GALANTUOMO, MARIA SILVANA
GALANTUOMO, MARIA SILVANA
DIPARTIMENTO DI SCIENZE CHIRURGICHE
A NOVEL MUTATION IN TRP1 GENE IN AN OCULAR CUTANEOUS ALBINISM PATIENT
2007-01-01 Galantuomo, MARIA SILVANA; Zucca, IGNAZIO ALBERTO; Gargiulo, A; Surace, Em; Fossarello, Maurizio
A NR2E3 Mutation (R309G) Associated With a Mild Form of Enhanced S-Cone Syndrome
2008-01-01 Galantuomo, MARIA SILVANA; Zucca, IGNAZIO ALBERTO; S., Banfi; C., Ziviello; G., Carboni; G., Forma; Y., Titi; Fossarello, Maurizio
A parafoveal ring of autofluorescence is a marker of disease in a large family with autosomal dominant sector RP associated with rhodopsin gene codon 190 mutation
2004-01-01 Fossarello, Maurizio; Mura, M; Carta, M; Galantuomo, MARIA SILVANA; Zucca, IGNAZIO ALBERTO; Serra, A.
A perifoveal ring of autofluorescence is a marker of disease in a large family with autosomal dominant sector RP associated with rhodopsin gene codon 190 mutation
2004-01-01 Fossarello, Maurizio; Mura, M; Carta, M; Galantuomo, MARIA SILVANA; Zucca, IGNAZIO ALBERTO; Serra, A.
Analysis of Fundus Autofluorescence in Patients With Different Genotypes and Phenotypes of Retinitis Pigmentosa (RP)
2005-01-01 Fossarello, Maurizio; Galantuomo, MARIA SILVANA; Malloci, C; Cappai, G; Carta, M; Serra, V; Loudianos, J; Peiretti, Enrico; Zucca, IGNAZIO ALBERTO
Analysis of Fundus Autofluorescence in Patients with Different Genotypes and Phenotypes of Retinitis Pigmentosa (RP)
2004-01-01 Fossarello, Maurizio; Galantuomo, MARIA SILVANA; Malloci, C; Cappai, G; Carta, M; Serra, V; Loudianos, G; Peiretti, Enrico; Zucca, IGNAZIO ALBERTO
Classification system of clearance of lipids in human tears according to optical coherence tomography parameters
2015-01-01 Galantuomo, MARIA SILVANA; Napoli, PIETRO EMANUELE; Coronella, Franco; Satta, GIOVANNI MARIA; Fossarello, Maurizio
Clinical and genetic study of miopia in St. Peter Island (Sardinia)
2003-01-01 Fossarello, Maurizio; Galantuomo, MARIA SILVANA; Zucca, IGNAZIO ALBERTO; Sulis, R; Mura, M; Mallocci, C; Serra, A; Siniscalco, M.
Clinical and genetic study of myopia in St. Peter island (Sardinia)
2006-01-01 Zucca, IGNAZIO ALBERTO; Galantuomo, MARIA SILVANA; Malloci, Mc; Stanbolian, D; Fossarello, Maurizio
Clinical and genetic study of myopia in St. Peter Island(Sardinia)
2003-01-01 Fossarello, Maurizio; Zucca, IGNAZIO ALBERTO; Galantuomo, MARIA SILVANA; Sulis, R.; Mura, M; Mallocci, C.; Serra, A.; Siniscalco, M.
CLINICAL AND MOLECULAR GENETICS OF LEBER'S CONGENITAL AMAUROSIS: A MULTICENTER STUDY OF ITALIAN PATIENTS
2007-01-01 Simonelli, F; Ziviello, C; Testa, F; Rossi, S; Fazzi, E; Bianchi, Pe; Fossarello, Maurizio; Signorini, S; Bertone, C; Galantuomo, MARIA SILVANA; Brancati, F; Valente, Em; Ciccodicola, A; Rinaldi, E; Auricchio, A; Banfi, S.
Colour Vision Deficiencies in two Sardinian families with butterfly-shaped macular distrophy
1995-01-01 Fossarello, Maurizio; Zucca, IGNAZIO ALBERTO; Pirastu, M.; Bertini, C.; Galantuomo, MARIA SILVANA; Serra, A.
Colour vision deficiencies in two unrelated Sardinian families with butterfly-shaped macular dystrophy
1997-01-01 Fossarello, Maurizio; Zucca, IGNAZIO ALBERTO; Bertini, C.; Pirastu, M.; Galantuomo, MARIA SILVANA; Contu, G. M.; Serra, A.
