Detalhe da pesquisa
1.
Physical activity practiced at a young age is associated with a less severe subsequent clinical presentation in facioscapulohumeral muscular dystrophy.
BMC Musculoskelet Disord
; 25(1): 35, 2024 Jan 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38183077
2.
Distal upper limb involvement in myasthenia-myositis association.
Neurol Sci
; 44(2): 719-722, 2023 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-36336775
3.
Comparison of quantitative muscle ultrasound and whole-body muscle MRI in facioscapulohumeral muscular dystrophy type 1 patients.
Neurol Sci
; 44(11): 4057-4064, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37311950
4.
Muscle magnetic resonance imaging in myotonic dystrophy type 1 (DM1): Refining muscle involvement and implications for clinical trials.
Eur J Neurol
; 29(3): 843-854, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34753219
5.
Gender effect on cardiac involvement in myotonic dystrophy type 1.
Eur J Neurol
; 28(4): 1366-1374, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33283405
6.
An Age-Standardized Prevalence Estimate and a Sex and Age Distribution of Myotonic Dystrophy Types 1 and 2 in the Rome Province, Italy.
Neuroepidemiology
; 46(3): 191-7, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-26882032
7.
Large scale genotype-phenotype analyses indicate that novel prognostic tools are required for families with facioscapulohumeral muscular dystrophy.
Brain
; 136(Pt 11): 3408-17, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-24030947
8.
Changes of clinical, neurophysiological and nerve ultrasound characteristics in CIDP over time: a 3-year follow-up.
J Neurol
; 268(8): 3011-3019, 2021 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-33638679
9.
Novel ACTA1 mutation causes late-presenting nemaline myopathy with unusual dark cores.
Neuromuscul Disord
; 31(2): 139-148, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33384202
10.
A 5-year clinical follow-up study from the Italian National Registry for FSHD.
J Neurol
; 268(1): 356-366, 2021 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-32813049
11.
Muscle involvement in myasthenia gravis: Expanding the clinical spectrum of Myasthenia-Myositis association from a large cohort of patients.
Autoimmun Rev
; 19(4): 102498, 2020 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-32062029
12.
Phenotypic Variability Among Patients With D4Z4 Reduced Allele Facioscapulohumeral Muscular Dystrophy.
JAMA Netw Open
; 3(5): e204040, 2020 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32356886
13.
Large genotype-phenotype study in carriers of D4Z4 borderline alleles provides guidance for facioscapulohumeral muscular dystrophy diagnosis.
Sci Rep
; 10(1): 21648, 2020 12 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-33303865
14.
Prevalence and predictor factors of respiratory impairment in a large cohort of patients with Myotonic Dystrophy type 1 (DM1): A retrospective, cross sectional study.
J Neurol Sci
; 399: 118-124, 2019 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30798109
15.
A 34-year longitudinal study on long-term cardiac outcomes in DM1 patients with normal ECG at baseline at an Italian clinical centre.
J Neurol
; 265(4): 885-895, 2018 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-29429070
16.
Increased risk of tumor in DM1 is not related to exposure to common lifestyle risk factors.
J Neurol
; 263(3): 492-8, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26739382
17.
"I Know that You Know that I Know": Neural Substrates Associated with Social Cognition Deficits in DM1 Patients.
PLoS One
; 11(6): e0156901, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27258100
18.
Clinical expression of facioscapulohumeral muscular dystrophy in carriers of 1-3 D4Z4 reduced alleles: experience of the FSHD Italian National Registry.
BMJ Open
; 6(1): e007798, 2016 Jan 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-26733561
19.
A novel clinical tool to classify facioscapulohumeral muscular dystrophy phenotypes.
J Neurol
; 263(6): 1204-14, 2016 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-27126453
20.
Peripheral nerve ultrasound changes in CIDP and correlations with nerve conduction velocity.
Neurology
; 84(8): 803-9, 2015 Feb 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-25632087