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Willy Renier

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Hal A Droogleever Fortuyn; Rolf Fronczek; Joke Kalkman; Gert Jan Lammers; Martijn Lappenschaar; Sebastiaan Overeem; Willy O Renier; Mirjan Smitshoek; Jan Buitelaar; Gijs Bleijenberg
Severe fatigue in narcolepsy with cataplexy.
Hal A Droogleever Fortuyn; Willy O Renier; Jan K Buitelaar; P C Mulders; Sebastiaan Overeem
Narcolepsy and psychiatry: an evolving association of increasing interest.
Nienke E Verbeek; Marjan J A van Kempen; W Boudewijn Gunning; Willy O Renier; Birgit Westland; Dick Lindhout; Eva H Brilstra
Adults with a history of possible Dravet syndrome: an illustration of the importance of analysis of the SCN1A gene.

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2012: Hal A Droogleever Fortuyn; Rolf Fronczek; Joke Kalkman; Gert Jan Lammers; Martijn Lappenschaar; Sebastiaan Overeem; Willy O Renier; Mirjan Smitshoek; Jan Buitelaar; Gijs Bleijenberg
Severe fatigue in narcolepsy with cataplexy.
Journal of sleep research 2012;21(2):163-9.
2011: Hal A Droogleever Fortuyn; Willy O Renier; Jan K Buitelaar; P C Mulders; Sebastiaan Overeem
Narcolepsy and psychiatry: an evolving association of increasing interest.
Sleep medicine 2011;12(7):714-9.
2011: Nienke E Verbeek; Marjan J A van Kempen; W Boudewijn Gunning; Willy O Renier; Birgit Westland; Dick Lindhout; Eva H Brilstra
Adults with a history of possible Dravet syndrome: an illustration of the importance of analysis of the SCN1A gene.
Epilepsia 2011;52(4):e23-5.
2010: Rianne P Reijs; Nora M de la Parra; Saskia G M van Mil; Mariette H J A van Hall; Johan B A M Arends; Jacobiene W Weber; Willy O Renier; Albert P Aldenkamp
Motor function in children with cryptogenic localization related epilepsy.
Seizure : the journal of the British Epilepsy Association 2010;19(8):467-9.
2010: H A Droogleever Fortuyn; Martijn A Lappenschaar; Joop W Furer; Paul P Hodiamont; Cees A Th Rijnders; Willy O Renier; Jan K Buitelaar; Sebastiaan Overeem
Anxiety and mood disorders in narcolepsy: a case-control study.
General hospital psychiatry 2010;32(1):49-56.
2009: Hal A Droogleever Fortuyn; G A Lappenschaar; Fokko J Nienhuis; Joop W Furer; Paul P Hodiamont; Cees A Rijnders; Gert Jan Lammers; Willy O Renier; Jan K Buitelaar; Sebastiaan Overeem
Psychotic symptoms in narcolepsy: phenomenology and a comparison with schizophrenia.
General hospital psychiatry 2009;31(2):146-54.
2008: T Antonius; J Draaisma; Elena N Levtchenko; Nine V A M Knoers; Willy O Renier; Conny van Ravenswaaij-Arts
Growth charts for Wolf-Hirschhorn syndrome (0-4 years of age).
European journal of pediatrics 2008;167(7):807-10.
2007: Rianne P Reijs; Saskia G M van Mil; Mariette H J A van Hall; Johan B A M Arends; Jacobiene W Weber; Willy O Renier; Albert P Aldenkamp
The validity of a separate classification of cryptogenic localization related epilepsy amongst childhood epilepsies.
Seizure : the journal of the British Epilepsy Association 2007;16(5):438-44.
2007: Rianne P Reijs; Saskia G M van Mil; Johan B A M Arends; Mariette H J A van Hall; Jacobiene W Weber; Willy O Renier; Albert P Aldenkamp
Cryptogenic localization related epilepsy in children from a tertiary outpatient clinic: is neurological and neuropsychological outcome predictable?
Clinical neurology and neurosurgery 2007;109(5):422-30.
2007: Pieter D Knoester; Charles L P Deckers; Eveline H Termeer; Arjo J Boendermaker; Irene A W Kotsopoulos; M C T F M de Krom; Toine Keyser; Willy O Renier; Yechiel A Hekster; Hans L Severens
A cost-effectiveness decision model for antiepileptic drug treatment in newly diagnosed epilepsy patients.
Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research 2007;10(3):173-82.
