Onderzoeker
Daniele Hasaerts
- Trefwoorden:Geneeskunde
- Disciplines:Pediatrie
Affiliaties
- Pediatrie (Departement)
Lid
Vanaf1 jan 2023 → Heden - Groei en ontwikkeling (Onderzoeksgroep)
Lid
Vanaf21 okt 2022 → Heden - Pediatrie (Departement)
Lid
Vanaf1 jan 2023 → 3 jan 2024 - Pediatrie (kind) (Departement)
Lid
Vanaf1 jan 2008 → 31 dec 2022
Publicaties
1 - 9 van 9
- Prevalence of cerebral palsy and factors associated with cerebral palsy subtype(2023)
Auteurs: Evy Dhondt, Bernard Dan, Frank S. Plasschaert, Marc Degelaen, Charlotte Dielman, Delphine Dispa, Iulia Ebetiuc, Daniele Hasaerts, Sandra Kenis, Costanza Lombardo, et al.
Pagina's: 8-23 - Normal EEG during the neonatal period(2021)
Auteurs: Emilie Bourel-Ponchel, Sophie Gueden, Daniele Hasaerts, Claire Héberlé, Geneviève Malfilâtre, Luc Mony, Patricia Vignolo-Diard, Marie-Dominique Lamblin
Pagina's: 61-88 - Behavioral-state development and sleep-state differentiation during early ontogenesis(2021)
Auteurs: Emilie Bourel-Ponchel, Daniele Hasaerts, Marie-Josèphe Challamel, Marie-Dominique Lamblin
Pagina's: 89-98 - Technical recommendations and interpretation guidelines for electroencephalography for premature and full-term newborns(2021)
Auteurs: Geneviève Malfilâtre, Luc Mony, Daniele Hasaerts, Patricia Vignolo-Diard, Marie-Dominique Lamblin, Emilie Bourel-Ponchel
Pagina's: 35-60 - Cranial ultrasound and neurophysiological testing to predict neurological outcome in infants born very preterm(2018)
Auteurs: Helen Maria A Franckx, Daniele Hasaerts, Koen Huysentruyt, Filip Cools
Pagina's: 1232-1238 - Identification of prenatal behavioral patterns of the gross motor movements within the early stages of fetal development(2017)
Auteurs: Elisabeth Van Merendonk, Jeroen J. W. M. Brouwers, Luc De Catte, Daniele Hasaerts, Maria W. G. Nijhuis-van der Sanden, Eric Kerckhofs
- Reduction of seizure frequency after epilepsy surgery in a patient with STXBP1 encephalopathy and clinical description of six novel mutation carriers(2013)
Auteurs: S. Weckhuysen, Philippe Holmgren, Rik Hendrickx, Anna C Jansen, Daniele Hasaerts, Charlotte Dielman, Julitta De Bellescize, Nadia Boutry-Kryza, Gaetan Lesca, Sarah Von Spiczak, et al.
Pagina's: 74-80 - Identification of two de novo mutations responsible for type I antithrombin deficiency.
Auteurs: Willy Lissens, Daniele Hasaerts
Pagina's: 187-189 - KCNQ2 encephalopathy: Emerging phenotype of a neonatal epileptic encephalopathy
Auteurs: Bert M. Weckhuysen, Simone Mandelstam, Arvid Suls, D. Audenaert, T. De Coninck, Lieve Claes, L. Deprez, K. Smets, Dimitrina Hristova, Iglika Yordanova, et al.
Pagina's: 15-25