K Takki

The Retinal Pigment Epithelium in Visual Function

The Ocular Hypertension Treatment Study

The molecular basis of human retinal and vitreoretinal diseases

Ocular Drug Delivery

Cellular signaling and factors involved in Müller cell gliosis: Neuroprotective and detrimental effects

Factors for Glaucoma Progression and the Effect of Treatment

Reduction of Intraocular Pressure and Glaucoma Progression

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

Müller cells in the healthy and diseased retina

The Quality of Medical Evidence and Medical Practice

Immunohistochemical characterization of retinal glial cell changes in areas of vascular occlusion secondary to diabetic retinopathy

Randomized Clinical Trials on Medical Treatment of Glaucoma

Retinopathy induced in mice by targeted disruption of the rhodopsin gene

Clinical Variation of Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy (APECED) in a Series of 68 Patients

Lens opacity induced by lipid peroxidation products as a model of cataract associated with retinal disease

Retinitis pigmentosa

Fundus albipunctatus: A clinical study of the fundus lesions, the physiologic deficit, and the vitamin a metabolism

Hepatic zonation of the catabolism of arginine and ornithine in the perfused rat liver

Gyrate atrophy of the choroid and retina with hyperornithinemia. Deficient formation of guanidinoacetic acid from arginine.

Ornithinemia, Hyperammonemia, and Homocitrullinuria

Inhibition of arginine-glycine amidinotransferase by ornithine. A possible mechanism for the muscular and chorioretinal atrophies in gyrate atrophy of the choroid and retina with hyperornithinemia

Gyrate Atrophy of the Choroid and Retina

At least two mutant alleles of ornithine delta-aminotransferase cause gyrate atrophy of the choroid and retina in Finns.

Prevention of Ornithine Cytotoxicity by Nonpolar Side Chain Amino Acids in Retinal Pigment Epithelial Cells

Supplementary Creatine as a Treatment for Gyrate Atrophy of the Choroid and Retina

Ornithine delta-aminotransferase mutations in gyrate atrophy. Allelic heterogeneity and functional consequences.

Gyrate atrophy of the choroid and retina: deficiency of ornithine aminotransferase in transformed lymphocytes.

Arginine metabolism: nitric oxide and beyond

Creatine and Creatinine Metabolism

A Double-Masked Study of Timolol and Pilocarpine Combined

Timolol treatment of chronic open-angle glaucoma and ocular hypertension

The Natural History of Gyrate Atrophy of the Choroid and Retina

Expression defect of ornithine aminotransferase gene in gyrate atrophy.

Genetic aspects in gyrate atrophy of the choroid and retina with hyperornithinaemia.

Gyrate atrophy of the choroid and retina with hyperornithinemia HOGA.

Differential diagnosis between the primary total choroidal vascular atrophies.

Systemic Manifestations of Gyrate Atrophy of the Choroid and Retina

RAISED PLASMA-ORNITHINE AND GYRATE ATROPHY OF THE CHOROID AND RETINA

Gyrate atrophy of the choroid and retina associated with hyperornithinaemia.

Cataract in gyrate atrophy: clinical and morphologic studies.

Gyrate Atrophy of the Choroid and Retina