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Items: 39

1.

Altered Expression of Circulating Cdc42 in Frontotemporal Lobar Degeneration.

Saraceno C, Catania M, Paterlini A, Fostinelli S, Ciani M, Zanardini R, Binetti G, Di Fede G, Caroppo P, Benussi L, Ghidoni R, Bolognin S.

J Alzheimers Dis. 2018;61(4):1477-1483. doi: 10.3233/JAD-170722.

PMID:
29376863
2.

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.

3.

Factors influencing the age at onset in familial frontotemporal lobar dementia: Important weight of genetics.

Barbier M, Camuzat A, Houot M, Clot F, Caroppo P, Fournier C, Rinaldi D, Pasquier F, Hannequin D, Pariente J, Larcher K; French Clinical and Genetic Research Network on FTD/FTD-ALS*; Predict-PGRN & PrevDemAls Study Groups†, Brice A, Génin E, Sabbagh A, Le Ber I.

Neurol Genet. 2017 Dec 13;3(6):e203. doi: 10.1212/NXG.0000000000000203. eCollection 2017 Dec.

4.

Early Cognitive, Structural, and Microstructural Changes in Presymptomatic C9orf72 Carriers Younger Than 40 Years.

Bertrand A, Wen J, Rinaldi D, Houot M, Sayah S, Camuzat A, Fournier C, Fontanella S, Routier A, Couratier P, Pasquier F, Habert MO, Hannequin D, Martinaud O, Caroppo P, Levy R, Dubois B, Brice A, Durrleman S, Colliot O, Le Ber I; Predict to Prevent Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis (PREV-DEMALS) Study Group.

JAMA Neurol. 2018 Feb 1;75(2):236-245. doi: 10.1001/jamaneurol.2017.4266.

PMID:
29197216
5.

Missense mutation in GRN gene affecting RNA splicing and plasma progranulin level in a family affected by frontotemporal lobar degeneration.

Luzzi S, Colleoni L, Corbetta P, Baldinelli S, Fiori C, Girelli F, Silvestrini M, Caroppo P, Giaccone G, Tagliavini F, Rossi G.

Neurobiol Aging. 2017 Jun;54:214.e1-214.e6. doi: 10.1016/j.neurobiolaging.2017.02.008. Epub 2017 Feb 20.

PMID:
28285794
6.

Alzheimer neuropathology without frontotemporal lobar degeneration hallmarks (TAR DNA-binding protein 43 inclusions) in missense progranulin mutation Cys139Arg.

Redaelli V, Rossi G, Maderna E, Kovacs GG, Piccoli E, Caroppo P, Cacciatore F, Spinello S, Grisoli M, Sozzi G, Salmaggi A, Tagliavini F, Giaccone G.

Brain Pathol. 2018 Jan;28(1):72-76. doi: 10.1111/bpa.12480. Epub 2017 Feb 15.

PMID:
27997711
7.

17q21.31 duplication causes prominent tau-related dementia with increased MAPT expression.

Le Guennec K, Quenez O, Nicolas G, Wallon D, Rousseau S, Richard AC, Alexander J, Paschou P, Charbonnier C, Bellenguez C, Grenier-Boley B, Lechner D, Bihoreau MT, Olaso R, Boland A, Meyer V, Deleuze JF, Amouyel P, Munter HM, Bourque G, Lathrop M, Frebourg T, Redon R, Letenneur L, Dartigues JF, Martinaud O, Kalev O, Mehrabian S, Traykov L, Ströbel T, Le Ber I, Caroppo P, Epelbaum S, Jonveaux T, Pasquier F, Rollin-Sillaire A, Génin E, Guyant-Maréchal L, Kovacs GG, Lambert JC, Hannequin D, Campion D, Rovelet-Lecrux A.

Mol Psychiatry. 2017 Aug;22(8):1119-1125. doi: 10.1038/mp.2016.226. Epub 2016 Dec 13.

