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Items: 1 to 50 of 170

1.

ATXN2 intermediate repeat expansions influence the clinical phenotype in frontotemporal dementia.

Rubino E, Mancini C, Boschi S, Ferrero P, Ferrone M, Bianca S, Zucca M, Orsi L, Pinessi L, Govone F, Vacca A, Gai A, Giordana MT, Brusco A, Rainero I.

Neurobiol Aging. 2019 Jan;73:231.e7-231.e9. doi: 10.1016/j.neurobiolaging.2018.09.009. Epub 2018 Sep 22.

PMID:
30342763
2.

Migraine: Genetic Variants and Clinical Phenotypes.

Rainero I, Vacca A, Govone F, Gai A, Pinessi L, Rubino E.

Curr Med Chem. 2018 Jul 19. doi: 10.2174/0929867325666180719120215. [Epub ahead of print]

PMID:
30027842
3.

Noninvasive Vagal Nerve Stimulation in Chronic Migraine with Medication Overuse Headache.

Vacca A, Gai A, Govone F, Rubino E, De Martino P, Gentile S, Pinessi L, Rainero I.

Pain Med. 2018 Dec 1;19(12):2575-2577. doi: 10.1093/pm/pny084. No abstract available.

PMID:
29767791
4.

Subclinical hypothyroidism is associated with migraine: A case-control study.

Rubino E, Rainero I, Garino F, Vicentini C, Govone F, Vacca A, Gai A, Gentile S, Govone G, Ragazzoni F, Pinessi L, Giordana MT, Limone P.

Cephalalgia. 2019 Jan;39(1):15-20. doi: 10.1177/0333102418769917. Epub 2018 Apr 22.

PMID:
29682977
5.

Corrigendum to "Neural correlates of reduced awareness in instrumental activities of daily living in frontotemporal dementia" [Exp. Gerontol. 83 (2016) 158-164].

Amanzio M, D'Agata F, Palermo S, Rubino E, Zucca M, Galati A, Pinessi L, Castellano G, Rainero I.

Exp Gerontol. 2017 Oct 1;96:164-165. doi: 10.1016/j.exger.2017.05.022. Epub 2017 Jun 17. No abstract available.

PMID:
28633865
6.

Recent advances in the molecular genetics of frontotemporal lobar degeneration.

Rainero I, Rubino E, Michelerio A, D'Agata F, Gentile S, Pinessi L.

Funct Neurol. 2017 Jan/Mar;32(1):7-16. Review.

7.

O057. Altered plasma adipokines concentrations in chronic migraine.

Rubino E, Govone F, Vacca A, Gai A, Boschi S, Zucca M, Pinessi L, Rainero I.

J Headache Pain. 2015 Dec;16(Suppl 1):A56. doi: 10.1186/1129-2377-16-S1-A56. No abstract available.

8.

P055. Prevalence of migraine in subclinical hypothyroidism: a case-control study.

Rainero I, Rubino E, Vicentini C, Garino F, Ragazzoni F, Pinessi L, Limone P.

J Headache Pain. 2015 Dec;16(Suppl 1):A81. doi: 10.1186/1129-2377-16-S1-A81. No abstract available.

9.

P014. Migraine and hypnosis.

Ardore M, Pinessi L, Savi L.

J Headache Pain. 2015 Dec;16(Suppl 1):A86. doi: 10.1186/1129-2377-16-S1-A86. No abstract available.

10.

O056. Migraine as presenting symptom of SLC20A2gene mutations.

Rubino E, Giorgio E, Rainero I, Ferrero P, Gallone S, Govone F, Pinessi L, Orsi L, Duca S, Brusco A.

J Headache Pain. 2015 Dec;16(Suppl 1):A121. doi: 10.1186/1129-2377-16-S1-A121. No abstract available.

11.

Effects of Multiple Genetic Loci on Age at Onset in Frontotemporal Dementia.

Ferrari R, Grassi M, Graziano F, Palluzzi F, Archetti S, Bonomi E, Bruni AC, Maletta RG, Bernardi L, Cupidi C, Colao R, Rainero I, Rubino E, Pinessi L, Galimberti D, Scarpini E, Serpente M, Nacmias B, Piaceri I, Bagnoli S, Rossi G, Giaccone G, Tagliavini F, Benussi L, Binetti G, Ghidoni R, Singleton A, Hardy J, Momeni P, Padovani A, Borroni B.

J Alzheimers Dis. 2017;56(4):1271-1278. doi: 10.3233/JAD-160949.

