Research Explorer

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Researcher

Helene Verhelst

Awards & Distinctions

92 Results

2024

Disease course and psychosocial outcome for children and adolescents with anti-N-methyl-D-aspartate receptor encephalitis

Joke DepreitereInge AntropHelene Verhelst

A1 Journal Article in CLINICAL CHILD PSYCHOLOGY AND PSYCHIATRY

Hypotonia : out of balance? The relation between hypotonia and vestibular dysfunction in children : a scoping review

Lena Van den BosscheLeen MaesFrederic AckeMarieke FontaineHelene VerhelstAnna OostraIngeborg Dhooge

Hypotonia: out of balance? The relation between hypotonia and vestibular dysfunction in children: a scoping review

Lena Van den BosscheLeen MaesFrederic AckeMarieke FontaineHelene VerhelstAnna OostraIngeborg Dhooge

Seizure quantification in sunflower syndrome by a wrist‐worn device

Jo SourbronRenee ProostJan VandenneuckerValentina TiccinelliFilip RoelensAn‐Sofie SchoonjansEls SercuHelene VerhelstKatrien JansenLieven Lagae

U Journal Article in Epileptic Disorders

The diagnostic workup of children with the radiologically isolated syndrome differs by age and by sex

Naila MakhaniChristine Lebrun-FrenayAksel SivaVeronika ShabanovaEvangeline WassmerJonathan D. SantoroSona NarulaJ. Nicholas BrentonSoe MarFrancoise Durand-Dubief et al.

U Journal Article in Journal of Neurology

2023

Anti-SOX1 antibodies in a 3-year-old girl, post-varicella

Aline WijnandHelene Verhelst

A2 Journal Article in CHILD NEUROLOGY OPEN

Atypical psychiatric presentation of relapsing anti-N-methyl-D-aspartate receptor encephalitis in childhood

Joke DepreitereJan De MeulenaereHelene Verhelst

A1 Journal Article in CLINICAL CHILD PSYCHOLOGY AND PSYCHIATRY

EpiCare@Home : remote wearable seizure monitoring for people with epilepsy can improve delivery of care

J. NysW. HarveyB. De RidderN. ZablerG. FonteynJ. DelbecqC. DepondtR. El TahryS. Ferrao SantosS. Weckhuysen et al.

2022

Blood transcriptomics to facilitate diagnosis and stratification in pediatric rheumatic diseases : a proof of concept study

My Kieu HaEsther BartholomeusLuc Van OsJulie DandelooyJulie LeysenOlivier AertsVasiliki SiozopoulouEline De SmetJan GielenKhadija Guerti et al.

A1 Journal Article in PEDIATRIC RHEUMATOLOGY

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

Anne-Sophie WeynsAnnelies A. J. VerlaetAnnelies BreynaertTania NaessensErik FransenHelene VerhelstDirk Van WestIngrid Van IngelghemAn I. JonckheereDiane Beysen et al.

A1 Journal Article in JOURNAL OF FUNCTIONAL FOODS

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

Anne-Sophie WeynsAnnelies A. J. VerlaetMaxim Van HerrewegheAnnelies BreynaertErik FransenIngrid De MeesterEmilie LogieWim Vanden BergheHelene VerhelstDirk Van West et al.

A1 Journal Article in JOURNAL OF FUNCTIONAL FOODS

Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications

Katrine M. JohannesenYuanyuan LiuMahmoud KokoCathrine E. GjerulfsenLukas SonnenbergJulian SchubertChristina D. FengerAhmed EltokhiMaert RannapNils A. Koch et al.

A1 Journal Article in BRAIN

Mental health outcomes among parents of children with a chronic disease during the COVID-19 pandemic : the role of parental burn-out

Aline WautersTine VervoortKarlien DhondtBart SoenensMaarten VansteenkisteSofie MorbéeJoachim WaterschootFilomeen HaerynckKristof VandekerckhoveHelene Verhelst et al.

