Shogo Ito
Nagoya, Japan
Last Updated: 09/26/2026
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Found 16 publications
Lipolysis-Stimulated Lipoprotein Receptor Gene Variants as a Cause of Progressive Familial Intrahepatic Cholestasis: A Case Report.
Journal: Hepatology research : the official journal of the Japan Society of Hepatology
Published: December 10, 2024
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.
Journal: Internal medicine (Tokyo, Japan)
Published: July 26, 2023
Living donor liver transplantation for myocerebrohepatopathy spectrum due to POLG mutations.
Journal: Pediatric transplantation
Published: June 06, 2023
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.
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.
Journal: JPGN reports
Published: August 27, 2021
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
Peripheral nerves are involved in hypomyelinating leukodystrophy-3 caused by a homozygous AIMP1 variant.
Journal: Brain & development
Published: October 22, 2020
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
Successful treatment of adult-onset type II citrullinemia with a low-carbohydrate diet and L-arginine after DNA analysis produced a definitive diagnosis.
Journal: Clinical journal of gastroenterology
Published: May 16, 2019
Last Updated: 09/26/2026