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Page 1
Panencephalopathic Creutzfeldt-Jakob disease with distinct pattern of prion protein deposition in a patient with D178N mutation and homozygosity for valine at codon 129 of the prion protein Gene.
Marcon G, Indaco A, Di Fede G, Suardi S, Finato N, Moretti V, Micoli S, Fociani P, Zerbi P, Pincherle A, Redaelli V, Tagliavini F, Giaccone G. Marcon G, et al. Among authors: suardi s. Brain Pathol. 2014 Mar;24(2):148-51. doi: 10.1111/bpa.12095. Epub 2013 Nov 27. Brain Pathol. 2014. PMID: 24118545 Free PMC article.
MM2-thalamic Creutzfeldt-Jakob disease: neuropathological, biochemical and transmission studies identify a distinctive prion strain.
Moda F, Suardi S, Di Fede G, Indaco A, Limido L, Vimercati C, Ruggerone M, Campagnani I, Langeveld J, Terruzzi A, Brambilla A, Zerbi P, Fociani P, Bishop MT, Will RG, Manson JC, Giaccone G, Tagliavini F. Moda F, et al. Among authors: suardi s. Brain Pathol. 2012 Sep;22(5):662-9. doi: 10.1111/j.1750-3639.2012.00572.x. Epub 2012 Feb 21. Brain Pathol. 2012. PMID: 22288561 Free PMC article.
A novel phenotype of sporadic Creutzfeldt-Jakob disease.
Giaccone G, Di Fede G, Mangieri M, Limido L, Capobianco R, Suardi S, Grisoli M, Binelli S, Fociani P, Bugiani O, Tagliavini F. Giaccone G, et al. Among authors: suardi s. J Neurol Neurosurg Psychiatry. 2007 Dec;78(12):1379-82. doi: 10.1136/jnnp.2007.115444. J Neurol Neurosurg Psychiatry. 2007. PMID: 18024694 Free PMC article.
Doxycycline in Creutzfeldt-Jakob disease: a phase 2, randomised, double-blind, placebo-controlled trial.
Haïk S, Marcon G, Mallet A, Tettamanti M, Welaratne A, Giaccone G, Azimi S, Pietrini V, Fabreguettes JR, Imperiale D, Cesaro P, Buffa C, Aucan C, Lucca U, Peckeu L, Suardi S, Tranchant C, Zerr I, Houillier C, Redaelli V, Vespignani H, Campanella A, Sellal F, Krasnianski A, Seilhean D, Heinemann U, Sedel F, Canovi M, Gobbi M, Di Fede G, Laplanche JL, Pocchiari M, Salmona M, Forloni G, Brandel JP, Tagliavini F. Haïk S, et al. Among authors: suardi s. Lancet Neurol. 2014 Feb;13(2):150-8. doi: 10.1016/S1474-4422(13)70307-7. Epub 2014 Jan 8. Lancet Neurol. 2014. PMID: 24411709 Clinical Trial.
Sporadic Creutzfeldt-Jakob disease: the extent of microglia activation is dependent on the biochemical type of PrPSc.
Puoti G, Giaccone G, Mangieri M, Limido L, Fociani P, Zerbi P, Suardi S, Rossi G, Iussich S, Capobianco R, Di Fede G, Marcon G, Cotrufo R, Filippini G, Bugiani O, Tagliavini F. Puoti G, et al. Among authors: suardi s. J Neuropathol Exp Neurol. 2005 Oct;64(10):902-9. doi: 10.1097/01.jnen.0000183346.19447.55. J Neuropathol Exp Neurol. 2005. PMID: 16215462
A novel phenotype of sporadic Creutzfeldt-Jakob disease.
Giaccone G, Di Fede G, Mangieri M, Limido L, Capobianco R, Suardi S, Grisoli M, Binelli S, Fociani P, Bugiani O, Tagliavini F. Giaccone G, et al. Among authors: suardi s. BMJ Case Rep. 2009;2009:bcr09.2008.0945. doi: 10.1136/bcr.09.2008.0945. Epub 2009 Feb 2. BMJ Case Rep. 2009. PMID: 21686549 Free PMC article.
Cerebrospinal fluid real-time quaking-induced conversion is a robust and reliable test for sporadic creutzfeldt-jakob disease: An international study.
McGuire LI, Poleggi A, Poggiolini I, Suardi S, Grznarova K, Shi S, de Vil B, Sarros S, Satoh K, Cheng K, Cramm M, Fairfoul G, Schmitz M, Zerr I, Cras P, Equestre M, Tagliavini F, Atarashi R, Knox D, Collins S, Haïk S, Parchi P, Pocchiari M, Green A. McGuire LI, et al. Among authors: suardi s. Ann Neurol. 2016 Jul;80(1):160-5. doi: 10.1002/ana.24679. Epub 2016 Jun 1. Ann Neurol. 2016. PMID: 27130376 Free PMC article.
Conversion of the BASE prion strain into the BSE strain: the origin of BSE?
Capobianco R, Casalone C, Suardi S, Mangieri M, Miccolo C, Limido L, Catania M, Rossi G, Di Fede G, Giaccone G, Bruzzone MG, Minati L, Corona C, Acutis P, Gelmetti D, Lombardi G, Groschup MH, Buschmann A, Zanusso G, Monaco S, Caramelli M, Tagliavini F. Capobianco R, et al. Among authors: suardi s. PLoS Pathog. 2007 Mar;3(3):e31. doi: 10.1371/journal.ppat.0030031. PLoS Pathog. 2007. PMID: 17352534 Free PMC article.
39 results