Yusuke Hamada

Suita, 5650087, Japan

Last Updated: 09/26/2026

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Found 11 publications

Successful trans-femoral retrieval of a stuck axillary Impella 5.0 device.

Successful trans-femoral retrieval of a stuck axillary Impella 5.0 device.

Journal: Journal of artificial organs : the official journal of the Japanese Society for Artificial Organs

Published: June 12, 2022

Successful Radical Pericardiectomy for Porcelain Constrictive Pericarditis.

Successful Radical Pericardiectomy for Porcelain Constrictive Pericarditis.

Journal: JACC. Case reports

Published: February 26, 2021

Mucolipidosis Ⅱ and III with neurological symptoms due to spinal cord compression.

Mucolipidosis Ⅱ and III with neurological symptoms due to spinal cord compression.

Journal: Brain & development

Published: January 07, 2021

Open-label clinical trial of bezafibrate treatment in patients with fatty acid oxidation disorders in Japan; 2nd report QOL survey.

Open-label clinical trial of bezafibrate treatment in patients with fatty acid oxidation disorders in Japan; 2nd report QOL survey.

Journal: Molecular genetics and metabolism reports

Published: July 01, 2019

Early juvenile Tay-Sachs disease with atypical symptoms.

Early juvenile Tay-Sachs disease with atypical symptoms.

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

Published: February 20, 2018

Open-label clinical trial of bezafibrate treatment in patients with fatty acid oxidation disorders in Japan.

Open-label clinical trial of bezafibrate treatment in patients with fatty acid oxidation disorders in Japan.

Journal: Molecular genetics and metabolism reports

Published: December 22, 2017

Newborn screening for carnitine palmitoyltransferase II deficiency using (C16+C18:1)/C2: Evaluation of additional indices for adequate sensitivity and lower false-positivity.

Newborn screening for carnitine palmitoyltransferase II deficiency using (C16+C18:1)/C2: Evaluation of additional indices for adequate sensitivity and lower false-positivity.

Journal: Molecular genetics and metabolism

Published: May 24, 2017

Mutation in VPS33A affects metabolism of glycosaminoglycans: a new type of mucopolysaccharidosis with severe systemic symptoms.

Mutation in VPS33A affects metabolism of glycosaminoglycans: a new type of mucopolysaccharidosis with severe systemic symptoms.

Journal: Human molecular genetics

Published: August 26, 2016

Intracellular fate of Ureaplasma parvum entrapped by host cellular autophagy.

Intracellular fate of Ureaplasma parvum entrapped by host cellular autophagy.

Journal: MicrobiologyOpen

Published: August 08, 2016

Late-onset Krabbe disease is predominant in Japan and its mutant precursor protein undergoes more effective processing than the infantile-onset form.

Late-onset Krabbe disease is predominant in Japan and its mutant precursor protein undergoes more effective processing than the infantile-onset form.

Journal: Gene

Published: August 16, 2013

Microdeletions of 3p21.31 characterized by developmental delay, distinctive features, elevated serum creatine kinase levels, and white matter involvement.

Microdeletions of 3p21.31 characterized by developmental delay, distinctive features, elevated serum creatine kinase levels, and white matter involvement.

Journal: American journal of medical genetics. Part A

Published: February 24, 2013

Showing 1-11 of 11

Last Updated: 09/26/2026