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Items: 1 to 50 of 176

1.

[The accuracy of hospital discharge records and their use in identifying and staging chronic kidney disease].

Gibertoni D, Mandreoli M, De Amicis S, Cantarelli C, Corradini M, Caruso F, Testa F, Gasperoni L, Orrico C, Brancaleoni F, Martelli D, Angelini ML, Ferri B, Flachi M, Iommi M, Santoro A.

G Ital Nefrol. 2019 Sep 24;36(5). pii: 2019-vol5. Italian.

PMID:
31580547
2.

TRPP2 dysfunction decreases ATP-evoked calcium, induces cell aggregation and stimulates proliferation in T lymphocytes.

Magistroni R, Mangolini A, Guzzo S, Testa F, Rapanà MR, Mignani R, Russo G, di Virgilio F, Aguiari G.

BMC Nephrol. 2019 Sep 13;20(1):355. doi: 10.1186/s12882-019-1540-6.

3.

Antecedents of environmental management system internalization: Assessing managerial interpretations and cognitive framings of sustainability issues.

Todaro NM, Testa F, Daddi T, Iraldo F.

J Environ Manage. 2019 Oct 1;247:804-815. doi: 10.1016/j.jenvman.2019.06.106. Epub 2019 Jul 9.

PMID:
31299556
4.

Full-field electroretinography, visual acuity and visual fields in Usher syndrome: a multicentre European study.

Stingl K, Kurtenbach A, Hahn G, Kernstock C, Hipp S, Zobor D, Kohl S, Bonnet C, Mohand-Saïd S, Audo I, Fakin A, Hawlina M, Testa F, Simonelli F, Petit C, Sahel JA, Zrenner E.

Doc Ophthalmol. 2019 Oct;139(2):151-160. doi: 10.1007/s10633-019-09704-8. Epub 2019 Jul 2.

PMID:
31267413
5.

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
6.

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
7.

Correction: Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease.

Van de Sompele S, Smith C, Karali M, Corton M, Van Schil K, Peelman F, Cherry T, Rosseel T, Verdin H, Derolez J, Van Laethem T, Khan KN, McKibbin M, Toomes C, Ali M, Torella A, Testa F, Jimenez B, Simonelli F, De Zaeytijd J, Van den Ende J, Leroy BP, Coppieters F, Ayuso C, Inglehearn CF, Banfi S, De Baere E.

Genet Med. 2019 Apr;21(4):1028. doi: 10.1038/s41436-018-0392-y.

8.

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
9.

Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease.

Van de Sompele S, Smith C, Karali M, Corton M, Van Schil K, Peelman F, Cherry T, Rosseel T, Verdin H, Derolez J, Van Laethem T, Khan KN, McKibbin M, Toomes C, Ali M, Torella A, Testa F, Jimenez B, Simonelli F, De Zaeytijd J, Van den Ende J, Leroy BP, Coppieters F, Ayuso C, Inglehearn CF, Banfi S, De Baere E.

Genet Med. 2019 Jun;21(6):1319-1329. doi: 10.1038/s41436-018-0345-5. Epub 2018 Oct 31. Erratum in: Genet Med. 2019 Apr;21(4):1028.

10.

Exploring waste prevention behaviour through empirical research.

Corsini F, Gusmerotti NM, Testa F, Iraldo F.

Waste Manag. 2018 Sep;79:132-141. doi: 10.1016/j.wasman.2018.07.037. Epub 2018 Jul 23.

PMID:
30343739
11.

Evolution and course of early life developmental encephalopathic epilepsies: Focus on Lennox-Gastaut syndrome.

Berg AT, Levy SR, Testa FM.

Epilepsia. 2018 Nov;59(11):2096-2105. doi: 10.1111/epi.14569. Epub 2018 Sep 26.

12.

Usher Syndrome and Color Vision.

Kurtenbach A, Hahn G, Kernstock C, Hipp S, Zobor D, Stingl K, Kohl S, Bonnet C, Mohand-Saïd S, Sliesoraityte I, Sahel JA, Audo I, Fakin A, Hawlina M, Testa F, Simonelli F, Petit C, Zrenner E.

Curr Eye Res. 2018 Oct;43(10):1295-1301. doi: 10.1080/02713683.2018.1501804. Epub 2018 Jul 30.

PMID:
30012035
13.

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
14.

