Manitto MP - Search Results

1

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. Simonelli F, et al. Among authors: manitto mp. Ophthalmic Res. 2001 Nov-Dec;33(6):325-8. doi: 10.1159/000055688. Ophthalmic Res. 2001. PMID: 11721184

2

Ocular pharmacokinetics of rufloxacin a new fluoroquinolone antibiotic.

Nucci P, Lombardo N, Cremonesi F, Manitto MP, Brancato R, Ghione M. Nucci P, et al. Among authors: manitto mp. Clin Ter. 1992 Jun;140(6):563-7. Clin Ter. 1992. PMID: 1322259

3

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. Nucci P, et al. Among authors: manitto mp. Int J Biol Markers. 1992 Oct-Dec;7(4):253-5. doi: 10.1177/172460089200700410. Int J Biol Markers. 1992. PMID: 1491183

4

[Neuron-specific enolase in ophthalmology].

Nucci P, Tredici G, Manitto MP, Alfarano R, Brancato R. Nucci P, et al. Among authors: manitto mp. Arch Ital Anat Embriol. 1991 Jan-Mar;96(1):73-6. Arch Ital Anat Embriol. 1991. PMID: 1781726 Review. Italian.

5

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

Nucci P, Manitto MP, Faiella A, Boncinelli E, Brancato R. Nucci P, et al. Among authors: manitto mp. Ophthalmic Genet. 1994 Sep-Dec;15(3-4):129-31. doi: 10.3109/13816819409057839. Ophthalmic Genet. 1994. PMID: 7749666

6

Macular dysplasia and pigmented paravenous retino-choroidal atrophy.

Nucci P, Manitto MP, Piantanida A, Brancato R. Nucci P, et al. Among authors: manitto mp. Ophthalmic Genet. 1994 Sep-Dec;15(3-4):161-4. doi: 10.3109/13816819409057844. Ophthalmic Genet. 1994. PMID: 7749671 Free article.

7

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. Manitto MP, et al. Eur J Ophthalmol. 1998 Jul-Sep;8(3):188-90. doi: 10.1177/112067219800800313. Eur J Ophthalmol. 1998. PMID: 9793775 Free article.

8

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

9

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. Lavorgna G, et al. Among authors: manitto mp. Biochem Biophys Res Commun. 2003 Aug 29;308(3):414-21. doi: 10.1016/s0006-291x(03)01410-4. Biochem Biophys Res Commun. 2003. PMID: 12914764

10

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. Simonelli F, et al. Among authors: manitto mp. Br J Ophthalmol. 2003 Sep;87(9):1130-4. doi: 10.1136/bjo.87.9.1130. Br J Ophthalmol. 2003. PMID: 12928282 Free PMC article.

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