Sfoglia per Autore
Creutzfeldt-Jakob disease with E200K PRNP mutation: a case report and revision of the literature
2009 Mancuso M.; Siciliano G.; Capellari S.; Orsucci D.; Moretti P.; Di Fede G.; Suardi S.; Strammiello R.; Parchi P.; Tagliavini F.; Murri L.
Magnetic resonance diagnostic markers in clinically sporadic prion disease: a combined brain magnetic resonance imaging and spectroscopy study.
2009 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.
Pathologic correlates of diffusion MRI changes in Creutzfeldt-Jakob disease
2009 Manners D.; Parchi P.; Tonon C.; Capellari S.; Strammiello R.; Testa C.; Tani G.; Malucelli E.; Spagnolo C.; Cortelli P.; Montagna P.; Lodi R.; Barbiroli B.
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
Benign tremulous parkinsonism in a patient with dardarin mutation.
2009 Rizzo G.; Marconi S.; Capellari S.; Scaglione C.; Martinelli P.
Striatal [123] FP-CIT SPECT demonstrates dopaminergic deficit in a sporadic case of Creutzfeldt-Jakob disease.
2009 Ragno M.; Scarcella M.G.; Cacchiò G.; Capellari S.; Di Marzio F.; Parchi P.; Trojano L.
The role of PrP and other proteins in prion diseases
2009 S. Principe; F. Cardone; L. Di Francesco; A. Giorgi; G. Mignogna; M. Sbriccoli; R. Galeno; S. Notari; S. Capellari; P. Parchi; J. Rappsilber; B. Maras; M.E. Schininà; M. Pocchiari
An update of the epidemiology of sporadic Creutzfeldt-Jakob disease in Italy based on neuropathologic and molecular typing of a large cohort of patients
2009 G. Giaccone; S. Capellari; L. Ingrosso; S. Ferrari; D. Imperiale; S. Taraglio; S. Monaco; M. Pocchiari; F. Tagliavini; P. Parchi
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.
A case of fatal familial insomnia in Africa.
2009 Baldin E.; Capellari S.; Provini F.; Corrado P.; Liguori R.; Parchi P.; Montagna P.; Cortelli P.
Sporadic CJD histotyping by means of activated microglia profiling
2009 R. Strammiello; S. Capellari; P. Parchi
"Agrypnia excitata'' in a case of sporadic Creutzfeldt-Jakob disease VV2
2009 La Morgia C.; Parchi P.; Capellari S.; Lodi R.; Tonon C.; Rinaldi R.; Mondini S.; Cirignotta F.
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.
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.
Lack of association between five serotonin metabolism-related genes and medication overuse headache
2010 Sabina Cevoli; Nadia Marzocchi; Sabina Capellari; Chiara Scapoli; Giulia Pierangeli; Daniela Grimaldi; Federica Naldi; L. Alberto Pini; Pasquale Montagna; Pietro Cortelli
Agent strain variation in human prion disease: insights from a molecular and pathological review of the National Institutes of Health series of experimentally transmitted disease.
2010 Parchi P.; Cescatti M.; Notari S.; Schulz-Schaeffer W.J.; Capellari S.; Giese A.; Zou W.Q.; Kretzschmar H.; Ghetti B.; Brown P.
Variably protease-sensitive prionopathy: A new sporadic disease of the prion protein.
2010 Zou W.Q.; Puoti G.; Xiao X.; Yuan J.; Qing L.; Cali I.; Shimoji M.; Langeveld J.P.; Castellani R.; Notari S.; Crain B.; Schmidt R.E.; Geschwind M.; Dearmond S.J.; Cairns N.J.; Dickson D.; Honig L.; Torres J.M.; Mastrianni J.; Capellari S.; Giaccone G.; Belay E.D.; Schonberger L.B.; Cohen M.; Perry G.; Kong Q.; Parchi P.; Tagliavini F.; Gambetti P.
