Frank Mainzer

The Retinal Pigment Epithelium in Visual Function

A proposed classification for spinal and cranial dural arteriovenous fistulous malformations and implications for treatment

Nephronophthisis

The molecular basis of human retinal and vitreoretinal diseases

The effect of initial management of hyperleukocytosis on early complications and outcome of children with acute lymphoblastic leukemia.

Nephronophthisis-Associated Ciliopathies

Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis

Leber congenital amaurosis: Genes, proteins and disease mechanisms

Therapeutic Effects of Xanthine Oxidase Inhibitors: Renaissance Half a Century after the Discovery of Allopurinol

Retinopathy induced in mice by targeted disruption of the rhodopsin gene

Retinitis pigmentosa

Guidelines on the Use of Therapeutic Apheresis in Clinical Practice – Evidence‐Based Approach from the Writing Committee of the American Society for Apheresis: The Eighth Special Issue

Keratoconus and related noninflammatory corneal thinning disorders

Congenital Leber Amaurosis, Keratoconus, and Mental Retardation in Familial Juvenile Nephronophtisis

Asymptomatic dural vascular anomalies

Neurological abnormalities in congenital amaurosis of Leber. Review of 30 cases.

Mutational analysis and clinical correlation in Leber congenital amaurosis

Early Venous Opacification in Cerebral Contusion

THYMIC ENLARGEMENT AND PLEURAL EFFUSION: AN UNUSUAL ROENTGENOGRAPHIC COMPLEX IN CHILDHOOD LEUKEMIA

Familial nephropathy associated with retinitis pigmentosa, cerebellar ataxia and skeletal abnormalities