A1 Journal Article in JOURNAL OF PEDIATRIC PSYCHOLOGY

Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenital

Annie LaquerriereDana JaberEmanuela AbiusiJerome MaluendaDan MejlachowiczAlexandre VivantiKlaus DieterichRadka StoevaLoic QuevarecFlora Nolent et al.

A1 Journal Article in JOURNAL OF MEDICAL GENETICS

2021

Is diffuse axonal injury on susceptibility weighted imaging a biomarker for executive functioning in adolescents with traumatic brain injury? (vol 23, pg 525, 2019)

Catharine Vander LindenHelene VerhelstEva GenbruggeEllen DeschepperKaren CaeyenberghsGuy VingerhoetsKarel Deblaere

Parental experience and emotional well-being in families with a child with a chronic disease during the COVID 19 pandemic

Eline Van HoeckeKarlien DhondtAnn RaesStephanie Van BiervlietBarbara De MoerlooseSara Van AkenFilomeen HaerynckLevi HosteHelene VerhelstBart Soenens et al.

Phenotypes and genotypes in non‐consanguineous and consanguineous primary microcephaly : high incidence of epilepsy

Sarah DuerinckxJulie DésirCamille PerazzoloCindy BadoerValérie JacqueminJulie SobletIsabelle MaystadtYusuf TuncaBettina BlaumeiserBerten Ceulemans et al.

A1 Journal Article in MOLECULAR GENETICS & GENOMIC MEDICINE

Plasma C3d levels as a diagnostic marker for complete complement factor I deficiency

Leslie NaesensJulie SmetSimon TavernierPetra SchelstraeteLevi HosteStijn LambrechtHelene VerhelstJutte van der Werff Ten BoschAlina FersterSophie Blumental et al.

A1 Journal Article in JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

Rare manifestations and malignancies in tuberous sclerosis complex : findings from the TuberOus SClerosis registry to increAse disease awareness (TOSCA)

Matthias SauterElena BelousovaMirjana P. BenedikTom CarterVincent CottinPaolo CuratoloMaria DahlinLisa D'AmatoGuillaume B. D'AugeresPetrus J. de Vries et al.

A1 Journal Article in ORPHANET JOURNAL OF RARE DISEASES

Safety and efficacy of teriflunomide in paediatric multiple sclerosis (TERIKIDS) : a multicentre, double-blind, phase 3, randomised, placebo-controlled trial

Tanuja ChitnisBrenda BanwellLudwig KapposDouglas L. ArnoldKivilcim GuecueyenerKumaran DeivaNatalia SkripchenkoLi-Ying CuiStephane SaubaduWenruo Hu et al.

A1 Journal Article in LANCET NEUROLOGY

2020

Defining the clinical, molecular and imaging spectrum of adaptor protein complex 4-associated hereditary spastic paraplegia

Darius Ebrahimi-FakhariJulian TeinertRobert BehneMiriam WimmerAngelica D'AmoreKathrin EberhardtBarbara BrechmannMarvin ZieglerDana M JensenPremsai Nagabhyrava et al.

A1 Journal Article in BRAIN

Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy

Holger HengelCélia Bosso-LefèvreGeorge GradyEmmanuelle Szenker-RaviHankun LiSarah PierceÉlise LebigotThong-Teck TanMichelle Y. EioGunaseelan Narayanan et al.

A1 Journal Article in NATURE COMMUNICATIONS

Natural clusters of tuberous sclerosis complex (TSC)-associated neuropsychiatric disorders (TAND) : new findings from the TOSCA TAND research project

Petrus J. de VriesElena BelousovaMirjana P. BenedikTom CarterVincent CottinPaolo CuratoloLisa D’AmatoGuillaume Beure d’AugèresJosé C. FerreiraMartha Feucht et al.

A1 Journal Article in JOURNAL OF NEURODEVELOPMENTAL DISORDERS

2019

Clinical characteristics of subependymal giant cell astrocytoma in tuberous sclerosis complex

Anna C. JansenElena BelousovaMirjana P. BenedikTom CarterVincent CottinPaolo CuratoloMaria DahlinLisa D'AmatoGuillaume Beaure d'AugèresPetrus J. de Vries et al.

