Detalhe da pesquisa
1.
Trial of Intravenous Immune Globulin in Dermatomyositis.
N Engl J Med
; 387(14): 1264-1278, 2022 10 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36198179
2.
Trial of Intravenous Immune Globulin in Dermatomyositis. Reply.
N Engl J Med
; 388(1): 94-95, 2023 01 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36599070
3.
Impact of the coronavirus disease 2019 pandemic on stroke teleconsultations in Germany in the first half of 2020.
Eur J Neurol
; 28(10): 3267-3278, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-33619788
4.
In vivo characterization of human myofibrillar myopathy genes in zebrafish.
Biochem Biophys Res Commun
; 461(2): 217-23, 2015 May 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-25866181
5.
Novel recessive myotilin mutation causes severe myofibrillar myopathy.
Neurogenetics
; 15(3): 151-6, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24928145
6.
Safety and tolerability of intravenous immunoglobulin in patients with active dermatomyositis: results from the randomised, placebo-controlled ProDERM study.
Arthritis Res Ther
; 26(1): 27, 2024 01 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-38233885
7.
Efficacy of intravenous immunoglobulins (IVIg) in improving skin symptoms in patients with dermatomyositis: a post-hoc analysis of the ProDERM study.
EClinicalMedicine
; 64: 102234, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37799613
8.
Unusually severe muscular dystrophy upon in-frame deletion of the dystrophin rod domain and lack of compensation by membrane-localized utrophin.
Med
; 4(4): 245-251.e3, 2023 04 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-36905929
9.
Patient-specific protein aggregates in myofibrillar myopathies: laser microdissection and differential proteomics for identification of plaque components.
Proteomics
; 12(23-24): 3598-609, 2012 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-23044792
10.
Novel ANO5 mutations causing hyper-CK-emia, limb girdle muscular weakness and Miyoshi type of muscular dystrophy.
Muscle Nerve
; 45(5): 740-2, 2012 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-22499103
11.
Proteomic identification of FHL1 as the protein mutated in human reducing body myopathy.
J Clin Invest
; 118(3): 904-12, 2008 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-18274675
12.
Prospective, double-blind, randomized, placebo-controlled phase III study evaluating efficacy and safety of octagam 10% in patients with dermatomyositis ("ProDERM Study").
Medicine (Baltimore)
; 100(1): e23677, 2021 Jan 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33429735
13.
Clinical, histological and genetic characterization of reducing body myopathy caused by mutations in FHL1.
Brain
; 132(Pt 2): 452-64, 2009 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-19181672
14.
Role of GluR1 in activity-dependent motor system development.
J Neurosci
; 28(40): 9953-68, 2008 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-18829953
15.
Deafferentation of neighbouring motor cortex areas does not further enhance saturated practice-dependent plasticity in healthy adults.
Clin Neurophysiol
; 119(4): 886-91, 2008 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-18282739
16.
Severe obstructive sleep apnea alleviated by oral appliance in a three-year-old boy.
Respiration
; 76(1): 112-6, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-17202808
17.
MRI in DNM2-related centronuclear myopathy: evidence for highly selective muscle involvement.
Neuromuscul Disord
; 17(1): 28-32, 2007 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-17134899
18.
Congenital muscular dystrophies and the extracellular matrix.
Semin Pediatr Neurol
; 13(2): 80-9, 2006 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-17027857
19.
Anti-GT1a IgG antibodies in a child with severe Guillain-Barré syndrome.
Pediatr Neurol
; 35(4): 277-9, 2006 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-16996403
20.
Orthodontic procedures in the treatment of obstructive sleep apnea in children.
J Orofac Orthop
; 67(1): 58-67, 2006 Jan.
Artigo
em Inglês, Alemão
| MEDLINE | ID: mdl-16447025