Results 71 to 80 of about 2,545 (213)

Accommodation [PDF]

open access: yes, 2001
Universidade de São Paulo Faculdade de Medicina Hospital das ClínicasUniversidade Federal de São Paulo (UNIFESP) Departamento de OftalmologiaUNIFESP, Depto.
Plutt, Mauro, Sá, Luís Carlos F. De
core   +3 more sources

Functional Convergence Spasm and Dysconjugate Eye Movements: A Vignette

open access: yes
Movement Disorders Clinical Practice, Volume 13, Issue 2, Page 563-564, February 2026.
Iryna Klopotovska   +2 more
wiley   +1 more source

Retrospective Study of Clinical and Genetic Profiles of Alpha‐Mannosidosis Patients From the UAE

open access: yesJIMD Reports, Volume 66, Issue 2, March 2025.
ABSTRACT Alpha‐mannosidosis (AM; OMIM 248500) is a rare autosomal recessive lysosomal storage disorder caused by mutations in MAN2B1, which codes for the lysosomal alpha‐mannosidase enzyme (LAMAN; EC:3.2.1.24). Clinical characteristics include developmental delay, hearing impairment, and recurrent infections.
Ali K. Saad   +6 more
wiley   +1 more source

Vision and Reading Difficulties Part 5: Clinical protocol and the role of the eye-care practitioner [PDF]

open access: yes, 2009
This series of articles has described various aspects of visual characteristics of reading difficulties and the background behind techniques such as the use of coloured filters in helping to reduce the difficulties that are experienced.
Allen, Peter M   +2 more
core  

Physical Therapy Management for Delayed Diagnosis of Developmental Dysplasia of the Hip: A Case Report

open access: yesCase Reports in Pediatrics, Volume 2025, Issue 1, 2025.
Background: Delayed diagnosis of developmental dysplasia of the hip (DDH)—defined as detection after 8 weeks of age using physical examination, ultrasound, or X‐ray—occurs in approximately 0.14%–0.26% of infants. This case report highlights the challenges of delayed DDH diagnosis and the role of physical therapy in rehabilitation.
Kai-Yu Ho   +3 more
wiley   +1 more source

Etiology, diagnosis, and management of partially accommodative esotropia

open access: yesKlinika Oczna
This paper presents an overview of partially accommodative esotro­pia focusing on its key characteristics, classification, and underlying mechanisms, primarily associated with uncorrected hyperopia and a high accommodative convergence to accommodation ...
Ewa Witowska-Jeleń
doaj   +1 more source

Repeatability of the measurement of the horizontal phoria in near vision with cover test and modified thorington method [PDF]

open access: yes, 2017
Objectiu- Estudiar la repetibilitat del cover test alternant i el mètode modificat de Thorington. Mètode- En aquest estudi han participat 10 persones joves i sanes amb agudesa visual de prop igual o superior a 20/20 amb la seva correcció habitual.
Gervilla Díaz, Gemma
core  

2024 UK and Ireland modified Delphi consensus on myopia management in children and young people

open access: yesOphthalmic and Physiological Optics, Volume 44, Issue 7, Page 1368-1391, November 2024.
Abstract Introduction This work aimed to establish the largest UK and Ireland consensus on myopia management in children and young people (CYP). Methods A modified Delphi consensus was conducted with a panel of 34 optometrists and ophthalmologists with expertise in myopia management.
Annegret H. Dahlmann‐Noor   +34 more
wiley   +1 more source

Treatment outcome in refractive accommodative esotropia

open access: yesDelta Journal of Ophthalmology
Background Accommodative esotropia (ET) usually presents in preschool years. It is often intermittent, and the deviation is typically eliminated by controlling the accommodative effort with optical correction of hypermetropia. Objective The aim of
Osama A Al-Morsy   +3 more
doaj   +1 more source

Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)

open access: yesAmerican Journal of Medical Genetics Part A, Volume 194, Issue 10, October 2024.
Abstract Myhre syndrome is an increasingly diagnosed ultrarare condition caused by recurrent germline autosomal dominant de novo variants in SMAD4. Detailed multispecialty evaluations performed at the Massachusetts General Hospital (MGH) Myhre Syndrome Clinic (2016–2023) and by collaborating specialists have facilitated deep phenotyping, genotyping and
Angela E. Lin   +94 more
wiley   +1 more source

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