PMID:
27956742
8.

A cluster of progranulin C157KfsX97 mutations in Southern Italy: clinical characterization and genetic correlations.

Coppola C, Saracino D, Puoti G, Lus G, Dato C, Le Ber I, Pariente J, Caroppo P, Piccoli E, Tagliavini F, Di Iorio G, Rossi G.

Neurobiol Aging. 2017 Jan;49:219.e5-219.e13. doi: 10.1016/j.neurobiolaging.2016.10.008. Epub 2016 Oct 11.

PMID:
27814992
9.

Cognitive and Neurophysiological Effects of Non-invasive Brain Stimulation in Stroke Patients after Motor Rehabilitation.

D'Agata F, Peila E, Cicerale A, Caglio MM, Caroppo P, Vighetti S, Piedimonte A, Minuto A, Campagnoli M, Salatino A, Molo MT, Mortara P, Pinessi L, Massazza G.

Front Behav Neurosci. 2016 Jun 24;10:135. doi: 10.3389/fnbeh.2016.00135. eCollection 2016.

10.

Defining the spectrum of frontotemporal dementias associated with TARDBP mutations.

Caroppo P, Camuzat A, Guillot-Noel L, Thomas-Antérion C, Couratier P, Wong TH, Teichmann M, Golfier V, Auriacombe S, Belliard S, Laurent B, Lattante S, Millecamps S, Clot F, Dubois B, van Swieten JC, Brice A, Le Ber I.

Neurol Genet. 2016 May 26;2(3):e80. doi: 10.1212/NXG.0000000000000080. eCollection 2016 Jun.

11.

Chemotherapy-Induced Neurotoxicity: Evidence of a Protective Role of CC Homozygosis in the Interleukin-1β Gene-511 C>T Polymorphism.

Peila E, D'Agata F, Caroppo P, Orsi L, Mortara P, Cauda S, Manfredi M, Caglio MM, Fenoglio P, Baudino B, Castellano G, Bisi G, Pinessi L, Gallone S.

Neurotox Res. 2016 Oct;30(3):521-9. doi: 10.1007/s12640-016-9637-1. Epub 2016 Jun 7.

12.

Semantic and nonfluent aphasic variants, secondarily associated with amyotrophic lateral sclerosis, are predominant frontotemporal lobar degeneration phenotypes in TBK1 carriers.

Caroppo P, Camuzat A, De Septenville A, Couratier P, Lacomblez L, Auriacombe S, Flabeau O, Jornéa L, Blanc F, Sellal F, Cretin B, Meininger V, Fleury MC, Couarch P, Dubois B, Brice A, Le Ber I.

Alzheimers Dement (Amst). 2015 Oct 30;1(4):481-6. doi: 10.1016/j.dadm.2015.10.002. eCollection 2015 Dec.

13.

Neuroimaging Correlates of Frontotemporal Dementia Associated with SQSTM1 Mutations.

Luis E, Ortiz A, Eudave L, Ortega-Cubero S, Borroni B, van der Zee J, Gazzina S, Caroppo P, Rubino E, D'Agata F, Le Ber I, Santana I, Cunha G, Almeida MR, Boutoleau-Bretonnière C, Hannequin D, Wallon D, Rainero I, Galimberti D, Van Broeckhoven C, Pastor MA, Pastor P.

J Alzheimers Dis. 2016 May 7;53(1):303-13. doi: 10.3233/JAD-160006.

14.

White matter lesions in FTLD: distinct phenotypes characterize GRN and C9ORF72 mutations.

Ameur F, Colliot O, Caroppo P, Ströer S, Dormont D, Brice A, Azuar C, Dubois B, Le Ber I, Bertrand A.

Neurol Genet. 2016 Jan 28;2(1):e47. doi: 10.1212/NXG.0000000000000047. eCollection 2016 Feb.

15.

