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The Genetic Variability of UCP4 Affects the Individual Susceptibility to Late-Onset Alzheimer's Disease and Modifies the Disease's Risk in APOE-ɛ4 Carriers. [electronic resource] by
- Montesanto, Alberto
- Crocco, Paolina
- Anfossi, Maria
- Smirne, Nicoletta
- Puccio, Gianfranco
- Colao, Rosanna
- Maletta, Raffaele
- Passarino, Giuseppe
- Bruni, Amalia C
- Rose, Giuseppina
Producer: 20161229
In:
Journal of Alzheimer's disease : JAD vol. 51
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3.
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Late onset familial Alzheimer's disease: novel presenilin 2 mutation and PS1 E318G polymorphism. [electronic resource] by
- Bernardi, Livia
- Tomaino, Carmine
- Anfossi, Maria
- Gallo, Maura
- Geracitano, Silvana
- Puccio, Gianfranco
- Colao, Rosanna
- Frangipane, Francesca
- Mirabelli, Maria
- Smirne, Nicoletta
- Maletta, Raffaele Giovanni
- Bruni, Amalia C
Producer: 20080701
In:
Journal of neurology vol. 255
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4.
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MAPT V363I variation in a sporadic case of frontotemporal dementia: variable penetrant mutation or rare polymorphism? [electronic resource] by
- Anfossi, Maria
- Bernardi, Livia
- Gallo, Maura
- Geracitano, Silvana
- Colao, Rosanna
- Puccio, Gianfranco
- Curcio, Sabrina A M
- Frangipane, Francesca
- Mirabelli, Maria
- Tomaino, Carmine
- Smirne, Nicoletta
- Maletta, Raffaele
- Bruni, Amalia Cecilia
Producer: 20110608
In:
Alzheimer disease and associated disorders vol. 25
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5.
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AbetaPP A713T mutation in late onset Alzheimer's disease with cerebrovascular lesions. [electronic resource] by
- Bernardi, Livia
- Geracitano, Silvana
- Colao, Rosanna
- Puccio, Gianfranco
- Gallo, Maura
- Anfossi, Maria
- Frangipane, Francesca
- Curcio, Sabrina A M
- Mirabelli, Maria
- Tomaino, Carmine
- Vasso, Franca
- Smirne, Nicoletta
- Maletta, Raffaele
- Bruni, Amalia C
Producer: 20091216
In:
Journal of Alzheimer's disease : JAD vol. 17
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6.
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Novel MAPT Val75Ala mutation and PSEN2 Arg62Hys in two siblings with frontotemporal dementia. [electronic resource] by
- Gallo, Maura
- Tomaino, Carmine
- Puccio, Gianfranco
- Frangipane, Francesca
- Curcio, Sabrina A M
- Bernardi, Livia
- Geracitano, Silvana
- Anfossi, Maria
- Mirabelli, Maria
- Colao, Rosanna
- Vasso, Franca
- Smirne, Nicoletta
- Maletta, Raffaele G
- Bruni, Amalia Cecilia
Producer: 20100413
In:
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology vol. 31
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Association of the variant Cys139Arg at GRN gene to the clinical spectrum of frontotemporal lobar degeneration. [electronic resource] by
- Piaceri, Irene
- Pradella, Silvia
- Cupidi, Chiara
- Nannucci, Serena
- Polito, Cristina
- Bagnoli, Silvia
- Tedde, Andrea
- Smirne, Nicoletta
- Anfossi, Maria
- Gallo, Maura
- Bernardi, Livia
- Colao, Rosanna
- Maletta, Raffaele
- Bruni, Amalia Cecilia
- Sorbi, Sandro
- Nacmias, Benedetta
Producer: 20141217
In:
Journal of Alzheimer's disease : JAD vol. 40
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8.
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Novel PSEN1 and PGRN mutations in early-onset familial frontotemporal dementia. [electronic resource] by
- Bernardi, Livia
- Tomaino, Carmine
- Anfossi, Maria
- Gallo, Maura
- Geracitano, Silvana
- Costanzo, Angela
- Colao, Rosanna
- Puccio, Gianfranco
- Frangipane, Francesca
- Curcio, Sabrina A M
- Mirabelli, Maria
- Smirne, Nicoletta
- Iapaolo, David
- Maletta, Raffaele Giovanni
- Bruni, Amalia C
Producer: 20091207
In:
Neurobiology of aging vol. 30
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PSEN1 and PRNP gene mutations: co-occurrence makes onset very early in a family with FTD phenotype. [electronic resource] by
- Bernardi, Livia
- Anfossi, Maria
- Gallo, Maura
- Geracitano, Silvana
- Cola, Rosanna
- Puccio, Gianfranco
- Curcio, Sabrina A M
- Frangipane, Francesca
- Mirabelli, Maria
- Clodomiro, Alessandra
- Di Lorenzo, Raffaele
- Smirne, Nicoletta
- Maletta, Raffaele
- Iapaolo, David
- Bruni, Amalia C
Producer: 20110919
In:
Journal of Alzheimer's disease : JAD vol. 24
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10.
