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Titolo Data di pubblicazione Autore(i) File
Drug points: Bilateral scopolamine mydriasis in a traveller 1-gen-1987 Marcon, Gabriella; Schiavo, Ferdinando
Bilateral scopolamine mydriasis in a traveller 1-gen-1987 Marcon, Gabriella; Schiavo, S.
Experience with phosphatidylserine treatment of patients with cognitive and behavioral decline 1-gen-1988 Marcon, Gabriella; Mascolo, Md
Linkage Analysis in familial Alzheimer Disease 1-gen-1990 Marcon, Gabriella
PRION PROTEIN GENE ANALYSIS IN PRE-SENILE DEMENTING AND ATAXlC 1-gen-1990 Sorbi, S; Mortilla, M; Nacmiae, B; Piacentini, S; Amaducci, L; St George Hyalop, Ph; Marcon, G
ANALYSIS OF CHROMOSOME-21 LINKAGE IN FAMILIAL ALZHEIMERS-DISEASE 1-gen-1990 Sorbi, S; Mortilla, M; Nacmias, B; Piacentini, S; Amaducci, L; Stgeorgehyslop, Phs; Marcon, G
Linkage Analysis in Italian Pedigrees with Autosomal Dominant Familial Alzheimer’s Disease 1-gen-1991 Sorbi, S.; Nacmias, B.; Mortilla, M.; Piacentini, S.; Marcon, G.; Piersanti, P.; Ballerini, C.; Forleo, P.; Latorraca, S.; Tesco, G.; Amaducci, L.
Hypomyelination neuropathy in an adult 1-gen-1991 Marcon, G; Polo, A; Simonati, A; Ferrari, S; Cavallaro, T; Rizzuto,
Serotoninergic fibres form dense synaptic contacts with Purkinje cells in the mouse cerebellar cortex--an immunohistochemical study 1-gen-1992 Crivellato, Enrico; Damiani, Daniela; Marcon, Gabriella; Fusaroli, Fp; Travan, Luciana; Mallardi, Franco
Expression of c-sis oncogene products in peripheral nerve tissue 1-gen-1992 Simonati, A; Marcon, G; Moretto, G; Stenta, G; Turazzi, T; Cavallaro, T; Rizzuto, N
Cytoskeletal markers in developmental disorders of human CNS 1-gen-1992 Marcon, G; Simonati, A; Rizzuto, N
Hereditary demyelinating neuropathies: autosomic recessive and sporadic forms 1-gen-1992 Simonati, A; Fenzi, F; Marcon, G; Rizzuto, N
Clinical – neuropathological correlations in Alzheimer’s disease: description of seven cases 1-gen-1993 Bracco, L; Campani, D; Piccini, D; Simonati, A; Marcon, G; Rizzuto, N
Subacute spongiform encephalopaty assiciated with amyloid deposits 1-gen-1994 Marcon, G; Cavallaro, T; Morbin, M; Bazan, D; Ragno, C; Tosi, L; Rizzuto, N
Clinico-Neuropathological correlations in AD 1-gen-1995 Campani, D; Bracco, L; Marcon, G; Simonati, A; Rizzuto, N
AD: role of clinical examinations in predicting neurpathological features 1-gen-1995 Campani, D; Marcon, G; Bracco, L; Simonati, A; Rizzuto, N; Piccininni, M; Piccini, D; Manfredi, G; Falcini, M; Notarelli, A; Amaducci, L
Neurotoxicity of a bPP peptide other than Ab 1-gen-1995 Marcon, G; Giaccone, G; Cajola, L; Rossi, G; Rizzuto, N; Bugiani, O; Tagliavini, F
The intronic polymorphism in presenilin-1 gene in familial Alzheimer’s disease with pathogenetic mutations in amyloid precursor protein and presenilin 1 and 2 genes 1-gen-1996 Sorbi, S; Nacmias, B; Forleo, P; Tedde, A; Latorraca, S; Piacentini, S; Marcon, G; Provinciali, L
Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrant 1-gen-1996 Sherrington, R; Froelich, S; Sorbi, S; Campion, D; Chi, H; Rogaeva, Ea; Levesque, G; Rogaev, Ei; Lin, C; Liang, Y; Ikeda, M; Mar, L; Brice, A; Agid, Y; Percy, Me; CLERGET DARPOUX, F; Piacentini, S; Marcon, Gabriella; Nacmias, B; Amaducci, L; Frebourg, T; Lannfelt, L; Rommens, Jm; ST GEORGE HYSLOP, Ph
Genetic and phenotypical analysis of presenilin genes-linked Familial Alzheimer’s disease in Italian kindreds 1-gen-1996 Forleo, P; Nacmias, B; Sorbi, S; Repice, Am; Tedde, A; Latorraca, S; Piacentini, S; Marcon, G; and Amaducci, L
Presenilin gene analysis in Italian familieswith early-onset Alzheimer’s disease 1-gen-1996 Sorbi, S; Nacmias, B; Forleo, P; Tedde, A; Latorraca, S; Liacentini, S; Marcon, G; Amaducci, L
PURE, ACUTE CEREBELAR SYNDROME ASSOCIATED WITH CYCLOSPORINE TREATMENT IN AN ADULT LIVER TRANSPLANT RECIPIENT 1-gen-1997 Risaliti, Andrea; Vitulli, D.; Marcon, Gabriella; Cautero, N.; Soardo, G.; Corno, V.; Bruschi, F.; Pirisi, M.
