Elevated Plasma Renin Activity Caused by Accelerated-malignant Hypertension in a Patient with Aldosterone-producing Adenoma Complicated with Renal Insufficiency

por Maruhashi, Tatsuya, Amioka, Michitaka, Kishimoto, Shinji, Ikenaga, Hiroki, Oki, Kenji, Ishida, Mari, Kihara, Yasuki, Higashi, Yukihito
Publicado 2019

Ser96Ala genetic variant of the human histidine-rich calcium-binding protein is a genetic predictor of recurrence after catheter ablation in patients with paroxysmal atrial fibrill...

por Amioka, Michitaka, Nakano, Yukiko, Ochi, Hidenori, Onohara, Yuko, Sairaku, Akinori, Tokuyama, Takehito, Motoda, Chikaaki, Matsumura, Hiroya, Tomomori, Shunsuke, Hironobe, Naoya, Okubo, Yousaku, Okamura, Sho, Chayama, Kazuaki, Kihara, Yasuki
Publicado 2019

Maintenance of low inflammation level by the ZFHX3 SNP rs2106261 minor allele contributes to reduced atrial fibrillation recurrence after pulmonary vein isolation

por Tomomori, Shunsuke, Nakano, Yukiko, Ochi, Hidenori, Onohara, Yuko, Sairaku, Akinori, Tokuyama, Takehito, Motoda, Chikaaki, Matsumura, Hiroya, Amioka, Michitaka, Hironobe, Naoya, Ookubo, Yousaku, Okamura, Shou, Kawazoe, Hiroshi, Chayama, Kazuaki, Kihara, Yasuki
Publicado 2018

H558R, a common SCN5A polymorphism, modifies the clinical phenotype of Brugada syndrome by modulating DNA methylation of SCN5A promoters

por Matsumura, Hiroya, Nakano, Yukiko, Ochi, Hidenori, Onohara, Yuko, Sairaku, Akinori, Tokuyama, Takehito, Tomomori, Shunsuke, Motoda, Chikaaki, Amioka, Michitaka, Hironobe, Naoya, Toshishige, Masaaki, Takahashi, Shinya, Imai, Katsuhiko, Sueda, Taijiro, Chayama, Kazuaki, Kihara, Yasuki
Publicado 2017

Chromosome 4q25 Variant rs6817105 Bring Sinus Node Dysfunction and Left Atrial Enlargement

por Tomomori, Shunsuke, Nakano, Yukiko, Ochi, Hidenori, Onohara, Yuko, Sairaku, Akinori, Tokuyama, Takehito, Motoda, Chikaaki, Matsumura, Hiroya, Amioka, Michitaka, Hironobe, Naoya, Okubo, Yousaku, Okamura, Shou, Kawazoe, Hiroshi, Nishiyama, Yukie, Tahara, Hidetoshi, Chayama, Kazuaki, Kihara, Yasuki
Publicado 2018

Genetic variations of aldehyde dehydrogenase 2 and alcohol dehydrogenase 1B are associated with the etiology of atrial fibrillation in Japanese

por Nakano, Yukiko, Ochi, Hidenori, Onohara, Yuko, Sairaku, Akinori, Tokuyama, Takehito, Matsumura, Hiroya, Tomomori, Shunsuke, Amioka, Michitaka, Hironomobe, Naoya, Motoda, Chikaaki, Oda, Nozomu, Chayama, Kazuaki, Chen, Che-Hong, Gross, Eric R., Mochly-Rosen, Daria, Kihara, Yasuki
Publicado 2016