Detalhe da pesquisa
1.
Reference curves of motor function outcomes in young steroid-naïve males with Duchenne muscular dystrophy.
Dev Med Child Neurol
; 66(5): 644-653, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-37885269
2.
Milestones of progression in myotonic dystrophy type 1 and type 2.
Muscle Nerve
; 66(4): 508-512, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35778789
3.
Effect of Different Corticosteroid Dosing Regimens on Clinical Outcomes in Boys With Duchenne Muscular Dystrophy: A Randomized Clinical Trial.
JAMA
; 327(15): 1456-1468, 2022 04 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-35381069
4.
Ankle bracing practices in ambulatory, corticosteroid-naive boys with Duchenne muscular dystrophy.
Muscle Nerve
; 61(1): 52-57, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31588574
5.
Electrical impedance myography in facioscapulohumeral muscular dystrophy: A 1-year follow-up study.
Muscle Nerve
; 58(2): 213-218, 2018 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-29543984
6.
Facioscapulohumeral muscular dystrophy functional composite outcome measure.
Muscle Nerve
; 2018 Jan 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-29381807
7.
Electrical impedance myography in facioscapulohumeral muscular dystrophy.
Muscle Nerve
; 54(4): 696-701, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-26840230
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.
Factors Associated With Early Motor Function Trajectories in DMD After Glucocorticoid Initiation: Post Hoc Analysis of the FOR-DMD Trial.
Neurology
; 102(10): e209206, 2024 May 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-38710006
11.
Lean tissue mass measurements by dual-energy X-ray absorptiometry and associations with strength and functional outcome measures in facioscapulohumeral muscular dystrophy.
Neuromuscul Disord
; 33(9): 63-68, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37400350
12.
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
13.
Validation of the Children's Hospital of Philadelphia Infant Test of Neuromuscular Disorders (CHOP INTEND).
Pediatr Phys Ther
; 23(4): 322-6, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-22090068
14.
Health related quality of life in young, steroid-naïve boys with Duchenne muscular dystrophy.
Neuromuscul Disord
; 31(11): 1161-1168, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34489153
15.
Psychometric properties of the PEDI-CAT for children and youth with spinal muscular atrophy.
J Pediatr Rehabil Med
; 14(3): 451-461, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34275913
16.
Nusinersen Treatment in Adults With Spinal Muscular Atrophy.
Neurol Clin Pract
; 11(3): e317-e327, 2021 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-34476123
17.
Evoked myotonia can be "dialed-up" by increasing stimulus train length in myotonic dystrophy type 1.
Muscle Nerve
; 41(2): 191-6, 2010 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-19750543
18.
Patient-Reported Symptoms in Facioscapulohumeral Muscular Dystrophy (PRISM-FSHD).
Neurology
; 93(12): e1180-e1192, 2019 09 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-31409737
19.
Reproductive Cancer Risk Factors in Women With Myotonic Dystrophy (DM): Survey Data From the US and UK DM Registries.
Front Neurol
; 10: 1071, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31681146
20.
A checklist for clinical trials in rare disease: obstacles and anticipatory actions-lessons learned from the FOR-DMD trial.
Trials
; 19(1): 291, 2018 May 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-29793540