Detalhe da pesquisa
1.
Optic nerve ultrasonography in the evaluation of the relationship between arachnoid cyst and headache.
Childs Nerv Syst
; 38(8): 1573-1579, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35460353
2.
A rare case of pontine and extrapontine myelinolysis in a pediatric patient with chronic renal failure.
Childs Nerv Syst
; 37(3): 1025-1027, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32504171
3.
Pediatric anti-NMDA receptor encephalitis associated with COVID-19.
Childs Nerv Syst
; 37(12): 3919-3922, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33852058
4.
Neurodevelopmental risk evaluation of premature closure of the anterior fontanelle.
Childs Nerv Syst
; 37(2): 561-566, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32737565
5.
A rare concurrence: gelastic seizures in a patient with right temporal nongalenic pial arteriovenous fistula.
Childs Nerv Syst
; 35(6): 1055-1058, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30783755
6.
Optic neuritis in Turkish children and adolescents: A multicenter retrospective study.
Mult Scler Relat Disord
; 81: 105149, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-38096730
7.
Short-Term and Long-Term Effects of Levetiracetam Monotherapy On Hematological Parameters in Children with Idiopathic Epilepsy.
Sisli Etfal Hastan Tip Bul
; 57(1): 46-53, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37064851
8.
Acute necrotizing encephalopathy associated with RANBP2 mutation: value of MRI findings for diagnosis and intervention.
Acta Neurol Belg
; 123(2): 571-582, 2023 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-36572756
9.
A rare cause of microcephaly, thin corpus callosum and refractory epilepsy due to a novel SLC1A4 gene mutation.
Clin Neurol Neurosurg
; 218: 107283, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35605507
10.
Expanding Phenotype of Poirier-Bienvenu Syndrome: New Evidence from an Italian Multicentrical Cohort of Patients.
Genes (Basel)
; 13(2)2022 01 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-35205321
11.
Identification of a Novel Mutation in GRIN2A Gene with Global Developmental Delay and Refractory Epilepsy.
Ann Indian Acad Neurol
; 23(5): 696-699, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33623275
12.
A rare concurrence: Antibodies against Myelin Oligodendrocyte Glycoprotein and N-methyl-d-aspartate receptor in a child.
Mult Scler Relat Disord
; 28: 101-103, 2019 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-30590238
13.
A Rare Cause of Paroxysmal Movement Disorder Associated with TBC1D24 Gene Mutation in Two Siblings.
Ann Indian Acad Neurol
; 26(3): 290-293, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37538433