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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, Magnoni S, Chiari L, Cortelli P, Cevoli S; BOLOGNA PRO-HYDRO Study Group.

Parkinsonism Relat Disord. 2019 Jul 18. pii: S1353-8020(19)30311-6. doi: 10.1016/j.parkreldis.2019.07.021. [Epub ahead of print]


Age at onset in genetic prion disease and the design of preventive clinical trials.

Minikel EV, Vallabh SM, Orseth MC, Brandel JP, Haïk S, Laplanche JL, Zerr I, Parchi P, Capellari S, Safar J, Kenny J, Fong JC, Takada LT, Ponto C, Hermann P, Knipper T, Stehmann C, Kitamoto T, Ae R, Hamaguchi T, Sanjo N, Tsukamoto T, Mizusawa H, Collins SJ, Chiesa R, Roiter I, de Pedro-Cuesta J, Calero M, Geschwind MD, Yamada M, Nakamura Y, Mead S.

Neurology. 2019 Jul 9;93(2):e125-e134. doi: 10.1212/WNL.0000000000007745. Epub 2019 Jun 6.


A Novel Eight Octapeptide Repeat Insertion in PRNP Causing Prion Disease in a Danish Family.

Areškevičiūtė A, Høgh P, Bartoletti-Stella A, Melchior LC, Nielsen PR, Parchi P, Capellari S, Broholm H, Scheie D, Lund EL.

J Neuropathol Exp Neurol. 2019 Jul 1;78(7):595-604. doi: 10.1093/jnen/nlz037.


Predicting conversion from mild cognitive impairment to Alzheimer's disease using brain 1H-MRS and volumetric changes: A two- year retrospective follow-up study.

Mitolo M, Stanzani-Maserati M, Capellari S, Testa C, Rucci P, Poda R, Oppi F, Gallassi R, Sambati L, Rizzo G, Parchi P, Evangelisti S, Talozzi L, Tonon C, Lodi R, Liguori R.

Neuroimage Clin. 2019 Apr 30;23:101843. doi: 10.1016/j.nicl.2019.101843. [Epub ahead of print]


The characterization of AD/PART co-pathology in CJD suggests independent pathogenic mechanisms and no cross-seeding between misfolded Aβ and prion proteins.

Rossi M, Kai H, Baiardi S, Bartoletti-Stella A, Carlà B, Zenesini C, Capellari S, Kitamoto T, Parchi P.

Acta Neuropathol Commun. 2019 Apr 8;7(1):53. doi: 10.1186/s40478-019-0706-6.


Prion protein quantification in human cerebrospinal fluid as a tool for prion disease drug development.

Vallabh SM, Nobuhara CK, Llorens F, Zerr I, Parchi P, Capellari S, Kuhn E, Klickstein J, Safar JG, Nery FC, Swoboda KJ, Geschwind MD, Zetterberg H, Arnold SE, Minikel EV, Schreiber SL.

Proc Natl Acad Sci U S A. 2019 Apr 16;116(16):7793-7798. doi: 10.1073/pnas.1901947116. Epub 2019 Apr 1.


Understanding Prion Strains: Evidence from Studies of the Disease Forms Affecting Humans.

Rossi M, Baiardi S, Parchi P.

Viruses. 2019 Mar 29;11(4). pii: E309. doi: 10.3390/v11040309. Review.


Clinicopathological features of the rare form of Creutzfeldt-Jakob disease in R208H-V129V PRNP carrier.

Tiple D, Poleggi A, Mellina V, Morocutti A, Brusa L, Iani C, Colaizzo E, Vaianella L, Baiardi S, Ladogana A, Parchi P, Pocchiari M.

Acta Neuropathol Commun. 2019 Mar 21;7(1):47. doi: 10.1186/s40478-019-0699-1. No abstract available.


Revisiting the Cerebrospinal Fluid Biomarker Profile in Idiopathic Normal Pressure Hydrocephalus: The Bologna Pro-Hydro Study.

Abu-Rumeileh S, Giannini G, Polischi B, Albini-Riccioli L, Milletti D, Oppi F, Stanzani-Maserati M, Capellari S, Mantovani P, Palandri G, Cortelli P, Cevoli S, Parchi P.

J Alzheimers Dis. 2019;68(2):723-733. doi: 10.3233/JAD-181012.