Deletion in the Peripherin/RDS gene in two unrelated Sardinian families with autosomal dominant butterfly-shaped macular dystrophy
1996-01-01 Fossarello, Maurizio; Bertini, C.; Galantuomo, MARIA SILVANA; Cao, A.; Serra, A.; Pirastu, M.
Efficacy of oral acetazolamide and topical dorzolamide therapy for X-linked juvenile retinoschisis maculopathy
2014-01-01 Galantuomo, MARIA SILVANA; Cuccu, Alberto; Zucca, IGNAZIO ALBERTO; Preising, M. N.; Lorenz, B.; Fossarello, Maurizio
Evaluation of foveal avascular zone alterations in diabetic retinopathy with optical coherence tomography angiography
2017-01-01 Fossarello, Maurizio; Coscas, Florence; Napoli, PIETRO EMANUELE; Galantuomo, MARIA SILVANA; Farci, Roberta; Diaz, Giacomo
Evaluation of the adhesive properties of the cornea by means of optical coherence tomography in patients with meibomian gland dysfunction and lacrimal tear deficiency
2014-01-01 Napoli, PIETRO EMANUELE; Coronella, Franco; Satta, GIOVANNI MARIA; Galantuomo, MARIA SILVANA; Fossarello, Maurizio
Familial strabismus in Sardinia
2011-01-01 Galantuomo, MARIA SILVANA; Zucca, IGNAZIO ALBERTO; Cuccu, A; Fossarello, Maurizio
Fibroblasts isolated from human pterygia exhibit altered lipid metabolism characteristics
2006-01-01 Peiretti, Enrico; Dessì, S; Mulas M., F; Abete, Claudia; Galantuomo, MARIA SILVANA; Fossarello, Maurizio
Genetic analysis of autosomal dominant primary open angle glaucoma in Sardinia
1996-01-01 Pirastu, M.; Loi, A.; Cao, A.; Fossarello, Maurizio; Zucca, IGNAZIO ALBERTO; Galantuomo, MARIA SILVANA; Mureddu, E.; Serra, C.; Pilia, D.; Serra, A.
Titolo | Data di pubblicazione | Autore(i) | Rivista | Editore |
---|---|---|---|---|
A NOVEL MUTATION IN TRP1 GENE IN AN OCULAR CUTANEOUS ALBINISM PATIENT | 1-gen-2007 | Galantuomo, MARIA SILVANA; Zucca, IGNAZIO ALBERTO; Gargiulo, A; Surace, Em; Fossarello, Maurizio | - | Paul L. Kaufman, MD |
A NR2E3 Mutation (R309G) Associated With a Mild Form of Enhanced S-Cone Syndrome | 1-gen-2008 | Galantuomo, MARIA SILVANA; Zucca, IGNAZIO ALBERTO; S., Banfi; C., Ziviello; G., Carboni; G., Forma; Y., Titi; Fossarello, Maurizio | - | Paul L. Kaufman, MD |
A parafoveal ring of autofluorescence is a marker of disease in a large family with autosomal dominant sector RP associated with rhodopsin gene codon 190 mutation | 1-gen-2004 | Fossarello, Maurizio; Mura, M; Carta, M; Galantuomo, MARIA SILVANA; Zucca, IGNAZIO ALBERTO; Serra, A. | - | Robert N. Frank |
A perifoveal ring of autofluorescence is a marker of disease in a large family with autosomal dominant sector RP associated with rhodopsin gene codon 190 mutation | 1-gen-2004 | Fossarello, Maurizio; Mura, M; Carta, M; Galantuomo, MARIA SILVANA; Zucca, IGNAZIO ALBERTO; Serra, A. | - | - |
Analysis of Fundus Autofluorescence in Patients With Different Genotypes and Phenotypes of Retinitis Pigmentosa (RP) | 1-gen-2005 | Fossarello, Maurizio; Galantuomo, MARIA SILVANA; Malloci, C; Cappai, G; Carta, M; Serra, V; Loudianos, J; Peiretti, Enrico; Zucca, IGNAZIO ALBERTO | - | Robert N. Frank |
Analysis of Fundus Autofluorescence in Patients with Different Genotypes and Phenotypes of Retinitis Pigmentosa (RP) | 1-gen-2004 | Fossarello, Maurizio; Galantuomo, MARIA SILVANA; Malloci, C; Cappai, G; Carta, M; Serra, V; Loudianos, G; Peiretti, Enrico; Zucca, IGNAZIO ALBERTO | - | - |
Classification system of clearance of lipids in human tears according to optical coherence tomography parameters | 1-gen-2015 | Galantuomo, MARIA SILVANA; Napoli, PIETRO EMANUELE; Coronella, Franco; Satta, GIOVANNI MARIA; Fossarello, Maurizio | INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE | - |
