Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1955 5
1956 2
1957 1
1958 5
1959 4
1966 2
1967 4
1969 2
1970 2
1971 5
1973 2
1975 2
1978 1
1979 5
1980 1
1981 4
1982 1
1988 3
1989 4
1990 6
1991 1
1992 5
1993 3
1994 3
1995 8
1996 7
1997 2
1998 3
1999 9
2000 5
2001 12
2002 7
2003 6
2004 10
2005 7
2006 6
2007 11
2008 14
2009 9
2010 16
2011 18
2012 20
2013 9
2014 15
2015 17
2016 19
2017 14
2018 12
2019 11
2020 22
2021 19
2022 14
2023 15
2024 10
2025 9

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

392 results

Results by year

Filters applied: . Clear all
Page 1
Hereditary transthyretin amyloidosis overview.
Manganelli F, Fabrizi GM, Luigetti M, Mandich P, Mazzeo A, Pareyson D. Manganelli F, et al. Among authors: fabrizi gm. Neurol Sci. 2022 Dec;43(Suppl 2):595-604. doi: 10.1007/s10072-020-04889-2. Epub 2020 Nov 14. Neurol Sci. 2022. PMID: 33188616 Free PMC article. Review.
Acquired progressive hyperpigmentation.
Pagliarello C, Fabrizi G, Ricci R, Besagni F, DE Felici B, Boccaletti V, Feliciani C, DI Nuzzo S. Pagliarello C, et al. Among authors: fabrizi g. G Ital Dermatol Venereol. 2017 Jun;152(3):312-314. doi: 10.23736/S0392-0488.16.05195-6. G Ital Dermatol Venereol. 2017. PMID: 28409580 No abstract available.
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: fabrizi gm. Eur J Neurol. 2023 Aug;30(8):2461-2470. doi: 10.1111/ene.15860. Epub 2023 May 26. Eur J Neurol. 2023. PMID: 37170966
Role of the repeat expansion size in predicting age of onset and severity in RFC1 disease.
Currò R, Dominik N, Facchini S, Vegezzi E, Sullivan R, Galassi Deforie V, Fernández-Eulate G, Traschütz A, Rossi S, Garibaldi M, Kwarciany M, Taroni F, Brusco A, Good JM, Cavalcanti F, Hammans S, Ravenscroft G, Roxburgh RH; RFC1 repeat expansion study group; Parolin Schnekenberg R, Rugginini B, Abati E, Manini A, Quartesan I, Ghia A, Lòpez de Munaìn A, Manganelli F, Kennerson M, Santorelli FM, Infante J, Marques W, Jokela M, Murphy SM, Mandich P, Fabrizi GM, Briani C, Gosal D, Pareyson D, Ferrari A, Prados F, Yousry T, Khurana V, Kuo SH, Miller J, Troakes C, Jaunmuktane Z, Giunti P, Hartmann A, Basak N, Synofzik M, Stojkovic T, Hadjivassiliou M, Reilly MM, Houlden H, Cortese A. Currò R, et al. Among authors: fabrizi gm. Brain. 2024 May 3;147(5):1887-1898. doi: 10.1093/brain/awad436. Brain. 2024. PMID: 38193360 Free PMC article.
An update on juvenile dermatomyositis.
Boccaletti V, Di Nuzzo S, Feliciani C, Fabrizi G, Pagliarello C. Boccaletti V, et al. Among authors: fabrizi g. G Ital Dermatol Venereol. 2014 Oct;149(5):519-24. Epub 2014 Jul 18. G Ital Dermatol Venereol. 2014. PMID: 25034096 Review.
Hereditary neuropathies: A pathological perspective.
Cavallaro T, Tagliapietra M, Fabrizi GM, Bai Y, Shy ME, Vallat JM. Cavallaro T, et al. Among authors: fabrizi gm. J Peripher Nerv Syst. 2021 Nov;26 Suppl 2:S42-S60. doi: 10.1111/jns.12467. J Peripher Nerv Syst. 2021. PMID: 34499384
Cytochrome c oxidase deficiency.
DiMauro S, Lombes A, Nakase H, Mita S, Fabrizi GM, Tritschler HJ, Bonilla E, Miranda AF, DeVivo DC, Schon EA. DiMauro S, et al. Among authors: fabrizi gm. Pediatr Res. 1990 Nov;28(5):536-41. doi: 10.1203/00006450-199011000-00025. Pediatr Res. 1990. PMID: 2175026 Review.
Total Synthesis of (±)-Kuwanol E.
Iovine V, Benni I, Sabia R, D'Acquarica I, Fabrizi G, Botta B, Calcaterra A. Iovine V, et al. Among authors: fabrizi g. J Nat Prod. 2016 Oct 28;79(10):2495-2503. doi: 10.1021/acs.jnatprod.6b00350. Epub 2016 Sep 22. J Nat Prod. 2016. PMID: 27656763
CIDP, CMT1B, or CMT1B plus CIDP?
Cardellini D, Zanette G, Taioli F, Bertolasi L, Ferrari S, Cavallaro T, Fabrizi GM. Cardellini D, et al. Among authors: fabrizi gm. Neurol Sci. 2021 Mar;42(3):1127-1130. doi: 10.1007/s10072-020-04789-5. Epub 2020 Oct 18. Neurol Sci. 2021. PMID: 33070202
392 results