Detalhe da pesquisa
1.
Reduced specific force in patients with mild and severe facioscapulohumeral muscular dystrophy.
Muscle Nerve
; 63(1): 60-67, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32959362
2.
Pathogenic variants in TNNC2 cause congenital myopathy due to an impaired force response to calcium.
J Clin Invest
; 131(9)2021 05 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33755597
3.
KBTBD13 is an actin-binding protein that modulates muscle kinetics.
J Clin Invest
; 130(2): 754-767, 2020 02 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31671076
4.
Muscle fiber dysfunction contributes to weakness in inclusion body myositis.
Neuromuscul Disord
; 29(6): 468-476, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31101463
5.
KBTBD13 is an actin-binding protein that modulates muscle kinetics.
J Clin Invest
; 134(3)2024 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38299595
6.
Effect of levosimendan on the contractility of muscle fibers from nemaline myopathy patients with mutations in the nebulin gene.
Skelet Muscle
; 5: 12, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25949787
7.
Gene expression profile in the diaphragm following contractile inactivity during thoracic surgery.
Int J Physiol Pathophysiol Pharmacol
; 3(3): 167-75, 2011 Sep 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-21941608