Detalhe da pesquisa
1.
Epidemiology of seropositive myasthenia gravis in Sardinia: A population-based study in the district of Sassari.
Muscle Nerve
; 69(5): 637-642, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38456240
2.
Clinical application of ultra-high frequency ultrasound: Discovering a new imaging frontier.
J Clin Ultrasound
; 50(6): 817-825, 2022 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-35730639
3.
Cardiac and Neuromuscular Features of Patients With LMNA-Related Cardiomyopathy.
Ann Intern Med
; 171(7): 458-463, 2019 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31476771
4.
Videofluorography swallow study in patients with systemic sclerosis: correlation with clinical and radiological features.
Clin Exp Rheumatol
; 37 Suppl 119(4): 108-114, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31587696
5.
Muscle magnetic resonance imaging in congenital myasthenic syndromes.
Muscle Nerve
; 54(2): 211-9, 2016 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-26789134
6.
Influence of treatments in multiple sclerosis disability: a cohort study.
Mult Scler
; 21(4): 433-41, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25257611
7.
Congenital myasthenic syndromes due to mutations in ALG2 and ALG14.
Brain
; 136(Pt 3): 944-56, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23404334
8.
Genetic and clinical characteristics of skeletal and cardiac muscle in patients with lamin A/C gene mutations.
Muscle Nerve
; 48(2): 161-70, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23450819
9.
Advances in basic and clinical research in laminopathies.
Acta Myol
; 32(1): 18-22, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23853505
10.
Overlapping syndromes in laminopathies: a meta-analysis of the reported literature.
Acta Myol
; 32(1): 7-17, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23853504
11.
Unusual clinical presentations in subjects carrying novel NOTCH3 gene mutations.
J Stroke Cerebrovasc Dis
; 22(4): 539-44, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23465844
12.
White matter abnormalities in 15 subjects with SPG76.
J Neurol
; 270(12): 5784-5792, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37578488
13.
Prevalence of Spinal Muscular Atrophy in the Era of Disease-Modifying Therapies: An Italian Nationwide Survey.
Neurology
; 100(11): 522-528, 2023 03 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-36460469
14.
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
15.
O2-O3 chemodiscolysis: How much, how long? Retrospective outcome evaluation of different treatment sessions in partially-responder patients.
Interv Neuroradiol
; 28(4): 433-438, 2022 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-34516319
16.
Epidemiology of multiple sclerosis in south-western Sardinia.
Mult Scler
; 17(11): 1282-9, 2011 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-21652610
17.
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
18.
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
19.
Clinical and molecular characterization of limb-girdle muscular dystrophy due to LAMA2 mutations.
Muscle Nerve
; 44(5): 703-9, 2011 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-21953594
20.
Muscle imaging analogies in a cohort of patients with different clinical phenotypes caused by LMNA gene mutations.
Muscle Nerve
; 41(4): 458-63, 2010 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-19882644