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Muscle ceroid lipofuscin-like deposits in a patient with corticobasal syndrome due to a progranulin mutation. [electronic resource] by
- Terlizzi, Rossana
- Valentino, Maria Lucia
- Bartoletti-Stella, Anna
- Columbaro, Marta
- Piras, Silvia
- Stanzani-Maserati, Michelangelo
- Quadri, Marialuisa
- Breedveld, Guido J
- Bonifati, Vincenzo
- Martinelli, Paolo
- Parchi, Piero
- Capellari, Sabina
Producer: 20190219
In:
Movement disorders : official journal of the Movement Disorder Society vol. 32
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63.
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Non Fluent Variant of Primary Progressive Aphasia Due to the Novel GRN g.9543delA(IVS3-2delA) Mutation. [electronic resource] by
- Cioffi, Sara M G
- Galimberti, Daniela
- Barocco, Federica
- Spallazzi, Marco
- Fenoglio, Chiara
- Serpente, Maria
- Arcaro, Marina
- Gardini, Simona
- Scarpini, Elio
- Caffarra, Paolo
Producer: 20180126
In:
Journal of Alzheimer's disease : JAD vol. 54
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Exome sequencing reveals a novel partial deletion in the progranulin gene causing primary progressive aphasia. [electronic resource] by
- Rohrer, Jonathan D
- Beck, Jonathan
- Plagnol, Vincent
- Gordon, Elizabeth
- Lashley, Tammaryn
- Revesz, Tamas
- Janssen, John C
- Fox, Nick C
- Warren, Jason D
- Rossor, Martin N
- Mead, Simon
- Schott, Jonathan M
Producer: 20140109
In:
Journal of neurology, neurosurgery, and psychiatry vol. 84
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One novel GRN null mutation, two different aphasia phenotypes. [electronic resource] by
- Coppola, Cinzia
- Oliva, Mariano
- Saracino, Dario
- Pappatà, Sabina
- Zampella, Emilia
- Cimini, Sara
- Ricci, Martina
- Giaccone, Giorgio
- Di Iorio, Giuseppe
- Rossi, Giacomina
Producer: 20200914
In:
Neurobiology of aging vol. 87
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Progranulin locus deletion in frontotemporal dementia. [electronic resource] by
- Gijselinck, I
- van der Zee, J
- Engelborghs, S
- Goossens, D
- Peeters, K
- Mattheijssens, M
- Corsmit, E
- Del-Favero, J
- De Deyn, P P
- Van Broeckhoven, C
- Cruts, M
Producer: 20080206
In:
Human mutation vol. 29
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Increased serum GP88 (Progranulin) concentrations in rheumatoid arthritis. [electronic resource] by
- Yamamoto, Yasuko
- Takemura, Masao
- Serrero, Ginette
- Hayashi, Jun
- Yue, Binbin
- Tsuboi, Aya
- Kubo, Hisako
- Mitsuhashi, Takashi
- Mannami, Kenji
- Sato, Masao
- Matsunami, Hidetoshi
- Matuo, Yushi
- Saito, Kuniaki
Producer: 20150622
In:
Inflammation vol. 37
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Partial deletions of the GRN gene are a cause of frontotemporal lobar degeneration. [electronic resource] by
- Clot, Fabienne
- Rovelet-Lecrux, Anne
- Lamari, Foudil
- Noël, Sandrine
- Keren, Boris
- Camuzat, Agnès
- Michon, Agnès
- Jornea, Ludmila
- Laudier, Béatrice
- de Septenville, Anne
- Caroppo, Paola
- Campion, Dominique
- Cazeneuve, Cécile
- Brice, Alexis
- LeGuern, Eric
- Le Ber, Isabelle
Producer: 20150528
In:
Neurogenetics vol. 15
Availability: No items available.
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