2007: Charlotte A Haaxma; J J J van Eijk; A M van der Vilet; Willy O Renier; Bastiaan R Bloem
[Bilateral lesions of the basal ganglia as a sign of chronic carbon monoxide intoxication].
Nederlands tijdschrift voor geneeskunde 2007;151(15):868-73.
2006: Rianne P Reijs; Saskia G M van Mil; Mariette H J A van Hall; Johan B A M Arends; Jacobiene W Weber; Willy O Renier; Albert P Aldenkamp
Cryptogenic localization-related epilepsy with childhood onset: The problem of definition and prognosis.
Epilepsy & behavior : E&B 2006;8(4):693-702.
2006: JF van Ast; Willy O Renier; Jan Talmon; J M A Roos; Arie Hasman
Diagnostic reference frames for seizures: A validation study.
Journal of neurology 2006;253(3):372-6.
2005: Pieter D Knoester; Arjo J Boendermaker; Toine Egberts; Yechiel A Hekster; Antoine Keyser; Johan L Severens; Willy O Renier; Charles L P Deckers
Cost-effectiveness of add-on lamotrigine therapy in clinical practice.
Epilepsy research 2005;67(3):143-51.
2005: Nicol C Voermans; Machiel J Zwarts; Willy O Renier; Bastiaan R Bloem
[Epileptic seizures during childbirth in a patient with idiopathic generalised epilepsy].
Nederlands tijdschrift voor geneeskunde 2005;149(25):1406-11.
2005: Pieter D Knoester; Antoine Keyser; Willy O Renier; Toine Egberts; Yechiel A Hekster; Charles L P Deckers
Effectiveness of lamotrigine in clinical practice: results of a retrospective population-based study.
Epilepsy research 2005;65(1-2):93-100.
2005: Pieter D Knoester; SV Belitser; Charles L P Deckers; Antoine Keyser; Willy O Renier; Toine Egberts; Yechiel A Hekster
Recruitment of a cohort of lamotrigine users through community pharmacists: differences between patients who gave informed consent and those who did not.
Pharmacoepidemiology and drug safety 2005;14(2):107-12.
2004: David A Koolen; Joris Veltman; Willy O Renier; Richard P Droog; Ad Geurts van Kessel; Bert B A de Vries
Chromosome 22q11 deletion and pachygyria characterized by array-based comparative genomic hybridization.
American journal of medical genetics. Part A 2004;131(3):322-4.
2004: Pieter D Knoester; SV Belitser; Charles L P Deckers; Antoine Keyser; Willy O Renier; Toine Egberts; Yechiel A Hekster
Diffusion of the new antiepileptic drug lamotrigine in Dutch clinical practice.
European journal of clinical pharmacology 2004;60(10):751-8.
2004: Clementina van Rijn; Mei Shen Sun; Charles L P Deckers; Peter M Edelbroek; Antoine Keyser; Willy O Renier; Harry Meinardi
Effects of the combination of valproate and ethosuximide on spike wave discharges in WAG/Rij rats.
Epilepsy research 2004;59(2-3):181-9.
2004: Pieter D Knoester; SV Belitser; Charles L P Deckers; Antoine Keyser; Willy O Renier; Toine Egberts; Yechiel A Hekster
Patterns of lamotrigine use in daily clinical practice during the first 5 years after introduction in the Netherlands.
Journal of clinical pharmacy and therapeutics 2004;29(2):131-8.
2004: B M van der Sluijs; Willy O Renier; Arnoud C Kappelle
Brain tumour as a rare cause of cardiac syncope.
Journal of neuro-oncology 2004;67(1-2):241-4.
2004: JF van Ast; Jan Talmon; Willy O Renier; Arie Hasman
An approach to knowledge base construction based on expert opinions.
Methods of information in medicine 2004;43(4):427-32.
2004: Willy O Renier
Compulsive spitting as manifestation of temporal lobe epilepsy.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2004;8(1):61-2.
2003: Hans J ten Donkelaar; Martin Lammens; P Wesseling; Henk O M Thijssen; Willy O Renier
Development and developmental disorders of the human cerebellum.
Journal of neurology 2003;250(9):1025-36.
2003: JF van Ast; Jan Talmon; Willy O Renier; Harry Meinardi; P P M Ahles; Arie Hasman
Development of diagnostic reference frames for seizures. Part 2: are seizure descriptions discriminative?
International journal of medical informatics 2003;70(2-3):293-300.
2003: JF van Ast; Jan Talmon; Willy O Renier; P P M Ahles; Arie Hasman
Development of diagnostic reference frames for seizures. Part 1: inter-participant agreement in the selection of symptoms.