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
15.

Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber's hereditary optic neuropathy.

Caporali L, Iommarini L, La Morgia C, Olivieri A, Achilli A, Maresca A, Valentino ML, Capristo M, Tagliavini F, Del Dotto V, Zanna C, Liguori R, Barboni P, Carbonelli M, Cocetta V, Montopoli M, Martinuzzi A, Cenacchi G, De Michele G, Testa F, Nesti A, Simonelli F, Porcelli AM, Torroni A, Carelli V.

PLoS Genet. 2018 Feb 14;14(2):e1007210. doi: 10.1371/journal.pgen.1007210. eCollection 2018 Feb.

16.

Pope Innocent XI's renal stones: an example of medical correspondence.

Riva MA, Testa F, Cesana G, Castagna F.

Intern Emerg Med. 2018 Mar;13(2):307-308. doi: 10.1007/s11739-018-1800-7. Epub 2018 Feb 6. No abstract available.

PMID:
29411308
17.

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
18.

The prevalence of autosomal dominant polycystic kidney disease (ADPKD): A meta-analysis of European literature and prevalence evaluation in the Italian province of Modena suggest that ADPKD is a rare and underdiagnosed condition.

Solazzo A, Testa F, Giovanella S, Busutti M, Furci L, Carrera P, Ferrari M, Ligabue G, Mori G, Leonelli M, Cappelli G, Magistroni R.

PLoS One. 2018 Jan 16;13(1):e0190430. doi: 10.1371/journal.pone.0190430. eCollection 2018.

19.

Levers supporting tariff growth for water services: evidence from a contingent valuation analysis.

Guerrini A, Vigolo V, Romano G, Testa F.

J Environ Manage. 2018 Feb 1;207:23-31. doi: 10.1016/j.jenvman.2017.11.008. Epub 2017 Nov 15.

PMID:
29154005
20.

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.

21.

Study of the association of atmospheric temperature and relative humidity with bulk tank milk somatic cell count in dairy herds using Generalized additive mixed models.

Testa F, Marano G, Ambrogi F, Boracchi P, Casula A, Biganzoli E, Moroni P.

Res Vet Sci. 2017 Oct;114:511-517. doi: 10.1016/j.rvsc.2017.09.027. Epub 2017 Sep 28.

PMID:
28987958
22.

Should we withhold angiotensin converting enzyme inhibitors before anaesthesia? An updated debate on the pros and cons.

Vassallo MC, Tartamella F, Testa F.

J Clin Anesth. 2017 Nov;42:51-52. doi: 10.1016/j.jclinane.2017.07.008. Epub 2017 Aug 15. No abstract available.

PMID:
28821004
23.

Prevalence of macular abnormalities assessed by optical coherence tomography in patients with Usher syndrome.

Testa F, Melillo P, Rossi S, Marcelli V, de Benedictis A, Colucci R, Gallo B, Brunetti-Pierri R, Donati S, Azzolini C, Marciano E, Simonelli F.

Ophthalmic Genet. 2018 Jan-Feb;39(1):17-21. doi: 10.1080/13816810.2017.1329445. Epub 2017 Jul 13.

PMID:
28704163
24.

Acute demyelinating neuropathy associated with rituximab treatment in a patient with relapsing nephrotic syndrome.

Galassi G, Testa F, Bianchi F, Cappelli G, Chiari A.

CEN Case Rep. 2017 Nov;6(2):215-216. doi: 10.1007/s13730-017-0264-3. Epub 2017 Jun 20. No abstract available.

25.

Multilayer Microstructure of Idiopathic Epiretinal Macular Membranes.

Azzolini C, Congiu T, Donati S, Passi A, Basso P, Piantanida E, Mariotti C, Testa F, Caprani SM, Cattaneo J, Vinciguerra R.

Eur J Ophthalmol. 2017 Nov 8;27(6):762-768. doi: 10.5301/ejo.5000982.

PMID:
28525683
26.

Wearable Improved Vision System for Color Vision Deficiency Correction.

Melillo P, Riccio D, Di Perna L, Sanniti Di Baja G, De Nino M, Rossi S, Testa F, Simonelli F, Frucci M.

IEEE J Transl Eng Health Med. 2017 May 2;5:3800107. doi: 10.1109/JTEHM.2017.2679746. eCollection 2017.

27.

