PARCHI, PIERO
PARCHI, PIERO
DIPARTIMENTO DI SCIENZE BIOMEDICHE E NEUROMOTORIE
Docenti di ruolo di IIa fascia
"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.
4-Repeat tau seeds and templating subtypes as brain and CSF biomarkers of frontotemporal lobar degeneration
2020 Saijo E.; Metrick M.A.; Koga S.; Parchi P.; Litvan I.; Spina S.; Boxer A.; Rojas J.C.; Galasko D.; Kraus A.; Rossi M.; Newell K.; Zanusso G.; Grinberg L.T.; Seeley W.W.; Ghetti B.; Dickson D.W.; Caughey B.
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.
A CTNNA3 compound heterozygous deletion implicates a role for αT-catenin in susceptibility to autism spectrum disorder.
2014 Bacchelli E;Ceroni F;Pinto D;Lomartire S;Giannandrea M;D'Adamo P;Bonora E;Parchi P;Tancredi R;Battaglia A;Maestrini E
A Novel Eight Octapeptide Repeat Insertion in PRNP Causing Prion Disease in a Danish Family
2019 Areskeviciute A.; Hogh P.; Bartoletti-Stella A.; Melchior L.C.; Nielsen P.R.; Parchi P.; Capellari S.; Broholm H.; Scheie D.; Lund E.L.
A novel prion protein gene-truncating mutation causing autonomic neuropathy and diarrhea
2018 Bommarito, G.*; Cellerino, M.; Prada, V.; Venturi, C.; Capellari, S.; Cortelli, P.; Mancardi, G.L.; Parchi, P.; Schenone, A.
A novel seven-octapeptide repeat insertion in the prion protein gene (PRNP) in a Dutch pedigree with Gerstmann-Straussler-Scheinker disease phenotype: comparison with similar cases from the literature.
2011 Jansen C.; Voet W.; Head M.W.; Parchi P.; Yull H.; Verrips A.; Wesseling P.; Meulstee J.; Baas F.; van Gool W.A.; Ironside J.W.; Rozemuller A.J.
A prospective evaluation of clinical and instrumental features before and after ventriculo-peritoneal shunt in patients with idiopathic Normal pressure hydrocephalus: The Bologna PRO-Hydro study
2019 Giannini G.; Palandri G.; Ferrari A.; Oppi F.; Milletti D.; Albini-Riccioli L.; Mantovani P.; Magnoni S.; Chiari L.; Cortelli P.; Cevoli S.; Agati R.; Calandra-Buonaura G.; Capellari S.; Parchi P.; Stanzani-Maserati M.; Marliani A.F.; Merola M.; Piserchia V.A.; Sambati L.; Sturiale C.; Supino A.; Nicola M.; Urli T.
A refined method for molecular typing reveals that co-occurrence of PrP(Sc) types in Creutzfeldt-Jakob disease is not the rule.
2007 Notari S.; Capellari S.; Langeveld J.; Giese A.; Strammiello R.; Gambetti P.; Kretzschmar H.A.; Parchi P.
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.
Abnormal ADC in the brain of prion disease patients: variation between brain structures.
2005 D. N. Manners; R. Lodi; P. Parchi; C. Tonon; S. Capellari; A. Filla; G. Pierangeli; C. Testa; P. Cortelli; P. Montagna; B. Barbiroli
ADC and Proton Spectroscopy Reflect Cellular Pathology in Patients with Creutzfeldt-Jakob Disease
2006 D. N. Manners; P. Parchi; R. Lodi; C. Tonon; C. Testa; S. Capellari; G. Pierangeli; P. Cortelli; P. Montagna; B. Barbiroli
Age at onset in genetic prion disease and the design of preventive clinical trials
2019 Minikel E.V.; Vallabh S.M.; Orseth M.C.; Brandel J.-P.; Haik S.; Laplanche J.-L.; Zerr I.; Parchi P.; Capellari S.; Safar J.; Kenny J.; Fong J.C.; Takada L.T.; Ponto C.; Hermann P.; Knipper T.; Stehmann C.; Kitamoto T.; Ae R.; Hamaguchi T.; Sanjo N.; Tsukamoto T.; Mizusawa H.; Collins S.J.; Chiesa R.; Roiter I.; de Pedro-Cuesta J.; Calero M.; Geschwind M.D.; Yamada M.; Nakamura Y.; Mead S.
