Detalhe da pesquisa
1.
Anterior cervical discectomy and fusion for the treatment of pediatric Hirayama disease.
Childs Nerv Syst
; 40(5): 1427-1434, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38231402
2.
Differential responses of disease-related GRIN variants located in pore-forming M2 domain of N-methyl-D-aspartate receptor to FDA-approved inhibitors.
J Neurochem
; 2023 Aug 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-37649269
3.
Heterogeneous clinical and functional features of GRIN2D-related developmental and epileptic encephalopathy.
Brain
; 142(10): 3009-3027, 2019 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31504254
4.
De novo GRIN variants in NMDA receptor M2 channel pore-forming loop are associated with neurological diseases.
Hum Mutat
; 40(12): 2393-2413, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31429998
5.
De novo mutations in GRIN1 cause extensive bilateral polymicrogyria.
Brain
; 141(3): 698-712, 2018 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29365063
6.
Pediatric neuroinflammatory diseases in the intensive care unit.
Semin Pediatr Neurol
; 49: 101118, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38677797
7.
Assessing Needs and Perceptions of Research Participation in Pediatric-Onset Multiple Sclerosis: A Multistakeholder Survey.
Pediatr Neurol
; 151: 115-120, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38154238
8.
Biallelic variation in the choline and ethanolamine transporter FLVCR1 underlies a pleiotropic disease spectrum from adult neurodegeneration to severe developmental disorders.
medRxiv
; 2024 Feb 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-38405817
9.
Arterial Spin Labeling Changes Parallel Asymmetric Perisylvian and Perirolandic Symptoms in 3 Pediatric Cases of Anti-NMDAR Encephalitis.
Neurol Neuroimmunol Neuroinflamm
; 10(4)2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37094999
10.
Infectious profiles in pediatric anti-N-methyl-d-aspartate receptor encephalitis.
J Neuroimmunol
; 381: 578139, 2023 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-37364517
11.
Fulminant Anti-Myelin Oligodendrocyte Glycoprotein-Associated Cerebral Cortical Encephalitis: Case Series of a Severe Pediatric Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease Phenotype.
Pediatr Neurol
; 147: 36-43, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37544084