International journal of medical informatics 2003;70(2-3):285-92.
2003: W H P M Vissers; Maurice A M van Steensel; Peter M Steijlen; Willy O Renier; P C M van de Kerkhof; Carine Van Der Vleuten
Klippel-Trenaunay syndrome and Sturge-Weber syndrome: variations on a theme?
European journal of dermatology : EJD 2003;13(3):238-41.
2003: JF van Ast; Jan Talmon; Willy O Renier; Arie Hasman
How many neurologists/epileptologists are needed to provide reliable descriptions of seizure types?
Studies in health technology and informatics 2003;95():549-53.
2003: Charles L P Deckers; Pieter D Knoester; G J de Haan; Antoine Keyser; Willy O Renier; Yechiel A Hekster
Selection criteria for the clinical use of the newer antiepileptic drugs.
CNS drugs 2003;17(6):405-21.
2002: Lucille D A Dorresteijn; Arnoud C Kappelle; Willy O Renier; Johanna M M Gijtenbeek
Anti-amphiphysin associated limbic encephalitis: a paraneoplastic presentation of small-cell lung carcinoma.
Journal of neurology 2002;249(9):1307-8.
2002: Paul A T M Eling; Willy O Renier; Joern Pomper; Tallie Z Baram
The mystery of the Doctor's son, or the riddle of West syndrome.
Neurology 2002;58(6):953-5.
2001: Charles L P Deckers; Yechiel A Hekster; Antoine Keyser; HJ van Lier; Harry Meinardi; Willy O Renier
Monotherapy versus polytherapy for epilepsy: a multicenter double-blind randomized study.
Epilepsia 2001;42(11):1387-94.
2001: Hans J ten Donkelaar; Martin Lammens; P Wesseling; Henk O M Thijssen; Willy O Renier; Fons J M Gabreëls
[Development and developmental disorders of the human brain. III. Neuronal migration disorders of the cerebrum].
Nederlands tijdschrift voor geneeskunde 2001;145(10):466-74.
2001: Hans J ten Donkelaar; P Wesseling; Martin Lammens; Henk O M Thijssen; Willy O Renier; Fons J M Gabreëls
[Development and developmental disorders of the human brain. II. Development of the cerebral cortex and major tract systems].
Nederlands tijdschrift voor geneeskunde 2001;145(9):401-10.
2001: Hans J ten Donkelaar; P Wesseling; Martin Lammens; Willy O Renier; Reinier A Mullaart; Henk O M Thijssen
[Development and the developmental disorders of human brain. I. Early development of the cerebrum].
Nederlands tijdschrift voor geneeskunde 2001;145(8):345-53.
2001: Charles L P Deckers; Willy O Renier
Long-term treatment retention with topiramate.
Epilepsia 2001;42(2):290-1.
2000: Charles L P Deckers; S J Czuczwar; Yechiel A Hekster; Antoine Keyser; H Kubova; Harry Meinardi; Philip N Patsalos; Willy O Renier; Clementina van Rijn
Selection of antiepileptic drug polytherapy based on mechanisms of action: the evidence reviewed.
Epilepsia 2000;41(11):1364-74.
2000: Charles L P Deckers; Yechiel A Hekster; Antoine Keyser; Harry Meinardi; Willy O Renier
Carbamazepine in comparative trials: pharmacokinetic characteristics too often forgotten.
Neurology 2000;55(1):154-5.
1999: E Strijks; swibertus rudolfus poort; Willy O Renier; Fons J M Gabreëls; R M Bertina
Hereditary prothrombin deficiency presenting as intracranial haematoma in infancy.
Neuropediatrics 1999;30(6):320-4.
1999: M J Jongsma; J M Mommers; Willy O Renier; Harry Meinardi
Follow-up of psychogenic, non-epileptic seizures: a pilot study - experience in a Dutch special centre for epilepsy.
Seizure : the journal of the British Epilepsy Association 1999;8(3):146-8.
1998: Bart P C van de Warrenburg; S van Gulik; Willy O Renier; M Lammens; J C Doelman
The linear naevus sebaceus syndrome.
Clinical neurology and neurosurgery 1998;100(2):126-32.
1997: Charles L P Deckers; Yechiel A Hekster; Antoine Keyser; Harry Meinardi; Willy O Renier
Drug load in clinical trials: a neglected factor.
Clinical pharmacology and therapeutics 1997;62(6):592-5.
