PubMed

Age-dependent effects of RPE65 gene therapy for Leber's congenital amaurosis: a phase 1 dose-escalation trial.

Maguire AM, High KA, Auricchio A, Wright JF, Pierce EA, Testa F, Mingozzi F, Bennicelli JL, Ying GS, Rossi S, Fulton A, Marshall KA, Banfi S, Chung DC, Morgan JI, Hauck B, Zelenaia O, Zhu X, Raffini L, Coppieters F, De Baere E, Shindler KS, Volpe NJ, Surace EM, Acerra C, Lyubarsky A, Redmond TM, Stone E, Sun J, McDonnell JW, Leroy BP, Simonelli F, Bennett J.

Lancet. 2009 Nov 7;374(9701):1597-605. Epub 2009 Oct 23.PMID: 19854499 [PubMed - in process]Related articles

Frequency, prognosis and surgical treatment of structural abnormalities seen with magnetic resonance imaging in childhood epilepsy.

Berg AT, Mathern GW, Bronen RA, Fulbright RK, DiMario F, Testa FM, Levy SR.

Brain. 2009 Oct;132(Pt 10):2785-97. Epub 2009 Jul 28.PMID: 19638447 [PubMed - in process]Related articles

Redox properties of the oxygen-detoxifying flavodiiron protein from the human parasite Giardia intestinalis.

Vicente JB, Testa F, Mastronicola D, Forte E, Sarti P, Teixeira M, Giuffrè A.

Arch Biochem Biophys. 2009 Aug 1;488(1):9-13. Epub 2009 Jun 21.PMID: 19545535 [PubMed - indexed for MEDLINE]Related articles

Remission of epilepsy after two drug failures in children: a prospective study.

Berg AT, Levy SR, Testa FM, D'Souza R.

Ann Neurol. 2009 May;65(5):510-9.PMID: 19475671 [PubMed - indexed for MEDLINE]Related articles

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. Epub 2008 Aug 14.PMID: 18703557 [PubMed - indexed for MEDLINE]Related articles

Residual cognitive effects of uncomplicated idiopathic and cryptogenic epilepsy.

Berg AT, Langfitt JT, Testa FM, Levy SR, DiMario F, Westerveld M, Kulas J.

Epilepsy Behav. 2008 Nov;13(4):614-9. Epub 2008 Aug 19.PMID: 18675938 [PubMed - indexed for MEDLINE]Related articles

Pulmonary arteriovenous malformations: percutaneous treatment preserving parenchyma in high-flow fistulae.

Grosso M, Groppo Marchisio F, Testa F, Gallarato G, Balderi A, Lingua G, Mondino I, Pedrazzini F, Danesino C, Buscarini E.

Radiol Med. 2008 Apr;113(3):395-413. Epub 2008 Jul 9. English, Italian. PMID: 18493776 [PubMed - indexed for MEDLINE]Related articles

Safety and efficacy of gene transfer for Leber's congenital amaurosis.

Maguire AM, Simonelli F, Pierce EA, Pugh EN Jr, Mingozzi F, Bennicelli J, Banfi S, Marshall KA, Testa F, Surace EM, Rossi S, Lyubarsky A, Arruda VR, Konkle B, Stone E, Sun J, Jacobs J, Dell'Osso L, Hertle R, Ma JX, Redmond TM, Zhu X, Hauck B, Zelenaia O, Shindler KS, Maguire MG, Wright JF, Volpe NJ, McDonnell JW, Auricchio A, High KA, Bennett J.

N Engl J Med. 2008 May 22;358(21):2240-8. Epub 2008 Apr 27.PMID: 18441370 [PubMed - indexed for MEDLINE]Related articlesFree article

The O2-scavenging flavodiiron protein in the human parasite Giardia intestinalis.

Di Matteo A, Scandurra FM, Testa F, Forte E, Sarti P, Brunori M, Giuffrè A.

J Biol Chem. 2008 Feb 15;283(7):4061-8. Epub 2007 Dec 12.PMID: 18077462 [PubMed - indexed for MEDLINE]Related articlesFree article

Global cognitive function in children with epilepsy: a community-based study.

Berg AT, Langfitt JT, Testa FM, Levy SR, DiMario F, Westerveld M, Kulas J.

Epilepsia. 2008 Apr;49(4):608-14. Epub 2007 Dec 6.PMID: 18070088 [PubMed - indexed for MEDLINE]Related articles

Silica-based mesoporous materials as drug delivery system for methotrexate release.

Carino IS, Pasqua L, Testa F, Aiello R, Puoci F, Iemma F, Picci N.