The RET51/FKBP52 complex and its involvement in Parkinson disease.
2010 Fusco D; Vargiolu M; Vidone M; Mariani E; Pennisi LF; Bonora E; Capellari S; Dirnberger D; Baumeister R; Martinelli P; Romeo G.
An atypical phenotype of CJD associated with the E200K mutation in the prion protein gene.
2010 Masullo C; Bizzarro A; Guglielmi V; Iannaccone E; Minicuci G; Vita MG; Capellari S; Parchi P; Servidei S
Cathepsin D (C224T) Polymorphism in Sporadic and Genetic Creutzfeldt-Jakob Disease
2010 Kovacs GG; Sanchez-Juan P; Ströbel T; Schuur M; Poleggi A; Nocentini S; Giannattasio C; Belay G; Bishop M; Capellari S; Parchi P; Gelpi E; Gal A; Bakos A; Molnar MJ; Heinemann U; Zerr I; Knight RS; Mitrova E; van Duijn C; Budka H.
| Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
|---|---|---|---|---|---|---|
| Creutzfeldt-Jakob disease with E200K PRNP mutation: a case report and revision of the literature | Mancuso M.; Siciliano G.; Capellari S.; Orsucci D.; Moretti P.; Di Fede G.; Suardi S.; Strammiell...o R.; Parchi P.; Tagliavini F.; Murri L. | 2009-01-01 | NEUROLOGICAL SCIENCES | - | 1.01 Articolo in rivista | - |
| 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.; Mal...ucelli E.; Mostacci B.; Rizzo G.; Pierangeli G.; Cortelli P.; Montagna P.; Barbiroli B. | 2009-01-01 | BRAIN | - | 1.01 Articolo in rivista | - |
| Pathologic correlates of diffusion MRI changes in Creutzfeldt-Jakob disease | Manners D.; Parchi P.; Tonon C.; Capellari S.; Strammiello R.; Testa C.; Tani G.; Malucelli E.; S...pagnolo C.; Cortelli P.; Montagna P.; Lodi R.; Barbiroli B. | 2009-01-01 | NEUROLOGY | - | 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) | - |
| Benign tremulous parkinsonism in a patient with dardarin mutation. | Rizzo G.; Marconi S.; Capellari S.; Scaglione C.; Martinelli P. | 2009-01-01 | MOVEMENT DISORDERS | - | 1.01 Articolo in rivista | - |
| Striatal [123] FP-CIT SPECT demonstrates dopaminergic deficit in a sporadic case of Creutzfeldt-Jakob disease. | Ragno M.; Scarcella M.G.; Cacchiò G.; Capellari S.; Di Marzio F.; Parchi P.; Trojano L. | 2009-01-01 | ACTA NEUROLOGICA SCANDINAVICA | - | 1.01 Articolo in rivista | - |
| The role of PrP and other proteins in prion diseases | S. Principe; F. Cardone; L. Di Francesco; A. Giorgi; G. Mignogna; M. Sbriccoli; R. Galeno; S. Not...ari; S. Capellari; P. Parchi; J. Rappsilber; B. Maras; M.E. Schininà; M. Pocchiari | 2009-01-01 | CLINICAL NEUROPATHOLOGY | - | 4.02 Riassunto (Abstract) | - |
| An update of the epidemiology of sporadic Creutzfeldt-Jakob disease in Italy based on neuropathologic and molecular typing of a large cohort of patients | G. Giaccone; S. Capellari; L. Ingrosso; S. Ferrari; D. Imperiale; S. Taraglio; S. Monaco; M. Pocc...hiari; F. Tagliavini; P. Parchi | 2009-01-01 | CLINICAL NEUROPATHOLOGY | - | 4.02 Riassunto (Abstract) | - |
| 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 | - |
