Detalhe da pesquisa
1.
Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome.
Am J Hum Genet
; 111(1): 200-210, 2024 Jan 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-38118446
2.
Lactoferrin versus iron hydroxide polymaltose complex for the treatment of iron deficiency anemia in children with cerebral palsy: a randomized controlled trial.
Eur J Pediatr
; 180(8): 2609-2618, 2021 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-34101010
3.
Clinical Characteristics and Appropriateness of Investigations in Children With Headaches at the Emergency Department.
Pediatr Neurol
; 154: 58-65, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38531164
4.
Adapting Evidence-Based Practice Guidelines for Emergency Management of Seizures in Children Beyond the Neonatal Period.
Pediatr Neurol
; 157: 14-18, 2024 May 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-38838593
5.
Unravelling undiagnosed rare disease cases by HiFi long-read genome sequencing.
medRxiv
; 2024 May 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-38746462
6.
Knowledge, Skills, and Attitudes Towards Children with Epilepsy Among Egyptian Parents: A Comparative Cross-Sectional Study.
Epilepsy Res
; 172: 106573, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33714865