Detalhe da pesquisa
1.
Fate of melatonin orally administered in preterm newborns: Antioxidant performance and basis for neuroprotection.
J Pineal Res
; 76(1): e12932, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-38111174
2.
A PUS7 gene pathogenic variant causing self-injurious behavior, sleep disturbances, and developmental delay: A case report.
Am J Med Genet A
; 191(7): 1953-1958, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37067188
3.
Unmet needs and gaps in the identification of secondary progression in multiple sclerosis: a Southern Italy healthcare professionals' perspective.
Neurol Sci
; 44(1): 45-58, 2023 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-36114980
4.
Cerebral folate transporter deficiency syndrome in three siblings: Why genetic testing for developmental and epileptic encephalopathies should be performed early and include the FOLR1 gene.
Am J Med Genet A
; 185(8): 2526-2531, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-34008900
5.
Childhood Absence Epilepsy evolving to Eyelid Myoclonia with Absence Epilepsy.
Seizure
; 61: 1-3, 2018 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-30029089
6.
Neonatal Assessment Visual European Grid (NAVEG): Unveiling neurological risk.
Infant Behav Dev
; 49: 21-30, 2017 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-28688291