Monthly Intramuscular Neridronate for the Treatment of Postmenopausal Osteoporosis: Results of a 6-Year Prospective Italian Study.

Guiducci L, Vassalle C, Parchi P, Maffei S.

Int J Endocrinol. 2019 Feb 6;2019:9802827. doi: 10.1155/2019/9802827. eCollection 2019.


Antemortem CSF Aβ42/Aβ40 ratio predicts Alzheimer's disease pathology better than Aβ42 in rapidly progressive dementias.

Baiardi S, Abu-Rumeileh S, Rossi M, Zenesini C, Bartoletti-Stella A, Polischi B, Capellari S, Parchi P.

Ann Clin Transl Neurol. 2018 Dec 14;6(2):263-273. doi: 10.1002/acn3.697. eCollection 2019 Feb.


Claims in total hip arthroplasty: analysis of the instigating factors, costs and possible solution.

Novi M, Vanni C, Parchi PD, Di Paolo M, Piolanti N, Scaglione M.

Musculoskelet Surg. 2019 Feb 13. doi: 10.1007/s12306-019-00590-6. [Epub ahead of print]


Sudden cardiac death in a patient with LGI1 antibody-associated encephalitis.

Rizzi R, Fisicaro F, Zangrandi A, Ghidoni E, Baiardi S, Ragazzi M, Parchi P.

Seizure. 2019 Feb;65:148-150. doi: 10.1016/j.seizure.2019.01.013. Epub 2019 Jan 25. No abstract available.


The 50 most cited articles about wrist surgery.

Piolanti N, Poggetti A, Nucci AM, Nesti A, Marchetti S, Parchi PD, Scaglione M.

Orthop Rev (Pavia). 2018 Dec 6;10(4):7715. doi: 10.4081/or.2018.7715. eCollection 2018 Dec 6.


Polymethylmethacrylate-augmented fenestreted pedicle-screw fixation in low bone quality patients: a case series and literature review.

Ghermandi R, Pipola V, Colangeli S, Parchi P, Andreani L, Capanna R, Gasbarrini A.

J Biol Regul Homeost Agents. 2018 Nov-Dec;32(6 Suppl. 1):71-76. Review.


Cryotherapy efficacy and safety as local therapy in surgical treatment of musculoskeletal tumours. A retrospective case series of 143 patients.

Colangeli S, Parchi P, Andreani L, Beltrami G, Scoccianti G, Sacchetti F, Ceccoli M, Totti F, Campanacci DA, Capanna R.

J Biol Regul Homeost Agents. 2018 Nov-Dec;32(6 Suppl. 1):65-70.


A local anesthesia without tourniquet for distal fibula hardware removal after open reduction and internal fixation: the safe use of epinephrine in the foot. A randomized clinical study.

Poggetti A, Del Chiaro A, Nicastro M, Parchi P, Piolanti N, Scaglione M.

J Biol Regul Homeost Agents. 2018 Nov-Dec;32(6 Suppl. 1):57-63.


Recent advances in the histo-molecular pathology of human prion disease.

Baiardi S, Rossi M, Capellari S, Parchi P.

Brain Pathol. 2019 Mar;29(2):278-300. doi: 10.1111/bpa.12695. Epub 2019 Jan 22. Review.


Variable Protease-Sensitive Prionopathy Transmission to Bank Voles.

Nonno R, Notari S, Di Bari MA, Cali I, Pirisinu L, d'Agostino C, Cracco L, Kofskey D, Vanni I, Lavrich J, Parchi P, Agrimi U, Gambetti P.

Emerg Infect Dis. 2019 Jan;25(1):73-81. doi: 10.3201/eid2501.180807.


How to Build a Patient-Specific Hybrid Simulator for Orthopaedic Open Surgery: Benefits and Limits of Mixed-Reality Using the Microsoft HoloLens.

Condino S, Turini G, Parchi PD, Viglialoro RM, Piolanti N, Gesi M, Ferrari M, Ferrari V.

J Healthc Eng. 2018 Nov 1;2018:5435097. doi: 10.1155/2018/5435097. eCollection 2018.


Analysis of RNA Expression Profiles Identifies Dysregulated Vesicle Trafficking Pathways in Creutzfeldt-Jakob Disease.

Bartoletti-Stella A, Corrado P, Mometto N, Baiardi S, Durrenberger PF, Arzberger T, Reynolds R, Kretzschmar H, Capellari S, Parchi P.