Diagnosis of Alzheimer's disease 1-gen-1997 Marcon, Gabriella; Giaccone, G; Tagliavini, F; Bugiani, O.
Implication of α1-antichimotrypsin polymorphism in familial Alazheimer’s disease 1-gen-1998 Nacmias, B; Tedde, A; Marcon, G; Latorraca, S; Forleo, P; Piacentini, S; Amaducci, L; Sorbi, S
Implication of alpha1-antichymotrypsin polymorphism in familial Alzheimer's disease 1-gen-1998 Nacmias, B; Marcon, Gabriella; Tedde, A; Forleo, P; Latorraca, S; Piacentini, S; Amaducci, L; Sorbi, S.
Implication of α1-antichimotrypsin polymorphism in familial Alazheimer’s disease 1-gen-1998 Nacmias, B; Tedde, A; Marcon, G; Latorraca, S; Forleo, P; Piacentini, S; Sorbi, S
Clinical and neuropathological findings of an Italian Family with Alzheimer’s disease and M239V mutation of PS2 gene 1-gen-1998 Marcon, G; Giaccone, G; Tagliavini, F; Bergonzi, P; Sorbi, S; Nacmias, B; Beltrami, Ca; Bugiani, O
Neuropsychological and psychometric findings in a large Italian Family with the M239V mutation of the PSEN2 gene 1-gen-1998 Marcon, G; Nacmias, B; Sorbi, S; Bergonzi, P; Balestrieri, M
A betaPP peptide carboxyl-terminal to Abeta is neurotoxic 1-gen-1999 Marcon, Gabriella; Giaccone, G; Canciani, B; Cajola, L; Rossi, G; DE GIOIA, L; Salmona, M; Bugiani, O; Tagliavini, F.
HLA A2 allele is associated with age at onset of Alzheimer's disease 1-gen-1999 Ballerini, C; Nacmias, B; Rombola, G; Marcon, Gabriella; Massacesi, L; Sorbi, S.
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22 1-gen-1999 Simonati, A; Fabrizi, Gm; Pasquinelli, A; Taioli, F; Cavallaro, T; Morbin, M; Marcon, Gabriella; Papini, M; Rizzuto, N.
Association between 5-HT2A receptor polymorphism and psychotic symptoms in Alzheimer’s disease 1-gen-1999 Sorbi, S; Nacmias, B; Tedde, A; Marcon, G; Piacentini, S
An Italian family with Alzhiemer’s disease and M239V mutation in PS2 1-gen-1999 Marcon, G; Giaccone, G; Tagliavini, F; Balestrieri, M; Beltrami, Ca; Bergonzi, P; Bugiani, O
Localisation of presenilin 2 in human and rodent pancreatic islet beta-cells; Met239Val presenilin 2 variant is not associated with diabetes in man 1-gen-1999 Jaikaran, Et; Marcon, Gabriella; Levesque, L; GEORGE HYSLOP, Ps; Fraser, Pe; Clark, A.
