Portal de recerca
REVISIÓN DE LA TROMBOSIS VENOSA CEREBRAL EN PEDIATRÍA. SERIE DE CASOS DE UN HOSPITAL TERCIARIO.
Dades bàsiques
- Protocol:
- HFV-TRO-2020-01
- EURDRACT:
- NCT:
- Centre:
- HOSPITAL UNIVERSITARI I POLITÈCNIC LA FE
- Any inici:
- 2020
- Any de finalització:
- 2020
Documents
- No hi ha documents
Participants
Grups d'Investigació
Finançadors - Promotors
Resultats de l'Assaig Clínic
A microRNA signature for valproate-induced steatosis in human hepatocytes and its application to predict fatty liver in paediatric epileptic patients on valproate therapy.
Soluyanova P; (...); Jover R
Article. 10.1016/j.tox.2024.153974. 2024
Apparent Radiological Improvement in an Infant With Labrune Syndrome Treated With Bevacizumab
Martinez-Matilla, Marina; (...); Pedrola, Laia
Letter. 10.1016/j.pediatrneurol.2020.07.011. 2020
Case Report: Novel Homozygous Likely Pathogenic SCN1A Variant With Autosomal Recessive Inheritance and Review of the Literature.
Marco Hernández AV; (...); Martinez F
Case Reports. 10.3389/fneur.2021.784892. 2021
Clinical Parameters in the First 5 Minutes after Birth Have a Predictive Value for Survival of Extremely Preterm Infants
Torrejon-Rodriguez, Laura; (...); Vento, Maximo
Review. 10.1097/FM9.0000000000000206. 2023
Early molecular markers of ventilator-associated pneumonia in bronchoalveolar lavage in preterm infants
Pinilla-Gonzalez, Alejandro; (...); Cernada, Maria
Article. 10.1038/s41390-022-02271-w. 2023
Effect of autologous umbilical cord blood transfusion in the development of retinopathy of prematurity: randomized clinical trial - study protocol.
Torrejon-Rodriguez L; (...); Aguar Carrascosa M
Article. 10.3389/fped.2023.1269797. 2023
Energetic and Spectroscopic Properties of the Low-Lying Isomers of C5H: A High-Level Ab Initio Study
Torrejon-Rodriguez, Laura; (...); Torres, Maximo Vento
Article. 10.3390/atoms11090115. 2023
Extending the Phenotype Related to SCN1A Gene: Arthrogryposis, Movement Disorders, and Malformations of Cortical Development.
Marco-Hernandez, Ana Victoria; (...); Martinez, Francisco
Article. 10.1177/08830738211072694. 2022
Genetic Heterogeneity Underlying Phenotypes with Early-Onset Cerebellar Atrophy
Martinez-Rubio, Dolores; (...); Espinos, Carmen
Article. 10.3390/ijms242216400. 2023
Genetics of Paroxysmal Dyskinesia: Novel Variants Corroborate the Role of KCNA1 in Paroxysmal Dyskinesia and Highlight the Diverse Phenotypic Spectrum of KCNA1- and SLC2A1-Related Disorders
Kegele J; (...); Lauxmann S
Article. 10.3389/fneur.2021.701351. 2021
Hidden etiology of cerebral palsy: genetic and clinical heterogeneity and efficient diagnosis by next-generation sequencing.
Rosello M; (...); Tomás M
Review. 10.1038/s41390-020-01250-3. 2020
Mitochondrial developmental encephalopathy with bilateral optic neuropathy related to homozygous variants in IMMT gene.
Marco-Hernández AV; (...); Martínez-Castellano F
Article. 10.1111/cge.14093. 2022
Neonatal skin antisepsis with alcohol-based compared to aqueous 2% chlorhexidine, used in moderate preterm infants or extremely preterm infants after the first week of life, is safe and may be associated with a reduced incidence of catheter-related bloodstream infections.
Pinilla-Gonzalez, Alejandro; (...); Cernada, Maria
Article. 10.1136/archdischild-2024-327728. 2025
New variants expand the neurological phenotype of COQ7 deficiency.
Fabra, Maria Alcazar; (...); Santos-Ocana, Carlos
Article. 10.1002/jimd.12776. 2024
N-Type Ca Channel in Epileptic Syndromes and Epilepsy: A Systematic Review of Its Genetic Variants
Mayo, Sonia; (...); Martinez, Francisco
Review. 10.3390/ijms24076100. 2023
The effect of inhaled nitric oxide treatment on biomarkers of oxidative/nitrosative damage to proteins and DNA/RNA.
Albiach-Delgado, Abel; (...); Vento, Maximo
Article. 10.1016/j.freeradbiomed.2025.01.020. 2025
The LINCE Project: A Pathway for Diagnosing NCL2 Disease.
Rodrigues, Daniel; (...); Colon, Cristobal
Article. 10.3389/fped.2022.876688. 2022
Transfusion practices of blood products in preterm infants: National survey
Torrejon-Rodriguez, Laura; (...); Aguar, Marta
Letter. 10.1016/j.anpedi.2023.07.003. 2023
Variant in CACNA1G as a Possible Genetic Modifier of Neonatal Epilepsy in an Infant with a De Novo SCN2A Mutation
Nieto-Barcelo, Juan Jose; (...); Tomas Vila, Miguel
Article. 10.1055/s-0041-1723958. 2021
Venous sinus thrombosis in pediatrics. Case series of a tertiary hospital.
Rubio Atienza Y; (...); Tomás Vila M
Article. 10.32641/andespediatr.v92i3.3344. 2021