1997: Charles L P Deckers; Yechiel A Hekster; Antoine Keyser; Harry Meinardi; Willy O Renier
Pharmacotherapy of epilepsy: state of the art and developments.
Journal of clinical pharmacy and therapeutics 1997;22(5-6):309-22.
1997: Charles L P Deckers; Yechiel A Hekster; Antoine Keyser; Harry Meinardi; Willy O Renier
Reappraisal of polytherapy in epilepsy: a critical review of drug load and adverse effects.
Epilepsia 1997;38(5):570-5.
1997: Charles L P Deckers; Yechiel A Hekster; Antoine Keyser; M W Lammers; Harry Meinardi; Willy O Renier
Adverse effects in epilepsy therapy. Wait and see or go for it?
Acta neurologica Scandinavica 1997;95(4):248-52.
1996: Y Geerts; Willy O Renier; J Bakkeren; J de Jong
2-Hydroxyglutaric aciduria: a case report on an infant with the D-isomeric form with review of the literature.
Journal of the neurological sciences 1996;143(1-2):166-9.
1996: Q H Leyten; Fons J M Gabreëls; Willy O Renier; Henk ter Laak
Congenital muscular dystrophy: a review of the literature.
Clinical neurology and neurosurgery 1996;98(4):267-80.
1996: A F van Heijst; Ron A Wevers; A Tangerman; J R M Cruysberg; Willy O Renier; J J M Tolboom
Chronic diarrhoea as a dominating symptom in two children with cerebrotendinous xanthomatosis.
Acta paediatrica (Oslo, Norway : 1992) 1996;85(8):932-6.
1996: Q H Leyten; Willy O Renier; Fons J M Gabreëls; H G Brunner; Henk ter Laak; Reinier A Mullaart
Association of congenital muscular dystrophy with hypoplasia of the lateral abdominal wall musculature and hypoplasia of the external genitalia.
Neuropediatrics 1996;27(2):108-10.
1996: M W Lammers; Yechiel A Hekster; Antoine Keyser; Harry Meinardi; Willy O Renier; Ron Herings
Use of antiepileptic drugs in a community-dwelling Dutch population.
Neurology 1996;46(1):62-7.
1995: M W Lammers; Yechiel A Hekster; Antoine Keyser; H van Lier; Harry Meinardi; Willy O Renier
Neither dosage nor serum levels of antiepileptic drugs are predictive for efficacy and adverse effects.
Pharmacy world & science : PWS 1995;17(6):201-6.
1995: Karel J B Lamers; F J Gabreëls; Willy O Renier; R A Wevers; W H Doesburg
Fasting studies in cerebrospinal fluid and blood in children with epilepsy of unknown origin.
Epilepsy research 1995;21(1):59-63.
1995: M W Lammers; Yechiel A Hekster; Antoine Keyser; Harry Meinardi; Willy O Renier; H van Lier
Monotherapy or polytherapy for epilepsy revisited: a quantitative assessment.
Epilepsia 1995;36(5):440-6.
1995: Q H Leyten; Fons J M Gabreëls; Willy O Renier; B G M van Engelen; Henk ter Laak; R C Sengers; H O Thijssen
White matter abnormalities in congenital muscular dystrophy.
Journal of the neurological sciences 1995;129(2):162-9.
1995: B G M van Engelen; Corry M R Weemaes; Willy O Renier; Jan Bakkeren; G F Borm; P F Strengers
A dysbalanced immune system in cryptogenic Lennox-Gastaut syndrome.
Scandinavian journal of immunology 1995;41(2):209-13.
1995: Q H Leyten; P G Barth; Fons J M Gabreëls; K Renkawek; Willy O Renier; A A W M Gabreëls-Festen; Henk ter Laak; M G Smits
Congenital muscular dystrophy and severe central nervous system atrophy in two siblings.
Acta neuropathologica 1995;90(6):650-6.
1994: B G M van Engelen; Willy O Renier; Corry M R Weemaes; F J Gabreels; H Meinardi
Immunoglobulin treatment in epilepsy, a review of the literature.
Epilepsy research 1994;19(3):181-90.
1994: M W Lammers; Yechiel A Hekster; Antoine Keyser; Harry Meinardi; Willy O Renier; H Van Lier; D J Wijsman
Clinimetric analysis of treatment objectives and clinical status: individualized treatment in epileptic patients.
Epilepsia 1994;35(6):1271-8.
1994: B G M van Engelen; Willy O Renier; Corry M R Weemaes
Immunoglobulin treatment in human and experimental epilepsy.
