Detalhe da pesquisa
1.
Axon guidance cue SEMA3A promotes the aggressive phenotype of basal-like PDAC.
Gut
; 2024 Apr 26.
Artigo
Inglês
| MEDLINE | ID: mdl-38670629
2.
Adaptive behaviour in adolescents and adults with Dravet syndrome.
Dev Med Child Neurol
; 65(6): 838-846, 2023 06.
Artigo
Inglês
| MEDLINE | ID: mdl-36316303
3.
Dysfunctional telomeres and hematological disorders.
Differentiation
; 100: 1-11, 2018.
Artigo
Inglês
| MEDLINE | ID: mdl-29331736
4.
Refractory tonic-myoclonic status epilepticus with catamenial recurrence in epilepsy with myoclonic atonic seizures: A case report.
Heliyon
; 10(2): e24747, 2024 Jan 30.
Artigo
Inglês
| MEDLINE | ID: mdl-38304836
5.
Long-term organoid culture of a small intestinal neuroendocrine tumor.
Front Endocrinol (Lausanne)
; 14: 999792, 2023.
Artigo
Inglês
| MEDLINE | ID: mdl-37082125
6.
Non-convulsive febrile status epilepticus mimicking a postictal state after a febrile seizure: an ictal electroclinical and evolutive study.
Epileptic Disord
; 24(2): 387-396, 2022 Apr 01.
Artigo
Inglês
| MEDLINE | ID: mdl-35014611
7.
Loss of FGFR4 promotes the malignant phenotype of PDAC.
Oncogene
; 41(38): 4371-4384, 2022 09.
Artigo
Inglês
| MEDLINE | ID: mdl-35963908
8.
Epilepsy Course and Developmental Trajectories in STXBP1-DEE.
Neurol Genet
; 8(3): e676, 2022 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-35655584
9.
The anti-tumoral effect of lenalidomide is increased in vivo by hypoxia-inducible factor (HIF)-1α inhibition in myeloma cells.
Haematologica
; 101(3): e107-10, 2016 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-26659917
10.
Early-onset bradykinetic rigid syndrome and reflex seizures in a child with PURA syndrome.
Epileptic Disord
; 23(5): 745-748, 2021 Oct 01.
Artigo
Inglês
| MEDLINE | ID: mdl-34583915
11.
Remote Teamwork Management of NORSE During the COVID-19 Lockdown.
Neurol Clin Pract
; 11(2): e170-e173, 2021 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-33842087
12.
Migrating Focal Seizures and Myoclonic Status in ARV1-Related Encephalopathy.
Neurol Genet
; 7(3): e593, 2021 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-34017911
13.
Epilepsy features in ARID1B-related Coffin-Siris syndrome.
Epileptic Disord
; 23(6): 865-874, 2021 Dec 01.
Artigo
Inglês
| MEDLINE | ID: mdl-34730517
14.
Hematopoiesis under telomere attrition at the single-cell resolution.
Nat Commun
; 12(1): 6850, 2021 11 25.
Artigo
Inglês
| MEDLINE | ID: mdl-34824242
15.
Basal Ganglia Dysmorphism in Patients With Aicardi Syndrome.
Neurology
; 96(9): e1319-e1333, 2021 03 02.
Artigo
Inglês
| MEDLINE | ID: mdl-33277420
16.
Modeling Cell Communication in Cancer With Organoids: Making the Complex Simple.
Front Cell Dev Biol
; 8: 166, 2020.
Artigo
Inglês
| MEDLINE | ID: mdl-32258040
17.
Ring chromosome 20 syndrome: a link between epilepsy onset and neuropsychological impairment in three children.
Epilepsia
; 50(11): 2420-7, 2009 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-19583784
18.
Pure Red Cell Aplasia (PRCA) and Cerebellar Hypoplasia as Atypical Features of Polyglandular Autoimmune Syndrome Type I (APS-1): Two Sisters With the Same AIRE Mutation but Different Phenotypes.
Front Pediatr
; 7: 51, 2019.
Artigo
Inglês
| MEDLINE | ID: mdl-30863741
19.
Migrating focal seizures in infancy: analysis of the electroclinical patterns in 17 patients.
J Child Neurol
; 23(5): 497-506, 2008 May.
Artigo
Inglês
| MEDLINE | ID: mdl-18230844
20.
Childhood absence epilepsy and electroencephalographic focal abnormalities with or without clinical manifestations.
Seizure
; 17(7): 617-24, 2008 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-18524634