Sfoglia per Autore
A novel mutation in the VMD2 gene in an Italian family with Best maculopathy.
2007 Sodi A;Passerini I;Simonelli F;Testa F;Menchini U;Torricelli F
Retinal astrocytic hamartoma and Stargardt's disease: unusual association in a patient with ABCR mutation without phacomatosis.
2007 Bini A;Sodi A;Passerini I;Menchini U;Torricelli F
A normal electro-oculography in a family affected by best disease with a novel spontaneous mutation of the BEST1 gene.
2008 Testa F;Rossi S;Passerini I;Sodi A;Di Iorio V;Interlandi E;Della Corte M;Menchini U;Rinaldi E;Torricelli F;Simonelli F
Novel RDH12 sequence variations in Leber congenital amaurosis.
2010 Sodi A;Caputo R;Passerini I;Bacci GM;Menchini U
Different patterns of fundus autofluorescence related to ABCA4 gene mutations in Stargardt disease.
2010 Sodi A;Bini A;Passerini I;Forconi S;Menchini U;Torricelli F
Ocular phenothypes associated with biallelic mutations in BEST in Italian patients
2011 A.Sodi;F.Menchini;M.P.Manitto;I.Passerini;V.Murro;F.Torricelli;U.Menchini
Correlation between Photoreceptor Layer Integrity and Visual Function in Patients with Stargardt Disease: Implications for Gene Therapy.
2012 Testa F;Rossi S;Sodi A;Passerini I;Di Iorio V;Corte MD;Banfi S;Surace EM;Menchini U;Auricchio A;Simonelli F
MYO7A and USH2A gene sequence variants in Italian patients with Usher syndrome
2014 Sodi, Andrea; Mariottini, Alessandro; Passerini, Ilaria; Murro, Vittoria; Tachyla, Iryna; Bianchi, Benedetta; Menchini, Ugo; Torricelli, Francesca
Long-Term Results of Photodynamic Therapy for Choroidal Neovascularization in Pediatric Patients with Best Vitelliform Macular Dystrophy
2015 Sodi, Andrea*; Murro, Vittoria; Caporossi, Orsola; Passerini, Ilaria; Bacci, Giacomo Maria; Caputo, Roberto; Menchini, Ugo
A novel GRK1 mutation in an Italian patient with Oguchi disease
2017 Mucciolo, Dario Pasquale*; Sodi, Andrea; Murro, Vittoria; Passerini, Ilaria; Palchetti, Simona; Pelo, Elisabetta; Virgili, Gianni; Rizzo, Stanislao
Retinal dystrophy and subretinal drusenoid deposits in female choroideremia carriers
2017 Murro, Vittoria; Mucciolo, Dario Pasquale; Passerini, Ilaria; Palchetti, Simona; Sodi, Andrea; Virgili, Gianni; Rizzo, Stanislao
EDI-OCT evaluation of choroidal thickness in retinitis pigmentosa
2018 Sodi, Andrea; Lenzetti, Chiara; Murro, Vittoria; Caporossi, Orsola; Mucciolo, Dario P; Bacherini, Daniela; Cipollini, Francesca; Passerini, Ilaria; Virgili, Gianni; Rizzo, Stanislao
CFH Y402H polymorphism in Italian patients with age-related macular degeneration, retinitis pigmentosa, and Stargardt disease
2018 Andrea Sodi, Ilaria Passerini, Daniela Bacherini, Luca Boni, Simona Palchetti, Vittoria Murro, Orsola Caporossi, Dario Pasquale Mucciolo, Franco Fabrizio, Lorenzo Vannozzi, Francesca Torricelli, Elisabetta Pelo, Stanislao Rizzo, Gianni Virgili
EDI OCT evaluation of choroidal thickness in stargardt disease
2018 Sodi, Andrea; Bacherini, Daniela; Lenzetti, Chiara*; Caporossi, Orsola; Murro, Vittoria; Mucciolo, Dario Pasquale; Cipollini, Francesca; Passerini, Ilaria; Virgili, Gianni; Rizzo, Stanislao