Drug Deliv. 2007 Nov;14(8):491-5.PMID: 18027178 [PubMed - indexed for MEDLINE]Related articles

Intrafamilial clinical heterogeneity associated with a novel mutation of the retinal degeneration slow/peripherin gene.

Simonelli F, Testa F, Marini V, Interlandi E, Rossi S, Pognuz DR, Virgili G, Garrè C, Bandello F.

Ophthalmic Res. 2007;39(5):255-9. Epub 2007 Sep 12.PMID: 17851265 [PubMed - indexed for MEDLINE]Related articles

Clinical and molecular genetics of Leber's congenital amaurosis: a multicenter study of Italian patients.

Simonelli F, Ziviello C, Testa F, Rossi S, Fazzi E, Bianchi PE, Fossarello M, Signorini S, Bertone C, Galantuomo S, Brancati F, Valente EM, Ciccodicola A, Rinaldi E, Auricchio A, Banfi S.

Invest Ophthalmol Vis Sci. 2007 Sep;48(9):4284-90.PMID: 17724218 [PubMed - indexed for MEDLINE]Related articlesFree article

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.

J Fr Ophtalmol. 2007 Jun;30(6):616-20.PMID: 17646752 [PubMed - indexed for MEDLINE]Related articlesFree article

Behavior and social competency in idiopathic and cryptogenic childhood epilepsy.

Berg AT, Vickrey BG, Testa FM, Levy SR, Shinnar S, DiMario F.

Dev Med Child Neurol. 2007 Jul;49(7):487-92.PMID: 17593118 [PubMed - indexed for MEDLINE]Related articles

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 [PubMed - indexed for MEDLINE]Related articles

Polymorphism p.402Y>H in the complement factor H protein is a risk factor for age related macular degeneration in an Italian population.

Simonelli F, Frisso G, Testa F, di Fiore R, Vitale DF, Manitto MP, Brancato R, Rinaldi E, Sacchetti L.

Br J Ophthalmol. 2006 Sep;90(9):1142-5. Epub 2006 Jun 14.PMID: 16774956 [PubMed - indexed for MEDLINE]Related articlesFree article

Intra-arterial hepatic chemotherapy: management of liver tumors by percutaneous port-a-cath positioning.

Grosso M, Scarrone A, Pedrazzini F, Priotto R, Testa F, Lingua G, Mondino I, Zanon C.

J Exp Clin Cancer Res. 2003 Dec;22(4 Suppl):171-5.PMID: 16767926 [PubMed - indexed for MEDLINE]Related articles

How long does it take for epilepsy to become intractable? A prospective investigation.

Berg AT, Vickrey BG, Testa FM, Levy SR, Shinnar S, DiMario F, Smith S.

Ann Neurol. 2006 Jul;60(1):73-9.PMID: 16685695 [PubMed - indexed for MEDLINE]Related articles

Selective binding and enrichment for low-molecular weight biomarker molecules in human plasma after exposure to nanoporous silica particles.

Terracciano R, Gaspari M, Testa F, Pasqua L, Tagliaferri P, Cheng MM, Nijdam AJ, Petricoin EF, Liotta LA, Cuda G, Ferrari M, Venuta S.

Proteomics. 2006 Jun;6(11):3243-50.PMID: 16645983 [PubMed - indexed for MEDLINE]Related articles

Special education needs of children with newly diagnosed epilepsy.

Berg AT, Smith SN, Frobish D, Levy SR, Testa FM, Beckerman B, Shinnar S.

Dev Med Child Neurol. 2005 Nov;47(11):749-53.PMID: 16225738 [PubMed - indexed for MEDLINE]Related articles

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.

Br J Ophthalmol. 2005 Aug;89(8):1066-8. No abstract available. PMID: 16024869 [PubMed - indexed for MEDLINE]Related articlesFree article

Molecular genetics of autosomal dominant retinitis pigmentosa (ADRP): a comprehensive study of 43 Italian families.

Ziviello C, Simonelli F, Testa F, Anastasi M, Marzoli SB, Falsini B, Ghiglione D, Macaluso C, Manitto MP, Garrè C, Ciccodicola A, Rinaldi E, Banfi S.

J Med Genet. 2005 Jul;42(7):e47.PMID: 15994872 [PubMed - indexed for MEDLINE]Related articlesFree article

Genotype-phenotype correlation in Italian families with Stargardt disease.

Simonelli F, Testa F, Zernant J, Nesti A, Rossi S, Allikmets R, Rinaldi E.

Ophthalmic Res. 2005 May-Jun;37(3):159-67. Epub 2005 May 7.PMID: 15942264 [PubMed - indexed for MEDLINE]Related articles

Sleep episodes and daytime somnolence as result of individual susceptibility to different dopaminergic drugs in a PD patient: a polysomnographic study.

