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Items: 26

1.

CAPILLARY NETWORK ALTERATIONS IN X-LINKED RETINOSCHISIS IMAGED ON OPTICAL COHERENCE TOMOGRAPHY ANGIOGRAPHY.

Romano F, Arrigo A, Chʼng SW, Battaglia Parodi M, Manitto MP, Martina E, Bandello F, Stanga PE.

Retina. 2018 Jun 5. doi: 10.1097/IAE.0000000000002222. [Epub ahead of print]

PMID:
29877903
2.

Integration of multigene panels for the diagnosis of hereditary retinal disorders using Next Generation Sequencing and bioinformatics approaches.

Di Resta C, Spiga I, Presi S, Merella S, Pipitone GB, Manitto MP, Querques G, Parodi MB, Ferrari M, Carrera P.

EJIFCC. 2018 Apr 30;29(1):15-25. eCollection 2018 Apr.

3.

Resolution of cystoid macular edema following arginine-restricted diet and vitamin B6 supplementation in a case of gyrate atrophy.

Casalino G, Pierro L, Manitto MP, Michaelides M, Bandello F.

J AAPOS. 2018 Aug;22(4):321-323. doi: 10.1016/j.jaapos.2017.12.016. Epub 2018 Apr 12.

PMID:
29654911
4.

VASCULAR ALTERATIONS REVEALED WITH OPTICAL COHERENCE TOMOGRAPHY ANGIOGRAPHY IN PATIENTS WITH CHOROIDEREMIA.

Battaglia Parodi M, Arrigo A, MacLaren RE, Aragona E, Toto L, Mastropasqua R, Manitto MP, Bandello F.

Retina. 2019 Jun;39(6):1200-1205. doi: 10.1097/IAE.0000000000002118.

PMID:
29543633
5.

OPTICAL COHERENCE TOMOGRAPHY AND OPTICAL COHERENCE TOMOGRAPHY ANGIOGRAPHY EVALUATION OF COMBINED HAMARTOMA OF THE RETINA AND RETINAL PIGMENT EPITHELIUM.

Arrigo A, Corbelli E, Aragona E, Manitto MP, Martina E, Bandello F, Parodi MB.

Retina. 2019 May;39(5):1009-1015. doi: 10.1097/IAE.0000000000002053.

PMID:
29370036
6.

Regressive Retinal Flecks in CRX-Mutated Early-Onset Retinal Dystrophy.

Cicinelli MV, Manitto MP, Parodi MB, Bandello F.

Optom Vis Sci. 2016 Oct;93(10):1315-1318.

PMID:
27668495
7.

Clinical Utility Gene Card for: autosomal recessive cone-rod dystrophy.

Manitto MP, Roosing S, Boon CJ, Souied EH, Bandello F, Querques G.

Eur J Hum Genet. 2015 Dec;23(12). doi: 10.1038/ejhg.2015.67. Epub 2015 Apr 15. No abstract available.

8.

Morpho-functional correlation of fundus autofluorescence in Stargardt disease.

Parodi MB, Iacono P, Triolo G, La Spina C, Zucchiatti I, Cicinelli MV, Borrelli E, Manitto MP, Martina E, Bandello F.

Br J Ophthalmol. 2015 Oct;99(10):1354-9. doi: 10.1136/bjophthalmol-2014-306237. Epub 2015 Apr 2.

PMID:
25837607
9.

Posterior polymorphous corneal dystrophy concomitant to large colloid drusen.

Del Turco C, Pierro L, Querques G, Gagliardi M, Corvi F, Manitto MP, Bandello FM.

Eur J Ophthalmol. 2015 Mar-Apr;25(2):177-9. doi: 10.5301/ejo.5000526. Epub 2014 Oct 8.

PMID:
25363852
10.

Spectral domain optical coherence tomography findings in patients with retinitis pigmentosa.

Triolo G, Pierro L, Parodi MB, De Benedetto U, Gagliardi M, Manitto MP, Bandello F.

Ophthalmic Res. 2013;50(3):160-4. doi: 10.1159/000351681. Epub 2013 Aug 28.

PMID:
23989166
11.

Ocular phenotypes associated with biallelic mutations in BEST1 in Italian patients.

Sodi A, Menchini F, Manitto MP, Passerini I, Murro V, Torricelli F, Menchini U.

Mol Vis. 2011;17:3078-87. Epub 2011 Nov 24.

12.

Are microarrays useful in the screening of ABCA4 mutations in Italian patients affected by macular degenerations?

Stenirri S, Alaimo G, Manitto MP, Brancato R, Ferrari M, Cremonesi L.

