Passerini I - Search Results

1

A novel mutation in the VMD2 gene in an Italian family with Best maculopathy.

Sodi A, Passerini I, Simonelli F, Testa F, Menchini U, Torricelli F. Sodi A, et al. Among authors: passerini i. J Fr Ophtalmol. 2007 Jun;30(6):616-20. doi: 10.1016/s0181-5512(07)89667-7. J Fr Ophtalmol. 2007. PMID: 17646752

2

Melting temperature assay for a UGT1A gene variant in Gilbert syndrome.

Marziliano N, Pelo E, Minuti B, Passerini I, Torricelli F, Da Prato L. Marziliano N, et al. Among authors: passerini i. Clin Chem. 2000 Mar;46(3):423-5. Clin Chem. 2000. PMID: 10702534 No abstract available.

3

Identification of seven novel mutations of F8C by DHPLC.

Frusconi S, Passerini I, Girolami F, Masieri M, Linari S, Longo G, Morfini M, Torricelli F. Frusconi S, et al. Among authors: passerini i. Hum Mutat. 2002 Sep;20(3):231-2. doi: 10.1002/humu.9052. Hum Mutat. 2002. PMID: 12203998

4

Prevalence and clinical profile of troponin T mutations among patients with hypertrophic cardiomyopathy in tuscany.

Torricelli F, Girolami F, Olivotto I, Passerini I, Frusconi S, Vargiu D, Richard P, Cecchi F. Torricelli F, et al. Among authors: passerini i. Am J Cardiol. 2003 Dec 1;92(11):1358-62. doi: 10.1016/j.amjcard.2003.08.031. Am J Cardiol. 2003. PMID: 14636924

5

Occurrence of full-thickness macular hole complicating Stargardt disease with ABCR mutation.

Sodi A, Bini A, Passerini I, Menchini U, Torricelli F. Sodi A, et al. Among authors: passerini i. Eur J Ophthalmol. 2006 Mar-Apr;16(2):335-8. doi: 10.1177/112067210601600223. Eur J Ophthalmol. 2006. PMID: 16703556

6

A molecular screening strategy based on beta-myosin heavy chain, cardiac myosin binding protein C and troponin T genes in Italian patients with hypertrophic cardiomyopathy.

Girolami F, Olivotto I, Passerini I, Zachara E, Nistri S, Re F, Fantini S, Baldini K, Torricelli F, Cecchi F. Girolami F, et al. Among authors: passerini i. J Cardiovasc Med (Hagerstown). 2006 Aug;7(8):601-7. doi: 10.2459/01.JCM.0000237908.26377.d6. J Cardiovasc Med (Hagerstown). 2006. PMID: 16858239

7

Retinal astrocytic hamartoma and Stargardt's disease: unusual association in a patient with ABCR mutation without phacomatosis.

Bini A, Sodi A, Passerini I, Menchini U, Torricelli F. Bini A, et al. Among authors: passerini i. Clin Exp Ophthalmol. 2007 Nov;35(8):777-9. doi: 10.1111/j.1442-9071.2007.01582.x. Clin Exp Ophthalmol. 2007. PMID: 17997789

8

Phenotypic intrafamilial variability associated with S212G mutation in the RDS/peripherin gene.

Passerini I, Sodi A, Giambene B, Menchini U, Torricelli F. Passerini I, et al. Eur J Ophthalmol. 2007 Nov-Dec;17(6):1000-3. doi: 10.1177/112067210701700624. Eur J Ophthalmol. 2007. PMID: 18050133

9

A normal electro-oculography in a family affected by best disease with a novel spontaneous mutation of the BEST1 gene.

Testa F, Rossi S, Passerini I, Sodi A, Di Iorio V, Interlandi E, Della Corte M, Menchini U, Rinaldi E, Torricelli F, Simonelli F. Testa F, et al. Among authors: passerini i. Br J Ophthalmol. 2008 Nov;92(11):1467-70. doi: 10.1136/bjo.2008.143776. Epub 2008 Aug 14. Br J Ophthalmol. 2008. PMID: 18703557

10

Novel mutations in of the ABCR gene in Italian patients with Stargardt disease.

Passerini I, Sodi A, Giambene B, Mariottini A, Menchini U, Torricelli F. Passerini I, et al. Eye (Lond). 2010 Jan;24(1):158-64. doi: 10.1038/eye.2009.35. Epub 2009 Mar 6. Eye (Lond). 2010. PMID: 19265867

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

61 results

Search Page

Filters