12.

Genetic analysis of CHCHD2 and CHCHD10 in Italian patients with Parkinson's disease.

Rubino E, Brusa L, Zhang M, Boschi S, Govone F, Vacca A, Gai A, Pinessi L, Lopiano L, Rogaeva E, Rainero I.

Neurobiol Aging. 2017 May;53:193.e7-193.e8. doi: 10.1016/j.neurobiolaging.2016.12.027. Epub 2017 Jan 5.

PMID:
28108040
13.

Successful use of bevacizumab in an adult primary diffuse leptomeningeal glioneuronal tumor.

Pellerino A, Rudà R, Bertero L, Magistrello M, Franchino F, Cassoni P, Pasqualetti F, Pinessi L, Giangaspero F, Soffietti R.

J Neurosurg Sci. 2018 Apr;62(2):229-232. doi: 10.23736/S0390-5616.16.03804-2. Epub 2016 Sep 27. No abstract available.

PMID:
27676284
14.

Spinal melanocytoma with leptomeningeal spread and long survival following surgery and chemotherapy.

Nicolotto E, Presas-Rodriguez S, Morra I, Franchino F, Magistrello M, Pellerino A, Massaro F, Pinessi L, Rudà R, Soffietti R.

J Neurosurg Sci. 2018 Jun;62(3):375-378. doi: 10.23736/S0390-5616.16.03687-0. Epub 2016 Sep 27. No abstract available.

PMID:
27676283
15.

Investigating the role of adipokines in chronic migraine.

Rubino E, Vacca A, Govone F, Gai A, Boschi S, Zucca M, De Martino P, Gentile S, Pinessi L, Rainero I.

Cephalalgia. 2017 Oct;37(11):1067-1073. doi: 10.1177/0333102416665871. Epub 2016 Aug 22.

16.

Neural correlates of reduced awareness in instrumental activities of daily living in frontotemporal dementia.

Amanzio M, D'Agata F, Palermo S, Rubino E, Zucca M, Galati A, Pinessi L, Castellano G, Rainero I.

Exp Gerontol. 2016 Oct;83:158-64. doi: 10.1016/j.exger.2016.08.008. Epub 2016 Aug 14.

PMID:
27534380
17.

Reversible disconnection syndrome in a case of acute tumefactive demyelinating lesion: a PET study.

Chiavazza C, Cistaro A, Fania P, Bertolotto A, Cavalla P, Rudà R, Pinessi L, Soffietti R.

Neurol Sci. 2016 Dec;37(12):2019-2023. Epub 2016 Jul 25. No abstract available.

PMID:
27457655
18.

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.

19.

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.

20.

Clinical and neuroradiological features of spinocerebellar ataxia 38 (SCA38).

Borroni B, Di Gregorio E, Orsi L, Vaula G, Costanzi C, Tempia F, Mitro N, Caruso D, Manes M, Pinessi L, Padovani A, Brusco A, Boccone L.

Parkinsonism Relat Disord. 2016 Jul;28:80-6. doi: 10.1016/j.parkreldis.2016.04.030. Epub 2016 Apr 27.

21.

PRNP P39L Variant is a Rare Cause of Frontotemporal Dementia in Italian Population.

Oldoni E, Fumagalli GG, Serpente M, Fenoglio C, Scarioni M, Arighi A, Bruno G, Talarico G, Confaloni A, Piscopo P, Nacmias B, Sorbi S, Rainero I, Rubino E, Pinessi L, Binetti G, Ghidoni R, Benussi L, Grande G, Arosio B, Bursey D, Kauwe JS, Cioffi SM, Arcaro M, Mari D, Mariani C, Scarpini E, Galimberti D.

J Alzheimers Dis. 2016;50(2):353-7. doi: 10.3233/JAD-150863.

22.

The rehabilitative effects on written language of a combined language and parietal dual-tDCS treatment in a stroke case.

De Tommaso B, Piedimonte A, Caglio MM, D'Agata F, Campagnoli M, Orsi L, Raimondo S, Vighetti S, Mortara P, Massazza G, Pinessi L.

Neuropsychol Rehabil. 2017 Sep;27(6):904-918. doi: 10.1080/09602011.2015.1103759. Epub 2015 Oct 22.

23.

Progranulin genetic polymorphisms influence progression of disability and relapse recovery in multiple sclerosis.

Vercellino M, Fenoglio C, Galimberti D, Mattioda A, Chiavazza C, Binello E, Pinessi L, Giobbe D, Scarpini E, Cavalla P.

