Rinaldi M - Search Results

1

Clinical phenotype of an Italian family with a new mutation in the PRPF8 gene.

Testa F, Ziviello C, Rinaldi M, Rossi S, Di Iorio V, Interlandi E, Ciccodicola A, Banfi S, Simonelli F. Testa F, et al. Among authors: rinaldi m. Eur J Ophthalmol. 2006 Sep-Oct;16(5):779-81. doi: 10.1177/112067210601600524. Eur J Ophthalmol. 2006. PMID: 17061239

2

Galactokinase activity in patients with idiopathic presenile and senile cataract.

Simonelli F, Giovane A, Frunzio S, Balestrieri P, Amicone A, Rinaldi M, Cotticelli L, Rinaldi E. Simonelli F, et al. Among authors: rinaldi e, rinaldi m. Metab Pediatr Syst Ophthalmol (1985). 1992;15(4):53-6. Metab Pediatr Syst Ophthalmol (1985). 1992. PMID: 1305705

3

[Measurement of the erythrocyte galactokinase activity in patients with presenile and senile idiopathic cataract. Preliminary study].

Simonelli F, Frunzio S, Rinaldi M, Balestrieri P, Giovane A, Cotticelli L, Rinaldi E. Simonelli F, et al. Among authors: rinaldi e, rinaldi m. Boll Soc Ital Biol Sper. 1990 Sep;66(9):887-92. Boll Soc Ital Biol Sper. 1990. PMID: 2073390 Italian.

4

Ocular signs associated with a rhodopsin mutation (Cys-167-->Arg) in a family with autosomal dominant retinitis pigmentosa.

Simonelli F, Rinaldi M, Nesti A, Testa F, Rinaldi E, Ciccodicola A, Flagiello L, Miano MG, Ventruto V, D'Urso M. Simonelli F, et al. Among authors: rinaldi e, rinaldi m. Br J Ophthalmol. 1998 Jun;82(6):709. doi: 10.1136/bjo.82.6.709. Br J Ophthalmol. 1998. PMID: 9797678 Free PMC article. No abstract available.

5

Mutation in the nerve-specific 5'non-coding region of Cx32 gene and absence of specific mRNA in a CMTX1 Italian family. Mutations in brief no. 195. Online.

Flagiello L, Cirigliano V, Strazzullo M, Cappa V, Ciccodicola A, D'Esposito M, Torrente I, Werner R, Di Iorio G, Rinaldi M, Dallapiccola A, Forabosco A, Ventruto V, D'Urso M. Flagiello L, et al. Among authors: rinaldi m. Hum Mutat. 1998;12(5):361. Hum Mutat. 1998. PMID: 10671058

6

Serum oxidative and antioxidant parameters in a group of Italian patients with age-related maculopathy.

Simonelli F, Zarrilli F, Mazzeo S, Verde V, Romano N, Savoia M, Testa F, Vitale DF, Rinaldi M, Sacchetti L. Simonelli F, et al. Among authors: rinaldi m. Clin Chim Acta. 2002 Jun;320(1-2):111-5. doi: 10.1016/s0009-8981(02)00056-6. Clin Chim Acta. 2002. PMID: 11983208

7

Sjögren reticular dystrophy of the retinal pigment epithelium: a case report.

Rinaldi M, Villani A, Borrelli M, Russo S, Cotticelli L. Rinaldi M, et al. Eur J Ophthalmol. 2003 Jun;13(5):491-5. doi: 10.1177/112067210301300512. Eur J Ophthalmol. 2003. PMID: 12841574

8

A novel mutation in the RDS gene in an Italian family with pattern dystrophy.

Testa F, Marini V, Rossi S, Interlandi E, Nesti A, Rinaldi M, Varano M, Garré C, Simonelli F. Testa F, et al. Among authors: rinaldi m. Br J Ophthalmol. 2005 Aug;89(8):1066-8. doi: 10.1136/bjo.2004.064188. Br J Ophthalmol. 2005. PMID: 16024869 Free PMC article. No abstract available.

9

Clinical evolution of neuroretinitis in Parry-Romberg syndrome.

de Crecchio G, Forte R, Strianese D, Rinaldi M, D'Aponte A. de Crecchio G, et al. Among authors: rinaldi m. J Pediatr Ophthalmol Strabismus. 2008 Mar-Apr;45(2):125-6. doi: 10.3928/01913913-20080301-04. J Pediatr Ophthalmol Strabismus. 2008. PMID: 18404964

10

Verteporfin photodynamic therapy for subfoveal choroidal neovascularization in pathologic myopia: a 12-month retrospective review.

Costagliola C, Campa C, Incorvaia C, Parmeggiani F, Menzione M, Della Corte M, Rinaldi M, Romano M, Semeraro F. Costagliola C, et al. Among authors: rinaldi m. Eur J Ophthalmol. 2008 Nov-Dec;18(6):955-9. doi: 10.1177/112067210801800616. Eur J Ophthalmol. 2008. PMID: 18988168

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