Detalhe da pesquisa
1.
The CINRG Becker Natural History Study: Baseline characteristics.
Muscle Nerve
; 62(3): 369-376, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32564389
2.
Twice-weekly glucocorticosteroids in infants and young boys with Duchenne muscular dystrophy.
Muscle Nerve
; 59(6): 650-657, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30706490
3.
Fixed dynamometry is more sensitive than vital capacity or ALS rating scale.
Muscle Nerve
; 56(4): 710-715, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28120413
4.
Clinical phenotypes as predictors of the outcome of skipping around DMD exon 45.
Ann Neurol
; 77(4): 668-74, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25612243
5.
Clinical trial readiness in non-ambulatory boys and men with duchenne muscular dystrophy: MDA-DMD network follow-up.
Muscle Nerve
; 54(4): 681-9, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-26930423
6.
Electrical impedance myography in Duchenne muscular dystrophy and healthy controls: A multicenter study of reliability and validity.
Muscle Nerve
; 52(4): 592-7, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25702806
7.
Outcome reliability in non-ambulatory boys/men with Duchenne muscular dystrophy.
Muscle Nerve
; 51(4): 522-32, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25056178
8.
LTBP4 genotype predicts age of ambulatory loss in Duchenne muscular dystrophy.
Ann Neurol
; 73(4): 481-8, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23440719
9.
Rasch analysis of clinical outcome measures in spinal muscular atrophy.
Muscle Nerve
; 49(3): 422-30, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23836324
10.
Ataluren treatment of patients with nonsense mutation dystrophinopathy.
Muscle Nerve
; 50(4): 477-87, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25042182
11.
A randomized study of alglucosidase alfa in late-onset Pompe's disease.
N Engl J Med
; 362(15): 1396-406, 2010 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-20393176
12.
Developing normalized strength scores for neuromuscular research.
Muscle Nerve
; 47(2): 177-82, 2013 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23168880
13.
The cooperative international neuromuscular research group Duchenne natural history study: glucocorticoid treatment preserves clinically meaningful functional milestones and reduces rate of disease progression as measured by manual muscle testing and other commonly used clinical trial outcome measures.
Muscle Nerve
; 48(1): 55-67, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23649481
14.
The 6-minute walk test and other clinical endpoints in duchenne muscular dystrophy: reliability, concurrent validity, and minimal clinically important differences from a multicenter study.
Muscle Nerve
; 48(3): 357-68, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23674289
15.
The cooperative international neuromuscular research group Duchenne natural history study--a longitudinal investigation in the era of glucocorticoid therapy: design of protocol and the methods used.
Muscle Nerve
; 48(1): 32-54, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23677550
16.
The 6-minute walk test and other endpoints in Duchenne muscular dystrophy: longitudinal natural history observations over 48 weeks from a multicenter study.
Muscle Nerve
; 48(3): 343-56, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23681930
17.
Development of the Performance of the Upper Limb module for Duchenne muscular dystrophy.
Dev Med Child Neurol
; 55(11): 1038-45, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-23902233
18.
Therapeutic exercise for people with amyotrophic lateral sclerosis or motor neuron disease.
Cochrane Database Syst Rev
; (5): CD005229, 2013 May 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-23728653
19.
Nonsense mutation-associated Becker muscular dystrophy: interplay between exon definition and splicing regulatory elements within the DMD gene.
Hum Mutat
; 32(3): 299-308, 2011 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21972111
20.
Qualitative and quantitative skeletal muscle ultrasound in late-onset acid maltase deficiency.
Muscle Nerve
; 44(3): 418-23, 2011 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-21755514