A1 Journal Article in FRONTIERS IN NEUROLOGY

Clinical trials of disease-modifying agents in pediatric MS : opportunities, challenges, and recommendations from the IPMSSG

Emmanuelle WaubantBrenda BanwellEvangeline WassmerMaria-Pia SormaniMaria-Pia AmatoRogier HintzenLauren KruppKevin RostásySilvia TenembaumTanuja Chitnis et al.

A1 Journal Article in NEUROLOGY

Diagnosing enterovirus meningitis via blood transcriptomics : an alternative for lumbar puncture?

Esther BartholomeusNicolas De NeuterAnnelies LemayLuc PattynDavid TuerlinckxDavid WeynantsKoen Van LedeGerlant van BerlaerDominique BulckaertTine Boiy et al.

A1 Journal Article in JOURNAL OF TRANSLATIONAL MEDICINE

Neuroinflammatory disorders in childhood : focus on specific clinical entities, genetic susceptibility and immunomodulatory treatment

Helene VerhelstRudy Van Coster

Newly diagnosed and growing subependymal giant cell astrocytoma in adults with tuberous sclerosis complex : results from the international TOSCA study

Anna C. JansenElena BelousovaMirjana P. BenedikTom CarterVincent CottinPaolo CuratoloLisa D'AmatoGuillaume Beaure d'AugèresPetrus J. de VriesJosé C. Ferreira et al.

A1 Journal Article in FRONTIERS IN NEUROLOGY

Recurrent arterial ischemic stroke with good response to mycophenolate mofetil

Benedikte Van DriesschePATRICK VERLOONele HerregodsVeerle MondelaersJo DehoorneRudy Van CosterHelene Verhelst

A1 Journal Article in EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY

Treatment patterns and use of resources in patients with tuberous sclerosis complex : insights from the TOSCA registry

Ruben MarquesElena BelousoyeMirjana P. BenedikTom CarterVincent CottinPaolo CuratoloMaria DahlinLisa D'AmatoGuillaume Beaure d'AugeresPetrus J. de Vries et al.

A1 Journal Article in FRONTIERS IN NEUROLOGY

2018

Efficacy and safety of the AspireSR (R) VNS at Ghent University Hospital, Belgium

Ann MertensKristl VonckVeerle De HerdtAlfred MeursStephanie HödlStefanie GadeyneHelene VerhelstFrank DewaelePaul Boon

Genotype-phenotype correlation in NF1 : evidence for a more severe phenotype associated with missense mutations affecting NF1 codons 844–848

Magdalena KoczkowskaYunjia ChenTom CallensAlicia GomesAngela SharpSherrell JohnsonMeng-Chang HsiaoZhenbin ChenMeena BalasubramanianChristopher P Barnett et al.

A1 Journal Article in AMERICAN JOURNAL OF HUMAN GENETICS

Megalencephalic leukoencephalopathy with subcortical cysts : characterization of disease variants

Eline MC HamiltonPinar TekturkFia CialdellaDiane F van RappardNicole I WolfCengiz YalcinkayaÜmran ÇetinçelikAhmad RajaeeAdriana KariminejadJustyna Paprocka et al.

A1 Journal Article in NEUROLOGY

Paediatric acute disseminated encephalomyelitis followed by optic neuritis : disease course, treatment response and outcome

YYM WongY HacohenT ArmangueE WassmerHelene VerhelstC HemingwayED van PeltCE Catsman-BerrevoetsRQ HintzenK Deiva et al.

A1 Journal Article in EUROPEAN JOURNAL OF NEUROLOGY

TSC-associated neuropsychiatric disorders (TAND) : findings from the TOSCA natural history study

Petrus J de VriesElena BelousovaMirjana P BenedikTom CarterVincent CottinPaolo CuratoloMaria DahlinLisa D'AmatoGuiillaume B d'AugèresJose C Ferreira et al.

