Detalhe da pesquisa
1.
Early treatment of type II SMA slows rate of progression of scoliosis.
J Neurol Neurosurg Psychiatry
; 95(3): 235-240, 2024 Feb 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-37739783
2.
Early neurological signs in infants identified through neonatal screening for SMA: do they predict outcome?
Eur J Pediatr
; 2024 Apr 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-38634892
3.
Longitudinal Motor Functional Outcomes and Magnetic Resonance Imaging Patterns of Muscle Involvement in Upper Limbs in Duchenne Muscular Dystrophy.
Medicina (Kaunas)
; 57(11)2021 Nov 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-34833484
4.
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
5.
Revised upper limb module for spinal muscular atrophy: Development of a new module.
Muscle Nerve
; 55(6): 869-874, 2017 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27701745
6.
Content validity and clinical meaningfulness of the HFMSE in spinal muscular atrophy.
BMC Neurol
; 17(1): 39, 2017 Feb 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-28231823
7.
Gain and loss of upper limb abilities in Duchenne muscular dystrophy patients: A 24-month study.
Neuromuscul Disord
; 34: 75-82, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-38157655
8.
Patient reported outcome measure for upper limb in Duchenne muscular dystrophy: correlation with PUL2.0.
Neuromuscul Disord
; 33(9): 69-73, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37612177
9.
Longitudinal Analysis of PUL 2.0 Domains in Ambulant and Non-Ambulant Duchenne Muscular Dystrophy Patients: How do they Change in Relation to Functional Ability?
J Neuromuscul Dis
; 10(4): 567-574, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37066919
10.
Point-of-care lung and diaphragm ultrasound in a patient with spinal muscular atrophy with respiratory distress type 1.
J Ultrasound
; 25(2): 395-398, 2022 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-33847972
11.
Oral and Swallowing Abilities Tool (OrSAT) in nusinersen treated patients.
Arch Dis Child
; 2022 May 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-35577540
12.
Long term follow-up of scoliosis progression in type II SMA patients.
Neuromuscul Disord
; 32(11-12): 879-885, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36456406
13.
Early Gross Motor Milestones in Duchenne Muscular Dystrophy.
J Neuromuscul Dis
; 8(4): 453-456, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33935100
14.
Oral and Swallowing Abilities Tool (OrSAT) for Type 1 SMA Patients: Development of a New Module.
J Neuromuscul Dis
; 8(4): 589-601, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34024771
15.
Respiratory function and therapeutic expectations in DMD: families experience and perspective.
Acta Myol
; 39(3): 121-129, 2020 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-33305168
16.
Ultrasound assessment of diaphragmatic function in type 1 spinal muscular atrophy.
Pediatr Pulmonol
; 55(7): 1781-1788, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32394611
17.
Long-term progression in type II spinal muscular atrophy: A retrospective observational study.
Neurology
; 93(13): e1241-e1247, 2019 09 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-31451515
18.
Clinical phenotypes and trajectories of disease progression in type 1 spinal muscular atrophy.
Neuromuscul Disord
; 28(1): 24-28, 2018 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29174525
19.
Functional levels and MRI patterns of muscle involvement in upper limbs in Duchenne muscular dystrophy.
PLoS One
; 13(6): e0199222, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29924868
20.
Ambulatory function in spinal muscular atrophy: Age-related patterns of progression.
PLoS One
; 13(6): e0199657, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29944707