Masanori Kouwaki

Toyohashi, Japan

Last Updated: 09/26/2026

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Found 15 publications

Pulmonary hypertension with bronchopulmonary dysplasia: Aichi cohort study.

Pulmonary hypertension with bronchopulmonary dysplasia: Aichi cohort study.

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

Published: February 02, 2022

A Novel α-Spectrin Pathogenic Variant in Trans to α-Spectrin LELY Causing Neonatal Jaundice With Hemolytic Anemia From Hereditary Pyropoikilocytosis Coexisting With Gilbert Syndrome.

A Novel α-Spectrin Pathogenic Variant in Trans to α-Spectrin LELY Causing Neonatal Jaundice With Hemolytic Anemia From Hereditary Pyropoikilocytosis Coexisting With Gilbert Syndrome.

Journal: Journal of pediatric hematology/oncology

Published: August 13, 2019

Echovirus Type 7 Virus-Associated Hemophagocytic Syndrome in a Neonate Successfully Treated With Intravenous Immunoglobulin Therapy: A Case Report.

Echovirus Type 7 Virus-Associated Hemophagocytic Syndrome in a Neonate Successfully Treated With Intravenous Immunoglobulin Therapy: A Case Report.

Journal: Frontiers in pediatrics

Published: July 24, 2019

Natural histories of patients with Wolf-Hirschhorn syndrome derived from variable chromosomal abnormalities.

Natural histories of patients with Wolf-Hirschhorn syndrome derived from variable chromosomal abnormalities.

Journal: Congenital anomalies

Published: June 17, 2018

Prognostic factors of hydrops fetalis with pleural effusion.

Prognostic factors of hydrops fetalis with pleural effusion.

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

Published: March 19, 2017

Neurodevelopmental outcomes at 3 years old for infants with birth weights under 500 g.

Neurodevelopmental outcomes at 3 years old for infants with birth weights under 500 g.

Journal: Pediatrics and neonatology

Published: February 14, 2017

Single nucleotide polymorphisms in AGTR1, TFAP2B, and TRAF1 are not associated with the incidence of patent ductus arteriosus in Japanese preterm infants.

Single nucleotide polymorphisms in AGTR1, TFAP2B, and TRAF1 are not associated with the incidence of patent ductus arteriosus in Japanese preterm infants.

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

Published: August 25, 2015

A novel mutation Ser344Cys in FGFR3 causes achondroplasia with severe platyspondyly.

A novel mutation Ser344Cys in FGFR3 causes achondroplasia with severe platyspondyly.

Journal: American journal of medical genetics. Part A

Published: December 05, 2014

Nemaline myopathy with KLHL40 mutation presenting as congenital totally locked-in state.

Nemaline myopathy with KLHL40 mutation presenting as congenital totally locked-in state.

Journal: Brain & development

Published: November 17, 2014

Hypoxic ischemic encephalopathy in a case of intranuclear rod myopathy without any prenatal sentinel event.

Hypoxic ischemic encephalopathy in a case of intranuclear rod myopathy without any prenatal sentinel event.

Journal: Brain & development

Published: November 30, 2013

Spontaneous movements in the supine position of preterm infants with intellectual disability.

Spontaneous movements in the supine position of preterm infants with intellectual disability.

Journal: Brain & development

Published: February 04, 2013

Effects of exchange transfusion on cytokine profiles in necrotizing enterocolitis.

Effects of exchange transfusion on cytokine profiles in necrotizing enterocolitis.

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

Published: January 03, 2013

Showing 1-12 of 15

Last Updated: 09/26/2026