Long-term follow-up of a CRB1-associated maculopathy
2018 Mucciolo, Dario Pasquale*; Murro, Vittoria; Giorgio, Dario; Passerini, Ilaria; Sodi, Andrea; Virgili, Gianni; Rizzo, Stanislao
Fundus phenotype in retinitis pigmentosa associated with EYS mutations
2018 Dario Pasquale Mucciolo and Andrea Sodi and Ilaria Passerini and Vittoria Murro and Francesca Cipollini and Isabella Borg and Elisabetta Pelo and Elisa Contini and Gianni Virgili and Stanislao Rizzo
OCTA Imaging of Choroidal Neovascularization Treated Using Photodynamic Therapy in a Young Patient With Best Macular Dystrophy
2018 Murro, Vittoria; Mucciolo, Dario Pasquale; Giorgio, Dario; Sodi, Andrea; Passerini, Ilaria; Virgili, Gianni; Rizzo, Stanislao
Novel clinical findings in autosomal recessive NR2E3-related retinal dystrophy
2018 Vittoria Murro, Dario Pasquale Mucciolo, Andrea Sodi, Ilaria Passerini, Dario Giorgio, Gianni Virgili, Stanislao Rizzo
Multimodal imaging of benign yellow dot maculopathy
2019 Murro, Vittoria; Mucciolo, Dario Pasquale; Giorgio, Dario; Sodi, Andrea; Passerini, Ilaria; Pacini, Bianca; Finocchio, Lucia; Virgili, Gianni; Rizzo, Stanislao
Optical Coherence Tomography Angiography (OCT-A) in young choroideremia (CHM) patients
2019 Murro, Vittoria; Mucciolo, Dario Pasquale; Giorgio, Dario; Sodi, Andrea; Passerini, Ilaria; Virgili, Gianni; Rizzo, Stanislao
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
A novel mutation in the VMD2 gene in an Italian family with Best maculopathy. | 2007 | Sodi A;Passerini I;Simonelli F;Testa F;Menchini U;Torricelli F | |
Retinal astrocytic hamartoma and Stargardt's disease: unusual association in a patient with ABCR mutation without phacomatosis. | 2007 | Bini A;Sodi A;Passerini I;Menchini U;Torricelli F | |
A normal electro-oculography in a family affected by best disease with a novel spontaneous mutation of the BEST1 gene. | 2008 | Testa F;Rossi S;Passerini I;Sodi A;Di Iorio V;Interlandi E;Della Corte M;Menchini U;Rinaldi E;Torricelli F;Simonelli F | |
Novel RDH12 sequence variations in Leber congenital amaurosis. | 2010 | Sodi A;Caputo R;Passerini I;Bacci GM;Menchini U | |
Different patterns of fundus autofluorescence related to ABCA4 gene mutations in Stargardt disease. | 2010 | Sodi A;Bini A;Passerini I;Forconi S;Menchini U;Torricelli F | |
Ocular phenothypes associated with biallelic mutations in BEST in Italian patients | 2011 | A.Sodi;F.Menchini;M.P.Manitto;I.Passerini;V.Murro;F.Torricelli;U.Menchini | |
Correlation between Photoreceptor Layer Integrity and Visual Function in Patients with Stargardt Disease: Implications for Gene Therapy. | 2012 | Testa F;Rossi S;Sodi A;Passerini I;Di Iorio V;Corte MD;Banfi S;Surace EM;Menchini U;Auricchio A;Simonelli F | |
MYO7A and USH2A gene sequence variants in Italian patients with Usher syndrome | 2014 | Sodi, Andrea; Mariottini, Alessandro; Passerini, Ilaria; Murro, Vittoria; Tachyla, Iryna; Bianchi, Benedetta; Menchini, Ugo; Torricelli, Francesca | |