A1 Journal Article in ORPHANET JOURNAL OF RARE DISEASES

The clinical heterogeneity of the NARS2 c.822G>C mutation clearly illustrated in two siblings : epilepsy and myopathy

Arnaud VanlanderHelene VerhelstElise VantroysJoél SmetBoel De PaepeSarah VergultBjörn MentenRudy Van Coster

Zuigeling met aseptische meningo-encefalitis gecompliceerd door een brachiale plexusneuritis

Delfien BogaertHelene VerhelstRuth Van Der LoovenNicola De ConoKatrien De Schynkel

2017

Effect of Pycnogenol® on attention-deficit hyperactivity disorder (ADHD) : study protocol for a randomised controlled trial

Annelies AJ VerlaetBerten CeulemansHelene VerhelstDirk Van WestTess De BruyneLuc PietersHuub FJ SavelkoulNina Hermans

A1 Journal Article in TRIALS

Inborn errors in RNA polymerase III underlie severe varicella zoster virus infections

Benson OgunjimiShen-Ying ZhangKatrine B SørensenKristian A SkipperMadalina Carter-TimofteGaspard KernerStefanie LueckeThaneas PrabakaranYujia CaiJosephina Meester et al.

A1 Journal Article in JOURNAL OF CLINICAL INVESTIGATION

Multiple sclerosis in Belgian children : a multicentre retrospective study

Helene VerhelstLiesbeth De WaeleNicolas DeconinckBerten CeulemansBarbara WillekensRudy Van Coster

A1 Journal Article in EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY

NR4A2 causes an autism spectrum disorder

Helene VerhelstPatrick VerlooAnnelies DheedeneBert CallewaertBjörn Menten

Nusinersen versus sham control in infantile-onset spinal muscular atrophy

RS FinkelE MercuriBT DarrasAM ConnellyNL KuntzJ KirschnerCA ChiribogaK SaitoL ServaisE Tizzano et al.

A1 Journal Article in NEW ENGLAND JOURNAL OF MEDICINE

Severe congenital microcephaly with AP4M1 mutation, a case report

Sarah DuerinckxHelene VerhelstCamille PerazzoloPhilippe DavidLaurence DesmyterIsabelle PirsonMarc Abramowicz

A1 Journal Article in BMC MEDICAL GENETICS

2016

EFFECTS : an expanded access program of everolimus for patients with subependymal giant cell astrocytoma associated with tuberous sclerosis complex

Andras FogarasiLiesbeth De WaeleGabriella BartaliniSergiusz JozwiakNicola LaforgiaHelene VerhelstBorivoj PetrakJean-Michel PedespanOlaf WittRamon Castellana et al.

A1 Journal Article in BMC NEUROLOGY

RC3H1 mutation with increased ICOS expression causes an autoinflammatory syndrome

Filomeen HaerynckPATRICK VERLOODelfien BogaertJoél SmetArnaud VanlanderMaria Bordon Cueto De BraemHelene VerhelstRudy Van CosterBjörn MentenMelissa Dullaers

STXBP1 encephalopathy : a neurodevelopmental disorder including epilepsy

Hannah StambergerMarina NikanorovaMarjolein H WillemsenPatrizia AccorsiMarco AngrimanHartmut BaierIra Benkel-HerrenbrueckValérie BenoitMauro BudettaAlmuth Caliebe et al.

A1 Journal Article in NEUROLOGY

2015

Intensive therapeutic plasma exchange in children with acute autoimmune neurological disorders

Agnieszka Prytula-EbelsJohan Vande WalleHelene VerhelstSTEFAAN CLAUSANNIK DE JAEGERJo DehoorneAnn Raes

Therapeutic plasma exchange in children with acute autoimmune central nervous system disorders

Agnieszka Prytula-EbelsJohan Vande WalleHelene VerhelstSunny ElootSTEFAAN CLAUSANNIK DE JAEGERJo DehoorneAnn Raes

A1 Journal Article in INTERNATIONAL JOURNAL OF ARTIFICIAL ORGANS

2014

Lambert-Eaton myasthenic syndrome in a 13-year-old girl with Xp11.22-p11.23 duplication

Sabine VerbeekOlivier VanakkerRudy MercelisAF LipkaFilomeen HaerynckMelissa DullaersPATRICK VERLOORudy Van CosterHelene Verhelst

A1 Journal Article in EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY

Polymicrogyria with dysmorphic basal ganglia? Think tubulin!

