CORRADO, PATRIZIA
CORRADO, PATRIZIA
DIP. DI SCIENZE NEUROLOGICHE
Analysis of RNA Expression Profiles Identifies Dysregulated Vesicle Trafficking Pathways in Creutzfeldt-Jakob Disease
2019 Bartoletti-Stella A.; Corrado P.; Mometto N.; Baiardi S.; Durrenberger P.F.; Arzberger T.; Reynolds R.; Kretzschmar H.; Capellari S.; Parchi P.
Corrigendum: Messenger RNA processing is altered in autosomal dominant leukodystrophy [Human Molecular Genetics, 24 (2015) (2746-2756)] DOI:10.1093/hmg/ddv034
2017 Bartoletti-Stella, Anna; Gasparini, Laura; Giacomini, Caterina; Corrado, Patrizia; Terlizzi, Rossana; Giorgio, Elisa; Magini, Pamela; Seri, Marco; Baruzzi, Agostino; Parchi, Piero; Brusco, Alfredo; Cortelli, Pietro; Capellari, Sabina
Messenger RNA processing is altered in autosomal dominant leukodystrophy
2015 Bartoletti Stella, A; Gasparini, L; Giacomini, C; Corrado, Patrizia; Terlizzi, R; Giorgio, E; Magini, P; Seri, Marco; Baruzzi, Agostino; Parchi, Piero; Brusco, A; Cortelli, Pietro; Capellari, Sabina
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.
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.
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.
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
Analysis of polymorphisms in PRNP 5' UTR region in sCJD subtypres
2008 Capellari S; Corrado P; Gambetti P; Parchi P
| Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
|---|---|---|---|---|---|---|
| Analysis of RNA Expression Profiles Identifies Dysregulated Vesicle Trafficking Pathways in Creutzfeldt-Jakob Disease | Bartoletti-Stella A.; Corrado P.; Mometto N.; Baiardi S.; Durrenberger P.F.; Arzberger T.; Reynol...ds R.; Kretzschmar H.; Capellari S.; Parchi P. | 2019-01-01 | MOLECULAR NEUROBIOLOGY | - | 1.01 Articolo in rivista | Bartoletti_et_al_.pdf |
| Corrigendum: Messenger RNA processing is altered in autosomal dominant leukodystrophy [Human Molecular Genetics, 24 (2015) (2746-2756)] DOI:10.1093/hmg/ddv034 | Bartoletti-Stella, Anna; Gasparini, Laura; Giacomini, Caterina; Corrado, Patrizia; Terlizzi, Ross...ana; Giorgio, Elisa; Magini, Pamela; Seri, Marco; Baruzzi, Agostino; Parchi, Piero; Brusco, Alfredo; Cortelli, Pietro; Capellari, Sabina | 2017-01-01 | HUMAN MOLECULAR GENETICS | - | 1.01 Articolo in rivista | - |
| Messenger RNA processing is altered in autosomal dominant leukodystrophy | Bartoletti Stella, A; Gasparini, L; Giacomini, C; Corrado, Patrizia; Terlizzi, R; Giorgio, E; Mag...ini, P; Seri, Marco; Baruzzi, Agostino; Parchi, Piero; Brusco, A; Cortelli, Pietro; Capellari, Sabina | 2015-01-01 | HUMAN MOLECULAR GENETICS | - | 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 |
| 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 | - |
| 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) | - |
| 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) | - |
| Analysis of polymorphisms in PRNP 5' UTR region in sCJD subtypres | Capellari S; Corrado P; Gambetti P; Parchi P | 2008-01-01 | - | sn | 4.02 Riassunto (Abstract) | - |