Detalhe da pesquisa
1.
Selective serotonin reuptake inhibitors ameliorate MEGF10 myopathy.
Hum Mol Genet;
28(14): 2365-2377, 2019 07 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31267131
2.
Late-onset Becker muscular dystrophy: Refining the clinical features and electrophysiological findings.
Muscle Nerve;
52(5): 885-7, 2015 Nov.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26179421
3.
Safety and clinical activity of autologous RNA chimeric antigen receptor T-cell therapy in myasthenia gravis (MG-001): a prospective, multicentre, open-label, non-randomised phase 1b/2a study.
Lancet Neurol;
22(7): 578-590, 2023 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37353278
4.
Coexisting sporadic late onset nemaline myopathy and AL amyloid myopathy - incidental or related?
Neuromuscul Disord;
32(6): 533-538, 2022 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35550111
5.
Unusual cases of Anti-SRP necrotizing myopathy with predominant distal leg weakness and atrophy.
Neuromuscul Disord;
32(2): 170-175, 2022 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35031192
6.
Editorial by concerned physicians: Unintended effect of the orphan drug act on the potential cost of 3,4-diaminopyridine.
Muscle Nerve;
53(2): 165-8, 2016 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26662952
7.
HIV lumbosacral radiculoplexus neuropathy mimicking lymphoma: diffuse infiltrative lymphocytosis syndrome (DILS) restricted to nerve?
Muscle Nerve;
41(2): 276-82, 2010 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-19882634
8.
Screening for genetic mutations in patients with neuropathy without definite etiology is useful.
J Neurol;
267(9): 2648-2654, 2020 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32399692
9.
Refractory CIDP: Clinical characteristics, antibodies and response to alternative treatment.
J Neurol Sci;
418: 117098, 2020 Nov 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32841917
10.
Nusinersen in adult patients with spinal muscular atrophy: Observations from a single center.
Neurology;
95(4): e413-e416, 2020 07 28.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32665408
11.
Diagnosis of paraproteinemic neuropathy: Room for improvement.
J Neurol Sci;
415: 116902, 2020 Aug 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32497875
12.
Bright tongue sign in patients with late-onset Pompe disease.
J Neurol;
266(10): 2518-2523, 2019 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31256280
13.
Neurosarcoidosis manifesting as focal sacral inflammatory radiculopathy.
BMJ Case Rep;
17(3)2024 Mar 19.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38508609
14.
A patient with mutation in the SCN4A p.M1592v presenting with fixed weakness, rhabdomyolysis, and episodic worsening of weakness.
Muscle Nerve;
48(2): 306-7, 2013 Aug.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23801527
15.
Diagnostic utility of exome sequencing in the evaluation of neuromuscular disorders.
Neurol Genet;
4(1): e212, 2018 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29417091
16.
Reader response: Sporadic late-onset nemaline myopathy: Clinical spectrum, survival, and treatment outcomes.
Neurology;
94(24): 1109-1110, 2020 06 16.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32540943
17.
Toxoplasmic encephalitis during mycophenolate mofetil immunotherapy of neuromuscular disease.
Neurol Neuroimmunol Neuroinflamm;
2(1): e63, 2015 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25635260
18.
Unwarranted, long term, alglucosidase alfa enzyme replacement therapy in two non-Pompe disease patients.
Clin Neurol Neurosurg;
196: 106048, 2020 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32623214
19.
Dermatomyositis as a presentation of neuromyelitis optica spectrum disorder.
J Neuroimmunol;
278: 108-11, 2015 Jan 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25595259
20.
Characteristics of magnetic resonance imaging biomarkers in a natural history study of golden retriever muscular dystrophy.
Neuromuscul Disord;
24(2): 178-91, 2014 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24295811