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Items: 35

1.

SUV95th as a Reliable Alternative to SUVmax for Determining Renal Uptake in [68Ga] PSMA PET/CT.

Baiocco S, Matteucci F, Mezzenga E, Caroli P, Di Iorio V, Cittanti C, Bevilacqua A, Paganelli G, Sarnelli A.

Mol Imaging Biol. 2019 Nov 22. doi: 10.1007/s11307-019-01451-1. [Epub ahead of print]

PMID:
31758510
2.

Carbonic anhydrase inhibitors in patients with X-linked retinoschisis: effects on macular morphology and function.

Testa F, Di Iorio V, Gallo B, Marchese M, Nesti A, De Rosa G, Melillo P, Simonelli F.

Ophthalmic Genet. 2019 Jun;40(3):207-212. doi: 10.1080/13816810.2019.1616303. Epub 2019 May 31.

PMID:
31149861
3.

CHM/REP1 Transcript Expression and Loss of Visual Function in Patients Affected by Choroideremia.

Di Iorio V, Esposito G, De Falco F, Boccia R, Fioretti T, Colucci R, De Rosa G, Melillo P, Salvatore F, Simonelli F, Testa F.

Invest Ophthalmol Vis Sci. 2019 Apr 1;60(5):1547-1555. doi: 10.1167/iovs.18-25501.

PMID:
30995293
4.

Dosimetry of 177Lu-PSMA-617 after Mannitol Infusion and Glutamate Tablet Administration: Preliminary Results of EUDRACT/RSO 2016-002732-32 IRST Protocol.

Sarnelli A, Belli ML, Di Iorio V, Mezzenga E, Celli M, Severi S, Tardelli E, Nicolini S, Oboldi D, Uccelli L, Cittanti C, Monti M, Ferrari M, Paganelli G.

Molecules. 2019 Feb 11;24(3). pii: E621. doi: 10.3390/molecules24030621.

5.

Early posterior vitreous detachment is associated with LAMA5 dominant mutation.

Napolitano F, Di Iorio V, Di Iorio G, Melone MAB, Gianfrancesco F, Simonelli F, Esposito T, Testa F, Sampaolo S.

Ophthalmic Genet. 2019 Feb;40(1):39-42. doi: 10.1080/13816810.2018.1558261. Epub 2018 Dec 27.

PMID:
30589377
6.

ASSOCIATION BETWEEN GENOTYPE AND DISEASE PROGRESSION IN ITALIAN STARGARDT PATIENTS: A Retrospective Natural History Study.

Di Iorio V, Orrico A, Esposito G, Melillo P, Rossi S, Sbordone S, Auricchio A, Testa F, Simonelli F.

Retina. 2019 Jul;39(7):1399-1409. doi: 10.1097/IAE.0000000000002151.

PMID:
29642238
7.

Visual Cortex Activation in Patients With Stargardt Disease.

Melillo P, Prinster A, Di Iorio V, Olivo G, D'Alterio FM, Cocozza S, Orrico A, Quarantelli M, Testa F, Brunetti A, Simonelli F.

Invest Ophthalmol Vis Sci. 2018 Mar 1;59(3):1503-1511. doi: 10.1167/iovs.17-22900.

PMID:
29625472
8.

Automatic segmentation of pigment deposits in retinal fundus images of Retinitis Pigmentosa.

Brancati N, Frucci M, Gragnaniello D, Riccio D, Di Iorio V, Di Perna L.

Comput Med Imaging Graph. 2018 Jun;66:73-81. doi: 10.1016/j.compmedimag.2018.03.002. Epub 2018 Mar 17.

PMID:
29573581
9.

The renal lesions in Bardet-Biedl Syndrome: history before and after the discovery of BBS genes.

Viggiano D, Zacchia M, Simonelli F, Di Iorio V, Anastasio P, Capasso G, De Santo NG.

G Ital Nefrol. 2018 Feb;35(Suppl 70):95-100. No abstract available.

10.

Autosomal-dominant myopia associated to a novel P4HA2 missense variant and defective collagen hydroxylation.

Napolitano F, Di Iorio V, Testa F, Tirozzi A, Reccia MG, Lombardi L, Farina O, Simonelli F, Gianfrancesco F, Di Iorio G, Melone MAB, Esposito T, Sampaolo S.

Clin Genet. 2018 May;93(5):982-991. doi: 10.1111/cge.13217. Epub 2018 Mar 5.

PMID:
29364500
11.

Clinical and Genetic Evaluation of a Cohort of Pediatric Patients with Severe Inherited Retinal Dystrophies.

Di Iorio V, Karali M, Brunetti-Pierri R, Filippelli M, Di Fruscio G, Pizzo M, Mutarelli M, Nigro V, Testa F, Banfi S, Simonelli F.

Genes (Basel). 2017 Oct 20;8(10). pii: E280. doi: 10.3390/genes8100280.

12.

[Patho-physiology of renal dysfunction in Bardet-Biedl Syndrome].

