Detalhe da pesquisa
1.
No evidence for an effect on brain atrophy rate of atorvastatin add-on to interferon ß1b therapy in relapsing-remitting multiple sclerosis (the ARIANNA study).
Mult Scler
; 22(9): 1163-73, 2016 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-26466947
2.
The burden of multiple sclerosis variants in continental Italians and Sardinians.
Mult Scler
; 21(11): 1385-95, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26438306
3.
Cardiac involvement in patients with lamin A/C gene mutations: a cohort observation.
Muscle Nerve
; 46(2): 187-92, 2012 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-22806367
4.
Epidemiology of multiple sclerosis in south-western Sardinia.
Mult Scler
; 17(11): 1282-9, 2011 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-21652610
5.
Dilated cardiomyopathy with conduction defects in a patient with partial merosin deficiency due to mutations in the laminin-α2-chain gene: a chance association or a novel phenotype?
Muscle Nerve
; 44(5): 826-8, 2011 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-22006699
6.
Aberrant splicing in the LMNA gene caused by a novel mutation on the polypyrimidine tract of intron 5.
Muscle Nerve
; 43(5): 688-93, 2011 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-21462202
7.
Evolution of the phenotype in a family with an LMNA gene mutation presenting with isolated cardiac involvement.
Muscle Nerve
; 41(1): 85-91, 2010 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-19768759
8.
Partial lipodystrophy associated with muscular dystrophy of unknown genetic origin.
Muscle Nerve
; 49(6): 928-30, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24375490
9.
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
10.
Effects of Six Months Training on Physical Capacity and Metaboreflex Activity in Patients with Multiple Sclerosis.
Front Physiol
; 7: 531, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27895592
11.
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
12.
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
13.
Chromosome 7q21-22 and multiple sclerosis: evidence for a genetic susceptibility effect in vicinity to the protachykinin-1 gene.
J Neuroimmunol
; 125(1-2): 141-8, 2002 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-11960650
14.
A novel LIPE nonsense mutation found using exome sequencing in siblings with late-onset familial partial lipodystrophy.
Can J Cardiol
; 30(12): 1649-54, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25475467
15.
Juvenile multiple sclerosis similar to type I diabetes mellitus has a seasonality of month of birth which differs from that in the general population.
J Pediatr Endocrinol Metab
; 21(5): 473-7, 2008 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-18655530
16.
Opposite roles of NMDA receptors in relapsing and primary progressive multiple sclerosis.
PLoS One
; 8(6): e67357, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23840674
17.
Cardiac and muscle imaging findings in a family with X-linked Emery-Dreifuss muscular dystrophy.
Neuromuscul Disord
; 22(2): 152-8, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-21993399
18.
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
19.
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
20.
Efficacy and safety of quetiapine treatment for delusional parasitosis: experience in an elderly patient.
Clin Neuropharmacol
; 31(5): 310-2, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-18836354