Mol Neurobiol. 2019 Jul;56(7):5009-5024. doi: 10.1007/s12035-018-1421-1. Epub 2018 Nov 16.


Prion-related peripheral neuropathy in sporadic Creutzfeldt-Jakob disease.

Baiardi S, Redaelli V, Ripellino P, Rossi M, Franceschini A, Moggio M, Sola P, Ladogana A, Fociani P, Magherini A, Capellari S, Giese A, Caughey B, Caroppo P, Parchi P.

J Neurol Neurosurg Psychiatry. 2019 Apr;90(4):424-427. doi: 10.1136/jnnp-2018-319221. Epub 2018 Oct 24.


Variably protease-sensitive prionopathy presenting within ALS/FTD spectrum.

Vicente-Pascual M, Rossi M, Gámez J, Lladó A, Valls J, Grau-Rivera O, Ávila Polo R, Llorens F, Zerr I, Ferrer I, Nos C, Parchi P, Sánchez-Valle R, Gelpí E.

Ann Clin Transl Neurol. 2018 Sep 21;5(10):1297-1302. doi: 10.1002/acn3.632. eCollection 2018 Oct.


Cerebrospinal Fluid Biomarkers in Patients with Frontotemporal Dementia Spectrum: A Single-Center Study.

Abu-Rumeileh S, Mometto N, Bartoletti-Stella A, Polischi B, Oppi F, Poda R, Stanzani-Maserati M, Cortelli P, Liguori R, Capellari S, Parchi P.

J Alzheimers Dis. 2018;66(2):551-563. doi: 10.3233/JAD-180409.


Clinical Reasoning: Rapidly progressive dementia in a patient with HIV after an exotic journey.

Abu-Rumeileh S, Baiardi S, D'Angelo R, Dentale N, Fasulo G, Guarino M, Parchi P.

Neurology. 2018 Oct 2;91(14):e1360-e1364. doi: 10.1212/WNL.0000000000006285. No abstract available.


Anterior Cruciate Ligament Reconstruction with LARS Artificial Ligament-Clinical Results after a Long-Term Follow-Up.

Parchi PD, Ciapini G, Paglialunga C, Giuntoli M, Picece C, Chiellini F, Lisanti M, Scaglione M.

Joints. 2018 May 23;6(2):75-79. doi: 10.1055/s-0038-1653950. eCollection 2018 Jun.


Sporadic Fatal Insomnia in Europe: Phenotypic Features and Diagnostic Challenges.

Abu-Rumeileh S, Redaelli V, Baiardi S, Mackenzie G, Windl O, Ritchie DL, Didato G, Hernandez-Vara J, Rossi M, Capellari S, Imperiale D, Rizzone MG, Belotti A, Sorbi S, Rozemuller AJM, Cortelli P, Gelpi E, Will RG, Zerr I, Giaccone G, Parchi P.

Ann Neurol. 2018 Sep;84(3):347-360. doi: 10.1002/ana.25300. Epub 2018 Aug 31.


Age at onset of genetic (E200K) and sporadic Creutzfeldt-Jakob diseases is modulated by the CYP4X1 gene.

Poleggi A, van der Lee S, Capellari S, Puopolo M, Ladogana A, De Pascali E, Lia D, Formato A, Bartoletti-Stella A, Parchi P, van Duijn C, Pocchiari M.

J Neurol Neurosurg Psychiatry. 2018 Dec;89(12):1243-1249. doi: 10.1136/jnnp-2018-318756. Epub 2018 Jul 21.


Unusual Clinical Presentations Challenging the Early Clinical Diagnosis of Creutzfeldt-Jakob Disease.

Baiardi S, Capellari S, Bartoletti Stella A, Parchi P.

J Alzheimers Dis. 2018;64(4):1051-1065. doi: 10.3233/JAD-180123. Review.


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 GL, Parchi P, Schenone A.

Eur J Neurol. 2018 Aug;25(8):e91-e92. doi: 10.1111/ene.13665. No abstract available.


Two novel PRNP truncating mutations broaden the spectrum of prion amyloidosis.

Capellari S, Baiardi S, Rinaldi R, Bartoletti-Stella A, Graziano C, Piras S, Calandra-Buonaura G, D'Angelo R, Terziotti C, Lodi R, Donadio V, Pironi L, Cortelli P, Parchi P.