Journal of neurology, neurosurgery, and psychiatry 1994;57 Suppl():72-5.
1994: B G M van Engelen; Willy O Renier; Corry M R Weemaes; P F Strengers; P J Bernsen; S L Notermans
High-dose intravenous immunoglobulin treatment in cryptogenic West and Lennox-Gastaut syndrome; an add-on study.
European journal of pediatrics 1994;153(10):762-9.
1994: M W Lammers; D J Wijsman; Yechiel A Hekster; Antoine Keyser; Willy O Renier; Harry Meinardi; H van Lier
Epilepsy treatment in The Netherlands. Comparison of matched groups of two medical centres.
Acta neurologica Scandinavica 1994;89(6):415-20.
1994: B G M van Engelen; Willy O Renier; Corry M R Weemaes; Karel J B Lamers; F J Gabreels; H Meinardi
Cerebrospinal fluid examinations in cryptogenic West and Lennox-Gastaut syndrome before and after intravenous immunoglobulin administration.
Epilepsy research 1994;18(2):139-47.
1994: H L Busard; J P Span; K Renkawek; Willy O Renier; Fons J M Gabreëls; J L Slooff; M A Van 't Hof
Polyglucosan bodies in brain tissue: a systematic study.
Clinical neuropathology 1994;13(2):60-3.
1994: B G M van Engelen; L P de Waal; Corry M R Weemaes; Willy O Renier
Serologic HLA typing in cryptogenic Lennox-Gastaut syndrome.
Epilepsy research 1994;17(1):43-7.
1993: H B van Lieshout; B G M van Engelen; E A Sanders; Willy O Renier
Diagnosing multiple sclerosis in childhood.
Acta neurologica Scandinavica 1993;88(5):339-43.
1993: D J Wijsman; M W Lammers; Yechiel A Hekster; Antoine Keyser; Willy O Renier; Harry Meinardi; H van Lier
Epilepsy treatment in The Netherlands. Comparison of two medical centres.
Acta neurologica Scandinavica 1993;87(6):438-42.
1993: Q H Leyten; Willy O Renier; Fons J M Gabreëls; Henk ter Laak; L H Hinkofer
Dystrophic myopathy of the diaphragm in a neonate with severe respiratory failure during infectious episodes.
Neuromuscular disorders : NMD 1993;3(1):51-5.
1993: Q H Leyten; Henk ter Laak; Fons J M Gabreëls; Willy O Renier; K Renkawek; R C Sengers
Congenital muscular dystrophy. A study on the variability of morphological changes and dystrophin distribution in muscle biopsies.
Acta neuropathologica 1993;86(4):386-92.
1992: Asgeir Haraldsson; B G M van Engelen; Willy O Renier; Jan Bakkeren; Corry M R Weemaes
Light chain ratios and concentrations of serum immunoglobulins in children with epilepsy.
Epilepsy research 1992;13(3):255-60.
1992: Q H Leyten; Fons J M Gabreëls; Willy O Renier; K Renkawek; Henk ter Laak; Reinier A Mullaart
Congenital muscular dystrophy with eye and brain malformations in six Dutch patients.
Neuropediatrics 1992;23(6):316-20.
1992: A A W M Gabreëls-Festen; Fons J M Gabreëls; E M Joosten; H M Vingerhoets; Willy O Renier
Hereditary neuropathy with liability to pressure palsies in childhood.
Neuropediatrics 1992;23(3):138-43.
1992: Ron A Wevers; J R M Cruysberg; A F Van Heijst; F S Janssen-Zijlstra; Willy O Renier; B G M van Engelen; J J M Tolboom
Paediatric cerebrotendinous xanthomatosis.
Journal of inherited metabolic disease 1992;15(3):374-6.
1992: K Renkawek; Willy O Renier; J J de Pont; O J Vogels; Fons J M Gabreëls
Neonatal status convulsivus, spongiform encephalopathy, and low activity of Na+/K(+)-ATPase in the brain.
Epilepsia 1992;33(1):58-64.
1991: D J Wijsman; Yechiel A Hekster; Antoine Keyser; Willy O Renier; Harry Meinardi
Clinimetrics and epilepsy care.
Pharmaceutisch weekblad. Scientific edition 1991;13(4):182-8.
1991: Gilles van Luijtelaar; S F de Bruijn; A C Declerck; Willy O Renier; J M H Vossen; Anton M L Coenen
Disturbances in time estimation during absence seizures in children.
Epilepsy research 1991;9(2):148-53.