Romigi A, Brusa L, Marciani MG, Pierantozzi M, Placidi F, Izzi F, Sperli F, Testa F, Stanzione P.

J Neurol Sci. 2005 Jan 15;228(1):7-10. Epub 2004 Nov 10.PMID: 15607203 [PubMed - indexed for MEDLINE]Related articles

Mortality in childhood-onset epilepsy.

Berg AT, Shinnar S, Testa FM, Levy SR, Smith SN, Beckerman B.

Arch Pediatr Adolesc Med. 2004 Dec;158(12):1147-52.PMID: 15583099 [PubMed - indexed for MEDLINE]Related articlesFree article

Genetics of diabetic retinopathy.

Simonelli F, Testa F, Bandello F.

Semin Ophthalmol. 2001 Mar;16(1):41-51. Review. No abstract available. PMID: 15487697 [PubMed - indexed for MEDLINE]Related articles

Status epilepticus after the initial diagnosis of epilepsy in children.

Berg AT, Shinnar S, Testa FM, Levy SR, Frobish D, Smith SN, Beckerman B.

Neurology. 2004 Sep 28;63(6):1027-34.PMID: 15452294 [PubMed - indexed for MEDLINE]Related articles

Longitudinal assessment of adaptive behavior in infants and young children with newly diagnosed epilepsy: influences of etiology, syndrome, and seizure control.

Berg AT, Smith SN, Frobish D, Beckerman B, Levy SR, Testa FM, Shinnar S.

Pediatrics. 2004 Sep;114(3):645-50.PMID: 15342834 [PubMed - indexed for MEDLINE]Related articlesFree article

Modeling remission and relapse in pediatric epilepsy: application of a Markov process.

Berg AT, Lin J, Ebrahimi N, Testa FM, Levy SR, Shinnar S.

Epilepsy Res. 2004 Jun;60(1):31-40.PMID: 15279868 [PubMed - indexed for MEDLINE]Related articles

Drug delivery devices based on mesoporous silicate.

Cavallaro G, Pierro P, Palumbo FS, Testa F, Pasqua L, Aiello R.

Drug Deliv. 2004 Jan-Feb;11(1):41-6.PMID: 15168790 [PubMed - indexed for MEDLINE]Related articles

Association of a homozygous nonsense mutation in the ABCA4 (ABCR) gene with cone-rod dystrophy phenotype in an Italian family.

Simonelli F, Testa F, Zernant J, Nesti A, Rossi S, Rinaldi E, Allikmets R.

Ophthalmic Res. 2004 Mar-Apr;36(2):82-8.PMID: 15017103 [PubMed - indexed for MEDLINE]Related articles

Genotyping microarray (gene chip) for the ABCR (ABCA4) gene.

Jaakson K, Zernant J, Külm M, Hutchinson A, Tonisson N, Glavac D, Ravnik-Glavac M, Hawlina M, Meltzer MR, Caruso RC, Testa F, Maugeri A, Hoyng CB, Gouras P, Simonelli F, Lewis RA, Lupski JR, Cremers FP, Allikmets R.

Hum Mutat. 2003 Nov;22(5):395-403.PMID: 14517951 [PubMed - indexed for MEDLINE]Related articles

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.

Br J Ophthalmol. 2003 Sep;87(9):1130-4.PMID: 12928282 [PubMed - indexed for MEDLINE]Related articlesFree article

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.

Biochem Biophys Res Commun. 2003 Aug 29;308(3):414-21.PMID: 12914764 [PubMed - indexed for MEDLINE]Related articles

Hypothalamic hamartomas: seven cases and review of the literature.

Nguyen D, Singh S, Zaatreh M, Novotny E, Levy S, Testa F, Spencer SS.

Epilepsy Behav. 2003 Jun;4(3):246-58.PMID: 12791326 [PubMed - indexed for MEDLINE]Related articles

Characterization of MPP4, a gene highly expressed in photoreceptor cells, and mutation analysis in retinitis pigmentosa.

Conte I, Lestingi M, den Hollander A, Miano MG, Alfano G, Circolo D, Pugliese M, Testa F, Simonelli F, Rinaldi E, Baiget M, Banfi S, Ciccodicola A.

Gene. 2002 Sep 4;297(1-2):33-8.PMID: 12384283 [PubMed - indexed for MEDLINE]Related articles

An Italian family affected by autosomal dominant microcephaly with chorioretinal degeneration.

Simonell F, Testa F, Nesti A, de Crecchio G, Bifani M, Cavaliere ML, Rinaldi E, Rinaldi MM.

