Detalhe da pesquisa
1.
Evaluation of body composition as a potential biomarker in spinal muscular atrophy.
Muscle Nerve
; 61(4): 530-534, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32012296
2.
Identification of a cytokine profile in serum and cerebrospinal fluid of pediatric and adult spinal muscular atrophy patients and its modulation upon nusinersen treatment.
Front Cell Neurosci
; 16: 982760, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36035258
3.
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
4.
Circulating MyomiRs as Potential Biomarkers to Monitor Response to Nusinersen in Pediatric SMA Patients.
Biomedicines
; 8(2)2020 Jan 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-31991852
5.
Evolution of bone mineral density, bone metabolism and fragility fractures in Spinal Muscular Atrophy (SMA) types 2 and 3.
Neuromuscul Disord
; 29(7): 525-532, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31266719
6.
Longitudinal natural history in young boys with Duchenne muscular dystrophy.
Neuromuscul Disord
; 29(11): 857-862, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31629611
7.
Outcome measures for children with movement disorders.
Eur J Paediatr Neurol
; 22(3): 346-353, 2018 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-29475818
8.
Two single cases treated by a new pseudoelastic upper-limb orthosis for secondary dystonia of the young.
IEEE Int Conf Rehabil Robot
; 2017: 1260-1265, 2017 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28813994
9.
Sleep disorders in spinal muscular atrophy.
Sleep Med
; 30: 160-163, 2017 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28215241
10.
Hand function assessment in the first years of life in unilateral cerebral palsy: Correlation with neuroimaging and cortico-spinal reorganization.
Eur J Paediatr Neurol
; 20(1): 114-24, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26439103
11.
Revised North Star Ambulatory Assessment for Young Boys with Duchenne Muscular Dystrophy.
PLoS One
; 11(8): e0160195, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27494024
12.
Timed Rise from Floor as a Predictor of Disease Progression in Duchenne Muscular Dystrophy: An Observational Study.
PLoS One
; 11(3): e0151445, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-26982196
13.
A novel homozygous ISPD gene mutation causing phenotype variability in a consanguineous family.
Neuromuscul Disord
; 25(1): 55-9, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25444434
14.
Bone and Spinal Muscular Atrophy.
Bone
; 79: 116-20, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26055105
15.
Long term natural history data in ambulant boys with Duchenne muscular dystrophy: 36-month changes.
PLoS One
; 9(10): e108205, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25271887
16.
6 Minute walk test in Duchenne MD patients with different mutations: 12 month changes.
PLoS One
; 9(1): e83400, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24421885
17.
Correction: Long Term Natural History Data in Ambulant Boys with Duchenne Muscular Dystrophy: 36-Month Changes.
PLoS One
; 10(12): e0144079, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26636671