Neurologic and cognitive outcomes after aortic arch operation with hypothermic circulatory arrest.

Centofanti P, Barbero C, D'Agata F, Caglio MM, Caroppo P, Cicerale A, Attisani M, La Torre M, Milan A, Contristano ML, Carlini E, Izzo G, Mortara P, Veglio F, Rinaldi M.

Surgery. 2016 Sep;160(3):796-804. doi: 10.1016/j.surg.2016.02.008. Epub 2016 Apr 3.

16.

TBK1 mutation frequencies in French frontotemporal dementia and amyotrophic lateral sclerosis cohorts.

Le Ber I, De Septenville A, Millecamps S, Camuzat A, Caroppo P, Couratier P, Blanc F, Lacomblez L, Sellal F, Fleury MC, Meininger V, Cazeneuve C, Clot F, Flabeau O, LeGuern E, Brice A; French Clinical and Genetic Research Network on FTLD/FTLD-ALS.

Neurobiol Aging. 2015 Nov;36(11):3116.e5-3116.e8. doi: 10.1016/j.neurobiolaging.2015.08.009. Epub 2015 Aug 14.

PMID:
26476236
17.

Lateral Temporal Lobe: An Early Imaging Marker of the Presymptomatic GRN Disease?

Caroppo P, Habert MO, Durrleman S, Funkiewiez A, Perlbarg V, Hahn V, Bertin H, Gaubert M, Routier A, Hannequin D, Deramecourt V, Pasquier F, Rivaud-Pechoux S, Vercelletto M, Edouart G, Valabregue R, Lejeune P, Didic M, Corvol JC, Benali H, Lehericy S, Dubois B, Colliot O, Brice A, Le Ber I; Predict-PGRN study group.

J Alzheimers Dis. 2015;47(3):751-9. doi: 10.3233/JAD-150270.

18.

Neurofunctional Signature of Hyperfamiliarity for Unknown Faces.

Negro E, D'Agata F, Caroppo P, Coriasco M, Ferrio F, Celeghin A, Diano M, Rubino E, de Gelder B, Rainero I, Pinessi L, Tamietto M.

PLoS One. 2015 Jul 8;10(7):e0129970. doi: 10.1371/journal.pone.0129970. eCollection 2015.

19.

Double-Cone Coil TMS Stimulation of the Medial Cortex Inhibits Central Pain Habituation.

D'Agata F, Cicerale A, Mingolla A, Caroppo P, Orsi L, Mortara P, Troni W, Pinessi L.

PLoS One. 2015 Jun 5;10(6):e0128765. doi: 10.1371/journal.pone.0128765. eCollection 2015.

20.

Brain correlates of alexithymia in eating disorders: A voxel-based morphometry study.

D'Agata F, Caroppo P, Amianto F, Spalatro A, Caglio MM, Bergui M, Lavagnino L, Righi D, Abbate-Daga G, Pinessi L, Mortara P, Fassino S.

Psychiatry Clin Neurosci. 2015 Nov;69(11):708-16. doi: 10.1111/pcn.12318. Epub 2015 Jun 26.

21.

Posterior cortical atrophy as an extreme phenotype of GRN mutations.

Caroppo P, Belin C, Grabli D, Maillet D, De Septenville A, Migliaccio R, Clot F, Lamari F, Camuzat A, Brice A, Dubois B, Le Ber I.

JAMA Neurol. 2015 Feb;72(2):224-8. doi: 10.1001/jamaneurol.2014.3308.

PMID:
25546130
22.

Extensive white matter involvement in patients with frontotemporal lobar degeneration: think progranulin.

Caroppo P, Le Ber I, Camuzat A, Clot F, Naccache L, Lamari F, De Septenville A, Bertrand A, Belliard S, Hannequin D, Colliot O, Brice A.

JAMA Neurol. 2014 Dec;71(12):1562-6. doi: 10.1001/jamaneurol.2014.1316.

