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Page 1
Retinal Photoreceptor Functions Are Compromised in Patients With Resistance to Thyroid Hormone Syndrome (RTHβ).
Campi I, Cammarata G, Bianchi Marzoli S, Beck-Peccoz P, Santarsiero D, Dazzi D, Bottari de Castello A, Taroni EG, Viola F, Mian C, Watutantrige-Fernando S, Pelusi C, Muzza M, Maffini MA, Persani L. Campi I, et al. Among authors: bianchi marzoli s. J Clin Endocrinol Metab. 2017 Jul 1;102(7):2620-2627. doi: 10.1210/jc.2016-3671. J Clin Endocrinol Metab. 2017. PMID: 28379567
Distributed abnormalities of brain white matter architecture in patients with dominant optic atrophy and OPA1 mutations.
Rocca MA, Bianchi-Marzoli S, Messina R, Cascavilla ML, Zeviani M, Lamperti C, Milesi J, Carta A, Cammarata G, Leocani L, Lamantea E, Bandello F, Comi G, Falini A, Filippi M. Rocca MA, et al. Among authors: bianchi marzoli s. J Neurol. 2015 May;262(5):1216-27. doi: 10.1007/s00415-015-7696-5. Epub 2015 Mar 21. J Neurol. 2015. PMID: 25794858
Leber's Hereditary Optic Neuropathy: A Report on Novel mtDNA Pathogenic Variants.
Peverelli L, Catania A, Marchet S, Ciasca P, Cammarata G, Melzi L, Bellino A, Fancellu R, Lamantea E, Capristo M, Caporali L, La Morgia C, Carelli V, Ghezzi D, Bianchi Marzoli S, Lamperti C. Peverelli L, et al. Among authors: bianchi marzoli s. Front Neurol. 2021 Jun 9;12:657317. doi: 10.3389/fneur.2021.657317. eCollection 2021. Front Neurol. 2021. PMID: 34177762 Free PMC article.
Adult-onset leukodystrophy with vanishing white matter: a case series of 19 patients.
Benzoni C, Moscatelli M, Farina L, Magri S, Ciano C, Scaioli V, Alverà S, Cammarata G, Bianchi-Marzoli S, Castellani M, Zito FM, Marotta G, Piacentini S, Villacara A, Mantegazza R, Gellera C, Durães J, Gouveia A, Matos A, do Carmo Macário M, Pareyson D, Taroni F, Di Bella D, Salsano E. Benzoni C, et al. Among authors: bianchi marzoli s. J Neurol. 2023 Sep;270(9):4219-4234. doi: 10.1007/s00415-023-11762-7. Epub 2023 May 12. J Neurol. 2023. PMID: 37171481
Early macular retinal ganglion cell loss in dominant optic atrophy: genotype-phenotype correlation.
Barboni P, Savini G, Cascavilla ML, Caporali L, Milesi J, Borrelli E, La Morgia C, Valentino ML, Triolo G, Lembo A, Carta A, De Negri A, Sadun F, Rizzo G, Parisi V, Pierro L, Bianchi Marzoli S, Zeviani M, Sadun AA, Bandello F, Carelli V. Barboni P, et al. Among authors: bianchi marzoli s. Am J Ophthalmol. 2014 Sep;158(3):628-36.e3. doi: 10.1016/j.ajo.2014.05.034. Epub 2014 Jun 5. Am J Ophthalmol. 2014. PMID: 24907432
Retinal dysfunction characterizes subtypes of dominant optic atrophy.
Cascavilla ML, Parisi V, Triolo G, Ziccardi L, Borrelli E, Di Renzo A, Balducci N, Lamperti C, Bianchi Marzoli S, Darvizeh F, Sadun AA, Carelli V, Bandello F, Barboni P. Cascavilla ML, et al. Among authors: bianchi marzoli s. Acta Ophthalmol. 2018 Mar;96(2):e156-e163. doi: 10.1111/aos.13557. Epub 2017 Sep 19. Acta Ophthalmol. 2018. PMID: 28926202 Free article.
Genotype-phenotype and OCT correlations in Autosomal Dominant Optic Atrophy related to OPA1 gene mutations: Report of 13 Italian families.
Pretegiani E, Rosini F, Rufa A, Gallus GN, Cardaioli E, Da Pozzo P, Bianchi S, Serchi V, Collura M, Franceschini R, Bianchi Marzoli S, Dotti MT, Federico A. Pretegiani E, et al. Among authors: bianchi s, bianchi marzoli s. J Neurol Sci. 2017 Nov 15;382:29-35. doi: 10.1016/j.jns.2017.09.018. Epub 2017 Sep 14. J Neurol Sci. 2017. PMID: 29111013
Optical coherence tomography is a useful tool in the differentiation between true edema and pseudoedema of the optic disc.
Carta A, Mora P, Aldigeri R, Gozzi F, Favilla S, Tedesco S, Calzetti G, Farci R, Barboni P, Bianchi-Marzoli S, Fossarello M, Gandolfi S, Sadun AA. Carta A, et al. Among authors: bianchi marzoli s. PLoS One. 2018 Nov 29;13(11):e0208145. doi: 10.1371/journal.pone.0208145. eCollection 2018. PLoS One. 2018. PMID: 30496251 Free PMC article.
47 results