List of works - Takaaki Hayashi

ABCC6 Gene Analysis in 20 Japanese Patients with Angioid Streaks Revealing Four Frequent and Two Novel Variants and Pseudodominant Inheritance

scientific article published on 20 August 2017

Characterization of GUCA1A-associated dominant cone/cone-rod dystrophy: low prevalence among Japanese patients with inherited retinal dystrophies

scientific article published on 14 November 2019

Clinical Course and Electron Microscopic Findings in Lymphocytes of Patients with DRAM2-Associated Retinopathy

scientific article published on 16 February 2020

Coexistence of GNAT1 and ABCA4 variants associated with Nougaret-type congenital stationary night blindness and childhood-onset cone-rod dystrophy

scientific article published on 03 October 2019

Color vision in an elderly patient with protanopic genotype and successfully treated unilateral age-related macular degeneration ⬇️

scientific article published on November 11, 2011

Electroretinographic abnormalities associated with pregabalin: a case report

scientific article published on 03 January 2020

Foveal Hypoplasia in Patients with Stickler Syndrome.

scientific article

Improvement in S-cone–mediated Visual Fields and Rod Function after Correction of Vitamin a Deficiency ⬇️

scientific article published on 01 September 2011

Improvement of central visual function following steroid pulse therapy in acute zonal occult outer retinopathy ⬇️

scientific article published on March 9, 2012

Long-term observation of a Japanese mucolipidosis IV patient with a novel homozygous p.F313del variant of MCOLN1

scientific article published on 27 March 2020

Macular Dysfunction in Oguchi Disease with the Frequent Mutation 1147delA in the <i>SAG</i> Gene ⬇️

scientific article published on March 29, 2011

Novel biallelic TRPM1 variants in an elderly patient with complete congenital stationary night blindness

scientific article published on 17 October 2020

Novel biallelic loss-of-function KCNV2 variants in cone dystrophy with supernormal rod responses

scientific article published on 15 March 2019

Novel biallelic splice-site BBS1 variants in Bardet-Biedle syndrome: a case report of the first Japanese patient

scientific article published on 29 January 2020

Novel homozygous CLN3 missense variant in isolated retinal dystrophy: A case report and electron microscopic findings

scientific article published on 22 May 2020

Novel use of Finesse Flex loop for macular hole retinal detachment

scientific article published on 19 April 2020

RHO Mutations (p.W126L and p.A346P) in Two Japanese Families with Autosomal Dominant Retinitis Pigmentosa.