| A case of fatal familial insomnia in Africa. | Baldin E.; Capellari S.; Provini F.; Corrado P.; Liguori R.; Parchi P.; Montagna P.; Cortelli P. | 2009-01-01 | JOURNAL OF NEUROLOGY | - | 1.04 Replica / breve intervento (e simili) | - |
| Sporadic CJD histotyping by means of activated microglia profiling | R. Strammiello; S. Capellari; P. Parchi | 2009-01-01 | CLINICAL NEUROPATHOLOGY | - | 4.02 Riassunto (Abstract) | - |
| "Agrypnia excitata'' in a case of sporadic Creutzfeldt-Jakob disease VV2 | La Morgia C.; Parchi P.; Capellari S.; Lodi R.; Tonon C.; Rinaldi R.; Mondini S.; Cirignotta F. | 2009-01-01 | JOURNAL OF NEUROLOGY, NEUROSURGERY AND PSYCHIATRY | - | 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 | - |
| 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 | - |
| Lack of association between five serotonin metabolism-related genes and medication overuse headache | Sabina Cevoli; Nadia Marzocchi; Sabina Capellari; Chiara Scapoli; Giulia Pierangeli; Daniela Grim...aldi; Federica Naldi; L. Alberto Pini; Pasquale Montagna; Pietro Cortelli | 2010-01-01 | THE JOURNAL OF HEADACHE AND PAIN | - | 1.01 Articolo in rivista | s10194-009-0168-5.pdf |
| Agent strain variation in human prion disease: insights from a molecular and pathological review of the National Institutes of Health series of experimentally transmitted disease. | Parchi P.; Cescatti M.; Notari S.; Schulz-Schaeffer W.J.; Capellari S.; Giese A.; Zou W.Q.; Kretz...schmar H.; Ghetti B.; Brown P. | 2010-01-01 | BRAIN | - | 1.01 Articolo in rivista | - |
| Variably protease-sensitive prionopathy: A new sporadic disease of the prion protein. | Zou W.Q.; Puoti G.; Xiao X.; Yuan J.; Qing L.; Cali I.; Shimoji M.; Langeveld J.P.; Castellani R....; Notari S.; Crain B.; Schmidt R.E.; Geschwind M.; Dearmond S.J.; Cairns N.J.; Dickson D.; Honig L.; Torres J.M.; Mastrianni J.; Capellari S.; Giaccone G.; Belay E.D.; Schonberger L.B.; Cohen M.; Perry G.; Kong Q.; Parchi P.; Tagliavini F.; Gambetti P. | 2010-01-01 | ANNALS OF NEUROLOGY | - | 1.01 Articolo in rivista | - |
| The RET51/FKBP52 complex and its involvement in Parkinson disease. |
Fusco D; Vargiolu M; Vidone M; Mariani E; Pennisi LF; Bonora E; Capellari S; Dirnberger D; Baume...ister R; Martinelli P; Romeo G. |
2010-01-01 | HUMAN MOLECULAR GENETICS | - | 1.01 Articolo in rivista | - |
| An atypical phenotype of CJD associated with the E200K mutation in the prion protein gene. | Masullo C; Bizzarro A; Guglielmi V; Iannaccone E; Minicuci G; Vita MG; Capellari S; Parchi P; Ser...videi S | 2010-01-01 | NEUROLOGICAL SCIENCES | - | 1.01 Articolo in rivista | - |
| Cathepsin D (C224T) Polymorphism in Sporadic and Genetic Creutzfeldt-Jakob Disease |
Kovacs GG; Sanchez-Juan P; Ströbel T; Schuur M; Poleggi A; Nocentini S; Giannattasio C; Belay G;... Bishop M; Capellari S; Parchi P; Gelpi E; Gal A; Bakos A; Molnar MJ; Heinemann U; Zerr I; Knight RS; Mitrova E; van Duijn C; Budka H. |
2010-01-01 | ALZHEIMER DISEASE & ASSOCIATED DISORDERS | - | 1.01 Articolo in rivista | - |
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