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

Year Number of Results
1990 1
1992 1
1993 1
1994 1
1995 3
1996 3
1997 4
1998 1
2000 1
2003 1
2005 1
2006 1
2008 1
2010 1
2012 1
2013 1
2014 1
2015 2
2016 1
2018 1
2019 1
2020 3
2021 3
2022 1
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35 results
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Page 1
Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion.
Campuzano V, Montermini L, Moltò MD, Pianese L, Cossée M, Cavalcanti F, Monros E, Rodius F, Duclos F, Monticelli A, Zara F, Cañizares J, Koutnikova H, Bidichandani SI, Gellera C, Brice A, Trouillas P, De Michele G, Filla A, De Frutos R, Palau F, Patel PI, Di Donato S, Mandel JL, Cocozza S, Koenig M, Pandolfo M. Campuzano V, et al. Science. 1996 Mar 8;271(5254):1423-7. doi: 10.1126/science.271.5254.1423. Science. 1996. PMID: 8596916
Frataxin fracas.
Cossée M, Campuzano V, Koutnikova H, Fischbeck K, Mandel JL, Koenig M, Bidichandani SI, Patel PI, Moltè MD, Cañizares J, De Frutos R, Pianese L, Cavalcanti F, Monticelli A, Cocozza S, Montermini L, Pandolfo M. Cossée M, et al. Among authors: campuzano v. Nat Genet. 1997 Apr;15(4):337-8. doi: 10.1038/ng0497-337. Nat Genet. 1997. PMID: 9090376 No abstract available.
Altered Neocortical Dynamics in a Mouse Model of Williams-Beuren Syndrome.
Dasilva M, Navarro-Guzman A, Ortiz-Romero P, Camassa A, Muñoz-Cespedes A, Campuzano V, Sanchez-Vives MV. Dasilva M, et al. Among authors: campuzano v. Mol Neurobiol. 2020 Feb;57(2):765-777. doi: 10.1007/s12035-019-01732-4. Epub 2019 Aug 30. Mol Neurobiol. 2020. PMID: 31471877 Free PMC article.
[Williams syndrome: its clinical aspects and molecular bases].
Antonell A, Del Campo M, Flores R, Campuzano V, Perez-Jurado LA. Antonell A, et al. Among authors: campuzano v. Rev Neurol. 2006 Jan 7;42 Suppl 1:S69-75. Rev Neurol. 2006. PMID: 16506136 Free article. Review. Spanish.
Anti-TGFβ (Transforming Growth Factor β) Therapy With Betaglycan-Derived P144 Peptide Gene Delivery Prevents the Formation of Aortic Aneurysm in a Mouse Model of Marfan Syndrome.
Arce C, Rodríguez-Rovira I, De Rycke K, Durán K, Campuzano V, Fabregat I, Jiménez-Altayó F, Berraondo P, Egea G. Arce C, et al. Among authors: campuzano v. Arterioscler Thromb Vasc Biol. 2021 Sep;41(9):e440-e452. doi: 10.1161/ATVBAHA.121.316496. Epub 2021 Jun 24. Arterioscler Thromb Vasc Biol. 2021. PMID: 34162229 Free article.
Metabolic abnormalities in Williams-Beuren syndrome.
Palacios-Verdú MG, Segura-Puimedon M, Borralleras C, Flores R, Del Campo M, Campuzano V, Pérez-Jurado LA. Palacios-Verdú MG, et al. Among authors: campuzano v. J Med Genet. 2015 Apr;52(4):248-55. doi: 10.1136/jmedgenet-2014-102713. Epub 2015 Feb 6. J Med Genet. 2015. PMID: 25663682
35 results