D AmromI TanyalçinHelene VerhelstN DeconinckGJ BrouhardJ-C DécarieT VanderhasseltS DasFF HamdanW Lissens et al.

A1 Journal Article in CLINICAL GENETICS

2013

Achieving anal pseudo-continence by colonic irrigations in patients with spina bifida

Saskia Vande VeldeDanny De LoozeStephanie Van BiervlietRuth De BruyneHelene VerhelstMyriam Van Winckel

Clinical and genetic aspects of PCDH19-related epilepsy syndromes and the possible role of PCDH19 mutations in males with autism spectrum disorders

JJT van HarsselS WeckhuysenMJA van KempenK HardiesNE VerbeekCGF de KovelWB GunningE van DaalenMV de JongeAC Jansen et al.

A1 Journal Article in NEUROGENETICS

Colon enemas for fecal incontinence in patients with spina bifida

Saskia Vande VeldeStephanie Van BiervlietErik Van LaeckeRuth De BruyneHelene VerhelstPiet HoebekeMyriam Van Winckel

A1 Journal Article in JOURNAL OF UROLOGY

Colon transit time and anorectal manometry in children and young adults with spina bifida

Saskia Vande VeldeLAURENCE PRATTEHelene VerhelstVALERIE MEERSSCHAUTNele HerregodsMyriam Van WinckelStephanie Van Biervliet

A1 Journal Article in INTERNATIONAL JOURNAL OF COLORECTAL DISEASE

Elaborating the phenotypic spectrum associated with mutations in ARFGEF2: case study and literature review

Ibrahim TanyalcinHelene VerhelstDickey JJ HalleyTim VanderhasseltLaurent VillardCyril GoizetWilly LissensGrazia M ManciniAnna C Jansen

A1 Journal Article in EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY

Expanding the spectrum of MERS type 2 lesions, a particular form of encephalitis

ANNELEEN NOTEBAERTJef WillemsLine CouckeRudy Van CosterHelene Verhelst

A1 Journal Article in PEDIATRIC NEUROLOGY

First line management of prolonged convulsive seizures in children and adults : good practice points

LIESBETH DE WAELEPaul BoonBerten CeulemansBernard DanAnna JansenBenjamin LegrosPatricia LeroyFrancoise DelmelleMichel OssemannSylvie De Raedt et al.

A1 Journal Article in ACTA NEUROLOGICA BELGICA

Hypocretin-1 deficiency in a girl with ROHHAD syndrome

Karlien DhondtPATRICK VERLOOHelene VerhelstRudy Van CosterSebastiaan Overeem

A1 Journal Article in PEDIATRICS

Temps du transit colique chez l'enfant atteint de dysraphisme ouvert

LAURENCE PRATTESaskia Vande VeldeVALERIE MEERSSCHAUTHelene VerhelstRuth De BruyneKoenraad VerstraeteMyriam Van WinckelStephanie Van Biervliet

A1 Journal Article in ARCHIVES DE PEDIATRIE

2012

Developing a modified 'quality of life' questionnaire for children with spina bifida

Saskia Vande VeldeJolien LaridaenJ DaelmanStephanie Van BiervlietMyriam Van WinckelHelene Verhelst

2011

Anti-NMDA-receptor encephalitis in a 3 year old patient with chromosome 6p21.32 microdeletion including the HLA cluster

Helene VerhelstPATRICK VERLOOKarlien DhondtBoel De PaepeBjörn MentenJosep DalmauRudy Van Coster

A1 Journal Article in EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY

Colon enemas in patients with spina bifida: practical approach

Saskia Vande VeldeStephanie Van BiervlietHelene VerhelstMyriam Van Winckel

Hashimoto encephalopathy and antibodies against dimethylargininase-1: a rare cause of cognitive decline in a pediatric Down's syndrome patient

Helene VerhelstPATRICK VERLOOBoel De PaepeBeatrice GiniBruno BonettiRudy Van Coster

A1 Journal Article in CLINICAL NEUROLOGY AND NEUROSURGERY

Palatal insufficiency as isolated sign of GQ1b antibody syndrome

Helene VerhelstMICHAELA MAESKarel DeblaereRudy Van Coster

A1 Journal Article in PEDIATRIC NEUROLOGY

TUBA1A mutations: from isolated lissencephaly to familial polymicrogyria

AC JansenAnn OostraB DesprechinsY De VlaeminckHelene VerhelstL RegalPATRICK VERLOON BockaertK KeymolenS Seneca et al.