Ann Clin Transl Neurol. 2018 Apr 26;5(6):777-783. doi: 10.1002/acn3.568. eCollection 2018 Jun.


LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study.

Quadri M, Mandemakers W, Grochowska MM, Masius R, Geut H, Fabrizio E, Breedveld GJ, Kuipers D, Minneboo M, Vergouw LJM, Carreras Mascaro A, Yonova-Doing E, Simons E, Zhao T, Di Fonzo AB, Chang HC, Parchi P, Melis M, Correia Guedes L, Criscuolo C, Thomas A, Brouwer RWW, Heijsman D, Ingrassia AMT, Calandra Buonaura G, Rood JP, Capellari S, Rozemuller AJ, Sarchioto M, Fen Chien H, Vanacore N, Olgiati S, Wu-Chou YH, Yeh TH, Boon AJW, Hoogers SE, Ghazvini M, IJpma AS, van IJcken WFJ, Onofrj M, Barone P, Nicholl DJ, Puschmann A, De Mari M, Kievit AJ, Barbosa E, De Michele G, Majoor-Krakauer D, van Swieten JC, de Jong FJ, Ferreira JJ, Cossu G, Lu CS, Meco G, Cortelli P, van de Berg WDJ, Bonifati V; International Parkinsonism Genetics Network.

Lancet Neurol. 2018 Jul;17(7):597-608. doi: 10.1016/S1474-4422(18)30179-0. Epub 2018 Jun 7.


Sporadic Creutzfeldt-Jakob disease.

Zerr I, Parchi P.

Handb Clin Neurol. 2018;153:155-174. doi: 10.1016/B978-0-444-63945-5.00009-X.


Rapidly Progressive Alzheimer's Disease: Contributions to Clinical-Pathological Definition and Diagnosis.

Abu-Rumeileh S, Capellari S, Parchi P.

J Alzheimers Dis. 2018;63(3):887-897. doi: 10.3233/JAD-171181. Review.


Identification of rare genetic variants in Italian patients with dementia by targeted gene sequencing.

Bartoletti-Stella A, Baiardi S, Stanzani-Maserati M, Piras S, Caffarra P, Raggi A, Pantieri R, Baldassari S, Caporali L, Abu-Rumeileh S, Linarello S, Liguori R, Parchi P, Capellari S.

Neurobiol Aging. 2018 Jun;66:180.e23-180.e31. doi: 10.1016/j.neurobiolaging.2018.02.006. Epub 2018 Feb 13.


The First Historically Reported Italian Family with FTD/ALS Teaches a Lesson on C9orf72 RE: Clinical Heterogeneity and Oligogenic Inheritance.

Giannoccaro MP, Bartoletti-Stella A, Piras S, Casalena A, Oppi F, Ambrosetto G, Montagna P, Liguori R, Parchi P, Capellari S.

J Alzheimers Dis. 2018;62(2):687-697. doi: 10.3233/JAD-170913.


Familial human prion diseases associated with prion protein mutations Y226X and G131V are transmissible to transgenic mice expressing human prion protein.

Race B, Williams K, Hughson AG, Jansen C, Parchi P, Rozemuller AJM, Chesebro B.

Acta Neuropathol Commun. 2018 Feb 20;6(1):13. doi: 10.1186/s40478-018-0516-2.


An in vivo 11C-PK PET study of microglia activation in Fatal Familial Insomnia.

Iaccarino L, Presotto L, Bettinardi V, Gianolli L, Roiter I, Capellari S, Parchi P, Cortelli P, Perani D.

Ann Clin Transl Neurol. 2017 Dec 9;5(1):11-18. doi: 10.1002/acn3.498. eCollection 2018 Jan.


The CSF neurofilament light signature in rapidly progressive neurodegenerative dementias.

Abu-Rumeileh S, Capellari S, Stanzani-Maserati M, Polischi B, Martinelli P, Caroppo P, Ladogana A, Parchi P.

Alzheimers Res Ther. 2018 Jan 11;10(1):3. doi: 10.1186/s13195-017-0331-1.


Cerebral Mitochondrial Microangiopathy Leads to Leukoencephalopathy in Mitochondrial Neurogastrointestinal Encephalopathy.

