Detalhe da pesquisa
1.
Determining minimal clinically important differences in the Hammersmith Functional Motor Scale Expanded for untreated spinal muscular atrophy patients: An international study.
Eur J Neurol
; : e16309, 2024 Apr 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-38656662
2.
Assessing Dysferlinopathy Patients Over Three Years With a New Motor Scale.
Ann Neurol
; 89(5): 967-978, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33576057
3.
Clinical Variability in Spinal Muscular Atrophy Type III.
Ann Neurol
; 88(6): 1109-1117, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32926458
4.
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
5.
Revised upper limb module for spinal muscular atrophy: 12 month changes.
Muscle Nerve
; 59(4): 426-430, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30677148
6.
Quantitative Evaluation of Lower Extremity Joint Contractures in Spinal Muscular Atrophy: Implications for Motor Function.
Pediatr Phys Ther
; 30(3): 209-215, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29924070
7.
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
8.
Is ongoing testosterone required after pubertal induction in Duchenne muscular dystrophy?
Endocr Connect
; 2023 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37768006
9.
Longitudinal Analysis of Respiratory Function of Different Types of Limb Girdle Muscular Dystrophies Reveals Independent Trajectories.
Neurol Genet
; 9(4): e200084, 2023 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-37440793
10.
Measuring Fatigue and Fatigability in Spinal Muscular Atrophy (SMA): Challenges and Opportunities.
J Clin Med
; 12(10)2023 May 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-37240564
11.
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
12.
Real-World Data on Access to Standards of Care for People With Spinal Muscular Atrophy in the UK.
Front Neurol
; 13: 866243, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35707038
13.
Validation of the North Star Assessment for Limb-Girdle Type Muscular Dystrophies.
Phys Ther
; 102(10)2022 10 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35932452
14.
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
15.
Assessing the Relationship of Patient Reported Outcome Measures With Functional Status in Dysferlinopathy: A Rasch Analysis Approach.
Front Neurol
; 13: 828525, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35359643
16.
Prevalence of Pain within Limb Girdle Muscular Dystrophy R9 and Implications for Other Degenerative Diseases.
J Clin Med
; 10(23)2021 Nov 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-34884219
17.
Pubertal induction in adolescents with DMD is associated with high satisfaction, gonadotropin release and increased muscle contractile surface area.
Eur J Endocrinol
; 184(1): 67-79, 2021 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-33112266
18.
Respiratory Trajectories in Type 2 and 3 Spinal Muscular Atrophy in the iSMAC Cohort Study.
Neurology
; 96(4): e587-e599, 2021 01 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-33067401
19.
Gain and loss of abilities in type II SMA: A 12-month natural history study.
Neuromuscul Disord
; 30(9): 765-771, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32893082
20.
Respiratory involvement in ambulant and non-ambulant patients with facioscapulohumeral muscular dystrophy.
J Neurol
; 264(6): 1271-1280, 2017 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-28550484