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	Validity of hospital morbidity records for amyotrophic lateral sclerosis. A population-based study	2002	Chiò A; Ciccone G; Calvo A; Vercellino M; Di Vito N; Ghiglione P; Mutani R; Plano F; Bertolotto A; Bottacchi E; Cocito D; Giordana MT; Leone M; Mazzini L; Mora G; Terreni A; Schiffer D; Bergamasco B; Rainero I; Tribolo A; Sciolla R; Mondino F; Gaviani P; Monaco F; De Mattei M; Morgando E; Sosso L; Gionco M; Morino U; Nobili M; Appendino L; Mazzini L; Piazza D; Oddenino E; Liboni W; Vaula G; Ferrari G; Favero M; Doriguzzi Bozzo C; Santamaria P; Massazza U; Bollani E; Villani A; Conti R; Balzarini C; Palermo M; Vergnano F; Cordera S; Buffa C; Penza MT; Fassio F; Meineri P; Cognazzo A; Mocellini C; Dutto A; Cucatto A; Cavestro C; Troni W; Corso G
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	TMEM106B genetic variability in patients with Alzheimer's Disease	2012	Serpente M; Fenoglio C; Villa C; Bonsi R; Cantoni C; Ridolfi E; Clerici F; Ghidoni R; Binussi L; Marcone A; Cerami C; Franceschi M; Gallone S; Cappa S; Binetti G; Rainero I; Bresolin N; Mariani C; Scarpini E; Galimberti D
13	Three novel missense mutations in SLC20A2 associated with idiopathic basal ganglia calcification	2017	Rubino, E; Giorgio, E; Godani, M; Grosso, E; Zibetti, M; Lopiano, L; Ferrero, P; Duca, S; Moretti, L; Gallone, S; Rainero, I; Brusco, A.
14	The use of the H reflex in serial evaluation of nerve conduction velocity	1983	Troni W; Cantello R; Rainero I
15	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
16	The NOS3 G894T (Glu298Asp) polymorphism is a risk factor for frontotemporal lobar degeneration	2009	Venturelli E; Villa C; Fenoglio C; Clerici F; Marcone A; Ghidoni R; Cortini F; Scalabrini D; Gallone S; Rainero I; Mandelli A; Restelli I; Binetti G; Cappa S; Mariani C; Giordana MT; Bresolin N; Scarpini E; Galimberti D
17	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
18	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
19	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
20	The genetics of migraine: An enigma in search of a solution	1997	Pinessi L; Rainero I; Savi L