Results 201 to 210 of about 354,098 (326)

A Blurred Vision of Health: Metabolic Syndrome as a Risk Factor for Glaucoma in a Large Taiwanese Population Study. [PDF]

Int J Med Sci
Chang SH, Lee JI, Chen SC, Huang SP, Geng JH.   +4 more
europepmc   +1 more source

Sturge-Weber Syndrome accompanied by epilepsy and congenital glaucoma: A case report

Junjie Ning
openalex   +1 more source

Visual Function Assessment in Geographic Atrophy: A Review

Clinical &Experimental Ophthalmology, EarlyView.
ABSTRACT Geographic atrophy (GA) causes significant vision impairment and reduction in vision‐related quality of life. Fundus autofluorescence (FAF) is the gold standard of structural assessment of GA but is a surrogate marker for vision loss, which can be assessed by tests of visual function and functional vision.
Ye Li, Lauren N. Ayton, Adrian T. Fung
wiley   +1 more source

Genetic Link Across Species: SIX6, a Major Human Glaucoma Gene, Confers Susceptibility to Glaucoma in Shiba-Inu Dogs. [PDF]

Invest Ophthalmol Vis Sci
Baba S, Meguro A, Kanemaki N, Maeda A, Takahashi H, Takeuchi M, Endo L, Nomura E, Nakamura J, Mizuki Y, Kanasashi S, Sakono T, Yamada N, Mizuki N.   +13 more
europepmc   +1 more source

The possibility of using optical coherent tomography of optical disc parameters and the peripapillary layer of retinal nerve fibers for the purposes of monitoring of primary open angle glaucoma patients

, 2011
А. П. Шахалова, Шахалова Анна Павловна   +1 more
openalex   +2 more sources

Industry‐Reported Financial Relationships Among American Ophthalmology Society Board Members

Clinical &Experimental Ophthalmology, EarlyView.
ABSTRACT Background To assess financial disclosures of American ophthalmology society board members by comparing self‐reported disclosures with industry‐reported payments and examining characteristics linked to larger financial relationships. Methods In this retrospective, cross‐sectional study, we assessed all governance board members from American ...
Mostafa Bondok, Leonardo Lando, Anne Xuan‐Lan Nguyen, Michael Knafo, Albert Y. Wu   +4 more
wiley   +1 more source

A Novel Homozygous Nonsense Pathogenic Variant of the CPAMD8 Gene Associated With Congenital Microcoria

Clinical Genetics, EarlyView.
A novel CPAMD8 nonsense mutation c.2679C>G (p.Tyr893*) was identified in a patient with congenital microcoria, leading to reduced mRNA expression and predicted protein truncation. ABSTRACT Congenital microcoria (MCOR) is a rare inherited ocular disorder. Here, we describe a novel nonsense variant in the CPAMD8 gene in a patient with MCOR.
Jing‐Fan Gao, Xin Jin, Jing‐Rao Wang, Shu Wang, Hong Zhang   +4 more
wiley   +1 more source

The impact of treatment modality on quality of life in glaucoma patients: findings from a clinical survey study in Augusta, GA. [PDF]

Int Ophthalmol
Edupuganti N, Chishom H, Bui T, Alevy D, Lee TJ, Franklin M, Töteberg-Harms M.   +6 more
europepmc   +1 more source

The Phenotypic and Genotypic Features of ADAMTSL4‐Related Ocular Disease

Clinical Genetics, EarlyView.
ADAMTSL4‐related ocular disease tends to present at a younger age and be associated with higher myopia than other forms of ectopia lentis (such as FBN1). A previously reported 20‐bp deletion (c.767_786del) was highly prevalent in this cohort (23/32), and all ectopia lentis et pupillae cases carried this variant. ABSTRACT Pathogenic variants in ADAMTSL4
Katie M. Williams, Wolfgang Berger, Samuel Koller, Fatma Kivrak Pfiffner, Alessandro Maspoli, Jiradet Gloggnitzer, Britta V. T. Brühwiler, Christina Stathopoulos, Francis Munier, Louise Allen, Christos Iosifidis, Graeme C. Black, Panagiotis I. Sergouniotis, Ian Christopher Lloyd, Christina Gerth‐Kahlert   +14 more
wiley   +1 more source

Indicators for effective glaucoma care coverage in adults: protocol for a scoping review. [PDF]

BMJ Open
Matayan EY, Burn H, Gordon I, Evans J, Toews I, Ramke J, Burton MJ, Philippin H, Mtuy T, Hu VH.   +9 more
europepmc   +1 more source