Zona E, Zacchia M, Di Iorio V, Capolongo G, Rinaldi L, Capasso G.

G Ital Nefrol. 2017 Sep 28;34(5):62-72. Review. Italian.

PMID:
28963828
13.

The Kidney in Bardet-Biedl Syndrome: Possible Pathogenesis of Urine Concentrating Defect.

Zacchia M, Di Iorio V, Trepiccione F, Caterino M, Capasso G.

Kidney Dis (Basel). 2017 Jul;3(2):57-65. doi: 10.1159/000475500. Epub 2017 May 17. Review.

14.

Reduction of 68Ga-PSMA renal uptake with mannitol infusion: preliminary results.

Matteucci F, Mezzenga E, Caroli P, Di Iorio V, Sarnelli A, Celli M, Fantini L, Moretti A, Galassi R, De Giorgi U, Paganelli G.

Eur J Nucl Med Mol Imaging. 2017 Dec;44(13):2189-2194. doi: 10.1007/s00259-017-3791-4. Epub 2017 Aug 11.

PMID:
28801787
15.

Mutations in the PCYT1A gene are responsible for isolated forms of retinal dystrophy.

Testa F, Filippelli M, Brunetti-Pierri R, Di Fruscio G, Di Iorio V, Pizzo M, Torella A, Barillari MR, Nigro V, Brunetti-Pierri N, Simonelli F, Banfi S.

Eur J Hum Genet. 2017 May;25(5):651-655. doi: 10.1038/ejhg.2017.23. Epub 2017 Mar 8.

16.

High Levels of Serum Ubiquitin and Proteasome in a Case of HLA-B27 Uveitis.

Rossi S, Gesualdo C, Maisto R, Trotta MC, Di Carluccio N, Brigida A, Di Iorio V, Testa F, Simonelli F, D'Amico M, Di Filippo C.

Int J Mol Sci. 2017 Feb 26;18(3). pii: E505. doi: 10.3390/ijms18030505.

17.

Genetic characterization of Italian patients with Bardet-Biedl syndrome and correlation to ocular, renal and audio-vestibular phenotype: identification of eleven novel pathogenic sequence variants.

Esposito G, Testa F, Zacchia M, Crispo AA, Di Iorio V, Capolongo G, Rinaldi L, D'Antonio M, Fioretti T, Iadicicco P, Rossi S, Franzè A, Marciano E, Capasso G, Simonelli F, Salvatore F.

BMC Med Genet. 2017 Feb 1;18(1):10. doi: 10.1186/s12881-017-0372-0.

18.

Implementing an evidence-based computerized decision support system linked to electronic health records to improve care for cancer patients: the ONCO-CODES study protocol for a randomized controlled trial.

Moja L, Passardi A, Capobussi M, Banzi R, Ruggiero F, Kwag K, Liberati EG, Mangia M, Kunnamo I, Cinquini M, Vespignani R, Colamartini A, Di Iorio V, Massa I, González-Lorenzo M, Bertizzolo L, Nyberg P, Grimshaw J, Bonovas S, Nanni O.

Implement Sci. 2016 Nov 25;11(1):153.

19.

Recombinant granulocyte colony-stimulating factor (rG-CSF) in the management of neutropenia induced by anthracyclines and ifosfamide in patients with soft tissue sarcomas (NEUSAR).

Bongiovanni A, Monti M, Foca F, Recine F, Riva N, Di Iorio V, Liverani C, De Vita A, Miserocchi G, Mercatali L, Amadori D, Ibrahim T.

Support Care Cancer. 2017 Jan;25(1):111-117. Epub 2016 Aug 27.

PMID:
27568305
20.

Renal phenotype in Bardet-Biedl syndrome: a combined defect of urinary concentration and dilution is associated with defective urinary AQP2 and UMOD excretion.

Zacchia M, Zacchia E, Zona E, Capolongo G, Raiola I, Rinaldi L, Trepiccione F, Ingrosso D, Perna A, Di Iorio V, Simonelli F, Moe OW, Capasso G.

Am J Physiol Renal Physiol. 2016 Oct 1;311(4):F686-F694. doi: 10.1152/ajprenal.00224.2016. Epub 2016 Aug 3.

21.

En Face Spectral-Domain Optical Coherence Tomography for the Monitoring of Lesion Area Progression in Stargardt Disease.

Melillo P, Testa F, Rossi S, Di Iorio V, Orrico A, Auricchio A, Simonelli F.

Invest Ophthalmol Vis Sci. 2016 Jul 1;57(9):OCT247-52. doi: 10.1167/iovs.15-18751.

22.

Sampling Optimization in Pharmacokinetic Bridging Studies: Example of the Use of Deferiprone in Children With β-Thalassemia.

Bellanti F, Di Iorio VL, Danhof M, Della Pasqua O.

J Clin Pharmacol. 2016 Sep;56(9):1094-103. doi: 10.1002/jcph.708. Epub 2016 Apr 1.

PMID:
26785826
23.

Peptide receptor radionuclide therapy with (177)Lu-DOTATATE in advanced bronchial carcinoids: prognostic role of thyroid transcription factor 1 and (18)F-FDG PET.