1991: H L Busard; A A W M Gabreëls-Festen; Willy O Renier; Fons J M Gabreëls; E M Joosten; M A van 't Hof; J B Rensing
Adult polyglucosan body disease: the diagnostic value of axilla skin biopsy.
Annals of neurology 1991;29(4):448-51.
1991: I F de Coo; Fons J M Gabreëls; Willy O Renier; J J de Pont; U J van Haelst; J H Veerkamp; J M F Trijbels; H H Jaspar; K Renkawek
Canavan disease: neuromorphological and biochemical analysis of a brain biopsy specimen.
Clinical neuropathology 1991;10(2):73-8.
1991: J L van Hellenberg Hubar; Fons J M Gabreëls; Wim Ruitenbeek; R C Sengers; Willy O Renier; H O Thijssen; Henk ter Laak
MELAS syndrome. Report of two patients, and comparison with data of 24 patients derived from the literature.
Neuropediatrics 1991;22(1):10-4.
1991: Q H Leyten; K Renkawek; Willy O Renier; Fons J M Gabreëls; C M Mooy; Henk ter Laak; Reinier A Mullaart
Neuropathological findings in muscle-eye-brain disease (MEB-D). Neuropathological delineation of MEB-D from congenital muscular dystrophy of the Fukuyama type.
Acta neuropathologica 1991;83(1):55-60.
1990: Willy O Renier; K Renkawek
Clinical and neuropathologic findings in a case of severe myoclonic epilepsy of infancy.
Epilepsia 1990;31(3):287-91.
1990: H L Busard; A A W M Gabreëls-Festen; M A van 't Hof; Willy O Renier; Fons J M Gabreëls
Polyglucosan bodies in sural nerve biopsies.
Acta neuropathologica 1990;80(5):554-7.
1990: Peter Praamstra; R A Wevers; Fons J M Gabreëls; J J Rotteveel; Willy O Renier; R C Sengers; Karel J B Lamers
GM2-gangliosidosis. Clinical and biochemical aspects of four cases.
Clinical neurology and neurosurgery 1990;92(2):143-8.
1989: J W Pasman; Fons J M Gabreëls; B Semmekrot; Willy O Renier; L A Monnens
Hyperkalemic periodic paralysis in Gordon's syndrome: a possible defect in atrial natriuretic peptide function.
Annals of neurology 1989;26(3):392-5.
1989: Q H Leyten; Fons J M Gabreëls; Willy O Renier; Henk ter Laak; R C Sengers; Reinier A Mullaart
Congenital muscular dystrophy.
The Journal of pediatrics 1989;115(2):214-21.
1989: H L Busard; Willy O Renier; Fons J M Gabreëls; J M F Trijbels; A J Janssen; Karel J B Lamers
Pyruvate metabolism in Lafora disease.
Epilepsia 1989;30(3):314-7.
1989: P M van Erven; Willy O Renier; Fons J M Gabreëls; H O Thijssen; W Ruitenbeek; Martin Horstink
Hypokinesia and rigidity as clinical manifestations of mitochondrial encephalomyopathy: report of three cases.
Developmental medicine and child neurology 1989;31(1):81-91.
1989: R A Bernsen; H L Busard; Henk ter Laak; Fons J M Gabreëls; Willy O Renier; E M Joosten; A G Theeuwes
Polyglucosan bodies in intramuscular motor nerves.
Acta neuropathologica 1989;77(6):629-33.
1988: Willy O Renier; Fons J M Gabreëls; H H Jaspar
Morphological and biochemical analysis of a brain biopsy in a case of idiopathic Lennox-Gastaut syndrome.
Epilepsia 1988;29(5):644-9.
1988: P M Van Erven; Fons J M Gabreëls; Wim Ruitenbeek; Willy O Renier; Henk ter Laak; A M Stadhouders
A mitochondrial encephalomyopathy with a partial cytochrome c oxidase deficiency of muscle.
Journal of neurology, neurosurgery, and psychiatry 1988;51(5):704-8.
1987: P H Jansen; Willy O Renier; G de Vaan; P Reekers; D M Vingerhoets; Fons J M Gabreëls
Effect of thymectomy on myasthenia gravis and autoimmune thrombocytopenic purpura in a 13-year-old girl.
European journal of pediatrics 1987;146(6):587-9.
1987: Karel J B Lamers; W H Doesburg; Fons J M Gabreëls; A C Romsom; Wim A J G Lemmens; Ron A Wevers; Willy O Renier
CSF concentration and CSF/blood ratio of fuel related components in children after prolonged fasting.
