Yasushi Tomita
Nagoya, 4600001, Japan
Last Updated: 09/26/2026
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Found 13 publications
The Efficacy and Safety of a Novel Extramedullary Guide Coordinated with 3D Surgical Assistive Software for Total Knee Arthroplasty: an Open-Label Single-Arm Trial.
Journal: The Kurume medical journal
Published: November 29, 2021
Extrinsic compression of the left main coronary artery: A rare cause of cardiogenic shock.
Journal: Radiology case reports
Published: December 22, 2020
The influence of frailty under direct oral anticoagulant use in patients with atrial fibrillation.
Journal: Heart Asia
Published: March 12, 2019
An Open-Label, Single-Arm Study of a Patient-Specific Femoral Guide for Total Hip Arthroplasty via the Anterolateral Supine Approach, Linked with Three-Dimensional Surgical Support Software: Study Protocol.
Journal: The Kurume medical journal
Published: September 11, 2018
An Open-label Single-arm Trial of a Novel Extramedullary Guide Coordinated with 3D Surgical Assistive Software for Total Knee Arthroplasty.
Journal: Acta medica Okayama
Published: August 25, 2018
Sunlight is merely a temporary modifier of dyschromatosis symmetrica hereditaria.
Journal: European journal of dermatology : EJD
Published: February 06, 2018
Dyschromatosis Symmetrica Hereditaria and Aicardi-Goutières Syndrome 6 Are Phenotypic Variants Caused by ADAR1 Mutations.
Journal: The Journal of investigative dermatology
Published: August 23, 2015
Effects of oral propranolol on a juxtapapillary capillary hemangioma: a single-subject pilot study.
Journal: Ophthalmic surgery, lasers & imaging retina
Published: February 24, 2014
Dyschromatosis symmetrica hereditaria by ADAR1 mutations and viral encephalitis: a hidden link?
Journal: International journal of dermatology
Published: November 23, 2013
Effects of oral propranolol on circumscribed choroidal hemangioma: a pilot study.
Journal: JAMA ophthalmology
Published: October 26, 2013
Whole-exome sequencing identifies ADAM10 mutations as a cause of reticulate acropigmentation of Kitamura, a clinical entity distinct from Dowling-Degos disease.
Journal: Human molecular genetics
Published: May 14, 2013
Four novel ADAR1 gene mutations in patients with dyschromatosis symmetrica hereditaria.
Journal: The Journal of dermatology
Published: January 23, 2013
Last Updated: 09/26/2026