Mult Scler. 2016 Jul;22(8):1007-12. doi: 10.1177/1352458515610646. Epub 2015 Oct 7.

PMID:
26447062
24.

Paroxysmal perceptual alteration in a schizophrenic patient treated with paliperidone: A case report.

Benna P, Rubino E, Marino C, Montalenti E, Giovanna Caprioli M, Rainero I, Pinessi L.

Ann Clin Psychiatry. 2015 Aug;27(3):223-4. No abstract available. Erratum in: Ann Clin Psychiatry. 2015 Nov;27(4):303. Caprioli, Maria Giovanna [corrected to Giovanna Caprioli, Maria].

PMID:
26247222
25.

Molecularly based management of gliomas in clinical practice.

Rudà R, Pellerino A, Magistrello M, Franchino F, Pinessi L, Soffietti R.

Neurol Sci. 2015 Sep;36(9):1551-7. doi: 10.1007/s10072-015-2332-9. Epub 2015 Jul 21. Review.

PMID:
26194534
26.

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.

27.

A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia.

Ferrari R, Grassi M, Salvi E, Borroni B, Palluzzi F, Pepe D, D'Avila F, Padovani A, Archetti S, Rainero I, Rubino E, Pinessi L, Benussi L, Binetti G, Ghidoni R, Galimberti D, Scarpini E, Serpente M, Rossi G, Giaccone G, Tagliavini F, Nacmias B, Piaceri I, Bagnoli S, Bruni AC, Maletta RG, Bernardi L, Postiglione A, Milan G, Franceschi M, Puca AA, Novelli V, Barlassina C, Glorioso N, Manunta P, Singleton A, Cusi D, Hardy J, Momeni P.

Neurobiol Aging. 2015 Oct;36(10):2904.e13-26. doi: 10.1016/j.neurobiolaging.2015.06.005. Epub 2015 Jun 12.

28.

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.

29.

A review of the recent advances in neuroimaging of frontotemporal lobar degeneration.

D'Agata F, Orsi L, Cicerale A, Rubino E, Rainero I, Bergui M, Pinessi L.

J Neurosurg Sci. 2017 Apr;61(2):180-192. doi: 10.23736/S0390-5616.16.03281-1. Epub 2015 May 20. Review.

30.

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.

31.

An atypical form of AOA2 with myoclonus associated with mutations in SETX and AFG3L2.

Mancini C, Orsi L, Guo Y, Li J, Chen Y, Wang F, Tian L, Liu X, Zhang J, Jiang H, Nmezi BS, Tatsuta T, Giorgio E, Di Gregorio E, Cavalieri S, Pozzi E, Mortara P, Caglio MM, Balducci A, Pinessi L, Langer T, Padiath QS, Hakonarson H, Zhang X, Brusco A.

BMC Med Genet. 2015 Mar 19;16:16. doi: 10.1186/s12881-015-0159-0.

32.

Efficacy of frovatriptan as compared to other triptans in migraine with aura.

Evers S, Savi L, Omboni S, Lisotto C, Zanchin G, Pinessi L.

J Headache Pain. 2015;16:514. doi: 10.1186/s10194-015-0514-8. Epub 2015 Apr 1.

33.

Two families with novel missense mutations in COL4A1: When diagnosis can be missed.

Giorgio E, Vaula G, Bosco G, Giacone S, Mancini C, Calcia A, Cavalieri S, Di Gregorio E, Rigault De Longrais R, Leombruni S, Pinessi L, Cerrato P, Brusco A, Brussino A.

J Neurol Sci. 2015 May 15;352(1-2):99-104. doi: 10.1016/j.jns.2015.03.042. Epub 2015 Apr 7.

34.

Mutation analysis of CHCHD10 in different neurodegenerative diseases.

Zhang M, Xi Z, Zinman L, Bruni AC, Maletta RG, Curcio SA, Rainero I, Rubino E, Pinessi L, Nacmias B, Sorbi S, Galimberti D, Lang AE, Fox S, Surace EI, Ghani M, Guo J, Sato C, Moreno D, Liang Y, Keith J, Traynor BJ, St George-Hyslop P, Rogaeva E.

Brain. 2015 Sep;138(Pt 9):e380. doi: 10.1093/brain/awv082. Epub 2015 Mar 31. No abstract available.

35.

Paroxysmal non-kinesigenic dyskinesia, post-streptococcal syndromes and psychogenic movement disorders: a diagnostic challenge.

