Hidenori Kawasaki

Kyoto, Japan

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 28 publications

Donor selection in living-donor lung transplantation for familial pulmonary fibrosis: A narrative review and single-center practical approach.

Donor selection in living-donor lung transplantation for familial pulmonary fibrosis: A narrative review and single-center practical approach.

Journal: Respiratory investigation

Published: April 27, 2026

Optimal Therapeutic Strategy for Ventricular Septal Defect Closure in Extremely Preterm Infants with Chronic Lung Disease and Severe Pulmonary Hypertension.

Optimal Therapeutic Strategy for Ventricular Septal Defect Closure in Extremely Preterm Infants with Chronic Lung Disease and Severe Pulmonary Hypertension.

Journal: International heart journal

Published: October 01, 2025

Familial Alveolar Capillary Dysplasia With Misalignment of Pulmonary Veins Caused by Paternal FOXF1 Upstream Enhancer Deletion: A Case Report.

Familial Alveolar Capillary Dysplasia With Misalignment of Pulmonary Veins Caused by Paternal FOXF1 Upstream Enhancer Deletion: A Case Report.

Journal: American journal of medical genetics. Part A

Published: December 19, 2024

Adult hypophosphatasia presenting with recurrent acute joint pain.

Adult hypophosphatasia presenting with recurrent acute joint pain.

Journal: Endocrinology, diabetes & metabolism case reports

Published: October 22, 2024

Case report: Duplication of the GCK gene is a novel cause of nesidioblastosis: evidence from a case with Silver-Russell syndrome-like phenotype related to chromosome 7.

Case report: Duplication of the GCK gene is a novel cause of nesidioblastosis: evidence from a case with Silver-Russell syndrome-like phenotype related to chromosome 7.

Journal: Frontiers in endocrinology

Published: May 12, 2024

Proactive Diagnosis and Tailor-Made Treatment of Patent Ductus Arteriosus in Very Preterm Infants with Routine Echocardiography in Japan: A post hoc Analysis of the PLASE Study.

Proactive Diagnosis and Tailor-Made Treatment of Patent Ductus Arteriosus in Very Preterm Infants with Routine Echocardiography in Japan: A post hoc Analysis of the PLASE Study.

Journal: Neonatology

Published: December 06, 2023

Living donor liver transplantation for myocerebrohepatopathy spectrum due to POLG mutations.

Living donor liver transplantation for myocerebrohepatopathy spectrum due to POLG mutations.

Journal: Pediatric transplantation

Published: June 06, 2023

Decision-making processes behind seeking regular cardiac checkups for individuals with Marfan syndrome: A grounded theory study.

Decision-making processes behind seeking regular cardiac checkups for individuals with Marfan syndrome: A grounded theory study.

Journal: Journal of genetic counseling

Published: April 30, 2023

Mortality and morbidity of infants with trisomy 21, weighing 1500 grams or less, in Japan.

Mortality and morbidity of infants with trisomy 21, weighing 1500 grams or less, in Japan.

Journal: Journal of human genetics

Published: February 21, 2022

Immature teratoma of the ovary associated with Cowden syndrome.

Immature teratoma of the ovary associated with Cowden syndrome.

Journal: Pediatric blood & cancer

Published: November 28, 2021

Valve-sparing Aortic Root Replacement for a Patient With Filamin A Mutation.

Valve-sparing Aortic Root Replacement for a Patient With Filamin A Mutation.

Journal: The Annals of thoracic surgery

Published: November 26, 2021

The association of ectopic craniopharyngioma in the fourth ventricle with familial adenomatous polyposis: illustrative case.

The association of ectopic craniopharyngioma in the fourth ventricle with familial adenomatous polyposis: illustrative case.

Journal: Journal of neurosurgery. Case lessons

Published: October 09, 2021

Showing 1-12 of 28

Last Updated: 09/26/2026