Long-Term Results of Photodynamic Therapy for Choroidal Neovascularization in Pediatric Patients with Best Vitelliform Macular Dystrophy | 2015 | Sodi, Andrea*; Murro, Vittoria; Caporossi, Orsola; Passerini, Ilaria; Bacci, Giacomo Maria; Caputo, Roberto; Menchini, Ugo | |
A novel GRK1 mutation in an Italian patient with Oguchi disease | 2017 | Mucciolo, Dario Pasquale*; Sodi, Andrea; Murro, Vittoria; Passerini, Ilaria; Palchetti, Simona; Pelo, Elisabetta; Virgili, Gianni; Rizzo, Stanislao | |
Retinal dystrophy and subretinal drusenoid deposits in female choroideremia carriers | 2017 | Murro, Vittoria; Mucciolo, Dario Pasquale; Passerini, Ilaria; Palchetti, Simona; Sodi, Andrea; Virgili, Gianni; Rizzo, Stanislao | |
EDI-OCT evaluation of choroidal thickness in retinitis pigmentosa | 2018 | Sodi, Andrea; Lenzetti, Chiara; Murro, Vittoria; Caporossi, Orsola; Mucciolo, Dario P; Bacherini, Daniela; Cipollini, Francesca; Passerini, Ilaria; Virgili, Gianni; Rizzo, Stanislao | |
CFH Y402H polymorphism in Italian patients with age-related macular degeneration, retinitis pigmentosa, and Stargardt disease | 2018 | Andrea Sodi, Ilaria Passerini, Daniela Bacherini, Luca Boni, Simona Palchetti, Vittoria Murro, Orsola Caporossi, Dario Pasquale Mucciolo, Franco Fabrizio, Lorenzo Vannozzi, Francesca Torricelli, Elisabetta Pelo, Stanislao Rizzo, Gianni Virgili | |
EDI OCT evaluation of choroidal thickness in stargardt disease | 2018 | Sodi, Andrea; Bacherini, Daniela; Lenzetti, Chiara*; Caporossi, Orsola; Murro, Vittoria; Mucciolo, Dario Pasquale; Cipollini, Francesca; Passerini, Ilaria; Virgili, Gianni; Rizzo, Stanislao | |
Long-term follow-up of a CRB1-associated maculopathy | 2018 | Mucciolo, Dario Pasquale*; Murro, Vittoria; Giorgio, Dario; Passerini, Ilaria; Sodi, Andrea; Virgili, Gianni; Rizzo, Stanislao | |
Fundus phenotype in retinitis pigmentosa associated with EYS mutations | 2018 | Dario Pasquale Mucciolo and Andrea Sodi and Ilaria Passerini and Vittoria Murro and Francesca Cipollini and Isabella Borg and Elisabetta Pelo and Elisa Contini and Gianni Virgili and Stanislao Rizzo | |
OCTA Imaging of Choroidal Neovascularization Treated Using Photodynamic Therapy in a Young Patient With Best Macular Dystrophy | 2018 | Murro, Vittoria; Mucciolo, Dario Pasquale; Giorgio, Dario; Sodi, Andrea; Passerini, Ilaria; Virgili, Gianni; Rizzo, Stanislao | |
Novel clinical findings in autosomal recessive NR2E3-related retinal dystrophy | 2018 | Vittoria Murro, Dario Pasquale Mucciolo, Andrea Sodi, Ilaria Passerini, Dario Giorgio, Gianni Virgili, Stanislao Rizzo | |
Multimodal imaging of benign yellow dot maculopathy | 2019 | Murro, Vittoria; Mucciolo, Dario Pasquale; Giorgio, Dario; Sodi, Andrea; Passerini, Ilaria; Pacini, Bianca; Finocchio, Lucia; Virgili, Gianni; Rizzo, Stanislao | |
Optical Coherence Tomography Angiography (OCT-A) in young choroideremia (CHM) patients | 2019 | Murro, Vittoria; Mucciolo, Dario Pasquale; Giorgio, Dario; Sodi, Andrea; Passerini, Ilaria; Virgili, Gianni; Rizzo, Stanislao |
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