To Stop Or Not? Withholding Anti-hypertensive Therapy Before Surgery Is Not Safe.

Vassallo MC, Tartamella F, Testa F.

J Cardiothorac Vasc Anesth. 2017 Dec;31(6):e92-e93. doi: 10.1053/j.jvca.2017.02.025. Epub 2017 Feb 3. No abstract available.

PMID:
28389189
28.

Identifying fallers among ophthalmic patients using classification tree methodology.

Melillo P, Orrico A, Chirico F, Pecchia L, Rossi S, Testa F, Simonelli F.

PLoS One. 2017 Mar 23;12(3):e0174083. doi: 10.1371/journal.pone.0174083. eCollection 2017.

29.

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.

30.

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.

31.

Surgical outcome in adolescents with mesial temporal sclerosis: Is it different?

Farooque P, Hirsch L, Levy S, Testa F, Mattson R, Spencer D.

Epilepsy Behav. 2017 Apr;69:24-27. doi: 10.1016/j.yebeh.2016.10.028. Epub 2017 Feb 20.

PMID:
28235653
32.

Macular hole surgery: the healing process of outer retinal layers to visual acuity recovery.

Caprani SM, Donati S, Bartalena L, Vinciguerra R, Mariotti C, Testa F, Porta G, Azzolini C.

Eur J Ophthalmol. 2017 Mar 10;27(2):235-239. doi: 10.5301/ejo.5000905. Epub 2017 Feb 22.

PMID:
28233890
33.

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.

34.

Melanocortin receptor agonists MCR1-5 protect photoreceptors from high-glucose damage and restore antioxidant enzymes in primary retinal cell culture.

Maisto R, Gesualdo C, Trotta MC, Grieco P, Testa F, Simonelli F, Barcia JM, D'Amico M, Di Filippo C, Rossi S.

J Cell Mol Med. 2017 May;21(5):968-974. doi: 10.1111/jcmm.13036. Epub 2016 Dec 20.

35.

Polarization insensitive silicon photonic ROADM with selectable communication direction for radio access networks.

Sorianello V, Angelis G, Cassese T, Preite MV, Velha P, Bianchi A, Romagnoli M, Testa F.

Opt Lett. 2016 Dec 15;41(24):5688-5691. doi: 10.1364/OL.41.005688.

PMID:
27973490
36.

Wide-band polarization controller for Si photonic integrated circuits.

Velha P, Sorianello V, Preite MV, De Angelis G, Cassese T, Bianchi A, Testa F, Romagnoli M.

Opt Lett. 2016 Dec 15;41(24):5656-5659. doi: 10.1364/OL.41.005656.

PMID:
27973482
37.

CLINICAL PRESENTATION AND DISEASE COURSE OF USHER SYNDROME BECAUSE OF MUTATIONS IN MYO7A OR USH2A.

Testa F, Melillo P, Bonnet C, Marcelli V, de Benedictis A, Colucci R, Gallo B, Kurtenbach A, Rossi S, Marciano E, Auricchio A, Petit C, Zrenner E, Simonelli F.

Retina. 2017 Aug;37(8):1581-1590. doi: 10.1097/IAE.0000000000001389.

PMID:
27828912
38.

Thromboelastographic predictors of venous thromboembolic events in critically ill patients: are we missing something?

Tartamella F, Vassallo MC, Berlot G, Grassi P, Testa F.

Blood Coagul Fibrinolysis. 2016 Oct;27(7):804-811.

PMID:
26895213
39.

Morphological and Functional Retinal Assessment in Epiretinal Membrane Surgery.

Donati S, Caprani SM, Semeraro F, Vinciguerra R, Virgili G, Testa F, Simonelli F, Azzolini C.

Semin Ophthalmol. 2017;32(6):751-758. doi: 10.1080/08820538.2016.1177097. Epub 2016 Aug 10.

PMID:
27715374
40.

Exploring the link between institutional pressures and environmental management systems effectiveness: An empirical study.

Daddi T, Testa F, Frey M, Iraldo F.

J Environ Manage. 2016 Dec 1;183(Pt 3):647-656. doi: 10.1016/j.jenvman.2016.09.025. Epub 2016 Sep 13.

PMID:
27637805
41.

Deciphering Variability of PKD1 and PKD2 in an Italian Cohort of 643 Patients with Autosomal Dominant Polycystic Kidney Disease (ADPKD).

