Detalhe da pesquisa
1.
Hexosamine biosynthetic pathway mutations cause neuromuscular transmission defect.
Am J Hum Genet
; 88(2): 162-72, 2011 Feb 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-21310273
2.
Contrasting disease patterns in seropositive and seronegative neuromyelitis optica: A multicentre study of 175 patients.
J Neuroinflammation
; 9: 14, 2012 Jan 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-22260418
3.
The European Lambert-Eaton Myasthenic Syndrome Registry: Long-Term Outcomes Following Symptomatic Treatment.
Neurol Ther
; 11(3): 1071-1083, 2022 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-35511347
4.
[Restless legs: recent advances in basic research and therapy]. / Restless Legs: Aktuelles zu Ursachen und Therapie.
Med Monatsschr Pharm
; 33(4): 133-9, 2010 Apr.
Artigo
em Alemão
| MEDLINE | ID: mdl-20429403
5.
Congenital myasthenic syndrome with tubular aggregates caused by GFPT1 mutations.
J Neurol
; 259(5): 838-50, 2012 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-21975507
6.
Congenital myasthenia in Brahman calves caused by homozygosity for a CHRNE truncating mutation.
Neurogenetics
; 4(2): 87-91, 2002 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-12481987