Clinica chimica acta; international journal of clinical chemistry 1987;167(2):135-45.
1987: P M van Erven; Fons J M Gabreëls; Wim Ruitenbeek; Willy O Renier; J C Fischer
Mitochondrial encephalomyopathy. Association with an NADH dehydrogenase deficiency.
Archives of neurology 1987;44(7):775-8.
1987: H L Busard; A A W M Gabreëls-Festen; Willy O Renier; Fons J M Gabreëls; A M Stadhouders
Axilla skin biopsy: a reliable test for the diagnosis of Lafora's disease.
Annals of neurology 1987;21(6):599-601.
1987: P M van Erven; Fons J M Gabreëls; Wim Ruitenbeek; Willy O Renier; Karel J B Lamers; J L Sloof
Familial Leigh's syndrome: association with a defect in oxidative metabolism probably restricted to brain.
Journal of neurology 1987;234(4):215-9.
1987: P M Van Erven; Fons J M Gabreëls; R A Wevers; W H Doesburg; Wim Ruitenbeek; Willy O Renier; Karel J B Lamers
Intravenous pyruvate loading test in Leigh syndrome.
Journal of the neurological sciences 1987;77(2-3):217-27.
1987: P H Jansen; H C Schoonderwaldt; Willy O Renier; R A Wevers; Fons J M Gabreëls
Mannosidosis: a study of two patients, presenting clinical heterogeneity.
Clinical neurology and neurosurgery 1987;89(3):185-92.
1987: P M van Erven; J P Cillessen; E M Eekhoff; Fons J M Gabreëls; W H Doesburg; Wim A J G Lemmens; J L Slooff; Willy O Renier; Wim Ruitenbeek
Leigh syndrome, a mitochondrial encephalo(myo)pathy. A review of the literature.
Clinical neurology and neurosurgery 1987;89(4):217-30.
1987: P J Jongen; Fons J M Gabreëls; J H Stekhoven; Willy O Renier; R le Coultre; J H Begeer
Early infantile form of neuronal ceroid lipofuscinosis. Four Dutch cases and review of the literature.
Clinical neurology and neurosurgery 1987;89(3):161-7.
1987: H L Busard; Willy O Renier; Fons J M Gabreëls; H H Jaspar; J L Slooff; A J Janssen; U J Van Haelst
Lafora disease: a quantitative morphological and biochemical study of the cerebral cortex.
Clinical neuropathology 1987;6(1):1-6.
1986: P M Van Erven; J C Fischer; Fons J M Gabreëls; Willy O Renier; J M F Trijbels; A J Janssen
Defect of NADH dehydrogenase in Leigh syndrome.
Acta neurologica Scandinavica 1986;74(2):167.
1986: B L Busard; Willy O Renier; Fons J M Gabreëls; H H Jaspar; U J van Haelst; J L Slooff
Lafora's disease. Comparison of inclusion bodies in skin and in brain.
Archives of neurology 1986;43(3):296-9.
1986: J C Fischer; Wim Ruitenbeek; Fons J M Gabreëls; A J Janssen; Willy O Renier; Rob C A Sengers; A M Stadhouders; Henk ter Laak; J M F Trijbels; J H Veerkamp
A mitochondrial encephalomyopathy: the first case with an established defect at the level of coenzyme Q.
European journal of pediatrics 1986;144(5):441-4.
1986: P M van Erven; Wim Ruitenbeek; Fons J M Gabreëls; Willy O Renier; J C Fischer; A J Janssen
Disturbed oxidative metabolism in subacute necrotizing encephalomyelopathy (Leigh syndrome).
Neuropediatrics 1986;17(1):28-32.
1986: Q H Leyten; Fons J M Gabreëls; E M Joosten; Willy O Renier; Henk ter Laak; B G Ter Haar; A M Stadhouders
An autosomal dominant type of congenital muscular dystrophy.
Brain & development 1986;8(5):533-7.
1985: Karel J B Lamers; W H Doesburg; Fons J M Gabreëls; Wim A J G Lemmens; A C Romsom; Ron A Wevers; Willy O Renier
The concentration of blood components related to fuel metabolism during prolonged fasting in children.
Clinica chimica acta; international journal of clinical chemistry 1985;152(1-2):155-63.
1985: P M Van Erven; Fons J M Gabreëls; Wim Ruitenbeek; M R Den Hartog; J C Fischer; Willy O Renier; J M F Trijbels; J L Slooff; A J Janssen
Subacute necrotizing encephalomyelopathy (Leigh syndrome) associated with disturbed oxidation of pyruvate, malate and 2-oxoglutarate in muscle and liver.
