Toru Meguro
Yamagata, Japan
Last Updated: 09/26/2026
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Found 11 publications
Bleeding Diathesis in Hypotrichosis-Lymphedema-Telangiectasia Syndrome due to Decreased von Willebrand Factor.
Journal: American journal of medical genetics. Part A
Published: September 27, 2025
Colorectal cancer in a patient with glutaric aciduria type 1.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: May 14, 2024
A retrospective analysis of azacitidine treatment for juvenile myelomonocytic leukemia.
Journal: International journal of hematology
Published: July 06, 2021
A surgical case of pediatric spinal medulloepithelioma.
Journal: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
Published: April 10, 2021
ALOX12 mutation in a family with dominantly inherited bleeding diathesis.
Journal: Journal of human genetics
Published: September 05, 2020
Raccoon eyes in an infant with neuroblastoma.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: May 20, 2020
Three Consecutive Cases of Familial Hemophagocytic Lymphohistiocytosis, Including a Case Due to Maternal Uniparental Disomy.
Journal: Journal of pediatric hematology/oncology
Published: December 03, 2019
Genotype-phenotype relationship in Japanese patients with congenital central hypoventilation syndrome.
Journal: Journal of human genetics
Published: February 22, 2015
Giant thymolipoma in a young child initially diagnosed as cardiomegaly.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: November 23, 2014
Successful treatment of acute myeloid leukaemia in a patient with ataxia telangiectasia.
Journal: European journal of haematology
Published: August 10, 2013
Inheritance of polyalanine expansion mutation of PHOX2B in congenital central hypoventilation syndrome.
Journal: Journal of human genetics
Published: March 23, 2012
Showing 1-11 of 11
Last Updated: 09/26/2026