Detalhe da pesquisa
1.
Phenotypic spectrum of the SCN1A mutation (from febrile seizures to Dravet syndrome).
Bratisl Lek Listy
; 123(7): 483-486, 2022.
Artigo
Inglês
| MEDLINE | ID: mdl-35907053
2.
MicroRNAs in the development of resistance to antiseizure drugs and their potential as biomarkers in pharmacoresistant epilepsy.
Epilepsia
; 62(11): 2573-2588, 2021 11.
Artigo
Inglês
| MEDLINE | ID: mdl-34486106
3.
The Direct Costs of Dravet's Syndrome before and after Diagnosis Assessment.
Neuropediatrics
; 52(1): 6-11, 2021 02.
Artigo
Inglês
| MEDLINE | ID: mdl-33049783
4.
Regional Incidence of Inflammatory Bowel Disease in a Czech Pediatric Population: 16 Years of Experience (2002-2017).
J Pediatr Gastroenterol Nutr
; 70(5): 586-592, 2020 05.
Artigo
Inglês
| MEDLINE | ID: mdl-32058417
5.
Subthalamic nucleus involvement in executive functions with increased cognitive load: a subthalamic nucleus and anterior cingulate cortex depth recording study.
J Neural Transm (Vienna)
; 121(10): 1287-96, 2014 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-24658745
6.
A Tagging Polymorphism in Fat Mass and Obesity-Associated (FTO) Gene Is Associated with Sepsis Status in Children.
Rom J Intern Med
; 2024 Mar 12.
Artigo
Inglês
| MEDLINE | ID: mdl-38470396
7.
Precision immuno-oncology approach for four malignant tumors in siblings with constitutional mismatch repair deficiency syndrome.
NPJ Precis Oncol
; 8(1): 110, 2024 May 21.
Artigo
Inglês
| MEDLINE | ID: mdl-38773265
8.
Multivariate linear mixture models for the prediction of febrile seizure risk and recurrence: a prospective case-control study.
Sci Rep
; 13(1): 17372, 2023 10 13.
Artigo
Inglês
| MEDLINE | ID: mdl-37833343
9.
CCL2/MCP-1, interleukin-8, and fractalkine/CXC3CL1: Potential biomarkers of epileptogenesis and pharmacoresistance in childhood epilepsy.
Eur J Paediatr Neurol
; 46: 48-54, 2023 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-37429062
10.
Current Management of Generalized Convulsive Status Epilepticus in Children.
Children (Basel)
; 9(10)2022 Oct 20.
Artigo
Inglês
| MEDLINE | ID: mdl-36291522
11.
Cytokine-chemokine profiles in the hippocampus of patients with mesial temporal lobe epilepsy and hippocampal sclerosis.
Epilepsy Res
; 180: 106858, 2022 02.
Artigo
Inglês
| MEDLINE | ID: mdl-35026708
12.
Novel mutations in TRPM6 gene associated with primary hypomagnesemia with secondary hypocalcemia. Case report.
Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub
; 165(4): 454-457, 2021 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-34012148
13.
Autosomal dominant temporal lobe epilepsy associated with heterozygous reelin mutation: 3â¯T brain MRI study with advanced neuroimaging methods.
Epilepsy Behav Case Rep
; 11: 39-42, 2019.
Artigo
Inglês
| MEDLINE | ID: mdl-30619712
14.
Prognostic factors and seizure outcome in posterior reversible encephalopathy syndrome (PRES) in children with hematological malignancies and bone marrow failure: A retrospective monocentric study.
Seizure
; 72: 1-10, 2019 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-31521834