Angiotensin converting enzyme polymorphism in sporadic and presenilin-linked Alzheimer's disease families 1-gen-1999 Nacmias, B; Tedde, A; Forleo, P; Marcon, Gabriella; Piacentini, S; Sorbi, S.
Are premorbid personality traits linked to the risk of Alzheimer's disease? A case series of subjects with familial mutation 1-gen-2000 Balestrieri, Matteo; Nacmias, B.; Sorbi, S.; Marcon, Gabriella
Guidelines for the diagnosis of dementia and Alzheimer’s disease 1-gen-2000 Marcon, Gabriella
No association between 2 Macroglobulin DNA polymorphism and sporadic Alzheimer’s Disease in Italy 1-gen-2000 Sorbi, S; Nacmias, B; Tedde, A; Forleo, P; Marcon, G; Petruzzi, C; Guarneri, B; Serio, A
Expression of activated caspase-3 in Alzheimer’s Disease and in Frontotemporal Dementia 1-gen-2000 Marcon, G; Atzori, C; Torta, I; Simonati, A; Bugiani, O; Ghetti, B; Migheli, A
Presenilin 2 mutation does not influence expression and concentration of APP forms in human platelets 1-gen-2000 Pastorino, L.; Colciaghi, F.; Marcon, Gabriella; Borroni, B.; Cottini, E.; Cattabeni, F.; Padovani, A.; Di Luca, M.
Enzyme polymorphism in presenilin linked Alzheimer’s disease families and sporadic Alzheimer’s disease 1-gen-2000 Tedde, A; Nacmias, B; Marcon, G; Et, Al
Angiotensin converting enzyme gene polymorphism in Presenilin linked Familial Alzhiemer’s Disease and Sporadic Alzheimer’s Disease 1-gen-2000 Forleo, P; Tedde, A; Nacmias, B; Cellini, E; Marcon, G; Orlacchio, A; Sorbi, S
Association between 5-HT 2° receptor polymorphism and psychotic symptoms in Alzheimer’s Disease 1-gen-2000 Sorbi, S; Nacmias, B; Tedde, A; Forleo, P; Marcon, G; Petruzzi, C; Guarnieri, Bm; Serio, A
Caspase-3 is activated in Alzheimer’s disease but not in Frontotemporal Dementia 1-gen-2000 Marcon, G; Atzori, C; Srinivasan, An; Okazawa, H; Ghetti, B; Migheli, A
Angiotensin converting enzyme gene polymorphism in Presenilin linked Familial Alzhiemer’s Disease and Sporadic Alzheimer’s Disease 1-gen-2000 Nacmias, B; Tedde, A; Forleo, P; Marcon, G; Orlacchio, A; Sorbi, S
ASSOCIATION BETWEEN 5-HT(2A) RECEPTOR POLYMORPHISM AND PSYCHOTIC SYMPTOMS IN ALZHEIMER'S DISEASE 1-gen-2001 Nacmias, B; Tedde, A; Forleo, P; Piacentini, S; Guarnieri, Bm; Bartoli, A; Ortenzi, L; Petruzzi, C; Serio, A; Marcon, Gabriella; Sorbi, S.
IL TRATTAMENTO FARMACOLOGICO DELLA MALATTIA DI ALZHEIMER. 1-gen-2003 Balestrieri, Matteo; Godeas, E.; Marcon, Gabriella
Nicastrin gene in familial and sporadic Alzheimer's disease 1-gen-2003 Confaloni, A; Terreni, L; Piscopo, P; Crestini, A; Campeggi, Lm; Frigerio, Cs; Blotta, I; Perri, M; DI NATALE, M; Maletta, R; Marcon, Gabriella; Franceschi, M; Bruni, Ac; Forloni, G; Cantafora, A.
Clinical and neuropathologic phenotype of a large Italian kindred with presenilin2 mutation M239V 1-gen-2003 Marcon, G; Giaccone, G; Mazzoleni, G; Cupidi, C; Spinello, S; Finato, N; Feltrami, Ca; Bergonzi, P; Sorbi, S; Tagliavini, F
La terapia nella malattia di Alzheimer 1-gen-2003 Marcon, G; Godeas, E; Mulè, P; Balestrieri, M
Mostrati risultati da 1 a 50 di 114
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