Age at onset of genetic (E200K) and sporadic Creutzfeldt-Jakob diseases is modulated by theCYP4X1gene
2018 Poleggi, Anna; van der Lee, Sven; Capellari, Sabina; Puopolo, Maria; Ladogana, Anna; De Pascali, Eleonora; Lia, Debora; Formato, Alessia; Bartoletti-Stella, Anna; Parchi, Piero; van Duijn, Cornelia; Pocchiari, Maurizio
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.
Agrypnia Excitata
2008 Cirignotta F; Mondini S; La Morgia C; Rinaldi R; Parchi P; Lodi R.
Amyloid-Beta Co-Pathology Is a Major Determinant of the Elevated Plasma GFAP Values in Amyotrophic Lateral Sclerosis
2023 Mastrangelo, Andrea; Vacchiano, Veria; Zenesini, Corrado; Ruggeri, Edoardo; Baiardi, Simone; Cherici, Arianna; Avoni, Patrizia; Polischi, Barbara; Santoro, Francesca; Capellari, Sabina; Liguori, Rocco; Parchi, Piero
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
An in vivo 11C-PK PET study of microglia activation in Fatal Familial Insomnia
2018 Iaccarino, Leonardo; Presotto, Luca; Bettinardi, Valentino; Gianolli, Luigi; Roiter, Ignazio; Capellari, Sabina; Parchi, Piero; Cortelli, Pietro; Perani, Daniela
An in vivo proton magnetic resonance spectroscopy study of thalamus in prion disease
2005 R. Lodi; P. Parchi; C. Tonon; D. N. Manners; S. Capellari; A. Filla; E. Malucelli; G. Pierangeli; P. Cortelli; P. Montagna; B. Barbiroli
| Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
|---|---|---|---|---|---|---|
| "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 | - |
| 4-Repeat tau seeds and templating subtypes as brain and CSF biomarkers of frontotemporal lobar degeneration | Saijo E.; Metrick M.A.; Koga S.; Parchi P.; Litvan I.; Spina S.; Boxer A.; Rojas J.C.; Galasko D....; Kraus A.; Rossi M.; Newell K.; Zanusso G.; Grinberg L.T.; Seeley W.W.; Ghetti B.; Dickson D.W.; Caughey B. | 2020-01-01 | ACTA NEUROPATHOLOGICA | - | 1.01 Articolo in rivista | s00401-019-02080-2.pdf |
| 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) | - |
| A CTNNA3 compound heterozygous deletion implicates a role for αT-catenin in susceptibility to autism spectrum disorder. | Bacchelli E;Ceroni F;Pinto D;Lomartire S;Giannandrea M;D'Adamo P;Bonora E;Parchi P;Tancredi R;Bat...taglia A;Maestrini E | 2014-01-01 | JOURNAL OF NEURODEVELOPMENTAL DISORDERS | - | 1.01 Articolo in rivista | 1866-1955-6-17.pdf |
| A Novel Eight Octapeptide Repeat Insertion in PRNP Causing Prion Disease in a Danish Family | Areskeviciute A.; Hogh P.; Bartoletti-Stella A.; Melchior L.C.; Nielsen P.R.; Parchi P.; Capellar...i S.; Broholm H.; Scheie D.; Lund E.L. | 2019-01-01 | JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY | - | 1.01 Articolo in rivista | - |
| A novel prion protein gene-truncating mutation causing autonomic neuropathy and diarrhea | Bommarito, G.*; Cellerino, M.; Prada, V.; Venturi, C.; Capellari, S.; Cortelli, P.; Mancardi, G.L....; Parchi, P.; Schenone, A. | 2018-01-01 | EUROPEAN JOURNAL OF NEUROLOGY | - | 1.01 Articolo in rivista | - |
| A novel seven-octapeptide repeat insertion in the prion protein gene (PRNP) in a Dutch pedigree with Gerstmann-Straussler-Scheinker disease phenotype: comparison with similar cases from the literature. | Jansen C.; Voet W.; Head M.W.; Parchi P.; Yull H.; Verrips A.; Wesseling P.; Meulstee J.; Baas F....; van Gool W.A.; Ironside J.W.; Rozemuller A.J. | 2011-01-01 | ACTA NEUROPATHOLOGICA | - | 1.01 Articolo in rivista | - |
