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1.
Novel ECHS1 mutations in Leigh syndrome identified by whole-exome sequencing in five Chinese families: case report.
BMC Med Genet
; 21(1): 149, 2020 07 16.
Artículo
en Inglés
| MEDLINE | ID: mdl-32677908
2.
Two novel ECHS1 variants, affecting splicing and reducing enzyme activity, is associated with mitochondrial encephalopathy in infant: a case report.
BMC Neurol
; 20(1): 165, 2020 Apr 30.
Artículo
en Inglés
| MEDLINE | ID: mdl-32354323
3.
Comparison of the effectiveness and safety of perampanel and oxcarbazepine as monotherapy in children and adolescents with newly diagnosed focal epilepsy.
Front Pharmacol
; 14: 1189058, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-37711169
4.
Corrigendum: Comparison of the effectiveness and safety of perampanel and oxcarbazepine as monotherapy in children and adolescents with newly diagnosed focal epilepsy.
Front Pharmacol
; 14: 1295784, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-37841932
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