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Page 1
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion.
Chiò A, Mora G, Sabatelli M, Caponnetto C, Lunetta C, Traynor BJ, Johnson JO, Nalls MA, Calvo A, Moglia C, Borghero G, Trojsi F, La Bella V, Volanti P, Simone I, Salvi F, Logullo FO, Riva N, Carrera P, Giannini F, Mandrioli J, Tanel R, Capasso M, Tremolizzo L, Battistini S, Murru MR, Origone P, Zollino M, Penco S; ITALSGEN consortium; SARDINIALS consortium; Mazzini L, D'Alfonso S, Restagno G, Brunetti M, Barberis M, Conforti FL. Chiò A, et al. Among authors: penco s. Neurobiol Aging. 2016 Mar;39:218.e5-8. doi: 10.1016/j.neurobiolaging.2015.11.027. Epub 2015 Dec 8. Neurobiol Aging. 2016. PMID: 26733254 Free PMC article.
An Italian dominant FALS Leu144Phe SOD1 mutation: genotype-phenotype correlation.
Ferrera L, Caponnetto C, Marini V, Rizzi D, Bordo D, Penco S, Amoroso A, Origone P, Garrè C. Ferrera L, et al. Among authors: penco s. Amyotroph Lateral Scler Other Motor Neuron Disord. 2003 Sep;4(3):167-70. doi: 10.1080/aml.4.3.167.170. Amyotroph Lateral Scler Other Motor Neuron Disord. 2003. PMID: 13129804
SOD1 mutations in amyotrophic lateral sclerosis. Results from a multicenter Italian study.
Battistini S, Giannini F, Greco G, Bibbò G, Ferrera L, Marini V, Causarano R, Casula M, Lando G, Patrosso MC, Caponnetto C, Origone P, Marocchi A, Del Corona A, Siciliano G, Carrera P, Mascia V, Giagheddu M, Carcassi C, Orrù S, Garrè C, Penco S. Battistini S, et al. Among authors: penco s. J Neurol. 2005 Jul;252(7):782-8. doi: 10.1007/s00415-005-0742-y. Epub 2005 Mar 29. J Neurol. 2005. PMID: 15789135
Variations in the coding and regulatory sequences of the angiogenin (ANG) gene are not associated to ALS (amyotrophic lateral sclerosis) in the Italian population.
Corrado L, Battistini S, Penco S, Bergamaschi L, Testa L, Ricci C, Giannini F, Greco G, Patrosso MC, Pileggi S, Causarano R, Mazzini L, Momigliano-Richiardi P, D'Alfonso S. Corrado L, et al. Among authors: penco s. J Neurol Sci. 2007 Jul 15;258(1-2):123-7. doi: 10.1016/j.jns.2007.03.009. Epub 2007 Apr 25. J Neurol Sci. 2007. PMID: 17462671
No association of DPP6 with amyotrophic lateral sclerosis in an Italian population.
Fogh I, D'Alfonso S, Gellera C, Ratti A, Cereda C, Penco S, Corrado L, Sorarù G, Castellotti B, Tiloca C, Gagliardi S, Cozzi L, Lupton MK, Ticozzi N, Mazzini L, Shaw CE, Al-Chalabi A, Powell J, Silani V. Fogh I, et al. Among authors: penco s. Neurobiol Aging. 2011 May;32(5):966-7. doi: 10.1016/j.neurobiolaging.2009.05.014. Epub 2009 Jun 13. Neurobiol Aging. 2011. PMID: 19525032
Mutations of FUS gene in sporadic amyotrophic lateral sclerosis.
Corrado L, Del Bo R, Castellotti B, Ratti A, Cereda C, Penco S, Sorarù G, Carlomagno Y, Ghezzi S, Pensato V, Colombrita C, Gagliardi S, Cozzi L, Orsetti V, Mancuso M, Siciliano G, Mazzini L, Comi GP, Gellera C, Ceroni M, D'Alfonso S, Silani V. Corrado L, et al. Among authors: penco s. J Med Genet. 2010 Mar;47(3):190-4. doi: 10.1136/jmg.2009.071027. Epub 2009 Oct 26. J Med Genet. 2010. PMID: 19861302
Cavernous malformation of the optic nerve mimicking optic neuritis.
Cerase A, Franceschini R, Battistini S, Maria Vallone I, Penco S, Venturi C. Cerase A, et al. Among authors: penco s. J Neuroophthalmol. 2010 Jun;30(2):126-31. doi: 10.1097/WNO.0b013e3181ceb428. J Neuroophthalmol. 2010. PMID: 20351573
Lack of association of PON polymorphisms with sporadic ALS in an Italian population.
Ricci C, Battistini S, Cozzi L, Benigni M, Origone P, Verriello L, Lunetta C, Cereda C, Milani P, Greco G, Patrosso MC, Causarano R, Caponnetto C, Giannini F, Corbo M, Penco S. Ricci C, et al. Among authors: penco s. Neurobiol Aging. 2011 Mar;32(3):552.e7-13. doi: 10.1016/j.neurobiolaging.2010.02.010. Epub 2010 Apr 9. Neurobiol Aging. 2011. PMID: 20381198
237 results