication type:
Article
Prevalence and development of idiopathic normal pressure hydrocephalus: A 16‐year longitudinal study in Japan.
Published in:
Acta Neurologica Scandinavica, 2022, v. 146, n. 5, p. 680, doi. 10.1111/ane.13710
By:
- Iseki, Chifumi;
- Takahashi, Yoshimi;
- Adachi, Michito;
- Igari, Ryosuke;
- Sato, Hiroyasu;
- Koyama, Shingo;
- Ishizawa, Kenichi;
- Ohta, Yasuyuki;
- Kato, Takeo
Publication type:
Article
A Segmental Copy Number Loss of the SFMBT1 Gene Is a Genetic Risk for Shunt-Responsive, Idiopathic Normal Pressure Hydrocephalus (iNPH): A Case-Control Study.
Published in:
PLoS ONE, 2016, v. 11, n. 11, p. 1, doi. 10.1371/journal.pone.0166615
By:
- Sato, Hidenori;
- Takahashi, Yoshimi;
- Kimihira, Luna;
- Iseki, Chifumi;
- Kato, Hajime;
- Suzuki, Yuya;
- Igari, Ryosuke;
- Sato, Hiroyasu;
- Koyama, Shingo;
- Arawaka, Shigeki;
- Kawanami, Toru;
- Miyajima, Masakazu;
- Samejima, Naoyuki;
- Sato, Shinya;
- Kameda, Masahiro;
- Yamada, Shinya;
- Kita, Daisuke;
- Kaijima, Mitsunobu;
- Date, Isao;
- Sonoda, Yukihiko
Publication type:
Article

Found: 6

Differing clinical features between Japanese siblings with cerebrotendinous xanthomatosis with a novel compound heterozygous CYP27A1 mutation: a case report.

Anti-IgLON5 Disease Showing an Improvement in Dysautonomia, Including Vocal Cord Palsy, via Combined Immunotherapy.

Paraneoplastic Cerebellar Degeneration Accompanied by Seropositivity for Anti-GAD65, Anti-SOX-1 and Anti-VGCC Antibodies Due to Small-cell Lung Cancer.

A Case with Anti-ganglioside Antibodies Showing Multiple Cranial Nerve Palsies Detected on Gadolinium-enhanced Magnetic Resonance Imaging.

Prevalence and development of idiopathic normal pressure hydrocephalus: A 16‐year longitudinal study in Japan.

A Segmental Copy Number Loss of the SFMBT1 Gene Is a Genetic Risk for Shunt-Responsive, Idiopathic Normal Pressure Hydrocephalus (iNPH): A Case-Control Study.