Libe Gradstein

ALFY-Controlled DVL3 Autophagy Regulates Wnt Signaling, Determining Human Brain Size

Huntington's disease

Amino acid transporters revisited: New views in health and disease

Ophthalmic and adnexal complications of radiotherapy

Mutations in FYCO1 Cause Autosomal-Recessive Congenital Cataracts

TFOS DEWS II pathophysiology report

Biological Functions of Autophagy Genes: A Disease Perspective

Repertoires of Autophagy in the Pathogenesis of Ocular Diseases

Cystine transporter SLC7A11/xCT in cancer: ferroptosis, nutrient dependency, and cancer therapy

Revised American Thyroid Association Guidelines for the Management of Medullary Thyroid Carcinoma

A missense mutation in LIM2 causes autosomal recessive congenital cataract.

Systematic review of effectiveness of different treatments for childhood retinoblastoma

Claudins and the Modulation of Tight Junction Permeability

A Literature Review of Late Complications of Radiation Therapy for Head and Neck Cancers: Incidence and Dose Response

Systematic reviews: CRD's guidance for undertaking reviews in health care

Neuroacanthocytosis

Isolated foveal hypoplasia with secondary nystagmus and low vision is associated with a homozygous SLC38A8 mutation

Ocular and Orbital Complications following the Treatment of Retinoblastoma

Eye Movements in Chorea-Acanthocytosis

HomozygousCRYBB1Deletion Mutation Underlies Autosomal Recessive Congenital Cataract