PMID:
25317628
23.

Homozygous TREM2 mutation in a family with atypical frontotemporal dementia.

Le Ber I, De Septenville A, Guerreiro R, Bras J, Camuzat A, Caroppo P, Lattante S, Couarch P, Kabashi E, Bouya-Ahmed K, Dubois B, Brice A.

Neurobiol Aging. 2014 Oct;35(10):2419.e23-2419.e25. doi: 10.1016/j.neurobiolaging.2014.04.010. Epub 2014 Apr 18.

24.

The Neurobiological Basis of the Distress Thermometer: A PET Study in Cancer Patients.

Castelli L, Tonello D, D'Agata F, Caroppo P, Baudino B, Zotta M, Cauda S, Pinessi L, Mortara P, Grassi L, Bisi G, Torta R.

Stress Health. 2015 Aug;31(3):197-203. doi: 10.1002/smi.2546. Epub 2013 Nov 6.

25.

Partial deletions of the GRN gene are a cause of frontotemporal lobar degeneration.

Clot F, Rovelet-Lecrux A, Lamari F, Noël S, Keren B, Camuzat A, Michon A, Jornea L, Laudier B, de Septenville A, Caroppo P, Campion D, Cazeneuve C, Brice A, LeGuern E, Le Ber I; French clinical and genetic research network on FTLD/FTLD-ALS.

Neurogenetics. 2014 May;15(2):95-100. doi: 10.1007/s10048-014-0389-x. Epub 2014 Jan 28.

PMID:
24469240
26.

DCTN1 mutation analysis in families with progressive supranuclear palsy-like phenotypes.

Caroppo P, Le Ber I, Clot F, Rivaud-Péchoux S, Camuzat A, De Septenville A, Boutoleau-Bretonnière C, Mourlon V, Sauvée M, Lebouvier T, Bonnet AM, Levy R, Vercelletto M, Brice A; French Clinical and Genetic Research Network on Frontotemporal Dementia/Frontotemporal Dementia–Amyotrophic Lateral Sclerosis.

JAMA Neurol. 2014 Feb;71(2):208-15. doi: 10.1001/jamaneurol.2013.5100.

27.

Brain volumetric abnormalities in patients with anorexia and bulimia nervosa: a voxel-based morphometry study.

Amianto F, Caroppo P, D'Agata F, Spalatro A, Lavagnino L, Caglio M, Righi D, Bergui M, Abbate-Daga G, Rigardetto R, Mortara P, Fassino S.

Psychiatry Res. 2013 Sep 30;213(3):210-6. doi: 10.1016/j.pscychresns.2013.03.010. Epub 2013 Jul 13.

PMID:
23856299
28.

Multivariate analysis of brain metabolism reveals chemotherapy effects on prefrontal cerebellar system when related to dorsal attention network.

D'Agata F, Costa T, Caroppo P, Baudino B, Cauda F, Manfredi M, Geminiani G, Mortara P, Pinessi L, Castellano G, Bisi G.

EJNMMI Res. 2013 Apr 4;3(1):22. doi: 10.1186/2191-219X-3-22.

29.

Intrinsic connectivity networks within cerebellum and beyond in eating disorders.

Amianto F, D'Agata F, Lavagnino L, Caroppo P, Abbate-Daga G, Righi D, Scarone S, Bergui M, Mortara P, Fassino S.

Cerebellum. 2013 Oct;12(5):623-31. doi: 10.1007/s12311-013-0471-1.

PMID:
23553468
30.

Brain metabolism changes after therapy with chenodeoxycholic acid in a case of cerebrotendinous xanthomatosis.

Caroppo P, D'Agata F, Mignarri A, Stromillo ML, Dotti MT, Mongini T.

Neurol Sci. 2013 Sep;34(9):1693-6. doi: 10.1007/s10072-012-1262-z. Epub 2012 Dec 5. No abstract available.

