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Molecular Genetics and Interferon Signature in the Italian Aicardi Goutières Syndrome Cohort: Report of 12 New Cases and Literature Review.
Garau J, Cavallera V, Valente M, Tonduti D, Sproviero D, Zucca S, Battaglia D, Battini R, Bertini E, Cappanera S, Chiapparini L, Crasà C, Crichiutti G, Dalla Giustina E, D'Arrigo S, De Giorgis V, De Simone M, Galli J, La Piana R, Messana T, Moroni I, Nardocci N, Panteghini C, Parazzini C, Pichiecchio A, Pini A, Ricci F, Saletti V, Salvatici E, Santorelli FM, Sartori S, Tinelli F, Uggetti C, Veneselli E, Zorzi G, Garavaglia B, Fazzi E, Orcesi S, Cereda C. Garau J, et al. Among authors: tinelli f. J Clin Med. 2019 May 26;8(5):750. doi: 10.3390/jcm8050750. J Clin Med. 2019. PMID: 31130681 Free PMC article.
Patient-reported outcomes measure for children born preterm: validation of the SOLE VLBWI Questionnaire, a new quality of life self-assessment tool.
Olivieri I, M Bova S, Fazzi E, Ricci D, Tinelli F, Montomoli C, Rezzani C, Balottin U, Orcesi S; SOLE VLBWI Questionnaire Study Group. Olivieri I, et al. Among authors: tinelli f. Dev Med Child Neurol. 2016 Sep;58(9):957-64. doi: 10.1111/dmcn.13122. Epub 2016 Apr 7. Dev Med Child Neurol. 2016. PMID: 27061508 Free article.
Next Generation Molecular Diagnosis of Hereditary Spastic Paraplegias: An Italian Cross-Sectional Study.
D'Amore A, Tessa A, Casali C, Dotti MT, Filla A, Silvestri G, Antenora A, Astrea G, Barghigiani M, Battini R, Battisti C, Bruno I, Cereda C, Dato C, Di Iorio G, Donadio V, Felicori M, Fini N, Fiorillo C, Gallone S, Gemignani F, Gigli GL, Graziano C, Guerrini R, Gurrieri F, Kariminejad A, Lieto M, Marques LourenḈo C, Malandrini A, Mandich P, Marcotulli C, Mari F, Massacesi L, Melone MAB, Mignarri A, Milone R, Musumeci O, Pegoraro E, Perna A, Petrucci A, Pini A, Pochiero F, Pons MR, Ricca I, Rossi S, Seri M, Stanzial F, Tinelli F, Toscano A, Valente M, Federico A, Rubegni A, Santorelli FM. D'Amore A, et al. Among authors: tinelli f. Front Neurol. 2018 Dec 4;9:981. doi: 10.3389/fneur.2018.00981. eCollection 2018. Front Neurol. 2018. PMID: 30564185 Free PMC article.
Vascular Remodeling in Moyamoya Angiopathy: From Peripheral Blood Mononuclear Cells to Endothelial Cells.
Tinelli F, Nava S, Arioli F, Bedini G, Scelzo E, Lisini D, Faragò G, Gioppo A, Ciceri EF, Acerbi F, Ferroli P, Vetrano IG, Esposito S, Saletti V, Pantaleoni C, Zibordi F, Nardocci N, Zedde ML, Pezzini A, Di Lazzaro V, Capone F, Dell'Acqua ML, Vajkoczy P, Tournier-Lasserve E, Parati EA, Bersano A, Gatti L. Tinelli F, et al. Int J Mol Sci. 2020 Aug 11;21(16):5763. doi: 10.3390/ijms21165763. Int J Mol Sci. 2020. PMID: 32796702 Free PMC article.
NGS in Hereditary Ataxia: When Rare Becomes Frequent.
Galatolo D, De Michele G, Silvestri G, Leuzzi V, Casali C, Musumeci O, Antenora A, Astrea G, Barghigiani M, Battini R, Battisti C, Caputi C, Cioffi E, De Michele G, Dotti MT, Fico T, Fiorillo C, Galosi S, Lieto M, Malandrini A, Melone MAB, Mignarri A, Natale G, Pegoraro E, Petrucci A, Ricca I, Riso V, Rossi S, Rubegni A, Scarlatti A, Tinelli F, Trovato R, Tedeschi G, Tessa A, Filla A, Santorelli FM. Galatolo D, et al. Among authors: tinelli f. Int J Mol Sci. 2021 Aug 6;22(16):8490. doi: 10.3390/ijms22168490. Int J Mol Sci. 2021. PMID: 34445196 Free PMC article.
Neurodevelopmental evolution of West syndrome: a 2-year prospective study.
Guzzetta F, Cioni G, Mercuri E, Fazzi E, Biagioni E, Veggiotti P, Bancale A, Baranello G, Epifanio R, Frisone MF, Guzzetta A, La Torre G, Mannocci A, Randò T, Ricci D, Signorini S, Tinelli F. Guzzetta F, et al. Among authors: tinelli f. Eur J Paediatr Neurol. 2008 Sep;12(5):387-97. doi: 10.1016/j.ejpn.2007.10.008. Epub 2007 Dec 11. Eur J Paediatr Neurol. 2008. PMID: 18063397
115 results