Norifumi Nakanishi

Design and Baseline Data for a Prospective Observational Study of Rivaroxaban in Patients with Venous Thromboembolism in Japan (XASSENT).

Journal: TH open : companion journal to thrombosis and haemostasis

Published: May 26, 2021

Selexipag for Chronic Thromboembolic Pulmonary Hypertension in Japanese Patients　- A Double-Blind, Randomized, Placebo-Controlled, Multicenter Phase II Study.

Journal: Circulation journal : official journal of the Japanese Circulation Society

Published: September 04, 2020

Long-term treatment of pulmonary arterial hypertension with macitentan in Japanese patients.

Journal: Current medical research and opinion

Published: April 17, 2020

Corrigendum to "Maternal and fetal outcomes in pregnancy complicated with Eisenmenger syndrome" [Taiwan J Obstet Gynecol 58 (2019) 183-187].

Journal: Taiwanese journal of obstetrics & gynecology

Published: February 11, 2020

Guidelines for the Treatment of Pulmonary Hypertension (JCS 2017/JPCPHS 2017).

Journal: Circulation journal : official journal of the Japanese Circulation Society

Published: March 12, 2019

Maternal and fetal outcomes in pregnancy complicated with Eisenmenger syndrome.

Journal: Taiwanese journal of obstetrics & gynecology

Published: July 10, 2018

Balloon pulmonary angioplasty for chronic thromboembolic pulmonary hypertension: A systematic review.

Journal: Respiratory investigation

Published: January 31, 2018

The Efficacy of a Genetic Analysis of the BMPR2 Gene in a Patient with Severe Pulmonary Arterial Hypertension and an Atrial Septal Defect Treated with Bilateral Lung Transplantation.

Journal: Internal medicine (Tokyo, Japan)

Published: October 13, 2017

Coexistence of a Double-Chambered Right Ventricle With Ebstein-Like Anomaly and Right Ventricular Apical Hypoplasia　- Usefulness of Multimodality Imaging.

Journal: Circulation journal : official journal of the Japanese Circulation Society

Published: September 05, 2017

Thalidomide for Hereditary Hemorrhagic Telangiectasia With Pulmonary Arterial Hypertension.

Journal: Circulation journal : official journal of the Japanese Circulation Society

Published: August 11, 2017

Left main coronary artery compression by a dilated main pulmonary artery and left coronary sinus of Valsalva aneurysm in a patient with heritable pulmonary arterial hypertension and FLNA mutation.

Journal: Pulmonary circulation

Published: June 30, 2017

Congenitally Corrected Transposition of the Great Arteries and Situs Inversus in an Octogenarian With Systemic Right Ventricular Failure.

Journal: International heart journal

Published: November 08, 2016

Design and Baseline Data for a Prospective Observational Study of Rivaroxaban in Patients with Venous Thromboembolism in Japan (XASSENT).

Design and Baseline Data for a Prospective Observational Study of Rivaroxaban in Patients with Venous Thromboembolism in Japan (XASSENT).

Selexipag for Chronic Thromboembolic Pulmonary Hypertension in Japanese Patients - A Double-Blind, Randomized, Placebo-Controlled, Multicenter Phase II Study.

Selexipag for Chronic Thromboembolic Pulmonary Hypertension in Japanese Patients - A Double-Blind, Randomized, Placebo-Controlled, Multicenter Phase II Study.

Long-term treatment of pulmonary arterial hypertension with macitentan in Japanese patients.

Long-term treatment of pulmonary arterial hypertension with macitentan in Japanese patients.

Corrigendum to "Maternal and fetal outcomes in pregnancy complicated with Eisenmenger syndrome" [Taiwan J Obstet Gynecol 58 (2019) 183-187].

Corrigendum to "Maternal and fetal outcomes in pregnancy complicated with Eisenmenger syndrome" [Taiwan J Obstet Gynecol 58 (2019) 183-187].

Guidelines for the Treatment of Pulmonary Hypertension (JCS 2017/JPCPHS 2017).

Guidelines for the Treatment of Pulmonary Hypertension (JCS 2017/JPCPHS 2017).

Maternal and fetal outcomes in pregnancy complicated with Eisenmenger syndrome.

Maternal and fetal outcomes in pregnancy complicated with Eisenmenger syndrome.

Balloon pulmonary angioplasty for chronic thromboembolic pulmonary hypertension: A systematic review.

Balloon pulmonary angioplasty for chronic thromboembolic pulmonary hypertension: A systematic review.

The Efficacy of a Genetic Analysis of the BMPR2 Gene in a Patient with Severe Pulmonary Arterial Hypertension and an Atrial Septal Defect Treated with Bilateral Lung Transplantation.

The Efficacy of a Genetic Analysis of the BMPR2 Gene in a Patient with Severe Pulmonary Arterial Hypertension and an Atrial Septal Defect Treated with Bilateral Lung Transplantation.

Coexistence of a Double-Chambered Right Ventricle With Ebstein-Like Anomaly and Right Ventricular Apical Hypoplasia - Usefulness of Multimodality Imaging.

Coexistence of a Double-Chambered Right Ventricle With Ebstein-Like Anomaly and Right Ventricular Apical Hypoplasia - Usefulness of Multimodality Imaging.

Thalidomide for Hereditary Hemorrhagic Telangiectasia With Pulmonary Arterial Hypertension.

Thalidomide for Hereditary Hemorrhagic Telangiectasia With Pulmonary Arterial Hypertension.

Left main coronary artery compression by a dilated main pulmonary artery and left coronary sinus of Valsalva aneurysm in a patient with heritable pulmonary arterial hypertension and FLNA mutation.

Left main coronary artery compression by a dilated main pulmonary artery and left coronary sinus of Valsalva aneurysm in a patient with heritable pulmonary arterial hypertension and FLNA mutation.

Congenitally Corrected Transposition of the Great Arteries and Situs Inversus in an Octogenarian With Systemic Right Ventricular Failure.

Congenitally Corrected Transposition of the Great Arteries and Situs Inversus in an Octogenarian With Systemic Right Ventricular Failure.

Selexipag for Chronic Thromboembolic Pulmonary Hypertension in Japanese Patients　- A Double-Blind, Randomized, Placebo-Controlled, Multicenter Phase II Study.

Selexipag for Chronic Thromboembolic Pulmonary Hypertension in Japanese Patients　- A Double-Blind, Randomized, Placebo-Controlled, Multicenter Phase II Study.

Coexistence of a Double-Chambered Right Ventricle With Ebstein-Like Anomaly and Right Ventricular Apical Hypoplasia　- Usefulness of Multimodality Imaging.

Coexistence of a Double-Chambered Right Ventricle With Ebstein-Like Anomaly and Right Ventricular Apical Hypoplasia　- Usefulness of Multimodality Imaging.