Peila E, Mortara P, Cicerale A, Pinessi L.

BMJ Case Rep. 2015 Mar 20;2015. pii: bcr2014207449. doi: 10.1136/bcr-2014-207449.

36.

The C9orf72 repeat expansion itself is methylated in ALS and FTLD patients.

Xi Z, Zhang M, Bruni AC, Maletta RG, Colao R, Fratta P, Polke JM, Sweeney MG, Mudanohwo E, Nacmias B, Sorbi S, Tartaglia MC, Rainero I, Rubino E, Pinessi L, Galimberti D, Surace EI, McGoldrick P, McKeever P, Moreno D, Sato C, Liang Y, Keith J, Zinman L, Robertson J, Rogaeva E.

Acta Neuropathol. 2015 May;129(5):715-27. doi: 10.1007/s00401-015-1401-8. Epub 2015 Feb 26.

37.

Pain beliefs and perceptions inventory: a cross-sectional study in chronic and episodic migraine.

Condello C, Piano V, Dadam D, Pinessi L, Lantéri-Minet M.

Headache. 2015 Jan;55(1):136-48. doi: 10.1111/head.12503. Epub 2014 Dec 29.

PMID:
25545038
38.

Parity is associated with a longer time to reach irreversible disability milestones in women with multiple sclerosis.

Masera S, Cavalla P, Prosperini L, Mattioda A, Mancinelli CR, Superti G, Chiavazza C, Vercellino M, Pinessi L, Pozzilli C.

Mult Scler. 2015 Sep;21(10):1291-7. doi: 10.1177/1352458514561907. Epub 2014 Dec 22.

PMID:
25533293
39.

Pharmacologic therapies for malignant glioma: a guide for clinicians.

Soffietti R, Bertero L, Pinessi L, Rudà R.

CNS Drugs. 2014 Dec;28(12):1127-37. doi: 10.1007/s40263-014-0215-x. Review.

PMID:
25403944
40.

KCNK18 (TRESK) genetic variants in Italian patients with migraine.

Rainero I, Rubino E, Gallone S, Zavarise P, Carli D, Boschi S, Fenoglio P, Savi L, Gentile S, Benna P, Pinessi L, Dalla Volta G.

Headache. 2014 Oct;54(9):1515-22. doi: 10.1111/head.12439.

PMID:
25324165
41.

Response to combined radiotherapy and chemotherapy of a leptomeningeal spread from choroid plexus carcinoma: case report.

Pellerino A, Cassoni P, Boldorini R, Pinessi L, Rudà R.

Neurol Sci. 2015 Apr;36(4):639-41. doi: 10.1007/s10072-014-1983-2. Epub 2014 Oct 12. No abstract available.

42.

Novel mutation of SLC20A2 in an Italian patient presenting with migraine.

Rubino E, Giorgio E, Gallone S, Pinessi L, Orsi L, Gentile S, Duca S, Brusco A.

J Neurol. 2014 Oct;261(10):2019-21. doi: 10.1007/s00415-014-7475-8. Epub 2014 Sep 2. No abstract available.

43.

Is HCRTR2 a genetic risk factor for Alzheimer's disease?

Gallone S, Boschi S, Rubino E, De Martino P, Scarpini E, Galimberti D, Fenoglio C, Acutis PL, Maniaci MG, Pinessi L, Rainero I.

Dement Geriatr Cogn Disord. 2014;38(3-4):245-53. doi: 10.1159/000359964. Epub 2014 Jun 25.

PMID:
24969517
44.

Frontotemporal dementia and its subtypes: a genome-wide association study.

