Detalhe da pesquisa
1.
Pilot study of a virtual weight management program for Duchenne muscular dystrophy.
Muscle Nerve
; 69(4): 459-466, 2024 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-38353295
2.
Exploring caregivers' attitudes and beliefs about nutrition and weight management for young people with Duchenne muscular dystrophy.
Muscle Nerve
; 69(4): 448-458, 2024 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-38353293
3.
Clinical practice guideline for the management of paediatric Charcot-Marie-Tooth disease.
J Neurol Neurosurg Psychiatry
; 93(5): 530-538, 2022 05.
Artigo
Inglês
| MEDLINE | ID: mdl-35140138
4.
Delivering multidisciplinary neuromuscular care for children via telehealth.
Muscle Nerve
; 66(1): 31-38, 2022 07.
Artigo
Inglês
| MEDLINE | ID: mdl-35426158
5.
Evaluation of Serial Casting for Boys with Duchenne Muscular Dystrophy: A Case Report.
Phys Occup Ther Pediatr
; 38(1): 88-96, 2018 02.
Artigo
Inglês
| MEDLINE | ID: mdl-28300461
6.
A phase 2 open-label study of the safety and efficacy of weekly dosing of ATL1102 in patients with non-ambulatory Duchenne muscular dystrophy and pharmacology in mdx mice.
PLoS One
; 19(1): e0294847, 2024.
Artigo
Inglês
| MEDLINE | ID: mdl-38271438
7.
Correlation between whole body muscle MRI and functional measures in paediatric patients with facioscapulohumeral muscular dystrophy.
Neuromuscul Disord
; 33(1): 15-23, 2023 01.
Artigo
Inglês
| MEDLINE | ID: mdl-36522253
8.
Therapeutic Options to Improve Bone Health Outcomes in Duchenne Muscular Dystrophy: Zoledronic Acid and Pubertal Induction.
J Paediatr Child Health
; 53(12): 1247-1248, 2017 12.
Artigo
Inglês
| MEDLINE | ID: mdl-29205648
9.
Characterising gait in paediatric neuromuscular disorders: an observational study of spatio-temporal gait in a clinical cohort.
Disabil Rehabil
; 44(23): 7023-7029, 2022 11.
Artigo
Inglês
| MEDLINE | ID: mdl-34546805
10.
The effects of calf massage in boys with Duchenne muscular dystrophy: a prospective interventional study.
Disabil Rehabil
; 43(26): 3803-3809, 2021 12.
Artigo
Inglês
| MEDLINE | ID: mdl-32356505
11.
Clinimetric properties of the alberta infant motor scale in infants born preterm.
Pediatr Phys Ther
; 22(3): 278-86, 2010.
Artigo
Inglês
| MEDLINE | ID: mdl-20699776
12.
268th ENMC workshop - Genetic diagnosis, clinical classification, outcome measures, and biomarkers in Facioscapulohumeral Muscular Dystrophy (FSHD): Relevance for clinical trials.
Neuromuscul Disord
; 33(5): 447-462, 2023 05.
Artigo
Inglês
| MEDLINE | ID: mdl-37099914
13.
Dejerine-Sottas disease in childhood-Genetic and sonographic heterogeneity.
Brain Behav
; 8(4): e00919, 2018 04.
Artigo
Inglês
| MEDLINE | ID: mdl-29670817
14.
A multinational study on motor function in early-onset FSHD.
Neurology
; 90(15): e1333-e1338, 2018 04 10.
Artigo
Inglês
| MEDLINE | ID: mdl-29540582
15.
Physical activity and the use of standard and complementary therapies in Duchenne and Becker muscular dystrophies.
J Pediatr Rehabil Med
; 9(1): 55-63, 2016.
Artigo
Inglês
| MEDLINE | ID: mdl-26966801
16.
Peripheral nerve ultrasound in pediatric Charcot-Marie-Tooth disease type 1A.
Neurology
; 84(6): 569-74, 2015 Feb 10.
Artigo
Inglês
| MEDLINE | ID: mdl-25576636
17.
Authors' Response to Commentary.
J Pediatr Rehabil Med
; 9(1): 77, 2016.
Artigo
Inglês
| MEDLINE | ID: mdl-26966804