PMID:
23212406
31.

The chemotherapy long-term effect on cognitive functions and brain metabolism in lymphoma patients.

Baudino B, D'agata F, Caroppo P, Castellano G, Cauda S, Manfredi M, Geda E, Castelli L, Mortara P, Orsi L, Cauda F, Sacco K, Ardito RB, Pinessi L, Geminiani G, Torta R, Bisi G.

Q J Nucl Med Mol Imaging. 2012 Dec;56(6):559-68. Epub 2012 Nov 21.

32.

A new NOTCH3 mutation presenting as primary intracerebral haemorrhage.

Pradotto L, Orsi L, Daniele D, Caroppo P, Lauro D, Milesi A, Sellitti L, Mauro A.

J Neurol Sci. 2012 Apr 15;315(1-2):143-5. doi: 10.1016/j.jns.2011.12.003. Epub 2011 Dec 27.

PMID:
22206696
33.

The recognition of facial emotions in spinocerebellar ataxia patients.

D'Agata F, Caroppo P, Baudino B, Caglio M, Croce M, Bergui M, Tamietto M, Mortara P, Orsi L.

Cerebellum. 2011 Sep;10(3):600-10. doi: 10.1007/s12311-011-0276-z.

34.

Linking coordinative and executive dysfunctions to atrophy in spinocerebellar ataxia 2 patients.

D'Agata F, Caroppo P, Boghi A, Coriasco M, Caglio M, Baudino B, Sacco K, Cauda F, Geda E, Bergui M, Geminiani G, Bradac GB, Orsi L, Mortara P.

Brain Struct Funct. 2011 Sep;216(3):275-88. doi: 10.1007/s00429-011-0310-4. Epub 2011 Apr 2.

35.

Neuropsychological picture of 33 spinocerebellar ataxia cases.

Orsi L, D'Agata F, Caroppo P, Franco A, Caglio MM, Avidano F, Manzone C, Mortara P.

J Clin Exp Neuropsychol. 2011 Mar;33(3):315-25. doi: 10.1080/13803395.2010.518139. Epub 2011 Feb 6.

PMID:
21302172
36.

Neuropsychological and functional study in a case of partial cerebellar agenesis.

Caroppo P, Orsi L, D'Agata F, Baudino B, Boghi A, Avidano F, Coriasco M, Bradac GB, Castellano G, Mutani R, Mortara P.

Neurocase. 2009 Oct;15(5):373-83. doi: 10.1080/13554790902842029. Epub 2009 Jul 15.

PMID:
19606387
37.

A previously undiagnosed case of Gerstmann-Sträussler-Scheinker disease revealed by PRNP gene analysis in patients with adult-onset ataxia.

Cagnoli C, Brussino A, Sbaiz L, Di Gregorio E, Atzori C, Caroppo P, Orsi L, Migone N, Buffa C, Imperiale D, Brusco A.

Mov Disord. 2008 Jul 30;23(10):1468-71. doi: 10.1002/mds.21953.

PMID:
18566986
38.

Mutations in the POLG1 gene are not a relevant cause of cerebellar ataxia in Italy.

Cagnoli C, Brussino A, Di Gregorio E, Caroppo P, Stola S, Dragone E, Ferrone M, Padovan S, Migone N, Orsi L, Brusco A.

J Neurol. 2008 Jul;255(7):1079-80. doi: 10.1007/s00415-008-0772-3. Epub 2008 May 5. No abstract available.

PMID:
18446310
39.

The effect of gender on planning: An fMRI study using the Tower of London task.

Boghi A, Rasetti R, Avidano F, Manzone C, Orsi L, D'Agata F, Caroppo P, Bergui M, Rocca P, Pulvirenti L, Bradac GB, Bogetto F, Mutani R, Mortara P.

Neuroimage. 2006 Nov 15;33(3):999-1010. Epub 2006 Sep 26.

PMID:
17005420

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