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Phenotypic variability of sporadic human prion disease and its molecular basis: past, present, and future.
Parchi P, Strammiello R, Giese A, Kretzschmar H. Parchi P, et al. Among authors: strammiello r. Acta Neuropathol. 2011 Jan;121(1):91-112. doi: 10.1007/s00401-010-0779-6. Epub 2010 Nov 24. Acta Neuropathol. 2011. PMID: 21107851 Review.
Regional pattern of microgliosis in sporadic Creutzfeldt-Jakob disease in relation to phenotypic variants and disease progression.
Franceschini A, Strammiello R, Capellari S, Giese A, Parchi P. Franceschini A, et al. Among authors: strammiello r. Neuropathol Appl Neurobiol. 2018 Oct;44(6):574-589. doi: 10.1111/nan.12461. Epub 2018 Feb 26. Neuropathol Appl Neurobiol. 2018. PMID: 29345730
Magnetic resonance diagnostic markers in clinically sporadic prion disease: a combined brain magnetic resonance imaging and spectroscopy study.
Lodi R, Parchi P, Tonon C, Manners D, Capellari S, Strammiello R, Rinaldi R, Testa C, Malucelli E, Mostacci B, Rizzo G, Pierangeli G, Cortelli P, Montagna P, Barbiroli B. Lodi R, et al. Among authors: strammiello r. Brain. 2009 Oct;132(Pt 10):2669-79. doi: 10.1093/brain/awp210. Epub 2009 Sep 15. Brain. 2009. PMID: 19755520 Free PMC article.
Human prion diseases in the Netherlands (1998-2009): clinical, genetic and molecular aspects.
Jansen C, Parchi P, Capellari S, Ibrahim-Verbaas CA, Schuur M, Strammiello R, Corrado P, Bishop MT, van Gool WA, Verbeek MM, Baas F, van Saane W, Spliet WG, Jansen GH, van Duijn CM, Rozemuller AJ. Jansen C, et al. Among authors: strammiello r. PLoS One. 2012;7(4):e36333. doi: 10.1371/journal.pone.0036333. Epub 2012 Apr 30. PLoS One. 2012. PMID: 22558438 Free PMC article.
Incidence and spectrum of sporadic Creutzfeldt-Jakob disease variants with mixed phenotype and co-occurrence of PrPSc types: an updated classification.
Parchi P, Strammiello R, Notari S, Giese A, Langeveld JP, Ladogana A, Zerr I, Roncaroli F, Cras P, Ghetti B, Pocchiari M, Kretzschmar H, Capellari S. Parchi P, et al. Acta Neuropathol. 2009 Nov;118(5):659-71. doi: 10.1007/s00401-009-0585-1. Epub 2009 Aug 29. Acta Neuropathol. 2009. PMID: 19718500 Free PMC article.
A refined method for molecular typing reveals that co-occurrence of PrP(Sc) types in Creutzfeldt-Jakob disease is not the rule.
Notari S, Capellari S, Langeveld J, Giese A, Strammiello R, Gambetti P, Kretzschmar HA, Parchi P. Notari S, et al. Lab Invest. 2007 Nov;87(11):1103-12. doi: 10.1038/labinvest.3700676. Epub 2007 Sep 24. Lab Invest. 2007. PMID: 17893675
Characterization of truncated forms of abnormal prion protein in Creutzfeldt-Jakob disease.
Notari S, Strammiello R, Capellari S, Giese A, Cescatti M, Grassi J, Ghetti B, Langeveld JP, Zou WQ, Gambetti P, Kretzschmar HA, Parchi P. Notari S, et al. J Biol Chem. 2008 Nov 7;283(45):30557-65. doi: 10.1074/jbc.M801877200. Epub 2008 Aug 27. J Biol Chem. 2008. PMID: 18753138 Free PMC article.
Prion protein amyloidosis with divergent phenotype associated with two novel nonsense mutations in PRNP.
Jansen C, Parchi P, Capellari S, Vermeij AJ, Corrado P, Baas F, Strammiello R, van Gool WA, van Swieten JC, Rozemuller AJ. Jansen C, et al. Among authors: strammiello r. Acta Neuropathol. 2010 Feb;119(2):189-97. doi: 10.1007/s00401-009-0609-x. Epub 2009 Nov 13. Acta Neuropathol. 2010. PMID: 19911184 Free PMC article.
Genetic Creutzfeldt-Jakob disease and fatal familial insomnia: insights into phenotypic variability and disease pathogenesis.
Capellari S, Strammiello R, Saverioni D, Kretzschmar H, Parchi P. Capellari S, et al. Among authors: strammiello r. Acta Neuropathol. 2011 Jan;121(1):21-37. doi: 10.1007/s00401-010-0760-4. Epub 2010 Oct 27. Acta Neuropathol. 2011. PMID: 20978903 Review.
Intracellular pH regulation in U-2 OS human osteosarcoma cells transfected with P-glycoprotein.
Porcelli AM, Scotlandi K, Strammiello R, Gislimberti G, Baldini N, Rugolo M. Porcelli AM, et al. Biochim Biophys Acta. 2002 Jan 30;1542(1-3):125-38. doi: 10.1016/s0167-4889(01)00173-2. Biochim Biophys Acta. 2002. PMID: 11853886
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