Mihoko Kawamura
Nagoya, Japan
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 12 publications
Twenty-Four Month Results of Intravitreal Ranibizumab for Macular Edema after Branch Retinal Vein Occlusion: Visual Outcomes and Resolution of Macular Edema.
Journal: Seminars in ophthalmology
Published: February 22, 2021
Genetic Background of Catecholaminergic Polymorphic Ventricular Tachycardia in Japan.
Journal: Circulation journal : official journal of the Japanese Circulation Society
Published: October 26, 2020
Macular hole and serous pigment epithelial detachment in bilateral acquired vitelliform lesions.
Journal: American journal of ophthalmology case reports
Published: June 12, 2019
Six-month results of intravitreal ranibizumab for macular edema after branch retinal vein occlusion in a single-center prospective study: visual outcomes and microaneurysm formation.
Journal: Clinical ophthalmology (Auckland, N.Z.)
Published: August 30, 2018
A Case of Euthyroid Graves' Ophthalmopathy in a Patient Sero-Negative for TSH Receptor Autoantibody.
A Case of Euthyroid Graves' Ophthalmopathy in a Patient Sero-Negative for TSH Receptor Autoantibody.
Journal: Case reports in endocrinology
Published: January 22, 2018
Exon 3 deletion of RYR2 encoding cardiac ryanodine receptor is associated with left ventricular non-compaction.
Journal: Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology
Published: January 08, 2014
Ethnic differences in GRHPR mutations in patients with primary hyperoxaluria type 2.
Journal: Clinical genetics
Published: May 23, 2013
Genetic background of catecholaminergic polymorphic ventricular tachycardia in Japan.
Journal: Circulation journal : official journal of the Japanese Circulation Society
Published: April 19, 2013
Seasonal and circadian distributions of cardiac events in genotyped patients with congenital long QT syndrome.
Journal: Circulation journal : official journal of the Japanese Circulation Society
Published: July 13, 2012
Phenotype variability in patients carrying KCNJ2 mutations.
Journal: Circulation. Cardiovascular genetics
Published: May 17, 2012
Successful catheter ablation of bidirectional ventricular premature contractions triggering ventricular fibrillation in catecholaminergic polymorphic ventricular tachycardia with RyR2 mutation.
Journal: Circulation. Arrhythmia and electrophysiology
Published: February 16, 2012
Showing 1-12 of 12
Last Updated: 09/26/2026