Results 251 to 260 of about 692,450 (357)

Empowering students to bridge basic and clinical sciences by creating innovative optometric tools. [PDF]

Med Educ
Leung TW.
europepmc   +1 more source

Vision Disorders and Visual Impairment

, 2008
Atkinson, J, Braddick, O
openaire   +2 more sources

Deciphering the Genetic Basis of Degenerative and Developmental Eye Disorders in 50 Pakistani Consanguineous Families Using Whole-Exome Sequencing. [PDF]

Int J Mol Sci
Zafar A, Baig RM, Arshad A, Rashid A, Oreshkov S, Frederiksen HN, Ansar M.   +6 more
europepmc   +1 more source

A model of the mammalian retina and the visual cortex. Disorders of vision [PDF]

, 2002
José A. Martín-Pereda, C. Sanchez-Guillen, Ana P. González-Marcos   +2 more
openalex   +1 more source

War-related eye trauma: a study of civilian and military cases from Ukraine's ongoing conflict. [PDF]

Front Public Health
Jonak K, Matysiak M, Choragiewicz T, Nowakowska D, Zimenkovsky A, Shybinskyi V, Sekh M, Karpiński R, Podkowiński A, Rejdak R.   +9 more
europepmc   +1 more source

Global trends in refractive disorders from 1990 to 2021: insights from the global burden of disease study and predictive modeling. [PDF]

Front Public Health
Huang L, Zhang D, Liu M.
europepmc   +1 more source

Authors' response. [PDF]

Optom Vis Sci, 2014
Ciner EB, Ying GS, Kulp MT, Maguire MG, Quinn GE, Orel-Bixler D, Cyert LA, Moore B, Huang J, Vision in Preschoolers (VIP) Study Group.   +9 more
europepmc   +1 more source

Editorial: Innovative prevention strategies for occupational health hazards. [PDF]

Front Public Health
Hon CY, Bergamaschi E.
europepmc   +1 more source

Advances in technology helps in early detection of vision disorders.

Indian J Ophthalmol, 2013
Natarajan S.
europepmc   +1 more source

Clinical Insights Into Nabais Sá‐De Vries Syndrome due to a Novel SPOP Mutation: Neuromotor, Cognitive, Adaptive, Behavioral, and Neurovisual Features

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Nabais Sá‐De Vries syndrome (NSDVS) is an extremely rare autosomal dominant disorder caused by SPOP mutations. To date, only 10 cases have been described presenting with intellectual disability, neurological signs and symptoms, and a variable association of dysmorphic features.
Jessica Galli, Erika Loi, Federica Zanardini, Giovanna Baldoni, Francesca Novara, Serena Panigada, Roberto Ciccone, Maria Rosa Cutrì, Alice Bertoletti, Lorenzo Pinelli, Elisa Fazzi   +10 more
wiley   +1 more source