MARCON, Gabriella
MARCON, Gabriella
DMED - DIPARTIMENTO DI MEDICINA
A betaPP peptide carboxyl-terminal to Abeta is neurotoxic
1999-01-01 Marcon, Gabriella; Giaccone, G; Canciani, B; Cajola, L; Rossi, G; DE GIOIA, L; Salmona, M; Bugiani, O; Tagliavini, F.
A novel Italian PSEN2 mutation with behavioral phenotype
2009-01-01 Marcon, Gabriella; G., Difede; G., Giaccone; G., Rossi; Giovagnoli, A. R.; E., Maccagnano; F., Tagliavini
A novel missense mutation in PSEN2 gene associated with a clinical phenotype of frontotemporal dementia
2008-01-01 Marcon, Gabriella; Giaccone, Giorgio; Difede, Giuseppe; Rita Giovagnoli, Anna; Tagliavini, Fabrizio
A novel PSEN2 mutation associated with a peculiar phenotype.
2008-01-01 Piscopo, P1; Marcon, G; Piras, Mr; Crestini, A; Campeggi, Lm; Deiana, E; Cherchi, R; Tanda, F; Deplano, A; Vanacore, N; Tagliavini, F; Pocchiari, M; Giaccone, G; Confaloni, A.
AD: role of clinical examinations in predicting neurpathological features
1995-01-01 Campani, D; Marcon, G; Bracco, L; Simonati, A; Rizzuto, N; Piccininni, M; Piccini, D; Manfredi, G; Falcini, M; Notarelli, A; Amaducci, L
Alzheimer disease: APP mutations are associated with high percentage of cerebral amyloid deposits containing Aβ40
2011-01-01 Marcon, G; Giaccone, G; Indaco, A; Moro, M; Moda, F; Cupidi, C; Bruni, A; Demarchi, A; Bogdanovic, N; Ghetti, B; Tagliavini, F
Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrant
1996-01-01 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
Amyotrophic Lateral Sclerosis, a Multisystem Pathology: Insights into the Role of TNFα
2017-01-01 Tortarolo, Massimo; Coco, Daniele Lo; Veglianese, Pietro; Vallarola, Antonio; Giordana, Maria Teresa; Marcon, Gabriella; Beghi, Ettore; Poloni, Marco; Strong, Michael J.; Iyer Anand, M.; Aronica, Eleonora; Bendotti, Caterina
An Italian family with Alzhiemer’s disease and M239V mutation in PS2
1999-01-01 Marcon, G; Giaccone, G; Tagliavini, F; Balestrieri, M; Beltrami, Ca; Bergonzi, P; Bugiani, O
ANALYSIS OF CHROMOSOME-21 LINKAGE IN FAMILIAL ALZHEIMERS-DISEASE
1990-01-01 Sorbi, S; Mortilla, M; Nacmias, B; Piacentini, S; Amaducci, L; Stgeorgehyslop, Phs; Marcon, G
Angiotensin converting enzyme gene polymorphism in Presenilin linked Familial Alzhiemer’s Disease and Sporadic Alzheimer’s Disease
2000-01-01 Forleo, P; Tedde, A; Nacmias, B; Cellini, E; Marcon, G; Orlacchio, A; Sorbi, S
Angiotensin converting enzyme gene polymorphism in Presenilin linked Familial Alzhiemer’s Disease and Sporadic Alzheimer’s Disease
2000-01-01 Nacmias, B; Tedde, A; Forleo, P; Marcon, G; Orlacchio, A; Sorbi, S
Angiotensin converting enzyme polymorphism in sporadic and presenilin-linked Alzheimer's disease families
1999-01-01 Nacmias, B; Tedde, A; Forleo, P; Marcon, Gabriella; Piacentini, S; Sorbi, S.
APE1/Ref-1 in Alzheimer's disease: An immunohistochemical study
2009-01-01 Marcon, Gabriella; Tell, Gianluca; Perrone, L; Garbelli, R; Quadrifoglio, Franco; Tagliavini, F; Giaccone, G.
APE1/Ref-1 regulates PTEN expression mediated by EGR-1
2008-01-01 Fantini, D; Vascotto, C.; Deganuto, M; Bivi, N; Gustincich, S; Marcon, G.; Quadrifoglio, F; Damante, G.; Bhakat, K. K; Mitra, S; Tell, G.