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Role of TOMM40 rs10524523 polymorphism in onset of alzheimer's disease caused by the PSEN1 M146L mutation. [electronic resource] by
- Bernardi, Livia
- Gallo, Maura
- Anfossi, Maria
- Conidi, Maria Elena
- Colao, Rosanna
- Puccio, Gianfranco
- Curcio, Sabrina A M
- Frangipane, Francesca
- Clodomiro, Alessandra
- Mirabelli, Maria
- Vasso, Franca
- Smirne, Nicoletta
- Di Lorenzo, Raffaele
- Maletta, Raffaele
- Bruni, Amalia C
Producer: 20140415
In:
Journal of Alzheimer's disease : JAD vol. 37
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11.
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Novel N-terminal domain mutation in prion protein detected in 2 patients diagnosed with frontotemporal lobar degeneration syndrome. [electronic resource] by
- Bernardi, Livia
- Cupidi, Chiara
- Frangipane, Francesca
- Anfossi, Maria
- Gallo, Maura
- Conidi, Maria Elena
- Vasso, Franca
- Colao, Rosanna
- Puccio, Gianfranco
- Curcio, Sabrina A M
- Mirabelli, Maria
- Clodomiro, Alessandra
- Di Lorenzo, Raffaele
- Smirne, Nicoletta
- Maletta, Raffaele
- Bruni, Amalia C
Producer: 20151019
In:
Neurobiology of aging vol. 35
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Identification of three novel LRRK2 mutations associated with Parkinson's disease in a Calabrian population. [electronic resource] by
- Anfossi, Maria
- Colao, Rosanna
- Gallo, Maura
- Bernardi, Livia
- Conidi, M Elena
- Frangipane, Francesca
- Vasso, Franca
- Puccio, Gianfranco
- Clodomiro, Alessandra
- Mirabelli, Maria
- Curcio, Sabrina A M
- Torchia, Giusi
- Smirne, Nicoletta
- Di Lorenzo, Raffaele
- Maletta, Raffaele
- Bruni, Amalia C
Producer: 20140627
In:
Journal of Alzheimer's disease : JAD vol. 38
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13.
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Presenilin 2 Ser130Leu mutation in a case of late-onset "sporadic" Alzheimer's disease. [electronic resource] by
- Tomaino, Carmine
- Bernardi, Livia
- Anfossi, Maria
- Costanzo, Angela
- Ferrise, Francesca
- Gallo, Maura
- Geracitano, Silvana
- Maletta, Raffaele
- Curcio, Sabrina A M
- Mirabelli, Maria
- Colao, Rosanna
- Frangipane, Francesca
- Puccio, Gianfranco
- Calignano, Cinzia
- Muraca, Maria Gabriella
- Paonessa, Annamaria
- Smirne, Nicoletta
- Leotta, Attilio
- Bruni, Amalia C
Producer: 20070706
In:
Journal of neurology vol. 254
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14.
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Compound heterozygosity of 2 novel MAPT mutations in frontotemporal dementia. [electronic resource] by
- Anfossi, Maria
- Vuono, Romina
- Maletta, Raffaele
- Virdee, Kanwar
- Mirabelli, Maria
- Colao, Rosanna
- Puccio, Gianfranco
- Bernardi, Livia
- Frangipane, Francesca
- Gallo, Maura
- Geracitano, Silvana
- Tomaino, Carmine
- Curcio, Sabrina Anna Maria
- Zannino, Giuseppa
- Lamenza, Francesco
- Duyckaerts, Charles
- Spillantini, Maria Grazia
- Losso, Maria Adele
- Bruni, Amalia C
Producer: 20110808
In:
Neurobiology of aging vol. 32
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15.
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Estimating the inheritance of frontotemporal lobar degeneration in the Italian population. [electronic resource] by
- Borroni, Barbara
- Grassi, Mario
- Bianchi, Marta
- Bruni, Amalia Cecilia
- Maletta, Raffaele Giovanni
- Anfossi, Maria
- Pepe, Daniele
- Cagnin, Annachiara
- Caffarra, Paolo
- Cappa, Stefano
- Clerici, Francesca
- Daniele, Antonio
- Frisoni, Giovanni B
- Galimberti, Daniela
- Parnetti, Lucilla
- Perri, Roberta
- Rainero, Innocenzo
- Tremolizzo, Lucio
- Turla, Marinella
- Zanetti, Orazio
- Padovani, Alessandro
Producer: 20150209
In:
Journal of Alzheimer's disease : JAD vol. 41
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16.
