GIORDANA, Maria Teresa

GIORDANA, Maria Teresa  

NEUROSCIENZE "RITA LEVI MONTALCINI"  

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Risultati 1 - 20 di 96 (tempo di esecuzione: 0.05 secondi).
Titolo Data di pubblicazione Autore(i) File
A defective L_MAG (large myelin-associated glycoprotein) is responsible for an adult-onset autosomal dominant orthochromatic leukodystrophy 2004 Giordana MT; Palmucci L; Piccinini M; Buccinnà B; Ramondetti C; Rinaudo MT
Adult medulloblastoma : an epidemiological study in Piemonte, Italy 1998 Giordana MT; Schiffer P; Juenemann C; Chio' A
An approach to the timing of altered localization of TDP-43 in ALS motor neurons during disease progression 2009 Giordana MT; Grifoni S; Piccinini M; Pellerino A; De Marco G ; Buccinnà B ; Lupino E ; Naldi A; Magistrello M; Rinaudo MT
Analysis of CHCHD2 and CHCHD10 genes in patients with Parkinson’s disease and mitochondrial myopathy. 2017 E. Rubino; S. Boschi; M. Zhang; L. Brusa; F. Govone; A. Vacca; A. Gai; L. Lopiano; E. Rogaeva; T. Mongini; M. Giordana; I. Rainero;
Analysis of forebrain progenitor markers in supratentorial primitive neuroectodermal tumors (st_PNETs) 2007 M Figus; E Salsano; E Maderna; R Paterra; MT Giordana; B Pollo; G Finocchiaro
Analysis of patched mutations in medulloblastoma of adults 2005 Pradotto L; D'Agostino C; Scirè A; Salsano E; Mauro A; Giordana MT
Assessment of TRKC mRNA levels by real time PCR may be useful in prediction of a favourable clinical outcome in medulloblastomas. 2004 Salsano E; Pollo B; Eoli M; Giordana MT; Finocchiaro G
Association analysis and influence between ORL1 rs1050283 variant and miRNA 369-3p in patients with Alzheimer’s disease. 2010 Serpente M; Fenoglio C; Clerici F; Marcone A; Benussi L; Ghidoni R; Gallone S; Scalabrini D; Cantoni C; Cappa S; Binetti G; Franceschi M; Rainero I; Giordana MT; Mariani C; Bresolin N; Scarpini E; Galimberti D.
Autosomal Dominant Frontotemporal Lobar Degeneration Due to the C9ORF72 Hexanucleotide Repeat Expansion: Late-Onset Psychotic Clinical Presentation 2013 Galimberti D; Fenoglio C; Serpente M; Villa C; Bonsi R; Arighi A; Fumagalli GG; Del Bo R; Bruni AC; Anfossi M; Clodomiro A; Cupidi C; Nacmias B; Sorbi S; Piaceri I; Bagnoli S; Bessi V; Marcone A; Cerami C; Cappa SF; Filippi M; Agosta F; Magnani G; Comi G; Franceschi M; Rainero I; Giordana M; Rubino E; Ferrero P; Rogaeva E; Xi Z; Confaloni A; Piscopo P; Bruno G; Talarico G; Cagnin A; Clerici F; Dell'osso B; Comi GP; Altamura AC; Mariani C; Scarpini E
Autosomal dominant Parkinson's disease: the neuropathological phenotype of a carrier of the novel Lrrk2 mutation (PI1371V) 2006 Giordana MT; D’Agostino C; Mauro A; Di Fonzo A; Bonifati V
Biomarker for Frontotemporal Lobar Degeneration (FTLD) with TDP-43 Pathology: the Circulating Lymphocytes 2012 Pellerino A; Lomartire A; Naldi A; Buccinna B; Maffeo E; Ramondetti C; Lupino E; Rinaudo MT; Piccinini M; Rainero I; De Marco G; Giordana MT
Brain metal levels in multiple system atrophy 2005 Herrero Hernandez E; Valentini C; Sacchetti A; Orsi L; D'Agostino C; Novero D; Giordana MT
Chemotherapy studies of various nitrosoureas: prevention of development of ethylnitrosourea-induced tumors in the nervous system 1977 Paoletti P; Giordana M T; Pezzotta S; Schiffer D
CHMP5 and BAG1 are protective factors for sporadic Frontotemporal Lobar Degeneration 2010 C. Villa; E. Venturelli; C. Fenoglio; F. Clerici; A. Marcone; L. Benussi; R. Ghidoni; S. Gallone; D. Scalabrini; F. Cortini; M. Serpente; C. Cantoni; S. Cappa; G. Binetti; I. Rainero; M.T. Giordana; C. Mariani; N. Bresolin; E. Scarpini; D. Galimberti
CHMP5 and BAG1 are protective factors for sporadic Frontotemporal Lobar Degeneration 2010 D. Galimberti; C. Villa; E. Venturelli; C. Fenoglio; F. Clerici; A. Marcone; L. Benussi; R. Ghidoni; S. Gallone; D. Scalabrini; F. Cortini; M. Serpente; C. Cantoni; S. Cappa; G. Binetti; I. Rainero; M.T. Giordana; C. Mariani; N. Bresolin; E. Scarpini
Chromosome 9 and sporadic Frontotemporal Lobar Degeneration: KIF24, but not UBAP1, is a risk factor in Italian population 2010 E. Venturelli; C. Villa; C. Fenoglio; F. Clerici; A. Marcone; L. Benussi; R. Ghidoni; S. Gallone; D. Scalabrini; F. Cortini; S. Cappa; G. Binetti; M. Franceschi; I. Rainero; M.T. Giordana; C. Mariani; N. Bresolin; E. Scarpini; D. Galimberti
Chromosome 9 and sporadic frontotemporal lobar degeneration: KIF24, but not UBAP1, is a risk factor in the Italian population 2010 Galimberti D; Venturelli E; Villa C; Fenoglio C; Clerici F; Marcone A; Benussi L; Ghidoni R; Gallone S; Scalabrini D; Cortini F; Cappa S; Binetti G; Franceschi M; Rainero I; Giordana MT; Mariani C; Bresolin N; Scarpini E.
Clinical and pathological findings in two familial cases of progressive muscular atrophy (PMA) 1985 Schiffer D; Brignolio F; Chio' A; Giordana MT; Leone M
Comparative morphometric analysis of nuclear size in medulloblastoma of children and adults 2006 D’Agostino C ; Giordana MT
Cortical pathology in multiple sclerosis: expression of glutamate transporter EAAT2 2006 Vercellino M; Merola A; Masera S; Plano F; Votta B; Capello E; Mancardi GL; Giordana MT; Mutani R; Cavalla P