Clin Chem Lab Med. 2008;46(9):1250-5. doi: 10.1515/CCLM.2008.248.

PMID:
18652558
13.

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 DF, Manitto MP, Brancato R, Rinaldi E, Sacchetti L.

Br J Ophthalmol. 2006 Sep;90(9):1142-5. Epub 2006 Jun 14.

14.

De novo deletion removes a conserved motif in the C-terminus of ABCA4 and results in cone-rod dystrophy.

Stenirri S, Battistella S, Fermo I, Manitto MP, Martina E, Brancato R, Ferrari M, Cremonesi L.

Clin Chem Lab Med. 2006;44(5):533-7.

PMID:
16681420
15.

Molecular genetics of autosomal dominant retinitis pigmentosa (ADRP): a comprehensive study of 43 Italian families.

Ziviello C, Simonelli F, Testa F, Anastasi M, Marzoli SB, Falsini B, Ghiglione D, Macaluso C, Manitto MP, Garrè C, Ciccodicola A, Rinaldi E, Banfi S.

J Med Genet. 2005 Jul;42(7):e47.

16.

Denaturing HPLC profiling of the ABCA4 gene for reliable detection of allelic variations.

Stenirri S, Fermo I, Battistella S, Galbiati S, Soriani N, Paroni R, Manitto MP, Martina E, Brancato R, Allikmets R, Ferrari M, Cremonesi L.

Clin Chem. 2004 Aug;50(8):1336-43. Epub 2004 Jun 10.

17.

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 MP, Ciccodicola A, Banfi S, Brancato R, Rinaldi E.

Br J Ophthalmol. 2003 Sep;87(9):1130-4.

18.

Identification and characterization of C1orf36, a transcript highly expressed in photoreceptor cells, and mutation analysis in retinitis pigmentosa.

Lavorgna G, Lestingi M, Ziviello C, Testa F, Simonelli F, Manitto MP, Brancato R, Ferrari M, Rinaldi E, Ciccodicola A, Banfi S.

Biochem Biophys Res Commun. 2003 Aug 29;308(3):414-21.

PMID:
12914764
19.

Apolipoprotein E polymorphisms in age-related macular degeneration in an Italian population.

Simonelli F, Margaglione M, Testa F, Cappucci G, Manitto MP, Brancato R, Rinaldi E.

Ophthalmic Res. 2001 Nov-Dec;33(6):325-8.

PMID:
11721184
20.

Mutational scanning of the ABCR gene with double-gradient denaturing-gradient gel electrophoresis (DG-DGGE) in Italian Stargardt disease patients.

Fumagalli A, Ferrari M, Soriani N, Gessi A, Foglieni B, Martina E, Manitto MP, Brancato R, Dean M, Allikmets R, Cremonesi L.

Hum Genet. 2001 Sep;109(3):326-38.

PMID:
11702214
21.

Ectopia lentis et pupillae with patchy depigmentation of the skin, hair and lashes: a new association.

Manitto MP, Brancato R, Lombardo N, Zarrella M, Nucci P.

Eur J Ophthalmol. 1998 Jul-Sep;8(3):188-90.

22.

Macular dysplasia and pigmented paravenous retino-choroidal atrophy.

Nucci P, Manitto MP, Piantanida A, Brancato R.

Ophthalmic Genet. 1994 Sep-Dec;15(3-4):161-4.

23.

Balanced translocation (t 2q; 10p) and ocular anomalies. A possible HOX gene defect.

Nucci P, Manitto MP, Faiella A, Boncinelli E, Brancato R.

Ophthalmic Genet. 1994 Sep-Dec;15(3-4):129-31.

PMID:
7749666
24.

Neuron-specific enolase and embryology of the trabecular meshwork of the rat eye: an immunohistochemical study.

Nucci P, Tredici G, Manitto MP, Pizzini G, Brancato R.

Int J Biol Markers. 1992 Oct-Dec;7(4):253-5.

PMID:
1491183
25.

Ocular pharmacokinetics of rufloxacin a new fluoroquinolone antibiotic.

Nucci P, Lombardo N, Cremonesi F, Manitto MP, Brancato R, Ghione M.

Clin Ter. 1992 Jun;140(6):563-7.

PMID:
1322259
26.

[Neuron-specific enolase in ophthalmology].

Nucci P, Tredici G, Manitto MP, Alfarano R, Brancato R.

Arch Ital Anat Embriol. 1991 Jan-Mar;96(1):73-6. Review. Italian.

PMID:
1781726

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