| A prospective evaluation of clinical and instrumental features before and after ventriculo-peritoneal shunt in patients with idiopathic Normal pressure hydrocephalus: The Bologna PRO-Hydro study | Giannini G.; Palandri G.; Ferrari A.; Oppi F.; Milletti D.; Albini-Riccioli L.; Mantovani P.; Mag...noni S.; Chiari L.; Cortelli P.; Cevoli S.; Agati R.; Calandra-Buonaura G.; Capellari S.; Parchi P.; Stanzani-Maserati M.; Marliani A.F.; Merola M.; Piserchia V.A.; Sambati L.; Sturiale C.; Supino A.; Nicola M.; Urli T. | 2019-01-01 | PARKINSONISM & RELATED DISORDERS | - | 1.01 Articolo in rivista | - |
| 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 H.A.; P...archi P. | 2007-01-01 | LABORATORY INVESTIGATION | - | 1.01 Articolo in rivista | - |
| 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 | - |
| Abnormal ADC in the brain of prion disease patients: variation between brain structures. | D. N. Manners; R. Lodi; P. Parchi; C. Tonon; S. Capellari; A. Filla; G. Pierangeli; C. Testa; P. ...Cortelli; P. Montagna; B. Barbiroli | 2005-01-01 | - | s.n | 4.02 Riassunto (Abstract) | - |
| ADC and Proton Spectroscopy Reflect Cellular Pathology in Patients with Creutzfeldt-Jakob Disease | D. N. Manners; P. Parchi; R. Lodi; C. Tonon; C. Testa; S. Capellari; G. Pierangeli; P. Cortelli; ...P. Montagna; B. Barbiroli | 2006-01-01 | - | s.n | 4.02 Riassunto (Abstract) | - |
| Age at onset in genetic prion disease and the design of preventive clinical trials | Minikel E.V.; Vallabh S.M.; Orseth M.C.; Brandel J.-P.; Haik S.; Laplanche J.-L.; Zerr I.; Parchi... P.; Capellari S.; Safar J.; Kenny J.; Fong J.C.; Takada L.T.; Ponto C.; Hermann P.; Knipper T.; Stehmann C.; Kitamoto T.; Ae R.; Hamaguchi T.; Sanjo N.; Tsukamoto T.; Mizusawa H.; Collins S.J.; Chiesa R.; Roiter I.; de Pedro-Cuesta J.; Calero M.; Geschwind M.D.; Yamada M.; Nakamura Y.; Mead S. | 2019-01-01 | NEUROLOGY | - | 1.01 Articolo in rivista | 401406.full.pdf |
| Age at onset of genetic (E200K) and sporadic Creutzfeldt-Jakob diseases is modulated by theCYP4X1gene | Poleggi, Anna; van der Lee, Sven; Capellari, Sabina; Puopolo, Maria; Ladogana, Anna; De Pascali, ...Eleonora; Lia, Debora; Formato, Alessia; Bartoletti-Stella, Anna; Parchi, Piero; van Duijn, Cornelia; Pocchiari, Maurizio | 2018-01-01 | JOURNAL OF NEUROLOGY, NEUROSURGERY AND PSYCHIATRY | - | 1.01 Articolo in rivista | - |
| 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 | - |
| Agrypnia Excitata | Cirignotta F; Mondini S; La Morgia C; Rinaldi R; Parchi P; Lodi R. | 2008-01-01 | SLEEP | - | 4.02 Riassunto (Abstract) | - |
| Amyloid-Beta Co-Pathology Is a Major Determinant of the Elevated Plasma GFAP Values in Amyotrophic Lateral Sclerosis | Mastrangelo, Andrea; Vacchiano, Veria; Zenesini, Corrado; Ruggeri, Edoardo; Baiardi, Simone; Cher...ici, Arianna; Avoni, Patrizia; Polischi, Barbara; Santoro, Francesca; Capellari, Sabina; Liguori, Rocco; Parchi, Piero | 2023-01-01 | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES | - | 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 | - |
| An in vivo 11C-PK PET study of microglia activation in Fatal Familial Insomnia | Iaccarino, Leonardo; Presotto, Luca; Bettinardi, Valentino; Gianolli, Luigi; Roiter, Ignazio; Cap...ellari, Sabina; Parchi, Piero; Cortelli, Pietro; Perani, Daniela | 2018-01-01 | ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY | - | 1.01 Articolo in rivista | acn3.498.pdf |
| An in vivo proton magnetic resonance spectroscopy study of thalamus in prion disease | R. Lodi; P. Parchi; C. Tonon; D. N. Manners; S. Capellari; A. Filla; E. Malucelli; G. Pierangeli;... P. Cortelli; P. Montagna; B. Barbiroli | 2005-01-01 | - | s.n | 4.02 Riassunto (Abstract) | - |