A1 Journal Article in NEUROLOGY

2010

Perisylvian polymicrogyria, infantile spasms and arthrogryposis : the severe end of the spectrum of congenital bilateral perisylvian polymicrogyria

ANJA DE COENERudy Van CosterHelene Verhelst

A1 Journal Article in EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY

Treatment and long term outcome in West syndrome : the clinical reality : a multicentre follow up study

Lieven LagaeHelene VerhelstBerten CeulemansLinda De MeirleirMarie-Cecile NassogneValerie De BorchgraveMarc D'HoogheMartine FoulonPatrick Van Bogaert

A1 Journal Article in SEIZURE-EUROPEAN JOURNAL OF EPILEPSY

2009

A missence mutation in complement factor I associated with recurrent aseptic meningoencephalitis

Joke DehoorneFilomeen HaerynckBart LoeysHelene VerhelstF MascartAnn RaesJohan Vande Walle

Childhood narcolepsy with partial facial cataplexy: a diagnostic dilemma

Karlien DhondtHelene VerhelstDirk PevernagieFlorence SlapRudy Van Coster

A1 Journal Article in SLEEP MEDICINE

Differential effects of atomoxetine on executive functioning and lexical decision in attention-deficit/hyperactivity disorder and reading disorder

Christien GW de JongSéverine Van De VoordeHerbert RoeyersRuth RaymaekersAlbert J AllenSimone KnijffHelene VerhelstAlfons H TemminkLeo ME SmitRob Rodriques-Pereira et al.

A1 Journal Article in JOURNAL OF CHILD AND ADOLESCENT PSYCHOPHARMACOLOGY

Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals

EK BijlsmaACJ GijsbersJHM Schuurs-HoeijmakersA van HaeringenDEF van de PutteBM AnderlidJ LundinP LapunzinaLAP JuradoBARBARA DELLE CHIAIE et al.

A1 Journal Article in EUROPEAN JOURNAL OF MEDICAL GENETICS

MECHANISM OF LACTIC ACIDOSIS IN PATIENTS WITH THE PROPOFOL INFUSION SYNDROME (PRIS)

Rudy Van CosterArnaud VanlanderJoél SmetHelene VerhelstPATRICK VERLOOANNIK DE JAEGER

Subcomplexes of mitochondrial complex V reveal mutations in mitochondrial DNA

Joél SmetSara SenecaBoel De PaepeAnn MeulemansHelene VerhelstJuliaan LeroyLinda De MeirleirWilly LissensRudy Van Coster

A1 Journal Article in ELECTROPHORESIS

2008

Hippocampal atrophy and developmental regression as first sign of linear scleroderma "en coup de sabre"

Helene VerhelstHilde BeeleRik JoosBenedicte VanneuvilleRudy Van Coster

A1 Journal Article in EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY

2007

Follow-up of a patient treated with vagus nerve stimulation for refractory status epilepticus

Kristl VonckVeerle De HerdtHelene VerhelstBart DermautIsabelle DewaeleLiesbeth WaterschootEvelien CarretteANNIK DE JAEGERRudy Van CosterDirk Van Roost et al.

Limbic encephalitis as presentation of a SAP deficiency

Helene VerhelstRudy Van CosterNele BockaertGenevieve LaureysSylvie LatourA FischerFilomeen Haerynck

Editorial material

Prospective screening of migraine criteria in Belgian patients with epilepsy

Evelien CarretteAnnelies Van DyckeIsabelle DewaeleKristl VonckVeerle De HerdtHelene VerhelstMichel Van ZandijckeLieven LagaeGunnar BuyseL Dom et al.

