Detalhe da pesquisa
1.
Association of genetic mutations and loss of ambulation in childhood-onset dystrophinopathy.
Muscle Nerve
; 63(2): 181-191, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33150975
2.
Left ventricular dysfunction in Duchenne muscular dystrophy.
Cardiol Young
; 30(2): 171-176, 2020 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-31964455
3.
The effect of steroid treatment on weight in nonambulatory males with Duchenne muscular dystrophy.
Am J Med Genet A
; 176(11): 2350-2358, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30256515
4.
Health profile of a cohort of adults with Duchenne muscular dystrophy.
Muscle Nerve
; 58(2): 219-223, 2018 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-29543994
5.
Corticosteroid Treatment and Growth Patterns in Ambulatory Males with Duchenne Muscular Dystrophy.
J Pediatr
; 173: 207-213.e3, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27039228
6.
Health services received by individuals with duchenne/becker muscular dystrophy.
Muscle Nerve
; 53(2): 191-7, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26044770
7.
Myotonic dystrophy health index: Correlations with clinical tests and patient function.
Muscle Nerve
; 53(2): 183-90, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26044513
8.
Rasch analysis of the Pediatric Evaluation of Disability Inventory-computer adaptive test (PEDI-CAT) item bank for children and young adults with spinal muscular atrophy.
Muscle Nerve
; 54(6): 1097-1107, 2016 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-27121348
9.
Spinal muscular atrophy functional composite score: A functional measure in spinal muscular atrophy.
Muscle Nerve
; 52(6): 942-7, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25846132
10.
Risk Factors for First Fractures Among Males With Duchenne or Becker Muscular Dystrophy.
J Pediatr Orthop
; 35(6): 640-4, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-25379822
11.
Splicing biomarkers of disease severity in myotonic dystrophy.
Ann Neurol
; 74(6): 862-72, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-23929620
12.
Sibling concordance for clinical features of Duchenne and Becker muscular dystrophies.
Muscle Nerve
; 49(6): 814-21, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24030636
13.
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
14.
Oral corticosteroids and onset of cardiomyopathy in Duchenne muscular dystrophy.
J Pediatr
; 163(4): 1080-4.e1, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23866715
15.
Corticosteroids in Duchenne muscular dystrophy: major variations in practice.
Muscle Nerve
; 48(1): 27-31, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23483575
16.
Role of disease severity, illness perceptions, and mood on quality of life in muscle disease.
Muscle Nerve
; 46(3): 351-9, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22907225
17.
A quantitative measure of handgrip myotonia in non-dystrophic myotonia.
Muscle Nerve
; 46(4): 482-9, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-22987687
18.
Differentiation of Pediatric-Onset Duchenne and Becker Muscular Dystrophy Subphenotypes Using Data from the Muscular Dystrophy Surveillance Tracking and Research Network (MD STARnet).
J Neuromuscul Dis
; 9(1): 171-178, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-34776418
19.
Selected clinical and demographic factors and all-cause mortality among individuals with Duchenne muscular dystrophy in the Muscular Dystrophy Surveillance, Tracking, and Research Network.
Neuromuscul Disord
; 32(6): 468-476, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35597713
20.
Role Attainment in Emerging Adulthood: Subjective Evaluation by Male Adolescents and Adults with Duchenne and Becker Muscular Dystrophy.
J Neuromuscul Dis
; 9(3): 447-456, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35275556