Akiko Hikoya

发表

Central corneal thickness in Japanese children

R. Asaoka, Miho Sato, Akiko Hikoya, 2008, Japanese Journal of Ophthalmology.

Visual Outcomes in Japanese Patients with Retinitis Pigmentosa and Usher Syndrome Caused by USH2A Mutations

H. Nakanishi, S. Minoshima, K. Mizuta, 2015, Seminars in ophthalmology.

Interaction between optineurin and the bZIP transcription factor NRL

S. Minoshima, M. Ohtsubo, Miho Sato, 2009, Cell biology international.

A case of siblings with juvenile retinitis pigmentosa associated with NEK1 gene variants

T. Ogata, H. Saitsu, Miho Sato, 2022, Ophthalmic genetics.

The first USH2A mutation analysis of Japanese autosomal recessive retinitis pigmentosa patients: a totally different mutation profile with the lack of frequent mutations found in Caucasian patients

H. Nakanishi, S. Minoshima, Y. Hirami, 2014, Journal of Human Genetics.

A case of aniridia with unilateral Peters anomaly.

S. Minoshima, Miho Sato, N. Azuma, 2011, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

Magnetic resonance imaging of the medial rectus muscle of patients with consecutive exotropia after medial rectus muscle recession.

H. Isoda, Miho Sato, Akiko Hikoya, 2010, Ophthalmology.

DNA Analysis for Diagnosis of X-Linked Juvenile Retinoschisis When Clinical Examination Is Difficult in a Young Child

Miho Sato, Akiko Hikoya, Y. Hotta, 2005, Japanese Journal of Ophthalmology.

Case of a Japanese patient with X-linked ocular albinism associated with the GPR143 gene mutation

S. Minoshima, M. Ohtsubo, Miho Sato, 2010, Japanese Journal of Ophthalmology.

Three novel mutations of the PAX6 gene in Japanese aniridia patients

S. Minoshima, N. Shimizu, M. Ohtsubo, 2007, Journal of Human Genetics.

A case of childhood glaucoma with a combined partial monosomy 6p25 and partial trisomy 18p11 due to an unbalanced translocation

S. Minoshima, H. Saitsu, T. Fukao, 2020, Ophthalmic genetics.

Two Novel Mutations in the EYS Gene Are Possible Major Causes of Autosomal Recessive Retinitis Pigmentosa in the Japanese Population

Shinsei Minoshima, Miho Sato, Tadashi Yokoi, 2012, PloS one.

Clinical features of a Japanese case with Bothnia dystrophy

S. Minoshima, M. Kondo, Akiko Hikoya, 2012, Ophthalmic genetics.

Effects of the Gaze Fixation Position on AS-OCT Measurements of the Limbus and Extraocular Muscle Insertion Site Distance.

Miho Sato, Akiko Hikoya, Y. Hotta, 2021, Journal of pediatric ophthalmology and strabismus.

Changes in conjunctival–scleral thickness after strabismus surgery measured with anterior segment optical coherence tomography

Miho Sato, Akiko Hikoya, Y. Hotta, 2018, Japanese Journal of Ophthalmology.

Characteristics and surgical outcomes of consecutive exotropia of different etiologies

Miho Sato, Akiko Hikoya, Y. Hotta, 2015, Japanese Journal of Ophthalmology.

Usefulness of handheld electroretinogram system for diagnosing blue-cone monochromatism in children

Miho Sato, Akiko Hikoya, Y. Hotta, 2020, Japanese Journal of Ophthalmology.

Evaluation of Surgical Strategy Based on the Intraoperative Superior Oblique Tendon Traction Test

Miho Sato, Akiko Hikoya, Y. Hotta, 2016, PloS one.

Superior oblique palsy with class III tendon anomaly.

Miho Sato, Akiko Hikoya, Yuka Maruyama Koide, 2008, American journal of ophthalmology.

Intraocular pressure at different gaze positions in patients with highly myopic strabismus

Miho Sato, Akiko Hikoya, Y. Hotta, 2022, Japanese Journal of Ophthalmology.

Clinical findings of acute acquired comitant esotropia in young patients

Miho Sato, Akiko Hikoya, Y. Hotta, 2021, Japanese Journal of Ophthalmology.

Two cases of acquired bilateral trochlea nerve palsy treated by simultaneous inferior rectus muscle nasal transposition and inferior oblique muscle myectomy

Miho Sato, Akiko Hikoya, Y. Hotta, 2021, American journal of ophthalmology case reports.

Clinical characteristics of a Japanese patient with Bardet-Biedl syndrome caused by BBS10 mutations

S. Minoshima, T. Ogata, H. Saitsu, 2018, Japanese Journal of Ophthalmology.

Molecular Diagnosis of 34 Japanese Families with Leber Congenital Amaurosis Using Targeted Next Generation Sequencing

S. Minoshima, H. Saitsu, Miho Sato, 2018, Scientific Reports.

Novel GUCY2D Gene Mutations in Japanese Male Twins with Leber Congenital Amaurosis

S. Minoshima, Miho Sato, Akiko Hikoya, 2015, Journal of ophthalmology.

Exophthalmos associated with chronic progressive external ophthalmoplegia

Miho Sato, Akiko Hikoya, Y. Hotta, 2022, Japanese Journal of Ophthalmology.