Gramegna LL, Pisano A, Testa C, Manners DN, D'Angelo R, Boschetti E, Giancola F, Pironi L, Caporali L, Capristo M, Valentino ML, Plazzi G, Casali C, Dotti MT, Cenacchi G, Hirano M, Giordano C, Parchi P, Rinaldi R, De Giorgio R, Lodi R, Carelli V, Tonon C.

AJNR Am J Neuroradiol. 2018 Mar;39(3):427-434. doi: 10.3174/ajnr.A5507. Epub 2018 Jan 18.


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.

Neuropathol Appl Neurobiol. 2018 Oct;44(6):574-589. doi: 10.1111/nan.12461. Epub 2018 Feb 26.


Iatrogenic Creutzfeldt-Jakob disease with Amyloid-β pathology: an international study.

Cali I, Cohen ML, Haik S, Parchi P, Giaccone G, Collins SJ, Kofskey D, Wang H, McLean CA, Brandel JP, Privat N, Sazdovitch V, Duyckaerts C, Kitamoto T, Belay ED, Maddox RA, Tagliavini F, Pocchiari M, Leschek E, Appleby BS, Safar JG, Schonberger LB, Gambetti P.

Acta Neuropathol Commun. 2018 Jan 8;6(1):5. doi: 10.1186/s40478-017-0503-z.


Bone cement implantation syndrome: a thromboelastographic study of the effect of bone cement on coagulation.

Mordà M, Pini S, Celli F, Casella F, Parchi P, Piolanti N, Marchetti S, Scaglione M.

J Biol Regul Homeost Agents. 2017 Oct-Dec,;31(4 suppl 1):121-127.


Use of autologous bone marrow cells concentrate enriched with platelet-fibrin on extensor mechanism allograft reconstruction for extensor mechanism failure following total knee arthroplasty.

Giannotti S, Parchi PD, Colasanti GB, Agostini G, Moreschini F, Cataldi C, Ferrata P, Capanna R.

J Biol Regul Homeost Agents. 2017 Oct-Dec;31(4 suppl 1):107-111.


Correlation between gamma glutamyltransferase fractions and bone quality.

Franzini M, Nesti A, Panetta D, Fierabracci V, Marchetti S, Parchi PD, Caponi L, Paolicchi A, Musetti V, Salvadori P, Edmin M, Pucci A, Bonicoli E, Scaglione M, Piolanti N.

J Biol Regul Homeost Agents. 2017 Oct-Dec,;31(4 suppl 1). pii: 14.


Complications and survival of megaprostheses after resection of bone metastases.

De Gori M, D’Arienzo A, Andreani L, Beltrami G, Campanacci DA, De Biase P, Frenos F, Giannotti S, Sacchetti F, Totti F, Parchi P, Capanna R.

J Biol Regul Homeost Agents. 2017 Oct-Dec,;31(4 suppl 1):43-50.


Clinical and radiographic short mid-term outcomes of primary total stabilizer knee arthroplasty.

Bonicoli E, Piolanti N, Giuntoli M, Polloni S, Ciapini G, Parchi PD, Scaglione M.

J Biol Regul Homeost Agents. 2017 Oct-Dec,;31(4 Suppl 1):7-14.


Atypical Creutzfeldt-Jakob disease with PrP-amyloid plaques in white matter: molecular characterization and transmission to bank voles show the M1 strain signature.

Rossi M, Saverioni D, Di Bari M, Baiardi S, Lemstra AW, Pirisinu L, Capellari S, Rozemuller A, Nonno R, Parchi P.

Acta Neuropathol Commun. 2017 Nov 23;5(1):87. doi: 10.1186/s40478-017-0496-7.


Messenger RNA processing is altered in autosomal dominant leukodystrophy.

Bartoletti-Stella A, Gasparini L, Giacomini C, Corrado P, Terlizzi R, Giorgio E, Magini P, Seri M, Baruzzi A, Parchi P, Brusco A, Cortelli P, Capellari S.

Hum Mol Genet. 2017 Oct 1;26(19):3868. doi: 10.1093/hmg/ddx225. No abstract available.


High diagnostic value of second generation CSF RT-QuIC across the wide spectrum of CJD prions.

Franceschini A, Baiardi S, Hughson AG, McKenzie N, Moda F, Rossi M, Capellari S, Green A, Giaccone G, Caughey B, Parchi P.

Sci Rep. 2017 Sep 6;7(1):10655. doi: 10.1038/s41598-017-10922-w.

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