Results
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1.
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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
Availability: No items available.
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2.
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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
Availability: No items available.
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3.
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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
Availability: No items available.
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4.
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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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5.
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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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6.
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Behavioral disorder, dementia, ataxia, and rigidity in a large family with TATA box-binding protein mutation. [electronic resource] by
- Bruni, Amalia C
- Takahashi-Fujigasaki, Junko
- Maltecca, Francesca
- Foncin, Jean Francois
- Servadio, Antonio
- Casari, Giorgio
- D'Adamo, Pio
- Maletta, Raffaele
- Curcio, Sabrina A M
- De Michele, Giuseppe
- Filla, Alessandro
- El Hachimi, Khalid H
- Duyckaerts, Charles
Producer: 20040907
In:
Archives of neurology vol. 61
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7.
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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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8.
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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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9.
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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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10.
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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
Availability: No items available.
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11.
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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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12.
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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
Availability: No items available.
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13.
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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
Availability: No items available.
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14.
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Mutation analysis of CHCHD10 in different neurodegenerative diseases. [electronic resource] by
- Zhang, Ming
- Xi, Zhengrui
- Zinman, Lorne
- Bruni, Amalia C
- Maletta, Raffaele G
- Curcio, Sabrina A M
- Rainero, Innocenzo
- Rubino, Elisa
- Pinessi, Lorenzo
- Nacmias, Benedetta
- Sorbi, Sandro
- Galimberti, Daniela
- Lang, Anthony E
- Fox, Susan
- Surace, Ezequiel I
- Ghani, Mahdi
- Guo, Jing
- Sato, Christine
- Moreno, Danielle
- Liang, Yan
- Keith, Julia
- Traynor, Bryan J
- St George-Hyslop, Peter
- Rogaeva, Ekaterina
Producer: 20151103
In:
Brain : a journal of neurology vol. 138
Availability: No items available.
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