APOLIPOPROTEIN E AND INFLAMMATORY CYTOKINES PROMOTER GENOTYPING IN A GROUP OF CENTENARIANS FROM THE “CaT: Centenari a Trieste” ONGOING STUDY
2019-01-01 Marcon, G
Are premorbid personality traits linked to the risk of Alzheimer's disease? A case series of subjects with familial mutation
2000-01-01 Balestrieri, Matteo; Nacmias, B.; Sorbi, S.; Marcon, Gabriella
Association between 5-HT 2° receptor polymorphism and psychotic symptoms in Alzheimer’s Disease
2000-01-01 Sorbi, S; Nacmias, B; Tedde, A; Forleo, P; Marcon, G; Petruzzi, C; Guarnieri, Bm; Serio, A
ASSOCIATION BETWEEN 5-HT(2A) RECEPTOR POLYMORPHISM AND PSYCHOTIC SYMPTOMS IN ALZHEIMER'S DISEASE
2001-01-01 Nacmias, B; Tedde, A; Forleo, P; Piacentini, S; Guarnieri, Bm; Bartoli, A; Ortenzi, L; Petruzzi, C; Serio, A; Marcon, Gabriella; Sorbi, S.
Association between 5-HT2A receptor polymorphism and psychotic symptoms in Alzheimer’s disease
1999-01-01 Sorbi, S; Nacmias, B; Tedde, A; Marcon, G; Piacentini, S
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
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. | |
A novel Italian PSEN2 mutation with behavioral phenotype | 1-gen-2009 | Marcon, Gabriella; G., Difede; G., Giaccone; G., Rossi; Giovagnoli, A. R.; E., Maccagnano; F., Tagliavini | |
A novel missense mutation in PSEN2 gene associated with a clinical phenotype of frontotemporal dementia | 1-gen-2008 | Marcon, Gabriella; Giaccone, Giorgio; Difede, Giuseppe; Rita Giovagnoli, Anna; Tagliavini, Fabrizio | |
A novel PSEN2 mutation associated with a peculiar phenotype. | 1-gen-2008 | Piscopo, P1; Marcon, G; Piras, Mr; Crestini, A; Campeggi, Lm; Deiana, E; Cherchi, R; Tanda, F; Deplano, A; Vanacore, N; Tagliavini, F; Pocchiari, M; Giaccone, G; Confaloni, A. | |
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 | |
Alzheimer disease: APP mutations are associated with high percentage of cerebral amyloid deposits containing Aβ40 | 1-gen-2011 | Marcon, G; Giaccone, G; Indaco, A; Moro, M; Moda, F; Cupidi, C; Bruni, A; Demarchi, A; Bogdanovic, N; Ghetti, B; Tagliavini, F | |
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 | |
Amyotrophic Lateral Sclerosis, a Multisystem Pathology: Insights into the Role of TNFα | 1-gen-2017 | Tortarolo, Massimo; Coco, Daniele Lo; Veglianese, Pietro; Vallarola, Antonio; Giordana, Maria Teresa; Marcon, Gabriella; Beghi, Ettore; Poloni, Marco; Strong, Michael J.; Iyer Anand, M.; Aronica, Eleonora; Bendotti, Caterina | |
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 | |
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 | |
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 | |
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 | |
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. | |
APE1/Ref-1 in Alzheimer's disease: An immunohistochemical study | 1-gen-2009 | Marcon, Gabriella; Tell, Gianluca; Perrone, L; Garbelli, R; Quadrifoglio, Franco; Tagliavini, F; Giaccone, G. | |
APE1/Ref-1 regulates PTEN expression mediated by EGR-1 | 1-gen-2008 | Fantini, D; Vascotto, C.; Deganuto, M; Bivi, N; Gustincich, S; Marcon, G.; Quadrifoglio, F; Damante, G.; Bhakat, K. K; Mitra, S; Tell, G. | |
APOLIPOPROTEIN E AND INFLAMMATORY CYTOKINES PROMOTER GENOTYPING IN A GROUP OF CENTENARIANS FROM THE “CaT: Centenari a Trieste” ONGOING STUDY | 1-gen-2019 | Marcon, G | |
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 | |
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 | |
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. | |
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 |