Vagus nerve stimulation for refractory epilepsy: a Belgian multicenter study

Veerle De HerdtPaul BoonBerten CeulemansHenri HaumanLieven LagaeBenjamin LegrosBernard SadzotPatrick Van BogaertKenou Van RijckevorselHelene Verhelst et al.

A1 Journal Article in EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY

Vagus nerve stimulation for refractory status epilepticus

Paul BoonVeerle De HerdtLiesbeth WaterschootHelene VerhelstANNIK DE JAEGERRudy Van CosterDirk Van RoostKristl Vonck

2006

CERVICAL INCARCERATION AND RADIAL NERVE ENTRAPMENT NEUROPATHY

Piet VanhaesebrouckAleksandra ZecicT BOVYNCatharine Vander LindenKoenraad SmetsClaudine De PraeterHelene VerhelstPaul Defoort

Limbic encephalitis as presentation of a SAP deficiency

Helene VerhelstRudy Van CosterN BOCKAERTGenevieve LaureysAlexandra FischerFilomeen Haerynck

2005

Hot-water epilepsy: a new Caucasian case

K KEYZERI CORTHOUTSRudy Van CosterHelene Verhelst

A1 Journal Article in EUROPEAN JOURNAL OF PEDIATRICS

Neuroradiologic findings in a young patient with characteristics of Sturge-Weber syndrome and Mippel-Mrenaunay syndrome

Helene VerhelstRudy Van Coster

A1 Journal Article in JOURNAL OF CHILD NEUROLOGY

Steroids in intractable childhood epilepsy: clinical experience and review of the literature

Helene VerhelstPaul BoonGunnar BuyseBerten CeulemansMarc D'HoogheLinda De MeirleirDanièle HasaertsAn JansenLieven LagaeAlfred Meurs et al.

A1 Journal Article in SEIZURE-EUROPEAN JOURNAL OF EPILEPSY

2004

Aicardi-Goutieres-like syndrome

Rudy Van CosterHelene VerhelstV RAMAEKERS

A1 Journal Article in ACTA NEUROLOGICA BELGICA

Auto-immune disorders of cerebral white matter in children

Helene VerhelstJoél SmetGoedele DhondtM SENEPARTRudy Van Coster

A1 Journal Article in ACTA NEUROLOGICA BELGICA

Prenatal phosphorus deficiency syndrome in type I SGA-infants

Piet VanhaesebrouckN VerburgKris De CoenClaudine De PraeterLinde GoossensKoenraad SmetsHelene VerhelstAleksandra Zecic

Severe haemorrhagic leucoencephalopathy in a young infant

Helene VerhelstRudy Van Coster

A1 Journal Article in ACTA NEUROLOGICA BELGICA

Two siblings with early presentation of Vanishing White Matter disease

NELE BOCKAERTM VAN DER KNAAPC VAN DEN BROECKEHelene VerhelstM LAMMENSRudy Van Coster

A1 Journal Article in ACTA NEUROLOGICA BELGICA

2003

Anti-epileptogenesis research: the clinical relevance

Lieven LagaeGunnar BuyseBerten CeulemansPieter ClaeysStefanie DedeurwaerdereLinda De MeirleirRudy HaumanAnna JanssenEric SchmeddingHelene Verhelst et al.

A1 Journal Article in ACTA NEUROLOGICA BELGICA

2001

Blue native polyacrylamide gel electrophoresis: A powerful tool in diagnosis of oxidative phosphorylation defects

Rudy Van CosterJoél SmetEDITH GEORGEL DE MEIRLEIRS SENECAJ VAN HOVEG SEBIREHelene VerhelstJan De BleeckerB VAN VLEM et al.

A1 Journal Article in PEDIATRIC RESEARCH

2000

A family with X-linked dominant Charcot-Marie-Tooth caused by a connexin32 mutation

Helene VerhelstAnn LofgrenRudy Van Coster

A2 Journal Article in EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY