Titolo	Data di pubblicazione	Autore(i)
1	α-Melanocyte-stimulating hormonelike immunoreactivity is increased in cerebrospinal fluid of patients with Parkinson's disease	1988	RAINERO I; KAYE JA; MAY C; DURSO R; KATZ DI; ALBERT ML; WOLFE N; PINESSI L; FRIEDLAND RP; RAPOPORT SI
2	Worldwide distribution of PSEN1 Met146Leu mutation: a large variability for a founder mutation	2010	Bruni AC; Bernardi L; Colao R; Rubino E; Smirne N; Frangipane F; Terni B; Curcio SA; Mirabelli M; Clodomiro A; Di Lorenzo R; Maletta R; Anfossi M; Gallo M; Geracitano S; Tomaino C; Muraca MG; Leotta A; Lio SG; Pinessi L; Rainero I; Sorbi S; Nee L; Milan G; Pappatà S; Postiglione A; Abbamondi N; Forloni G; St George Hyslop P; Rogaeva E; Bugiani O; Giaccone G; Foncin JF; Spillantini MG; Puccio G
3	Worldwide distribution of PSEN1 Met146Leu mutation: a large variability for a founder mutation	2011	Puccio G; Bernardi L; Colao R; Rubino E; Smirne N; Frangipane F; Terni B; Curcio S; Mirabelli M; Clodomiro A; Di Lorenzo R; Maletta R; Anfossi M; Gallo M; Geracitano S; Tomaino C; Muraca G; Leotta A; Lio S; Pinessi L; Rainero I; Sorbi S; Nee L; Milan G; Pappatà S; Postiglione A; Abbamondi N; Forloni G; St. George Hyslop P; Rogaeva E; Bugiani O; Giaccone G; Foncin JF; Spillantini MG; Bruni AC
4	Voxel-based morphometry reveals gray matter loss in patients with Paget's disease of the bone carrying SQSTM1 gene mutations	2014	Rainero I; Rubino E; D'Agata F; Rossetti S; Gastaldi L; Bergui M; Orsi L; Pinessi L; Isaia GC; Di Stefano M
5	Voxel-based Morphometry Reveals Gray Matter Loss in Patients with Paget's Disease of the Bone Carrying SQSTM1 Gene Mutations	2014	Innocenzo Rainero; Elisa Rubino; Federico D'Agata; Silvia Rossetti; Laura Gastaldi; Mauro Bergui; Laura Orsi; Lorenzo Pinessi; Giancarlo Isaia; Marco Di Stefano
6	Voxel-based Morphometry Reveals Gray Matter Abnormalities in Migraine	2008	VALFRE' W; RAINERO I; BERGUI M; PINESSI L
7	Vascular endothelial growth factor gene polymorphisms and intracranial aneurysms.	2013	Fontanella M;Gallone S;Panciani PP;Garbossa D;Stefini R;Latronico N;Rubino E;Marengo N;Ducati A;Pinessi L;Rainero I
8	Valutazione dell’asse ipotalamo-ipofiso-surrenalico in pazienti epilettici in trattamento con carbamazepina, fenobarbital ed acido valproico	1989	Gentile S; Buffa C; Piazza D; Lovera N; Manenti M; Frairia R; Rainero I; Pinessi L; Sacerdote I
9	Two families with novel missense mutations in COL4A1: When diagnosis can be missed.	2015	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
10	Tumor necrosis factor-alpha gene and cerebral aneurysms	2007	FONTANELLA M; RAINERO I; GALLONE S; RUBINO E; FENOGLIO P; VALFRÈ W; GARBOSSA D; CARLINO C; DUCATI A; PINESSI L
11	Triptani e funzioni neuroendocrine	2002	Rainero I; Ferrero M; Pinessi L
12	The power of systematic genealogical study in familial Alzheimer disease	1993	BRUNI AC ;MONTESI MP ;RAINERO I ;FERINI-STRAMBI L ;MACCIARDI F ;PINESSI L ;GEI G ;FRAGIACOMO D ;BERGAMINI L
13	The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease	2007	ROGAEVA E; MENG Y; LEE JH; GU Y; KAWARAI T; ZOU F; KATAYAMA T; BALDWIN CT; CHENG R; HASEGAWA H; CHEN F; SHIBATA N; LUNETTA KL; PARDOSSI-PIQUARD R; BOHM C; WAKUTANI Y; CUPPLES LA; CUENCO KT; GREEN RC; PINESSI L; RAINERO I; SORBI S; BRUNI A; DUARA R; FRIEDLAND RP; INZELBERG R; HAMPE W; BUJO H; SONG YQ; ANDERSEN OM; WILLNOW TE; GRAFF-RADFORD N; PETERSEN RC; DICKSON D; DER SD; FRASER PE; SCHMITT-ULMS G; YOUNKIN S; MAYEUX R; FARRER LA; ST GEORGE-HYSLOP P
14	The hypothalamo-hypophyso-adrenal axis in epileptic patients treated with sodium valproate	1987	GENTILE S; CARETTO M; MANENTI M; FRAIRIA R; RAINERO I; PINESSI L
15	The hemochromatosis (HFE) gene influences the clinical features of migraine	2006	Rubino E; Rainero I; Rivoiro C; Valfrè W; Binello E; Zampella E; De Martino P; Gentile S; Fenoglio P; Savi L; Gallone S; Pinessi L
16	The genetics of migraine: An enigma in search of a solution	1997	Pinessi L; Rainero I; Savi L
17	The genetics of Alzheimer's disease	1992	PINESSI L ;RAINERO I ;BRUNETTI E ;CERRATO P ;COSENTINO N ;MARTINO C ;VAULA G ;BERGAMINI L
18	The diagnosis of FTD-ALS: a longitudinal study in a specialized dementia unit	2009	Magistrello M; Rota E; Caglio M; Rizzi L; Rainero I; Ghiglione P; Calvo A; Chio’ A; Castellano G; Pinessi L; Giordana MT; Ferrero P
19	The 1246G-->A polymorphism of the HCRTR2 gene is not associated with migraine	2007	PINESSI L; BINELLO E; DE MARTINO P; GALLONE S; GENTILE S; RAINERO I; RIVOIRO C; RUBINO E; SAVI L; VALFRÈ W; VAULA G
20	Tardive dyskinesia	1985	SABBATINI F; GENTILE S; DE MATTEI M; PINESSI L; RAINERO I