Detalhe da pesquisa
1.
The clinical and biochemical hallmarks generally associated with GLUT1DS may be caused by defects in genes other than SLC2A1.
Clin Genet
; 102(1): 40-55, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35388452
2.
Childhood-Onset Chorea Caused by a Recurrent De Novo DRD2 Variant.
Mov Disord
; 36(6): 1472-1473, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34145635
3.
Classic and Atypical Late Infantile Neuronal Ceroid Lipofuscinosis in Latin America: Clinical and Genetic Aspects, and Treatment Outcome with Cerliponase Alfa.
Mol Genet Metab Rep
; 38: 101060, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38469103
4.
Transitional Care for Young People with Movement Disorders: Consensus-Based Recommendations from the MDS Task Force on Pediatrics.
Mov Disord Clin Pract
; 10(5): 748-755, 2023 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-37205244
5.
Aproximación clínica al diagnóstico diferencial de los trastornos del movimiento en la infancia / Clinical approach to the differential diagnosis of childhood movement disorders
Rev. chil. psiquiatr. neurol. infanc. adolesc. (Impr.)
; 27(2): 64-71, ago.2016.
Artigo
em Espanhol, Inglês
|
LILACS-Express
| ID: biblio-1413125
6.
¿Crisis febriles complejas o síndrome de Dravet?: Descripción de 3 casos clínicos / Complex febrile Seizures or Dravet syndrome?: Description of 3 case reports
Rev. chil. pediatr
; 85(5): 588-593, oct. 2014. tab
Artigo
em Espanhol
| LILACS | ID: lil-731647