Polymorphism p.402Y>H in the complement factor H protein is a risk factor for age related macular degeneration in an Italian population
Simonelli, F, Frisso, G, Testa, F, di Fiore, R, Vitale, D F, Manitto, M P, Brancato, R, Rinaldi, E, Sacchetti, L
Published in British journal of ophthalmology (01.09.2006)
Published in British journal of ophthalmology (01.09.2006)
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Molecular genetics of autosomal dominant retinitis pigmentosa (ADRP): a comprehensive study of 43 Italian families
Ziviello, C, Simonelli, F, Testa, F, Anastasi, M, Marzoli, S B, Falsini, B, Ghiglione, D, Macaluso, C, Manitto, M P, Garrè, C, Ciccodicola, A, Rinaldi, E, Banfi, S
Published in Journal of medical genetics (01.07.2005)
Published in Journal of medical genetics (01.07.2005)
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Clinical features of X linked juvenile retinoschisis associated with new mutations in the XLRS1 gene in Italian families
Simonelli, F, Cennamo, G, Ziviello, C, Testa, F, de Crecchio, G, Nesti, A, Manitto, M P, Ciccodicola, A, Banfi, S, Brancato, R, Rinaldi, E
Published in British journal of ophthalmology (01.09.2003)
Published in British journal of ophthalmology (01.09.2003)
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Mutational scanning of the ABCR gene with double-gradient denaturing-gradient gel electrophoresis (DG-DGGE) in Italian Stargardt disease patients
FUMAGALLI, Antonella, FERRARI, Maurizio, CREMONESI, Laura, SORIANI, Nadia, GESSI, Alessandra, FOGLIENI, Barbara, MARTINA, Elisabetta, MANITTO, Maria Pia, BRANCATO, Rosario, DEAN, Michael, ALLIKMETS, Rando
Published in Human genetics (01.09.2001)
Published in Human genetics (01.09.2001)
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Ectopia lentis et pupillae with patchy depigmentation of the skin, hair and lashes: a new association
Manitto, M P, Brancato, R, Lombardo, N, Zarrella, M, Nucci, P
Published in European journal of ophthalmology (01.07.1998)
Published in European journal of ophthalmology (01.07.1998)
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Apolipoprotein E Polymorphisms in Age-Related Macular Degeneration in an Italian Population
Simonelli, Francesca, Margaglione, Maurizio, Testa, Francesco, Cappucci, Giuseppe, Manitto, Maria Pia, Brancato, Rosario, Rinaldi, Ernesto
Published in Ophthalmic research (01.11.2001)
Published in Ophthalmic research (01.11.2001)
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Balanced translocation (t 2q; 10p) and ocular anomalies. A possible HOX gene defect
Nucci, P, Manitto, M P, Faiella, A, Boncinelli, E, Brancato, R
Published in Ophthalmic genetics (1994)
Published in Ophthalmic genetics (1994)
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Identification and characterization of C1orf36, a transcript highly expressed in photoreceptor cells, and mutation analysis in retinitis pigmentosa
Lavorgna, Giovanni, Lestingi, Marta, Ziviello, Carmela, Testa, Francesco, Simonelli, Francesca, Manitto, Maria Pia, Brancato, Rosario, Ferrari, Maurizio, Rinaldi, Ernesto, Ciccodicola, Alfredo, Banfi, Sandro
Published in Biochemical and biophysical research communications (29.08.2003)
Published in Biochemical and biophysical research communications (29.08.2003)
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Denaturing HPLC Profiling of the ABCA4 Gene for Reliable Detection of Allelic Variations
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
Published in Clinical chemistry (Baltimore, Md.) (01.08.2004)
Published in Clinical chemistry (Baltimore, Md.) (01.08.2004)
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Ocular pharmacokinetics of rufloxacin a new fluoroquinolone antibiotic
Nucci, P, Lombardo, N, Cremonesi, F, Manitto, M P, Brancato, R, Ghione, M
Published in Clinica terapeutica (01.06.1992)
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Published in Clinica terapeutica (01.06.1992)
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Neuron-specific enolase in ophthalmology
Nucci, P, Tredici, G, Manitto, M P, Alfarano, R, Brancato, R
Published in Archivio italiano di anatomia e di embriologia. Italian journal of anatomy and embryology (01.01.1991)
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Published in Archivio italiano di anatomia e di embriologia. Italian journal of anatomy and embryology (01.01.1991)
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