STRAMMIELLO, ROSARIA
STRAMMIELLO, ROSARIA
DIP. DI SCIENZE NEUROLOGICHE
Regional pattern of microgliosis in sporadic Creutzfeldt-Jakob disease in relation to phenotypic variants and disease progression
2018 Franceschini, A.; Strammiello, R.; Capellari, S.; Giese, A.; Parchi, P.
Human papillomavirus evaluation of vemurafenib induced skin epithelial tumors: a case series
2015 Dika Emi; Patrizi Annalisa; Venturoli Simona; Fanti Pier Alessandro; Barbieri Daniela; Strammiello Rosaria; Melotti Barbara; La Placa Michelangelo
Detection of HPV16 African variants and quantitative analysis of viral DNA methylation in oropharyngeal squamous cell carcinomas
2014 Barbieri D; Nebiaj A; Strammiello R; Agosti R; Sciascia S; Gallinella G; Landini MP; Caliceti U; Venturoli S
Human prion diseases in the Netherlands (1998-2009): clinical, genetic and molecular aspects.
2012 Jansen C.; Parchi P.; Capellari S.; Ibrahim-Verbaas C.A.; Schuur M.; Strammiello R.; Corrado P.; Bishop M.T.; van Gool W.A.; Verbeek M.M.; Baas F.; van Saane W.; Spliet W.G.; Jansen G.H.; van Duijn C.M.; Rozemuller A.J.
A second case of Gerstmann-Sträussler-Scheinker disease linked to the G131V mutation in the prion protein gene in a Dutch patient.
2011 Jansen C.; Parchi P.; Capellari S.; Strammiello R.; Dopper E.G.; van Swieten J.C.; Kamphorst W.; Rozemuller A.J.
Distribution of Diffusivity Changes in Subcortical Deep Gray Matter in Prion Diseases
2011 R Lodi; D N Manners; E Malucelli; C Testa; G Rizzo; S Capellari; R Strammiello; G Pierangeli; P Cortelli; P Montagna; B Barbiroli; C Tonon; P Parchi
Genetic Creutzfeldt-Jakob disease and fatal familial insomnia: Insights into phenotypic variability and disease pathogenesis.
2011 Capellari S.; Strammiello R.; Saverioni D.; Kretzschmar H.; Parchi P.
Phenotypic variability of sporadic human prion disease and its molecular basis: past, present, and future.
2011 Parchi P.; Strammiello R.; Giese A.; Kretzschmar H.
Prion protein amyloidosis with divergent phenotype associated with two novel nonsense mutations in PRNP.
2010 Jansen C.; Parchi P.; Capellari S.; Vermeij A.J.; Corrado P.; Baas F.; Strammiello R.; van Gool W.A.; van Swieten J.C.; Rozemuller A.J.
Incidence and spectrum of sporadic Creutzfeldt-Jakob disease variants with mixed phenotype and co-occurrence of PrP(Sc) types: an updated classification.
2009 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.
Inherited Creutzfeldt-Jakob disease in a Dutch patient with a novel five octapeptide repeat insertion and unusual cerebellar morphology.
2009 Jansen C.; van Swieten J.C.; Capellari S.; Strammiello R.; Parchi P.; Rozemuller A.J.
PROTEIN AMYLOIDOSIS ASSOCIATED WITH A NOVEL STOP CODON MUTATION IN PRNP
2009 C. Jansen; P. Parchi; S. Capellari; P. Corrado; R. Strammiello; J.C. van Swieten and A.J.M. Rozemuller
Sporadic CJD histotyping by means of activated microglia profiling
2009 R. Strammiello; S. Capellari; P. Parchi
Microglial activation in sporadic CJD: regional variability and the effect of disease subtype
2008 Strammiello R; Capellari S; Parchi P
PHYSICO-CHEMICAL PROPERTIES OF PRPRES IN PERIPHERAL TISSUES OF EXPERIMENTAL TSES.
