Maria Vadalà

Mutations in the Cone Photoreceptor G-Protein α-Subunit Gene GNAT2 in Patients with Achromatopsia

Susanne Kohl, Britta Baumann, Thomas Rosenberg et al. · The American Journal of Human Genetics · 2002 · 263 citations · Full text

Biology, Photoreceptor Cell, Genetic Disorder +6

Retinal and choroidal vasculature changes associated with chronic kidney disease

Maria Vadalà, Massimo Castellucci, Giulia Guarrasi et al. · Graefe s Archive for Clinical and Experimental Ophthalmology · 2019 · 87 citations

Glomerular Disease, Ocular Disease, Renal Disease +6

One year study of efficacy and safety of infliximab in the treatment of patients with ocular and neurological Behçet’s disease refractory to standard immunosuppressive drugs

Anna Giardina, Angelo Ferrante, Francesco Ciccia et al. · Rheumatology International · 2009 · 74 citations · Full text

Ocular Disease, Autoimmune Disease, Ophthalmology +12

Mutation Analysis Identifies<i>GUCY2D</i>as the Major Gene Responsible for Autosomal Dominant Progressive Cone Degeneration

Veronique Kitiratschky, Robert Wilke, Agnes B. Renner et al. · Investigative Ophthalmology & Visual Science · 2008 · 68 citations

PHOTODYNAMIC THERAPY WITH VERTEPORFIN FOR SUBFOVEAL CHOROIDAL NEOVASCULARIZATION SECONDARY TO PATHOLOGIC MYOPIA

Alfredo Pece, V. Isola, Maria Vadalà et al. · Retina · 2006 · 47 citations