Yuya Hashimura

Takatsuki, Japan

Last Updated: 09/26/2026

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Found 9 publications

Efficacy of primary treatment with immunoglobulin plus ciclosporin for prevention of coronary artery abnormalities in patients with Kawasaki disease predicted to be at increased risk of non-response to intravenous immunoglobulin (KAICA): a randomised controlled, open-label, blinded-endpoints, phase 3 trial.

Efficacy of primary treatment with immunoglobulin plus ciclosporin for prevention of coronary artery abnormalities in patients with Kawasaki disease predicted to be at increased risk of non-response to intravenous immunoglobulin (KAICA): a randomised controlled, open-label, blinded-endpoints, phase 3 trial.

Journal: Lancet (London, England)

Published: July 03, 2018

Segmental membranous nephropathy with severe IgG3 deposition.

Segmental membranous nephropathy with severe IgG3 deposition.

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

Published: August 04, 2017

Mitochondrial respiratory chain complex IV deficiency complicated with chronic intestinal pseudo-obstruction in a neonate.

Mitochondrial respiratory chain complex IV deficiency complicated with chronic intestinal pseudo-obstruction in a neonate.

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

Published: October 11, 2015

X-linked Alport syndrome caused by splicing mutations in COL4A5.

X-linked Alport syndrome caused by splicing mutations in COL4A5.

Journal: Clinical journal of the American Society of Nephrology : CJASN

Published: September 04, 2014

Natural history of genetically proven autosomal recessive Alport syndrome.

Natural history of genetically proven autosomal recessive Alport syndrome.

Journal: Pediatric nephrology (Berlin, Germany)

Published: January 12, 2014

A patient with autosomal recessive Alport syndrome due to segmental maternal isodisomy.

A patient with autosomal recessive Alport syndrome due to segmental maternal isodisomy.

Journal: Human genome variation

Published: January 01, 2014

Milder clinical aspects of X-linked Alport syndrome in men positive for the collagen IV α5 chain.

Milder clinical aspects of X-linked Alport syndrome in men positive for the collagen IV α5 chain.

Journal: Kidney international

Published: July 10, 2013

Metabolomics analysis of umbilical cord blood clarifies changes in saccharides associated with delivery method.

Metabolomics analysis of umbilical cord blood clarifies changes in saccharides associated with delivery method.

Journal: Early human development

Published: September 01, 2012

Renal transplantations from parents to siblings with autosomal recessive Alport syndrome caused by a rearrangement in an intronic antisense Alu element in the COL4A3 gene led to different outcomes.

Renal transplantations from parents to siblings with autosomal recessive Alport syndrome caused by a rearrangement in an intronic antisense Alu element in the COL4A3 gene led to different outcomes.

Journal: CEN case reports

Published: July 02, 2012

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Last Updated: 09/26/2026