Ianniello A, Sansovini M, Severi S, Nicolini S, Grana CM, Massri K, Bongiovanni A, Antonuzzo L, Di Iorio V, Sarnelli A, Caroli P, Monti M, Scarpi E, Paganelli G.

Eur J Nucl Med Mol Imaging. 2016 Jun;43(6):1040-6. doi: 10.1007/s00259-015-3262-8. Epub 2015 Nov 27.

PMID:
26611427
24.

Feasibility and utility of re-treatment with (177)Lu-DOTATATE in GEP-NENs relapsed after treatment with (90)Y-DOTATOC.

Severi S, Sansovini M, Ianniello A, Bodei L, Nicolini S, Ibrahim T, Di Iorio V, D'Errico V, Caroli P, Monti M, Paganelli G.

Eur J Nucl Med Mol Imaging. 2015 Dec;42(13):1955-63. doi: 10.1007/s00259-015-3105-7. Epub 2015 Jun 26.

PMID:
26112388
25.

Macular function and morphologic features in juvenile stargardt disease: longitudinal study.

Testa F, Melillo P, Di Iorio V, Orrico A, Attanasio M, Rossi S, Simonelli F.

Ophthalmology. 2014 Dec;121(12):2399-405. doi: 10.1016/j.ophtha.2014.06.032. Epub 2014 Aug 2.

26.

Macular abnormalities in Italian patients with retinitis pigmentosa.

Testa F, Rossi S, Colucci R, Gallo B, Di Iorio V, della Corte M, Azzolini C, Melillo P, Simonelli F.

Br J Ophthalmol. 2014 Jul;98(7):946-50. doi: 10.1136/bjophthalmol-2013-304082. Epub 2014 Feb 13.

27.

Correlation between photoreceptor layer integrity and visual function in patients with Stargardt disease: implications for gene therapy.

Testa F, Rossi S, Sodi A, Passerini I, Di Iorio V, Della Corte M, Banfi S, Surace EM, Menchini U, Auricchio A, Simonelli F.

Invest Ophthalmol Vis Sci. 2012 Jul 3;53(8):4409-15. doi: 10.1167/iovs.11-8201.

28.

The role of optical coherence tomography in an atypical case of oculocutaneous albinism: a case report.

Rossi S, Testa F, Gargiulo A, Di Iorio V, Pierri RB, D'Alterio FM, Corte MD, Surace E, Simonelli F.

Case Rep Ophthalmol. 2012 Jan;3(1):113-7. doi: 10.1159/000337489. Epub 2012 Mar 27.

29.

Translation of drug effects from experimental models of neuropathic pain and analgesia to humans.

Taneja A, Di Iorio VL, Danhof M, Della Pasqua O.

Drug Discov Today. 2012 Aug;17(15-16):837-49. doi: 10.1016/j.drudis.2012.02.010. Epub 2012 Mar 3. Review.

PMID:
22445930
30.

Evaluation of Italian patients with leber congenital amaurosis due to AIPL1 mutations highlights the potential applicability of gene therapy.

Testa F, Surace EM, Rossi S, Marrocco E, Gargiulo A, Di Iorio V, Ziviello C, Nesti A, Fecarotta S, Bacci ML, Giunti M, Della Corte M, Banfi S, Auricchio A, Simonelli F.

Invest Ophthalmol Vis Sci. 2011 Jul 29;52(8):5618-24. doi: 10.1167/iovs.10-6543.

PMID:
21474771
31.

Molecular and clinical characterization of albinism in a large cohort of Italian patients.

Gargiulo A, Testa F, Rossi S, Di Iorio V, Fecarotta S, de Berardinis T, Iovine A, Magli A, Signorini S, Fazzi E, Galantuomo MS, Fossarello M, Montefusco S, Ciccodicola A, Neri A, Macaluso C, Simonelli F, Surace EM.

Invest Ophthalmol Vis Sci. 2011 Mar 14;52(3):1281-9. doi: 10.1167/iovs.10-6091. Print 2011 Mar.

32.

Adaptive-optimal design in PET occupancy studies.

Zamuner S, Di Iorio VL, Nyberg J, Gunn RN, Cunningham VJ, Gomeni R, Hooker AC.

Clin Pharmacol Ther. 2010 May;87(5):563-71. doi: 10.1038/clpt.2010.9. Epub 2010 Mar 24.

PMID:
20336064
33.

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.

Br J Ophthalmol. 2008 Nov;92(11):1467-70. doi: 10.1136/bjo.2008.143776. Epub 2008 Aug 14.

PMID:
18703557
34.

Successful treatment of severe Behçet's disease with infliximab in an Italian Olympic athlete.

Olivieri I, Latanza L, Siringo S, Peruz G, Di Iorio V.

J Rheumatol. 2008 May;35(5):930-2.

PMID:
18464316
35.

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.

Eur J Ophthalmol. 2006 Sep-Oct;16(5):779-81.

PMID:
17061239

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