Acta neurologica Scandinavica 1985;72(1):36-42.
1985: Karel J B Lamers; W H Doesburg; Fons J M Gabreëls; A C Romsom; Willy O Renier; Ron A Wevers; Wim A J G Lemmens
Reference values of blood components related to fuel metabolism in children after an overnight fast.
Clinica chimica acta; international journal of clinical chemistry 1985;145(1):17-26.
1985: C J Stevering; Fons J M Gabreëls; R J Lippens; Willy O Renier; H O Thijssen; H J ter Laak
Treatment of leptomeningeal dissemination of medulloblastoma. Report of a case with a long-term survival.
Clinical neurology and neurosurgery 1985;87(4):291-6.
1984: Fons J M Gabreëls; M J Prick; J M F Trijbels; Willy O Renier; H H Jaspar; A J Janssen; J L Slooff
Defects in citric acid cycle and the electron transport chain in progressive poliodystrophy.
Acta neurologica Scandinavica 1984;70(3):145-54.
1983: Willy O Renier; F A Nabben; T W Hustinx; J H Veerkamp; B J Otten; Henk ter Laak; B G Ter Haar; Fons J M Gabreëls
Congenital adrenal hypoplasia, progressive muscular dystrophy, and severe mental retardation, in association with glycerol kinase deficiency, in male sibs.
Clinical genetics 1983;24(4):243-51.
1983: Willy O Renier; Fons J M Gabreëls; T W Hustinx; H O Thijssen; B G Ter Haar; E W Kroll; H Beckers
Cerebellar hypoplasia, communicating hydrocephalus and mental retardation in two brothers and a maternal uncle.
Brain & development 1983;5(1):41-5.
1983: M G Smits; Fons J M Gabreëls; P G Froeling; R A de Abreu; H O Thijssen; Willy O Renier
Calcium-phosphate metabolism in autosomal recessive idiopathic strio-pallido-dentate calcinosis and Cockayne's syndrome.
Clinical neurology and neurosurgery 1983;85(3):145-53.
1982: M G Smits; Fons J M Gabreëls; Willy O Renier; E M Joosten; A A W M Gabreëls-Festen; Henk ter Laak; Alfred J L G Pinckers; G C Hombergen; S L Notermans; H O Thijssen
Peripheral and central myelinopathy in Cockayne's syndrome. Report of 3 siblings.
Neuropediatrics 1982;13(3):161-7.
1982: M J Prick; Fons J M Gabreëls; Willy O Renier; J M F Trijbels; J L Willems; A J Janssen; J L Slooff; J A Geelen; J P de Jager
Progressive infantile poliodystrophy (Alpers' disease) with a defect in citric acid cycle activity in liver and fibroblasts.
Neuropediatrics 1982;13(2):108-11.
1982: Willy O Renier; Fons J M Gabreëls; H H Jasper; T W Hustinx; J A Geelen; U J van Haelst
An X-linked syndrome with microcephaly, severe mental retardation, spasticity, epilepsy and deafness.
Journal of mental deficiency research 1982;26(Pt 1):27-40.
1982: P M van Erven; Fons J M Gabreëls; H O Thijssen; Willy O Renier
The Moya-Moya syndrome: a report of two children.
Clinical neurology and neurosurgery 1982;84(3):179-89.
1982: Willy O Renier; B G Ter Haar; J L Slooff; T W Hustinx; Fons J M Gabreëls
X-linked congenital hydrocephalus.
Clinical neurology and neurosurgery 1982;84(2):113-23.
1981: M J Prick; Fons J M Gabreëls; Willy O Renier; J M F Trijbels; R C Sengers; J L Slooff
Progressive infantile poliodystrophy. Association with disturbed pyruvate oxidation in muscle and liver.
Archives of neurology 1981;38(12):767-72.
1981: Willy O Renier; Fons J M Gabreëls; T W Hustinx; H H Jaspar; J A Geelen; U J Van Haelst; E J Lommen; B G Ter Haar
Connatal Pelizaeus-Merzbacher disease with congenital stridor in two maternal cousins.
Acta neuropathologica 1981;54(1):11-7.
1981: S J Duinkerke; J L Slooff; Fons J M Gabreëls; Willy O Renier; H O Thijssen; J H Biesta
Melanotic rhabdomyomedulloblastoma or teratoid tumour of the cerebellar vermis.
Clinical neurology and neurosurgery 1981;83(1):29-33.