Manitto MP - Search Results

1

Multimodal imaging in Schubert-Bornschein congenital stationary night blindness.

Parodi MB, Arrigo A, Rajabian F, Mansour A, Mercuri S, Starace V, Bordato A, Manitto MP, Martina E, Bandello F. Parodi MB, et al. Among authors: manitto mp. Ophthalmic Genet. 2023 Aug;44(4):408-413. doi: 10.1080/13816810.2022.2135108. Epub 2022 Oct 13. Ophthalmic Genet. 2023. PMID: 36226416

2

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. Fumagalli A, et al. Among authors: manitto mp. Hum Genet. 2001 Sep;109(3):326-38. doi: 10.1007/s004390100583. Hum Genet. 2001. PMID: 11702214

3

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. Stenirri S, et al. Among authors: manitto mp. Clin Chem. 2004 Aug;50(8):1336-43. doi: 10.1373/clinchem.2004.033241. Epub 2004 Jun 10. Clin Chem. 2004. PMID: 15192030

4

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. Stenirri S, et al. Among authors: manitto mp. Clin Chem Lab Med. 2006;44(5):533-7. doi: 10.1515/CCLM.2006.116. Clin Chem Lab Med. 2006. PMID: 16681420

5

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. Triolo G, et al. Among authors: manitto mp. Ophthalmic Res. 2013;50(3):160-4. doi: 10.1159/000351681. Epub 2013 Aug 28. Ophthalmic Res. 2013. PMID: 23989166

6

Posterior polymorphous corneal dystrophy concomitant to large colloid drusen.

Del Turco C, Pierro L, Querques G, Gagliardi M, Corvi F, Manitto MP, Bandello FM. Del Turco C, et al. Among authors: manitto mp. Eur J Ophthalmol. 2015 Mar-Apr;25(2):177-9. doi: 10.5301/ejo.5000526. Epub 2014 Oct 8. Eur J Ophthalmol. 2015. PMID: 25363852

7

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. Parodi MB, et al. Among authors: manitto mp. Br J Ophthalmol. 2015 Oct;99(10):1354-9. doi: 10.1136/bjophthalmol-2014-306237. Epub 2015 Apr 2. Br J Ophthalmol. 2015. PMID: 25837607

8

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

Manitto MP, Roosing S, Boon CJ, Souied EH, Bandello F, Querques G. Manitto MP, et al. Eur J Hum Genet. 2015 Dec;23(12):1749-. doi: 10.1038/ejhg.2015.67. Epub 2015 Apr 15. Eur J Hum Genet. 2015. PMID: 25873014 Free PMC article. No abstract available.

9

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

Cicinelli MV, Manitto MP, Parodi MB, Bandello F. Cicinelli MV, et al. Among authors: manitto mp. Optom Vis Sci. 2016 Oct;93(10):1315-1318. doi: 10.1097/OPX.0000000000000944. Optom Vis Sci. 2016. PMID: 27668495

10

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. Arrigo A, et al. Among authors: manitto mp. Retina. 2019 May;39(5):1009-1015. doi: 10.1097/IAE.0000000000002053. Retina. 2019. PMID: 29370036

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