2006 R. Strammiello; M.Cescatti; C. Farquhar; A. Marshall; J. Mai; M. Beekes; P. Parchi
Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
---|---|---|---|---|---|---|
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. | 2018-01-01 | NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY | - | 1.01 Articolo in rivista | - |
Human papillomavirus evaluation of vemurafenib induced skin epithelial tumors: a case series | Dika Emi; Patrizi Annalisa; Venturoli Simona; Fanti Pier Alessandro; Barbieri Daniela; Strammiell...o Rosaria; Melotti Barbara; La Placa Michelangelo | 2015-01-01 | BRITISH JOURNAL OF DERMATOLOGY | - | 1.01 Articolo in rivista | - |
Detection of HPV16 African variants and quantitative analysis of viral DNA methylation in oropharyngeal squamous cell carcinomas | Barbieri D; Nebiaj A; Strammiello R; Agosti R; Sciascia S; Gallinella G; Landini MP; Caliceti U; ...Venturoli S | 2014-01-01 | JOURNAL OF CLINICAL VIROLOGY | - | 1.01 Articolo in rivista | - |
Human prion diseases in the Netherlands (1998-2009): clinical, genetic and molecular aspects. | Jansen C.; Parchi P.; Capellari S.; Ibrahim-Verbaas C.A.; Schuur M.; Strammiello R.; Corrado P.; ...Bishop M.T.; van Gool W.A.; Verbeek M.M.; Baas F.; van Saane W.; Spliet W.G.; Jansen G.H.; van Duijn C.M.; Rozemuller A.J. | 2012-01-01 | PLOS ONE | - | 1.01 Articolo in rivista | journal.pone.0036333.PDF |
A second case of Gerstmann-Sträussler-Scheinker disease linked to the G131V mutation in the prion protein gene in a Dutch patient. | Jansen C.; Parchi P.; Capellari S.; Strammiello R.; Dopper E.G.; van Swieten J.C.; Kamphorst W.; ...Rozemuller A.J. | 2011-01-01 | JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY | - | 1.01 Articolo in rivista | - |
Distribution of Diffusivity Changes in Subcortical Deep Gray Matter in Prion Diseases | R Lodi; D N Manners; E Malucelli; C Testa; G Rizzo; S Capellari; R Strammiello; G Pierangeli; P C...ortelli; P Montagna; B Barbiroli; C Tonon; P Parchi | 2011-01-01 | - | - | 4.02 Riassunto (Abstract) | - |
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. | 2011-01-01 | ACTA NEUROPATHOLOGICA | - | 1.01 Articolo in rivista | - |
Phenotypic variability of sporadic human prion disease and its molecular basis: past, present, and future. | Parchi P.; Strammiello R.; Giese A.; Kretzschmar H. | 2011-01-01 | ACTA NEUROPATHOLOGICA | - | 1.01 Articolo in rivista | - |
Prion protein amyloidosis with divergent phenotype associated with two novel nonsense mutations in PRNP. | Jansen C.; Parchi P.; Capellari S.; Vermeij A.J.; Corrado P.; Baas F.; Strammiello R.; van Gool W....A.; van Swieten J.C.; Rozemuller A.J. | 2010-01-01 | ACTA NEUROPATHOLOGICA | - | 1.01 Articolo in rivista | - |
Incidence and spectrum of sporadic Creutzfeldt-Jakob disease variants with mixed phenotype and co-occurrence of PrP(Sc) 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. | 2009-01-01 | ACTA NEUROPATHOLOGICA | - | 1.01 Articolo in rivista | - |
Inherited Creutzfeldt-Jakob disease in a Dutch patient with a novel five octapeptide repeat insertion and unusual cerebellar morphology. | Jansen C.; van Swieten J.C.; Capellari S.; Strammiello R.; Parchi P.; Rozemuller A.J. | 2009-01-01 | JOURNAL OF NEUROLOGY, NEUROSURGERY AND PSYCHIATRY | - | 1.01 Articolo in rivista | - |
PROTEIN AMYLOIDOSIS ASSOCIATED WITH A NOVEL STOP CODON MUTATION IN PRNP | C. Jansen; P. Parchi; S. Capellari; P. Corrado; R. Strammiello; J.C. van Swieten and A.J.M. Rozem...uller | 2009-01-01 | CLINICAL NEUROPATHOLOGY | - | 4.02 Riassunto (Abstract) | - |
Sporadic CJD histotyping by means of activated microglia profiling | R. Strammiello; S. Capellari; P. Parchi | 2009-01-01 | CLINICAL NEUROPATHOLOGY | - | 4.02 Riassunto (Abstract) | - |
Microglial activation in sporadic CJD: regional variability and the effect of disease subtype | Strammiello R; Capellari S; Parchi P | 2008-01-01 | - | sn | 4.02 Riassunto (Abstract) | - |
PHYSICO-CHEMICAL PROPERTIES OF PRPRES IN PERIPHERAL TISSUES OF EXPERIMENTAL TSES. | R. Strammiello; M.Cescatti; C. Farquhar; A. Marshall; J. Mai; M. Beekes; P. Parchi | 2006-01-01 | - | s.n | 4.02 Riassunto (Abstract) | - |