Detalhe da pesquisa
1.
Parent-proxy pediatric CMT quality of life outcome measure: Validation of the Italian version.
J Peripher Nerv Syst;
29(1): 107-110, 2024 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38329138
2.
Anti-pan-neurofascin nodopathy: cause of fulminant neuropathy.
Neurol Sci;
45(4): 1755-1759, 2024 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38190082
3.
Anterior lumbosacral polyradiculoneuropathy following intrathecal methotrexate administration: a case report and literature update.
Neurol Sci;
44(2): 715-718, 2023 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36418611
4.
Starting eculizumab as rescue therapy in refractory myasthenic crisis.
Neurol Sci;
44(10): 3707-3709, 2023 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37306795
5.
Validation of the Italian version of the pediatric CMT quality of life outcome measure.
J Peripher Nerv Syst;
27(2): 127-130, 2022 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35416371
6.
A Model to Study Myelinated Fiber Degeneration and Regeneration in Human Skin.
Ann Neurol;
87(3): 456-465, 2020 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31849107
7.
Different nerve ultrasound patterns in charcot-marie-tooth types and hereditary neuropathy with liability to pressure palsies.
Muscle Nerve;
57(1): E18-E23, 2018 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28802056
8.
Palatal tremor in a patient with prolonged vegetative state after ischemic stroke.
Neurol Sci;
44(12): 4545-4547, 2023 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37537417
9.
Relative lymphocyte count as an indicator of 3-year mortality in elderly people with severe COPD.
BMC Pulm Med;
18(1): 116, 2018 Jul 13.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30005642
10.
A novel NDRG1 mutation in a non-Romani patient with CMT4D/HMSN-Lom.
J Peripher Nerv Syst;
22(1): 47-50, 2017 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27982524
11.
Hereditary gelsolin amyloidosis (HGA): a neglected cause of bilateral progressive or recurrent facial palsy.
J Peripher Nerv Syst;
22(1): 59-63, 2017 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27982499
12.
Screening for SH3TC2 gene mutations in a series of demyelinating recessive Charcot-Marie-Tooth disease (CMT4).
J Peripher Nerv Syst;
21(3): 142-9, 2016 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27231023
13.
Genotype-phenotype characteristics and baseline natural history of heritable neuropathies caused by mutations in the MPZ gene.
Brain;
138(Pt 11): 3180-92, 2015 Nov.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26310628
14.
Mutational mechanisms in MFN2-related neuropathy: compound heterozygosity for recessive and semidominant mutations.
J Peripher Nerv Syst;
20(4): 380-6, 2015 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26306937
15.
Overlapping phenotypes in complex spastic paraplegias SPG11, SPG15, SPG35 and SPG48.
Brain;
137(Pt 7): 1907-20, 2014 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24833714
16.
Anti-amyloid ß autoantibodies in cerebral amyloid angiopathy-related inflammation: implications for amyloid-modifying therapies.
Ann Neurol;
73(4): 449-58, 2013 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23625526
17.
X-linked Charcot-Marie-Tooth type 1: stroke-like presentation of a novel GJB1 mutation.
J Peripher Nerv Syst;
19(2): 183-6, 2014 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24863494
18.
Psychometrics evaluation of Charcot-Marie-Tooth Neuropathy Score (CMTNSv2) second version, using Rasch analysis.
J Peripher Nerv Syst;
19(3): 192-6, 2014 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25400013
19.
Small fiber pathology parallels disease progression in Parkinson disease: a longitudinal study.
Acta Neuropathol;
136(3): 501-503, 2018 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29916036
20.
Coexistence of Charcot-Marie-Tooth disease type 1A and anti-MAG neuropathy.
J Peripher Nerv Syst;
18(2): 185-8, 2013 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23781967