Study of FTMT and ABCA4 genes in a patient affected by age-related macular degeneration: identification and analysis of new mutations von Stenirri, Stefania, Santambrogio, Paolo, Setaccioli, Marco, Erba, Benedetta Gaia, Pia Manitto, Maria, Rovida, Ermanna, Ferrari, Maurizio, Levi, Sonia, Cremonesi, Laura

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Gene Therapy in Inherited Retinal Diseases: An Update on Current State of the Art von Amato, Alessia, Arrigo, Alessandro, Aragona, Emanuela, Manitto, Maria Pia, Saladino, Andrea, Bandello, Francesco, Battaglia Parodi, Maurizio

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Morpho-functional correlation of fundus autofluorescence in Stargardt disease von Parodi, Maurizio Battaglia, Iacono, Pierluigi, Triolo, Giacinto, La Spina, Carlo, Zucchiatti, Ilaria, Cicinelli, Maria Vittoria, Borrelli, Enrico, Manitto, Maria Pia, Martina, Elisabetta, Bandello, Francesco

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Reviewing the Role of Ultra-Widefield Imaging in Inherited Retinal Dystrophies von Cicinelli, Maria Vittoria, Marchese, Alessandro, Bordato, Alessandro, Manitto, Maria Pia, Bandello, Francesco, Battaglia Parodi, Maurizio

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Are microarrays useful in the screening of ABCA4 mutations in Italian patients affected by macular degenerations? von Stenirri, Stefania, Alaimo, Georgia, Manitto, Maria Pia, Brancato, Rosario, Ferrari, Maurizio, Cremonesi, Laura

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Association Between Genotype and Phenotype Severity in ABCA4-Associated Retinopathy von Bianco, Lorenzo, Arrigo, Alessandro, Antropoli, Alessio, Manitto, Maria Pia, Martina, Elisabetta, Aragona, Emanuela, Bandello, Francesco, Battaglia Parodi, Maurizio

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Resolution of cystoid macular edema following arginine-restricted diet and vitamin B6 supplementation in a case of gyrate atrophy von Casalino, Giuseppe, Pierro, Luisa, Manitto, Maria Pia, Michaelides, Michel, Bandello, Francesco

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Multimodal imaging in pediatric arterial macroaneurysm: A case report von Pierro, Luisa, Battista, Marco, Arrigo, Alessandro, Manitto, Maria Pia, Bandello, Francesco

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Combined Optic Atrophy and Rod–Cone Dystrophy Expands the RTN4IP1 (Optic Atrophy 10) Phenotype von Rajabian, Firuzeh, Manitto, Maria Pia, Palombo, Flavia, Caporali, Leonardo, Grazioli, Alessio, Starace, Vincenzo, Arrigo, Alessandro, Cascavilla, Maria Lucia, La Morgia, Chiara, Barboni, Piero, Bandello, Francesco, Carelli, Valerio, Battaglia Parodi, Maurizio

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Spectral Domain Optical Coherence Tomography Findings in Patients with Retinitis Pigmentosa von Triolo, Giacinto, Pierro, Luisa, Parodi, Maurizio Battaglia, De Benedetto, Umberto, Gagliardi, Marco, Manitto, Maria Pia, Bandello, Francesco

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Optical Coherence Tomography Angiography in CRB1 -Associated Retinal Dystrophies von Rajabian, Firuzeh, Arrigo, Alessandro, Bianco, Lorenzo, Antropoli, Alessio, Manitto, Maria Pia, Martina, Elisabetta, Bandello, Francesco, Chhablani, Jay, Battaglia Parodi, Maurizio

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Clinical Utility Gene Card for: autosomal recessive cone-rod dystrophy von Manitto, Maria Pia, Roosing, Susanne, Boon, Camiel J F, Souied, Eric H, Bandello, Francesco, Querques, Giuseppe

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Posterior Polymorphous Corneal Dystrophy Concomitant to Large Colloid Drusen von Del Turco, Claudia, Pierro, Luisa, Querques, Giuseppe, Gagliardi, Marco, Corvi, Federico, Manitto, Maria Pia, Bandello, Francesco M.

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Integration of multigene panels for the diagnosis of hereditary retinal disorders using Next Generation Sequencing and bioinformatics approaches von Di Resta, Chiara, Spiga, Ivana, Presi, Silvia, Merella, Stefania, Pipitone, Giovanni Battista, Manitto, Maria Pia, Querques, Giuseppe, Parodi, Maurizio Battaglia, Ferrari, Maurizio, Carrera, Paola

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Ocular phenotypes associated with biallelic mutations in BEST1 in Italian patients von Sodi, Andrea, Menchini, Francesca, Manitto, Maria Pia, Passerini, Ilaria, Murro, Vittoria, Torricelli, Francesca, Menchini, Ugo

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Denaturing HPLC Profiling of the ABCA4 Gene for Reliable Detection of Allelic Variations von Stenirri, Stefania, Fermo, Isabella, Battistella, Stefania, Galbiati, Silvia, Soriani, Nadia, Paroni, Rita, Manitto, Maria Pia, Martina, Elisabetta, Brancato, Rosario, Allikmets, Rando, Ferrari, Maurizio, Cremonesi, Laura

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Mutational scanning of the ABCR gene with double-gradient denaturing-gradient gel electrophoresis (DG-DGGE) in Italian Stargardt disease patients von FUMAGALLI, Antonella, FERRARI, Maurizio, CREMONESI, Laura, SORIANI, Nadia, GESSI, Alessandra, FOGLIENI, Barbara, MARTINA, Elisabetta, MANITTO, Maria Pia, BRANCATO, Rosario, DEAN, Michael, ALLIKMETS, Rando

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De novo deletion removes a conserved motif in the C-terminus of ABCA4 and results in cone-rod dystrophy von Stenirri, Stefania, Battistella, Stefania, Fermo, Isabella, Manitto, Maria Pia, Martina, Elisabetta, Brancato, Rosario, Ferrari, Maurizio, Cremonesi, Laura

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Apolipoprotein E Polymorphisms in Age-Related Macular Degeneration in an Italian Population von Simonelli, Francesca, Margaglione, Maurizio, Testa, Francesco, Cappucci, Giuseppe, Manitto, Maria Pia, Brancato, Rosario, Rinaldi, Ernesto

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Identification and characterization of C1orf36, a transcript highly expressed in photoreceptor cells, and mutation analysis in retinitis pigmentosa von Lavorgna, Giovanni, Lestingi, Marta, Ziviello, Carmela, Testa, Francesco, Simonelli, Francesca, Manitto, Maria Pia, Brancato, Rosario, Ferrari, Maurizio, Rinaldi, Ernesto, Ciccodicola, Alfredo, Banfi, Sandro

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