J Pediatr Ophthalmol Strabismus. 2002 Sep-Oct;39(5):288-92. Review.PMID: 12353901 [PubMed - indexed for MEDLINE]Related articles

[Heart surgery interventions in chronic dialysis patients: short- and long-term results]

Luciani N, Nasso G, D'Alessandro C, Testa F, Glieca F, Gaudino M, Possati G.

Ital Heart J Suppl. 2002 Jul;3(7):746-52. Italian. PMID: 12187635 [PubMed - indexed for MEDLINE]Related articles

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.

Clin Chim Acta. 2002 Jun;320(1-2):111-5.PMID: 11983208 [PubMed - indexed for MEDLINE]Related articles

The ABCA4 2588G>C Stargardt mutation: single origin and increasing frequency from South-West to North-East Europe.

Maugeri A, Flothmann K, Hemmrich N, Ingvast S, Jorge P, Paloma E, Patel R, Rozet JM, Tammur J, Testa F, Balcells S, Bird AC, Brunner HG, Hoyng CB, Metspalu A, Simonelli F, Allikmets R, Bhattacharya SS, D'Urso M, Gonzàlez-Duarte R, Kaplan J, te Meerman GJ, Santos R, Schwartz M, Van Camp G, Wadelius C, Weber BH, Cremers FP.

Eur J Hum Genet. 2002 Mar;10(3):197-203.PMID: 11973624 [PubMed - indexed for MEDLINE]Related articlesFree article

Two-year remission and subsequent relapse in children with newly diagnosed epilepsy.

Berg AT, Shinnar S, Levy SR, Testa FM, Smith-Rapaport S, Beckerman B, Ebrahimi N.

Epilepsia. 2001 Dec;42(12):1553-62. Erratum in: Epilepsia 2002 Feb;43(2):207-8. PMID: 11879366 [PubMed - indexed for MEDLINE]Related articles

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.

Ophthalmic Res. 2001 Nov-Dec;33(6):325-8.PMID: 11721184 [PubMed - indexed for MEDLINE]Related articles

Properties of Portland cement--stabilised MSWI fly ashes.

Polettini A, Pomi R, Sirini P, Testa F.

J Hazard Mater. 2001 Nov 16;88(1):123-38.PMID: 11606245 [PubMed - indexed for MEDLINE]Related articles

Identification of novel RP2 mutations in a subset of X-linked retinitis pigmentosa families and prediction of new domains.

Miano MG, Testa F, Filippini F, Trujillo M, Conte I, Lanzara C, Millán JM, De Bernardo C, Grammatico B, Mangino M, Torrente I, Carrozzo R, Simonelli F, Rinaldi E, Ventruto V, D'Urso M, Ayuso C, Ciccodicola A.

Hum Mutat. 2001 Aug;18(2):109-19.PMID: 11462235 [PubMed - indexed for MEDLINE]Related articles

Early development of intractable epilepsy in children: a prospective study.

Berg AT, Shinnar S, Levy SR, Testa FM, Smith-Rapaport S, Beckerman B.

Neurology. 2001 Jun 12;56(11):1445-52. Erratum in: Neurology 2001 Sep 11;57(5):939. PMID: 11402099 [PubMed - indexed for MEDLINE]Related articles

Defining early seizure outcomes in pediatric epilepsy: the good, the bad and the in-between.

Berg AT, Shinnar S, Levy SR, Testa FM, Smith-Rapaport S, Beckerman B, Ebrahimi N.

Epilepsy Res. 2001 Jan;43(1):75-84.PMID: 11137389 [PubMed - indexed for MEDLINE]Related articles

How well can epilepsy syndromes be identified at diagnosis? A reassessment 2 years after initial diagnosis.

Berg AT, Shinnar S, Levy SR, Testa FM, Smith-Rapaport S, Beckerman B.

Epilepsia. 2000 Oct;41(10):1269-75.PMID: 11051121 [PubMed - indexed for MEDLINE]Related articles

Liebenberg syndrome: brachydactyly with joint dysplasia (MIM 186550): a second family.

Tiberio G, Diglio MC, Graziani M, Testa F, Giannotti A.

J Med Genet. 2000 Jul;37(7):548-51. No abstract available. PMID: 10970192 [PubMed - indexed for MEDLINE]Related articlesFree article

Neuroimaging in children with newly diagnosed epilepsy: A community-based study.

Berg AT, Testa FM, Levy SR, Shinnar S.

Pediatrics. 2000 Sep;106(3):527-32.PMID: 10969098 [PubMed - indexed for MEDLINE]Related articles