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Year Number of Results
1980 1
1985 1
1987 1
1988 1
1990 1
1992 1
1997 1
2000 2
2001 2
2003 1
2004 1
2006 1
2007 2
2008 2
2010 2
2011 1
2012 2
2013 4
2014 3
2015 3
2016 1
2017 3
2018 2
2019 4
2020 8
2021 7
2022 6
2023 4
2024 5

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65 results

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Page 1
Natural history of Charcot-Marie-Tooth disease type 2A: a large international multicentre study.
Pipis M, Feely SME, Polke JM, Skorupinska M, Perez L, Shy RR, Laura M, Morrow JM, Moroni I, Pisciotta C, Taroni F, Vujovic D, Lloyd TE, Acsadi G, Yum SW, Lewis RA, Finkel RS, Herrmann DN, Day JW, Li J, Saporta M, Sadjadi R, Walk D, Burns J, Muntoni F, Ramchandren S, Horvath R, Johnson NE, Züchner S, Pareyson D, Scherer SS, Rossor AM, Shy ME, Reilly MM; Inherited Neuropathies Consortium - Rare Disease Clinical Research Network (INC-RDCRN). Pipis M, et al. Brain. 2020 Dec 1;143(12):3589-3602. doi: 10.1093/brain/awaa323. Brain. 2020. PMID: 33415332 Free PMC article.
CADASIL: Treatment and Management Options.
Bersano A, Bedini G, Oskam J, Mariotti C, Taroni F, Baratta S, Parati EA. Bersano A, et al. Among authors: baratta s. Curr Treat Options Neurol. 2017 Sep;19(9):31. doi: 10.1007/s11940-017-0468-z. Curr Treat Options Neurol. 2017. PMID: 28741120 Review.
Cardiac Children's Hospital Early Warning Score: Italian Validation.
Simeone S, Platone N, Serra N, Assanta N, Guillari A, Rea T, Pucciarelli G, Da Valle P, Gargiulo G, Baratta S, McLellan M. Simeone S, et al. Among authors: baratta s. J Pediatr Nurs. 2020 Mar-Apr;51:e21-e26. doi: 10.1016/j.pedn.2019.06.011. Epub 2019 Jun 28. J Pediatr Nurs. 2020. PMID: 31262605
Clinical spectrum and frequency of Charcot-Marie-Tooth disease in Italy: Data from the National CMT Registry.
Pisciotta C, Bertini A, Tramacere I, Manganelli F, Fabrizi GM, Schenone A, Tozza S, Cavallaro T, Taioli F, Ferrarini M, Grandis M, Bellone E, Mandich P, Previtali SC, Falzone Y, Allegri I, Padua L, Pazzaglia C, Quattrone A, Valentino P, Gentile L, Russo M, Calabrese D, Moroni I, Pagliano E, Saveri P, Magri S, Baratta S, Taroni F, Mazzeo A, Santoro L, Vita G, Pareyson D; Italian CMT Network. Pisciotta C, et al. Among authors: baratta s. Eur J Neurol. 2023 Aug;30(8):2461-2470. doi: 10.1111/ene.15860. Epub 2023 May 26. Eur J Neurol. 2023. PMID: 37170966
Genetic analysis and natural history of Charcot-Marie-Tooth disease CMTX1 due to GJB1 variants.
Record CJ, Skorupinska M, Laura M, Rossor AM, Pareyson D, Pisciotta C, Feely SME, Lloyd TE, Horvath R, Sadjadi R, Herrmann DN, Li J, Walk D, Yum SW, Lewis RA, Day J, Burns J, Finkel RS, Saporta MA, Ramchandren S, Weiss MD, Acsadi G, Fridman V, Muntoni F, Poh R, Polke JM, Zuchner S, Shy ME, Scherer SS, Reilly MM; Inherited Neuropathies Consortium—Rare Disease Clinical Research Network. Record CJ, et al. Brain. 2023 Oct 3;146(10):4336-4349. doi: 10.1093/brain/awad187. Brain. 2023. PMID: 37284795 Free PMC article.
Hypomyelinating leukodystrophies in adults: Clinical and genetic features.
Di Bella D, Magri S, Benzoni C, Farina L, Maccagnano C, Sarto E, Moscatelli M, Baratta S, Ciano C, Piacentini SHMJ, Draghi L, Mauro E, Pareyson D, Gellera C, Taroni F, Salsano E. Di Bella D, et al. Among authors: baratta s. Eur J Neurol. 2021 Mar;28(3):934-944. doi: 10.1111/ene.14646. Epub 2020 Dec 3. Eur J Neurol. 2021. PMID: 33190326
[Specific pharmacological treatment guide for transthyretin amyloid cardiomyopathy, 2021].
Villanueva E, Carretero M, Aguirre MA, Negro A, Belziti CA, Posadas-Martínez ML, Nucifora EM, Baratta S, Costabel JP, Higa C, Rivas C, Fernández A, Quiroga A, Dumont CA, Volberg VI, Streitenberg GM, Perez de Arenaza D. Villanueva E, et al. Among authors: baratta s. Medicina (B Aires). 2022;82(2):275-288. Medicina (B Aires). 2022. PMID: 35417392 Free article. Spanish.
65 results