unspecified retinal defect

Vigabatrin (VGB) is a structural analogue of γ‐aminobutyric acid (GABA) that irreversibly inhibits GABA‐transaminase (GABA‐T… Expand

Approximately 10% of humans with anophthalmia (absent eye) or severe microphthalmia (small eye) show haploid insufficiency due to… Expand

Major malformations of the human eye, including microphthalmia and anophthalmia, are examples of phenotypes that recur in… Expand

To determine the function of VEGF-A in nervous system development, we have utilized the Nestin promoter-driven Cre recombinase… Expand

Aims: To evaluate the clinical significance of macular hole closure types assessed by optical coherence tomography (OCT). Methods… Expand

OBJECTIVE To investigate whether photocoagulation of the retinal pigment epithelium is possible with sparing of the… Expand

Usher syndrome type 1 (USH1) associates severe congenital deafness, vestibular dysfunction and progressive retinitis pigmentosa… Expand

The semidominant mutation Krd (kidney and retinal defects) was identified in transgenic line Tg8052. Krd/+ mice have a high… Expand

To explore the physiological roles of transforming growth factor alpha (TGF alpha), we disrupted the mouse gene by homologous… Expand

OBJECTIVE To compare the reports of scotomas and metamorphosia in standard and threshold Amsler grid testing with the location… Expand