Detalhe da pesquisa
1.
Bone health in Duchenne muscular dystrophy: clinical and biochemical correlates.
J Endocrinol Invest
; 45(3): 517-525, 2022 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-34524678
2.
Clinical Variability in Spinal Muscular Atrophy Type III.
Ann Neurol
; 88(6): 1109-1117, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32926458
3.
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
4.
Which are the factors influencing NIV adaptation and tolerance in ALS patients?
Neurol Sci
; 42(3): 1023-1029, 2021 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-32710206
5.
Nusinersen Modulates Proteomics Profiles of Cerebrospinal Fluid in Spinal Muscular Atrophy Type 1 Patients.
Int J Mol Sci
; 22(9)2021 Apr 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-33919289
6.
Effect of exercise on telomere length and telomere proteins expression in mdx mice.
Mol Cell Biochem
; 470(1-2): 189-197, 2020 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-32447718
7.
Is it the right time for an infant screening for Duchenne muscular dystrophy?
Neurol Sci
; 41(7): 1677-1683, 2020 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-32112218
8.
Practical approach to respiratory emergencies in neurological diseases.
Neurol Sci
; 41(3): 497-508, 2020 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-31792719
9.
Psychosocial impact of sport activity in neuromuscular disorders.
Neurol Sci
; 41(9): 2561-2567, 2020 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-32246354
10.
Genetic neuromuscular disorders: living the era of a therapeutic revolution. Part 2: diseases of motor neuron and skeletal muscle.
Neurol Sci
; 40(4): 671-681, 2019 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-30805745
11.
Genetic neuromuscular disorders: living the era of a therapeutic revolution. Part 1: peripheral neuropathies.
Neurol Sci
; 40(4): 661-669, 2019 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-30847674
12.
Clinical management of Duchenne muscular dystrophy: the state of the art.
Neurol Sci
; 39(11): 1837-1845, 2018 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-30218397
13.
Intrathecal administration of Nusinersen in type 1 SMA: successful psychological program in a single Italian center.
Neurol Sci
; 39(11): 1961-1964, 2018 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-30043247
14.
Molecular analysis of SMARD1 patient-derived cells demonstrates that nonsense-mediated mRNA decay is impaired.
J Neurol Neurosurg Psychiatry
; 93(8): 908-910, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35086940
15.
Burden, professional support, and social network in families of children and young adults with muscular dystrophies.
Muscle Nerve
; 52(1): 13-21, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25363165
16.
Psychological and practical difficulties among parents and healthy siblings of children with Duchenne vs. Becker muscular dystrophy: an Italian comparative study.
Acta Myol
; 33(3): 136-43, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25873782
17.
The IAAM LTBP4 Haplotype is Protective Against Dystrophin-Deficient Cardiomyopathy.
J Neuromuscul Dis
; 11(2): 285-297, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38363615
18.
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
19.
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
20.
Muscle fat-fraction and mapping in Duchenne muscular dystrophy: evaluation of disease distribution and correlation with clinical assessments. Preliminary experience.
Skeletal Radiol
; 41(8): 955-61, 2012 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-22069033