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 · 269 citations · Full text

Life Sciences, Genetics, Molecular Genetics +7

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 · 89 citations

Medicine, Nephrology, Ophthalmology +14

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 · 75 citations · Full text

Medicine, Immunology, Pharmacotherapy +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 · 69 citations

Life Sciences, Genetics, Molecular Genetics +17

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

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

Medicine, Ophthalmology, Vision Science +17