Detalhe da pesquisa
1.
Characteristics of myotonic dystrophy patients in the national registry of Japan.
J Neurol Sci;
432: 120080, 2022 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-34923335
2.
Metabolic complications in myotonic dystrophy type 1: A cross-sectional survey using the National Registry of Japan.
J Neurol Sci;
427: 117511, 2021 08 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-34082146
3.
EF hand-like motif mutations of Nav1.4 C-terminus cause myotonic syndrome by impairing fast inactivation.
Muscle Nerve;
61(6): 808-814, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32129495
4.
The expanding phenotype of hypokalemic periodic paralysis in a Japanese family with p.Val876Glu mutation in CACNA1S.
Mol Genet Genomic Med;
8(4): e1175, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32104981