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A novel pathogenic PSEN1 mutation in a family with Alzheimer's disease: phenotypical and neuropathological features. [electronic resource] by
- Gallo, Maura
- Marcello, Norina
- Curcio, Sabrina A M
- Colao, Rosanna
- Geracitano, Silvana
- Bernardi, Livia
- Anfossi, Maria
- Puccio, Gianfranco
- Frangipane, Francesca
- Clodomiro, Alessandra
- Mirabelli, Maria
- Vasso, Franca
- Smirne, Nicoletta
- Muraca, Gabriella
- Di Lorenzo, Raffaele
- Maletta, Raffaele
- Ghidoni, Enrico
- Bugiani, Orso
- Tagliavini, Fabrizio
- Giaccone, Giorgio
- Bruni, Amalia C
Producer: 20111115
In:
Journal of Alzheimer's disease : JAD vol. 25
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17.
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Role of Niemann-Pick Type C Disease Mutations in Dementia. [electronic resource] by
- Cupidi, Chiara
- Frangipane, Francesca
- Gallo, Maura
- Clodomiro, Alessandra
- Colao, Rosanna
- Bernardi, Livia
- Anfossi, Maria
- Conidi, Maria Elena
- Vasso, Franca
- Curcio, Sabrina Anna Maria
- Mirabelli, Maria
- Smirne, Nicoletta
- Torchia, Giusi
- Muraca, Maria Gabriella
- Puccio, Gianfranco
- Di Lorenzo, Raffaele
- Zampieri, Stefania
- Romanello, Milena
- Dardis, Andrea
- Maletta, Raffaele Giovanni
- Bruni, Amalia Cecilia
Producer: 20180220
In:
Journal of Alzheimer's disease : JAD vol. 55
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18.
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Homozygous carriers of APP A713T mutation in an autosomal dominant Alzheimer disease family. [electronic resource] by
- Conidi, Maria E
- Bernardi, Livia
- Puccio, Gianfranco
- Smirne, Nicoletta
- Muraca, Maria G
- Curcio, Sabrina A M
- Colao, Rosanna
- Piscopo, Paola
- Gallo, Maura
- Anfossi, Maria
- Frangipane, Francesca
- Clodomiro, Alessandra
- Mirabelli, Maria
- Vasso, Franca
- Cupidi, Chiara
- Torchia, Giusi
- Di Lorenzo, Raffaele
- Mandich, Paola
- Confaloni, Annamaria
- Maletta, Raffaele G
- Bruni, Amalia C
Producer: 20150819
In:
Neurology vol. 84
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Frequency of Cardiovascular Genetic Risk Factors in a Calabrian Population and Their Effects on Dementia. [electronic resource] by
- Maletta, Raffaele
- Smirne, Nicoletta
- Bernardi, Livia
- Anfossi, Maria
- Gallo, Maura
- Conidi, Maria Elena
- Colao, Rosanna
- Puccio, Gianfranco
- Curcio, Sabrina A M
- Laganà, Valentina
- Frangipane, Francesca
- Cupidi, Chiara
- Mirabelli, Maria
- Vasso, Franca
- Torchia, Giusi
- Muraca, Maria G
- Di Lorenzo, Raffaele
- Rose, Giuseppina
- Montesanto, Alberto
- Passarino, Giuseppe
- Bruni, Amalia C
Producer: 20190117
In:
Journal of Alzheimer's disease : JAD vol. 61
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The novel PSEN1 M84V mutation associated to frontal dysexecutive syndrome, spastic paraparesis, and cerebellar atrophy in a dominant Alzheimer's disease family. [electronic resource] by
- Gallo, Maura
- Frangipane, Francesca
- Cupidi, Chiara
- De Bartolo, Matteo
- Turone, Sabina
- Ferrari, Camilla
- Nacmias, Benedetta
- Grimaldi, Giuliana
- Laganà, Valentina
- Colao, Rosanna
- Bernardi, Livia
- Anfossi, Maria
- Conidi, Maria Elena
- Vasso, Franca
- Curcio, Sabrina Anna Maria
- Mirabelli, Maria
- Smirne, Nicoletta
- Torchia, Giusi
- Muraca, Maria Gabriella
- Puccio, Gianfranco
- Di Lorenzo, Raffaele
- Piccininni, Maristella
- Tedde, Andrea
- Maletta, Raffaele Giovanni
- Sorbi, Sandro
- Bruni, Amalia Cecilia
Producer: 20171116
In:
Neurobiology of aging vol. 56
Availability: No items available.
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