CELLINI, ELENA

CELLINI, ELENA  

SCIENZE NEUROLOGICHE E PSICHIATRICHE (attivo dal 01/08/1980 al 31/12/2012)  

Mostra records
Risultati 1 - 20 di 49 (tempo di esecuzione: 0.047 secondi).
Titolo Data di pubblicazione Autore(i) File
A family with spinocerebellar ataxia type 8 expansion and vitamin E deficiency ataxia. 2002 Elena Cellini; Silvia Piacentini; Benedetta Nacmias; Paolo Forleo; Andrea Tedde; Silvia Bagnoli; Monica Ciantelli; Sandro Sorbi
A2 macroglobulin polymorphisms in Italian sporadic and familial Alzheimer’s disease 2001 Nacmias B.; Tedde A.; Cellini E.; Forleo P.; Orlacchio A.; Guarnieri B.M.; Petruzzi C.; D’Andrea F.; Serio S.; Sorbi S.
Acylphosphatase expression during macrophage differentiation and activation of U-937 cell line 1999 D. DEGL'INNOCENTI; MARZOCCHINI R; ROSATI F; CELLINI E; RAUGEI G; RAMPONI G
Alzheimer's disease: role of size and location of white matter changes in determining cognitive deficits. 2005 BRACCO L; PICCINI C; MORETTI M; MASCALCHI M; SFORZA A; B. NACMIAS; CELLINI E; BAGNOLI S; SORBI S.
Angiotensin converting enzyme insertion/deletion polymorphism in sporadic and familial Alzheimer's disease and longevity 2007 Nacmias B; Bagnoli S; Tedde A; Cellini E; Bessi V; Guarnieri B; Ortensi L; Piacentini S; Bracco L; Sorbi S
Association analysis of the paraoxonase-1 gene with Alzheimer's disease 2006 Elena Cellini;Andrea Tedde;Silvia Bagnoli;Benedetta Nacmias;Silvia Piacentini;Valentina Bessi;Laura Bracco;Sandro Sorbi
Association of IL10 promoter polymorphism in Italian Alzheimer's disease. 2007 BAGNOLI S; CELLINI E; TEDDE A; NACMIAS B; PIACENTINI S; BESSI V; BRACCO L; S. SORBI
Association of NTRK3 and its interaction with NGF suggest an altered cross-regulation of the neurotrophin signaling pathway in eating disorders. 2008 Josep Maria Mercader; Ester Saus; Zaida Agüera; Mònica Bayés; Claudette Boni; Anna Carreras; E. Cellini; Rafael de Cid; Mara Dierssen; Geòrgia Escaramís; Fernando Fernández-Aranda; Laura Forcano; Xavier Gallego; Juan Ramón González; Philip Gorwood; Johannes Hebebrand; Anke Hinney; B. Nacmias; Anna Puig; Marta Ribasés; V. Ricca; Lucia Romo; S. Sorbi; Audrey Versini; Mònica Gratacòs; Xavier Estivill
Associations of individual and family eating patterns during childhood and early adolescence: a multicentre European study of associated eating disorder factors. 2009 Isabel Krug; Janet Treasure; Marija Anderluh; Laura Bellodi; Elena Cellini; David Collier; Milena di Bernardo; Roser Granero; Andreas Karwautz; Benedetta Nacmias; Eva Penelo; Valdo Ricca; Sandro Sorbi; Kate Tchanturia; Gudrun Wagner; Fernando Fernández-Aranda
Atypical Friedreich ataxia with a very late onset and an unusual limited GAA repeat. 2000 S. Sorbi; P. Forleo; E. Cellini; S. Piacentini; A. Serio; B. Guarnieri; C. Petruzzi
Brain metabolic differences between sporadic and familial Alzheimer's disease. 2003 Mosconi L; Sorbi S; Nacmias B; De Cristofaro MT; Fayyaz M; Cellini E; Bagnoli S; Bracco L; Herholz K; Pupi A
Brain-derived neurotrophic factor genetic variants are notsusceptibility factors to Alzheimer's disease in Italy. 2004 Bagnoli S; Nacmias B; Tedde A; Guarnieri BM; Cellini E; Petruzzi C; Bartoli A; Ortenzi L; Sorbi S
Brain-derived neurotrophic factor, apolipoprotein E genetic variants and cognitive performance in Alzheimer's disease. 2004 B. NACMIAS; PICCINI C; BAGNOLI S; TEDDE A; CELLINI E; BRACCO L; SORBI S.
Case-control and combined family trios analysis of three polymorphisms in the ghrelin gene in European patients with anorexia and bulimia nervosa. 2006 E. CELLINI; B. NACMIAS; C. ROTELLA; S. SORBI; V. RICCA; L. BELLODI
Cathepsin D polymorphism in Italian sporadic and familial Alzheimer's disease. 2002 BAGNOLI S; NACMIAS B; TEDDE A; GUARNIERI BM; CELLINI E; CIANTELLI M; PETRUZZI C; BARTOLI A; ORTENZI L; SERIO A; S. SORBI
Cholesteryl ester transfer protein (CETP) I405V polymorphism and longevity in Italian centenarians. 2005 CELLINI E; B. NACMIAS; OLIVIERI F; ORTENZI L; TEDDE A; BAGNOLI S; PETRUZZI C; FRANCESCHI C; SORBI S.
Clinical and genetic analysis of a Machado-Joseph Italian family 2000 Cellini E.; Forleo P.; Nacmias B.; Tedde A.; Parnetti L.; Gallai V.; Piacentini S.; Sorbi S.
Clinical features and outcome of 6 new patients carrying de novoKCNB1gene mutations 2017 Marini, Carla; Romoli, Michele; Parrini, Elena; Costa, Cinzia; Mei, Davide; Mari, Francesco; Parmeggiani, Lucio; Procopio, Elena; Metitieri, Tiziana; Cellini, Elena; Virdò, Simona; De Vita, Dalila; Gentile, Mattia; Prontera, Paolo; Calabresi, Paolo; Guerrini, Renzo
Codon 129 polymorphism of prion protein gene in sporadic Alzheimer's disease. 2008 A. Poleggi; A. Bizzarro; A. Acciarri; P. Antuono; S. Bagnoli; E. Cellini; G. Dal Forno; C. Giannattasio; A. Lauria; M. G. Matera; B. Nacmias; M. Puopolo; D. Seripa; S. Sorbi; D. R. Wekstein; M. Pocchiari; C. Masullo
Combined family trio and case-control analysis of the COMT Val158Met polymorphism in European patients with anorexia nervosa. 2004 M. Gabrovsek; M. Brecelj-Anderluh; L. Bellodi; E. Cellini; D. Di Bella; X. Estivill; F. Fernandez-Aranda; B. Freeman; F. Geller; M. Gratacos; R. Haigh; J. Hebebrand; A. Hinney; J. Holliday; X. Hu; A. Karwautz; B. Nacmias; M. Ribases; H. Remschmidt; R. Komel; S. Sorbi; M. Tomori; J. Treasure; G. Wagner; J. Zhao; D. A. Collier