Latest papers

Axenfeld's anomaly.

A novel mutation of PAX6 in Chinese patients with new clinical features of Peters' anomaly.

A missense mutation in CRYBA4 associated with congenital cataract and microcornea.

Identification, characterization, and effects of Xenopus laevis PNAS-4 gene on embryonic development.

Examination of SOX2 in variable ocular conditions identifies a recurrent deletion in microphthalmia and lack of mutations in other phenotypes.

Partial trisomy due to a de novo duplication 22q11.1-22q13.1: a cat-eye syndrome variant with brain anomalies.

Ocular manifestations of branchio-oculo-facial syndrome: report of a novel mutation and review of the literature.

What's your diagnosis? Diagnosis: Ankyloblepharon filiforme adnatum.

Collie Eye Anomaly in Switzerland.

Congenital Pupillary-Iris-Lens Membrane With Goniodysgenesis

Trisomy 13 mosaicism associated with cyclopia and cystic hygroma.

Rieger syndrome is not associated with PAX6 deletion: a correction to Acta Ophthalmol Scand 2001: 79: 201-203.

Optic nerve hypoplasia associated with chromosome 9 inversion

Importance of ophthalmological examination in children with congenital sensorineural hearing loss.

Eye abnormalities in fetal alcohol syndrome.

Intravitreal bevacizumab for CNV-complicated tilted disk syndrome.

Inducible 70 kDa heat shock proteins protect embryos from teratogen-induced exencephaly: Analysis using Hspa1a/a1b knockout mice.

Thalidomide and misoprostol: Ophthalmologic manifestations and associations both expected and unexpected.

The podosomal-adaptor protein SH3PXD2B is essential for normal postnatal development.

[Ultrasound in the evaluation of intrauterine infection during pregnancy]