Takao Togawa

Toyohashi, Japan

Last Updated: 09/26/2026

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Found 28 publications

Tandem duplication of 7q11.23-q22.1: Partial trisomy 7q in a very-low-birth-weight infant.

Tandem duplication of 7q11.23-q22.1: Partial trisomy 7q in a very-low-birth-weight infant.

Journal: Pediatrics international : official journal of the Japan Pediatric Society

Published: January 06, 2025

Antenatal Growth, Gestational Age, Birth, Enteral Feeding, and Blood Citrulline Levels in Very Low Birth Weight Infants.

Antenatal Growth, Gestational Age, Birth, Enteral Feeding, and Blood Citrulline Levels in Very Low Birth Weight Infants.

Journal: Nutrients

Published: December 25, 2023

Clinicopathologic Features, Genetics, Treatment, and Long-Term Outcomes in Japanese Children and Young Adults with Benign Recurrent Intrahepatic Cholestasis: A Multicenter Study.

Clinicopathologic Features, Genetics, Treatment, and Long-Term Outcomes in Japanese Children and Young Adults with Benign Recurrent Intrahepatic Cholestasis: A Multicenter Study.

Journal: Journal of clinical medicine

Published: July 30, 2023

Adult-onset Type II Citrullinemia Developed under Dietary Restrictions during Imprisonment.

Adult-onset Type II Citrullinemia Developed under Dietary Restrictions during Imprisonment.

Journal: Internal medicine (Tokyo, Japan)

Published: July 26, 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

Intraoperative indocyanine green fluorescence cholangiography can rule out biliary atresia: A preliminary report.

Intraoperative indocyanine green fluorescence cholangiography can rule out biliary atresia: A preliminary report.

Journal: Frontiers in pediatrics

Published: July 28, 2022

Case Report: A Rare Case of Benign Recurrent Intrahepatic Cholestasis-Type 1 With a Novel Heterozygous Pathogenic Variant of ATP8B1.

Case Report: A Rare Case of Benign Recurrent Intrahepatic Cholestasis-Type 1 With a Novel Heterozygous Pathogenic Variant of ATP8B1.

Journal: Frontiers in medicine

Published: March 08, 2022

Novel gene mutations in three Japanese patients with ARC syndrome associated mild phenotypes: a case series.

Novel gene mutations in three Japanese patients with ARC syndrome associated mild phenotypes: a case series.

Journal: Journal of medical case reports

Published: September 14, 2021

Real-life Progression of the Use of a Genetic Panel in to Diagnose Neonatal Cholestasis.

Real-life Progression of the Use of a Genetic Panel in to Diagnose Neonatal Cholestasis.

Journal: JPGN reports

Published: August 27, 2021

Urine bile acid profile of a Japanese patient with a bile acid amidation defect.

Urine bile acid profile of a Japanese patient with a bile acid amidation defect.

Journal: Pediatrics international : official journal of the Japan Pediatric Society

Published: August 24, 2021

Long-term Outcomes of Living-donor Liver Transplantation for Progressive Familial Intrahepatic Cholestasis Type 1.

Long-term Outcomes of Living-donor Liver Transplantation for Progressive Familial Intrahepatic Cholestasis Type 1.

Journal: Journal of pediatric gastroenterology and nutrition

Published: December 02, 2020

Assessment of Adenosine Triphosphatase Phospholipid Transporting 8B1 (ATP8B1) Function in Patients With Cholestasis With ATP8B1 Deficiency by Using Peripheral Blood Monocyte-Derived Macrophages.

Assessment of Adenosine Triphosphatase Phospholipid Transporting 8B1 (ATP8B1) Function in Patients With Cholestasis With ATP8B1 Deficiency by Using Peripheral Blood Monocyte-Derived Macrophages.

Journal: Hepatology communications

Published: April 30, 2020

Showing 1-12 of 28

Last Updated: 09/26/2026