Clinical and genetic study of miopia in St. Peter Island (Sardinia) | 1-gen-2003 | Fossarello, Maurizio; Galantuomo, MARIA SILVANA; Zucca, IGNAZIO ALBERTO; Sulis, R; Mura, M; Mallocci, C; Serra, A; Siniscalco, M. | - | - |
Clinical and genetic study of myopia in St. Peter island (Sardinia) | 1-gen-2006 | Zucca, IGNAZIO ALBERTO; Galantuomo, MARIA SILVANA; Malloci, Mc; Stanbolian, D; Fossarello, Maurizio | - | Einar Stefansson |
Clinical and genetic study of myopia in St. Peter Island(Sardinia) | 1-gen-2003 | Fossarello, Maurizio; Zucca, IGNAZIO ALBERTO; Galantuomo, MARIA SILVANA; Sulis, R.; Mura, M; Mallocci, C.; Serra, A.; Siniscalco, M. | - | - |
CLINICAL AND MOLECULAR GENETICS OF LEBER'S CONGENITAL AMAUROSIS: A MULTICENTER STUDY OF ITALIAN PATIENTS | 1-gen-2007 | Simonelli, F; Ziviello, C; Testa, F; Rossi, S; Fazzi, E; Bianchi, Pe; Fossarello, Maurizio; Signorini, S; Bertone, C; Galantuomo, MARIA SILVANA; Brancati, F; Valente, Em; Ciccodicola, A; Rinaldi, E; Auricchio, A; Banfi, S. | INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE | - |
Colour Vision Deficiencies in two Sardinian families with butterfly-shaped macular distrophy | 1-gen-1995 | Fossarello, Maurizio; Zucca, IGNAZIO ALBERTO; Pirastu, M.; Bertini, C.; Galantuomo, MARIA SILVANA; Serra, A. | - | - |
Colour vision deficiencies in two unrelated Sardinian families with butterfly-shaped macular dystrophy | 1-gen-1997 | Fossarello, Maurizio; Zucca, IGNAZIO ALBERTO; Bertini, C.; Pirastu, M.; Galantuomo, MARIA SILVANA; Contu, G. M.; Serra, A. | - | kluwer accademic publ. |
Deletion in the Peripherin/RDS gene in two unrelated Sardinian families with autosomal dominant butterfly-shaped macular dystrophy | 1-gen-1996 | Fossarello, Maurizio; Bertini, C.; Galantuomo, MARIA SILVANA; Cao, A.; Serra, A.; Pirastu, M. | ARCHIVES OF OPHTHALMOLOGY | - |
Efficacy of oral acetazolamide and topical dorzolamide therapy for X-linked juvenile retinoschisis maculopathy | 1-gen-2014 | Galantuomo, MARIA SILVANA; Cuccu, Alberto; Zucca, IGNAZIO ALBERTO; Preising, M. N.; Lorenz, B.; Fossarello, Maurizio | INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE | - |
Evaluation of foveal avascular zone alterations in diabetic retinopathy with optical coherence tomography angiography | 1-gen-2017 | Fossarello, Maurizio; Coscas, Florence; Napoli, PIETRO EMANUELE; Galantuomo, MARIA SILVANA; Farci, Roberta; Diaz, Giacomo | INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE | - |
Evaluation of the adhesive properties of the cornea by means of optical coherence tomography in patients with meibomian gland dysfunction and lacrimal tear deficiency | 1-gen-2014 | Napoli, PIETRO EMANUELE; Coronella, Franco; Satta, GIOVANNI MARIA; Galantuomo, MARIA SILVANA; Fossarello, Maurizio | PLOS ONE | - |
Familial strabismus in Sardinia | 1-gen-2011 | Galantuomo, MARIA SILVANA; Zucca, IGNAZIO ALBERTO; Cuccu, A; Fossarello, Maurizio | INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE | Paul L. Kaufman |
Fibroblasts isolated from human pterygia exhibit altered lipid metabolism characteristics | 1-gen-2006 | Peiretti, Enrico; Dessì, S; Mulas M., F; Abete, Claudia; Galantuomo, MARIA SILVANA; Fossarello, Maurizio | EXPERIMENTAL EYE RESEARCH | - |
Genetic analysis of autosomal dominant primary open angle glaucoma in Sardinia | 1-gen-1996 | Pirastu, M.; Loi, A.; Cao, A.; Fossarello, Maurizio; Zucca, IGNAZIO ALBERTO; Galantuomo, MARIA SILVANA; Mureddu, E.; Serra, C.; Pilia, D.; Serra, A. | - | - |