Sfoglia per Autore
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
Diagnosis of Alzheimer's disease
1997-01-01 Marcon, Gabriella; Giaccone, G; Tagliavini, F; Bugiani, O.
PURE, ACUTE CEREBELAR SYNDROME ASSOCIATED WITH CYCLOSPORINE TREATMENT IN AN ADULT LIVER TRANSPLANT RECIPIENT
1997-01-01 Risaliti, Andrea; Vitulli, D.; Marcon, Gabriella; Cautero, N.; Soardo, G.; Corno, V.; Bruschi, F.; Pirisi, M.
Neuropsychological and psychometric findings in a large Italian Family with the M239V mutation of the PSEN2 gene
1998-01-01 Marcon, G; Nacmias, B; Sorbi, S; Bergonzi, P; Balestrieri, M
Clinical and neuropathological findings of an Italian Family with Alzheimer’s disease and M239V mutation of PS2 gene
1998-01-01 Marcon, G; Giaccone, G; Tagliavini, F; Bergonzi, P; Sorbi, S; Nacmias, B; Beltrami, Ca; Bugiani, O
Implication of α1-antichimotrypsin polymorphism in familial Alazheimer’s disease
1998-01-01 Nacmias, B; Tedde, A; Marcon, G; Latorraca, S; Forleo, P; Piacentini, S; Sorbi, S
Implication of alpha1-antichymotrypsin polymorphism in familial Alzheimer's disease
1998-01-01 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
1998-01-01 Nacmias, B; Tedde, A; Marcon, G; Latorraca, S; Forleo, P; Piacentini, S; Amaducci, L; Sorbi, S
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
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.
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
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.
Localisation of presenilin 2 in human and rodent pancreatic islet beta-cells; Met239Val presenilin 2 variant is not associated with diabetes in man
1999-01-01 Jaikaran, Et; Marcon, Gabriella; Levesque, L; GEORGE HYSLOP, Ps; Fraser, Pe; Clark, A.
HLA A2 allele is associated with age at onset of Alzheimer's disease
1999-01-01 Ballerini, C; Nacmias, B; Rombola, G; Marcon, Gabriella; Massacesi, L; Sorbi, S.
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22
1999-01-01 Simonati, A; Fabrizi, Gm; Pasquinelli, A; Taioli, F; Cavallaro, T; Morbin, M; Marcon, Gabriella; Papini, M; Rizzuto, N.
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
Enzyme polymorphism in presenilin linked Alzheimer’s disease families and sporadic Alzheimer’s disease
2000-01-01 Tedde, A; Nacmias, B; Marcon, G; Et, Al
Caspase-3 is activated in Alzheimer’s disease but not in Frontotemporal Dementia
2000-01-01 Marcon, G; Atzori, C; Srinivasan, An; Okazawa, H; Ghetti, B; Migheli, A
No association between 2 Macroglobulin DNA polymorphism and sporadic Alzheimer’s Disease in Italy
2000-01-01 Sorbi, S; Nacmias, B; Tedde, A; Forleo, P; Marcon, G; Petruzzi, C; Guarneri, B; Serio, A
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
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
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 | |
Diagnosis of Alzheimer's disease | 1-gen-1997 | Marcon, Gabriella; Giaccone, G; Tagliavini, F; Bugiani, O. | |
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. | |
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 | |
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 | |
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 | |
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; Amaducci, L; Sorbi, 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 | |
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. | |
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 | |
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. | |
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. | |
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. | |
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 | |
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 | |
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 | |
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 | |
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 |
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