Detalhe da pesquisa
1.
Geographic differences in the incidence of Huntington's disease in Sardinia, Italy.
Neurol Sci
; 42(12): 5177-5181, 2021 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-33792825
2.
Phenotypic variability related to C9orf72 mutation in a large Sardinian kindred.
Amyotroph Lateral Scler Frontotemporal Degener
; 17(3-4): 245-8, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-26575405
3.
Constructional apraxia in frontotemporal dementia associated with the C9orf72 mutation: broadening the clinical and neuropsychological phenotype.
Amyotroph Lateral Scler Frontotemporal Degener
; 16(1-2): 8-15, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25285776
4.
Clinical phenotypes and radiological findings in frontotemporal dementia related to TARDBP mutations.
J Neurol
; 262(2): 375-84, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25408367
5.
Progressive apraxia of speech in a patient with a C9orf72 mutation.
Amyotroph Lateral Scler Frontotemporal Degener
; 17(7-8): 608-609, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27166164
6.
A patient carrying a homozygous p.A382T TARDBP missense mutation shows a syndrome including ALS, extrapyramidal symptoms, and FTD.
Neurobiol Aging
; 32(12): 2327.e1-5, 2011 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-21803454
7.
Bipolar affective disorder preceding frontotemporal dementia in a patient with C9ORF72 mutation: is there a genetic link between these two disorders?
J Neurol
; 260(4): 1155-7, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23314407
8.
Frontotemporal dementia with psychosis, parkinsonism, visuo-spatial dysfunction, upper motor neuron involvement associated to expansion of C9ORF72: a peculiar phenotype?
J Neurol
; 259(8): 1749-51, 2012 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-22323211