Results 91 to 100 of about 1,654 (162)

Congenitally Impaired Disparity Vergence in Children With Infantile Esotropia. [PDF]

Invest Ophthalmol Vis Sci, 2016
Kelly KR, Felius J, Ramachandran S, John BA, Jost RM, Birch EE.   +5 more
europepmc   +1 more source

Prevalence of Strabismus and Decreased Stereopsis in Parents of Children with Strabismus. [PDF]

Ophthalmology
MacKinnon S, Zacks R, Barry B, Mackey DA, Hunter DG, Engle EC, Whitman MC, Strabismus Genetics Research Consortium.   +7 more
europepmc   +1 more source

Analysis of Convergence and Divergence Using an Eye Tracker in Acquired Comitant Esotropia. [PDF]

Invest Ophthalmol Vis Sci
Hiratake J, Mochizuki Y, Okita Y, Masuda A, Kanda H, Gomi F.   +5 more
europepmc   +1 more source

Ophthalmic Findings in a Child with Purine-Rich Element Binding Protein A (PURA)-Related Neurodevelopmental Disorder: A Case Report. [PDF]

Korean J Ophthalmol
Lee S, Chung SA.
europepmc   +1 more source

Visual and refractive pattern in patients with comitant large angle esotropia. [PDF]

BMC Ophthalmol
Khorrami-Nejad M, Akbari MR, Masoomian B, Saleh KK, Azizi E.   +4 more
europepmc   +1 more source

Subtype-Specific Macular Microvascular Changes in Accommodative Esotropia Assessed by Optical Coherence Tomography Angiography. [PDF]

Invest Ophthalmol Vis Sci
Güven S, Bozoklu M, Arikan S.
europepmc   +1 more source

Surgical Outcomes and Predictors of Success in Esotropia: A Five-Year Retrospective Review From a Large UK Tertiary Centre. [PDF]

Cureus
Chan SW, Yan CK, Masoodi H, Khan S, Shenoy BH.   +4 more
europepmc   +1 more source

Essential infantile esotropia with inferior oblique hyperfunction: long term follow-up of 6 muscles approach. [PDF]

Int J Ophthalmol, 2016
Magli A, Carelli R, Chiariello Vecchio E, Esposito F, Rombetto L, Esposito Veneruso P.   +5 more
europepmc   +1 more source

Use of Botulinum Toxin for Esotropia Treatment in Government Hospitals of Bahrain: A Cross-Sectional Study. [PDF]

Cureus
Alamari HM, Bucheery YA.
europepmc   +1 more source

Xq26.2 Contiguous Gene Deletion Involving <i>FRMD7</i> and <i>IGSF1</i>: Highly Penetrant Infantile Nystagmus with Variable Endocrine Involvement. [PDF]

Genes (Basel)
Poleg T, Carmon L, Brav E, Hadar N, Dolgin V, Amar S, Narkis G, Birk OS, Gradstein L.   +8 more
europepmc   +1 more source