Ferrari R, Hernandez DG, Nalls MA, Rohrer JD, Ramasamy A, Kwok JB, Dobson-Stone C, Brooks WS, Schofield PR, Halliday GM, Hodges JR, Piguet O, Bartley L, Thompson E, Haan E, Hernández I, Ruiz A, Boada M, Borroni B, Padovani A, Cruchaga C, Cairns NJ, Benussi L, Binetti G, Ghidoni R, Forloni G, Galimberti D, Fenoglio C, Serpente M, Scarpini E, Clarimón J, Lleó A, Blesa R, Waldö ML, Nilsson K, Nilsson C, Mackenzie IR, Hsiung GY, Mann DM, Grafman J, Morris CM, Attems J, Griffiths TD, McKeith IG, Thomas AJ, Pietrini P, Huey ED, Wassermann EM, Baborie A, Jaros E, Tierney MC, Pastor P, Razquin C, Ortega-Cubero S, Alonso E, Perneczky R, Diehl-Schmid J, Alexopoulos P, Kurz A, Rainero I, Rubino E, Pinessi L, Rogaeva E, St George-Hyslop P, Rossi G, Tagliavini F, Giaccone G, Rowe JB, Schlachetzki JC, Uphill J, Collinge J, Mead S, Danek A, Van Deerlin VM, Grossman M, Trojanowski JQ, van der Zee J, Deschamps W, Van Langenhove T, Cruts M, Van Broeckhoven C, Cappa SF, Le Ber I, Hannequin D, Golfier V, Vercelletto M, Brice A, Nacmias B, Sorbi S, Bagnoli S, Piaceri I, Nielsen JE, Hjermind LE, Riemenschneider M, Mayhaus M, Ibach B, Gasparoni G, Pichler S, Gu W, Rossor MN, Fox NC, Warren JD, Spillantini MG, Morris HR, Rizzu P, Heutink P, Snowden JS, Rollinson S, Richardson A, Gerhard A, Bruni AC, Maletta R, Frangipane F, Cupidi C, Bernardi L, Anfossi M, Gallo M, Conidi ME, Smirne N, Rademakers R, Baker M, Dickson DW, Graff-Radford NR, Petersen RC, Knopman D, Josephs KA, Boeve BF, Parisi JE, Seeley WW, Miller BL, Karydas AM, Rosen H, van Swieten JC, Dopper EG, Seelaar H, Pijnenburg YA, Scheltens P, Logroscino G, Capozzo R, Novelli V, Puca AA, Franceschi M, Postiglione A, Milan G, Sorrentino P, Kristiansen M, Chiang HH, Graff C, Pasquier F, Rollin A, Deramecourt V, Lebert F, Kapogiannis D, Ferrucci L, Pickering-Brown S, Singleton AB, Hardy J, Momeni P.

Lancet Neurol. 2014 Jul;13(7):686-99. doi: 10.1016/S1474-4422(14)70065-1.

45.

Lack of association between APOE gene polymorphisms and amyotrophic lateral sclerosis: a comprehensive meta-analysis.

Govone F, Vacca A, Rubino E, Gai A, Boschi S, Gentile S, Orsi L, Pinessi L, Rainero I.

Amyotroph Lateral Scler Frontotemporal Degener. 2014 Dec;15(7-8):551-6. doi: 10.3109/21678421.2014.918149. Epub 2014 Jun 11.

PMID:
24918518
46.

Hypermethylation of the CpG-island near the C9orf72 G₄C₂-repeat expansion in FTLD patients.

Xi Z, Rainero I, Rubino E, Pinessi L, Bruni AC, Maletta RG, Nacmias B, Sorbi S, Galimberti D, Surace EI, Zheng Y, Moreno D, Sato C, Liang Y, Zhou Y, Robertson J, Zinman L, Tartaglia MC, St George-Hyslop P, Rogaeva E.

Hum Mol Genet. 2014 Nov 1;23(21):5630-7. doi: 10.1093/hmg/ddu279. Epub 2014 Jun 6.

47.

Association between polymorphisms rs1333040 and rs7865618 of chromosome 9p21 and sporadic brain arteriovenous malformations.

Sturiale CL, Fontanella MM, Gatto I, Puca A, Giarretta I, D'Arrigo S, Lofrese G, Rainero I, Gallone S, Pinessi L, Ducati A, Maira G, Pola R.

Cerebrovasc Dis. 2014;37(4):290-5. doi: 10.1159/000360752. Epub 2014 May 7.

48.

Nonlinear analysis of electroencephalogram in frontotemporal lobar degeneration.

Carlino E, Frisaldi E, Rainero I, Asteggiano G, Cappa G, Tarenzi L, Vighetti S, Pollo A, Pinessi L, Benedetti F.

Neuroreport. 2014 May 7;25(7):496-500. doi: 10.1097/WNR.0000000000000123.

PMID:
24717666
49.

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.

50.

Occurrence of ecchymotic angioedema-like cutaneous lesions as a possible side effect of fingolimod.

Masera S, Chiavazza C, Mattioda A, Superti G, Beggiato E, Crosasso P, Broganelli P, Pinessi L, Cavalla P.

Mult Scler. 2014 Oct;20(12):1666-7. doi: 10.1177/1352458514525872. Epub 2014 Mar 6. No abstract available.

PMID:
24603883

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