Researcher
Helene Verhelst
- Keywords:pediatric MS, neural tube disorders, pediatric neurology, epilepsie, autoimmune, neuroinflammation
- Disciplines:Neurosciences not elsewhere classified, Behavioural neuroscience, Paediatrics, Autoimmunity, Neurophysiology, Neurological and neuromuscular diseases, Cognitive neuroscience, Developmental neuroscience
Affiliations
- Department of Internal Medicine and Pediatrics (Department)
Member
From1 Oct 2018 → Today - Department of Pediatrics and medical genetics (Department)
Member
From27 Jan 2009 → 30 Sep 2018
Publications
1 - 10 of 62
- Disease course and psychosocial outcome for children and adolescents with anti-N-methyl-D-aspartate receptor encephalitis(2024)
Authors: Inge Antrop, Helene Verhelst
Pages: 648 - 660 - Anti-SOX1 antibodies in a 3-year-old girl, post-varicella(2023)
Authors: Helene Verhelst
Pages: 1 - 5 - Clinical investigation of French maritime pine bark extract on attention-deficit hyperactivity disorder as compared to methylphenidate and placebo : part 1 : efficacy in a randomised trial(2022)
Authors: Anne-Sophie Weyns, Annelies A. J. Verlaet, Annelies Breynaert, Tania Naessens, Erik Fransen, Helene Verhelst, Dirk Van West, Ingrid Van Ingelghem, An I. Jonckheere, Diane Beysen, et al.
- Clinical investigation of French maritime pine bark extract on attention-deficit hyperactivity disorder as compared to methylphenidate and placebo : part 2 : oxidative stress and immunological modulation(2022)
Authors: Anne-Sophie Weyns, Annelies A. J. Verlaet, Maxim Van Herreweghe, Annelies Breynaert, Erik Fransen, Ingrid De Meester, Emilie Logie, Wim Vanden Berghe, Helene Verhelst, Dirk Van West, et al.
- Mental health outcomes among parents of children with a chronic disease during the COVID-19 pandemic : the role of parental burn-out(2022)
Authors: Aline Wauters, Tine Vervoort, Karlien Dhondt, Bart Soenens, Maarten Vansteenkiste, Sofie Morbée, Joachim Waterschoot, Filomeen Haerynck, Kristof Vandekerckhove, Helene Verhelst, et al.
Pages: 420 - 431 - Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications(2022)
Authors: Katrine M. Johannesen, Yuanyuan Liu, Mahmoud Koko, Cathrine E. Gjerulfsen, Lukas Sonnenberg, Julian Schubert, Christina D. Fenger, Ahmed Eltokhi, Maert Rannap, Nils A. Koch, et al.
Pages: 2991 - 3009 - Blood transcriptomics to facilitate diagnosis and stratification in pediatric rheumatic diseases : a proof of concept study(2022)
Authors: My Kieu Ha, Esther Bartholomeus, Luc Van Os, Julie Dandelooy, Julie Leysen, Olivier Aerts, Vasiliki Siozopoulou, Eline De Smet, Jan Gielen, Khadija Guerti, et al.
- Phenotypes and genotypes in non‐consanguineous and consanguineous primary microcephaly : high incidence of epilepsy(2021)
Authors: Sarah Duerinckx, Julie Désir, Camille Perazzolo, Cindy Badoer, Valérie Jacquemin, Julie Soblet, Isabelle Maystadt, Yusuf Tunca, Bettina Blaumeiser, Berten Ceulemans, et al.
- Plasma C3d levels as a diagnostic marker for complete complement factor I deficiency(2021)
Authors: Leslie Naesens, Julie Smet, Simon Tavernier, Levi Hoste, Helene Verhelst, Jutte van der Werff Ten Bosch, Alina Ferster, Sophie Blumental, Pascale Hilbert, Johan Van de Walle, et al.
Pages: 749 - 753.e2 - Rare manifestations and malignancies in tuberous sclerosis complex : findings from the TuberOus SClerosis registry to increAse disease awareness (TOSCA)(2021)
Authors: Matthias Sauter, Elena Belousova, Mirjana P. Benedik, Tom Carter, Vincent Cottin, Paolo Curatolo, Maria Dahlin, Lisa D'Amato, Guillaume B. D'Augeres, Petrus J. de Vries, et al.