Detalhe da pesquisa
1.
Quantitative Foot Muscle Magnetic Resonance Imaging Reliably Measures Disease Progression in Children and Adolescents with Charcot-Marie-Tooth Disease Type 1A.
Ann Neurol
; 2024 Apr 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-38613459
2.
Assessment of the upper limb function, strength, and mobility in treatment-naive children with spinal muscular atrophy Types 2 and 3.
Muscle Nerve
; 69(3): 340-348, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38238963
3.
Validation of the parent-proxy version of the pediatric Charcot-Marie-Tooth disease quality of life instrument for children aged 0-7 years.
J Peripher Nerv Syst
; 28(3): 382-389, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37166413
4.
Clinical Variability in Spinal Muscular Atrophy Type III.
Ann Neurol
; 88(6): 1109-1117, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32926458
5.
Longitudinal changes in respiratory and upper limb function in a pediatric type III spinal muscular atrophy cohort after loss of ambulation.
Muscle Nerve
; 64(5): 545-551, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34432301
6.
Different trajectories in upper limb and gross motor function in spinal muscular atrophy.
Muscle Nerve
; 64(5): 552-559, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34327716
7.
Quantifying Variability in Motor Function in Duchenne Muscular Dystrophy: UK Centiles for the NorthStar Ambulatory Assessment, 10âm Walk Run Velocity and Rise from Floor Velocity in GC Treated Boys.
J Neuromuscul Dis
; 11(1): 153-166, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-37980680
8.
Lower limb muscle MRI fat fraction is a responsive outcome measure in CMT X1, 1B and 2A.
Ann Clin Transl Neurol
; 11(3): 607-617, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38173284
9.
Disease Trajectories in the Revised Hammersmith Scale in a Cohort of Untreated Patients with Spinal Muscular Atrophy types 2 and 3.
J Neuromuscul Dis
; 11(3): 665-677, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38427497
10.
2-Year Change in Revised Hammersmith Scale Scores in a Large Cohort of Untreated Paediatric Type 2 and 3 SMA Participants.
J Clin Med
; 12(5)2023 Feb 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-36902710
11.
Revised upper limb module in type II and III spinal muscular atrophy: 24-month changes.
Neuromuscul Disord
; 32(1): 36-42, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34980538
12.
Functional outcome measures in young, steroid-naïve boys with Duchenne muscular dystrophy.
Neuromuscul Disord
; 32(6): 460-467, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35618576
13.
Ambulatory function in spinal muscular atrophy: Age-related patterns of progression.
PLoS One
; 13(6): e0199657, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29944707