Nirit Bourla

Vitamin K ₂ Is a Mitochondrial Electron Carrier That Rescues Pink1 Deficiency

Genetics and clinical characteristics of keratoconus.

The Roles of PINK1, Parkin, and Mitochondrial Fidelity in Parkinson’s Disease

Corneal Collagen Cross-Linking for Ectasia after LASIK and Photorefractive Keratectomy

The Role of the Reactive Oxygen Species and Oxidative Stress in the Pathomechanism of the Age‐Related Ocular Diseases and Other Pathologies of the Anterior and Posterior Eye Segments in Adults

Molecular bases of corneal endothelial dystrophies

Corneal collagen crosslinking: a systematic review.

Polymorphisms in COL4A3 and COL4A4 genes associated with keratoconus.

Insights into keratoconus from a genetic perspective

Keratoconus is Not Associated With Mutations in COL8A1 and COL8A2

Posterior polymorphous corneal dystrophy is associated with TCF8 gene mutations and abdominal hernia

Autosomal Recessive CHED Associated With Novel Compound Heterozygous Mutations in SLC4A11

Differences in the corneal biomechanical effects of surface ablation compared with laser in situ keratomileusis using a microkeratome or femtosecond laser

Identification of mutations in UBIAD1 following exclusion of coding mutations in the chromosome 1p36 locus for Schnyder crystalline corneal dystrophy.