Carrera P, Calzavara S, Magistroni R, den Dunnen JT, Rigo F, Stenirri S, Testa F, Messa P, Cerutti R, Scolari F, Izzi C, Edefonti A, Negrisolo S, Benetti E, Alibrandi MT, Manunta P, Boletta A, Ferrari M.

Sci Rep. 2016 Aug 8;6:30850. doi: 10.1038/srep30850.

42.

An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients.

Bonnet C, Riahi Z, Chantot-Bastaraud S, Smagghe L, Letexier M, Marcaillou C, Lefèvre GM, Hardelin JP, El-Amraoui A, Singh-Estivalet A, Mohand-Saïd S, Kohl S, Kurtenbach A, Sliesoraityte I, Zobor D, Gherbi S, Testa F, Simonelli F, Banfi S, Fakin A, Glavač D, Jarc-Vidmar M, Zupan A, Battelino S, Martorell Sampol L, Claveria MA, Catala Mora J, Dad S, Møller LB, Rodriguez Jorge J, Hawlina M, Auricchio A, Sahel JA, Marlin S, Zrenner E, Audo I, Petit C.

Eur J Hum Genet. 2016 Dec;24(12):1730-1738. doi: 10.1038/ejhg.2016.99. Epub 2016 Jul 27.

43.

Functional improvement assessed by multifocal electroretinogram after Ocriplasmin treatment for vitreomacular traction.

Rossi S, Testa F, Melillo P, Orrico A, Della Corte M, Simonelli F.

BMC Ophthalmol. 2016 Jul 18;16:110. doi: 10.1186/s12886-016-0284-3.

44.

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.

45.

Intrafamilial heterogeneity of congenital optic disc pit maculopathy.

Rossi S, De Rosa G, D'Alterio FM, Orrico A, Banfi S, Testa F, Simonelli F.

Ophthalmic Genet. 2017 May-Jun;38(3):267-272. doi: 10.1080/13816810.2016.1188120. Epub 2016 Jun 8.

PMID:
27268460
46.

Determinants of Social Outcomes in Adults With Childhood-onset Epilepsy.

Berg AT, Baca CB, Rychlik K, Vickrey BG, Caplan R, Testa FM, Levy SR.

Pediatrics. 2016 Apr;137(4). pii: e20153944. doi: 10.1542/peds.2015-3944. Epub 2016 Mar 16.

47.

Activation of Melanocortin Receptors MC 1 and MC 5 Attenuates Retinal Damage in Experimental Diabetic Retinopathy.

Rossi S, Maisto R, Gesualdo C, Trotta MC, Ferraraccio F, Kaneva MK, Getting SJ, Surace E, Testa F, Simonelli F, Grieco P, Merlino F, Perretti M, D'Amico M, Di Filippo C.

Mediators Inflamm. 2016;2016:7368389. doi: 10.1155/2016/7368389. Epub 2016 Jan 12.

48.

Antioxidant defence systems in the protozoan pathogen Giardia intestinalis.

Mastronicola D, Falabella M, Forte E, Testa F, Sarti P, Giuffrè A.

Mol Biochem Parasitol. 2016 Mar-Apr;206(1-2):56-66. doi: 10.1016/j.molbiopara.2015.12.002. Epub 2015 Dec 7. Review.

PMID:
26672398
49.

Cerebral Involvement in Stargardt's Disease: A VBM and TBSS Study.

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

Invest Ophthalmol Vis Sci. 2015 Nov;56(12):7388-97. doi: 10.1167/iovs.15-16899. Erratum in: Invest Ophthalmol Vis Sci. 2015 Dec 1;56(13):7867. Gaia, Olivo [corrected to Olivo, Gaia]; Sirio, Cocozza [corrected to Cocozza, Sirio].

PMID:
26574798
50.

Superoxide reductase from Giardia intestinalis: structural characterization of the first SOR from a eukaryotic organism shows an iron centre that is highly sensitive to photoreduction.

Sousa CM, Carpentier P, Matias PM, Testa F, Pinho F, Sarti P, Giuffrè A, Bandeiras TM, Romão CV.

Acta Crystallogr D Biol Crystallogr. 2015 Nov;71(Pt 11):2236-47. doi: 10.1107/S1399004715015825. Epub 2015 Oct 31.

PMID:
26527141

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