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Dick Lindhout

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Magdalena Harakalova; Xavier Jeunemaitre; Irene Joziasse; Dick Lindhout; Jelena Medic; Isaäc J Nijman; Gerard Pals; Martin Poot; Jolien W Roos-Hesselink; Jasper J van der Smagt; Ruben van't Slot; Marjan M Weiss; Marja W Wessels; Edwin Cuppen; Carolien G F de Kovel; Jaap Deckers; Lisa Golmard; Hubert F Baars; Annette F Baas
Incomplete segregation of MYH11 variants with thoracic aortic aneurysms and dissections and patent ductus arteriosus.
Dick Lindhout
Antiepileptic drugs during pregnancy and cognitive outcomes.
J J T van Harssel; Marjan J A van Kempen; N E Verbeek; H Verhelst; R J Vermeulen; S Weckhuysen; W F M Arts; M V de Jonge; Peter De Jonghe; Carolien G F de Kovel; JF de Rijk-van Andel; A Fogarasi; W B Gunning; K Hardies; A C Jansen; A Kelemen; Bobby P C Koeleman; Dick Lindhout; Arvid Suls; Emma van Daalen; Eva H Brilstra
Clinical and genetic aspects of PCDH19-related epilepsy syndromes and the possible role of PCDH19 mutations in males with autism spectrum disorders.

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All Publications

2013: Magdalena Harakalova; Xavier Jeunemaitre; Irene Joziasse; Dick Lindhout; Jelena Medic; Isaäc J Nijman; Gerard Pals; Martin Poot; Jolien W Roos-Hesselink; Jasper J van der Smagt; Ruben van't Slot; Marjan M Weiss; Marja W Wessels; Edwin Cuppen; Carolien G F de Kovel; Jaap Deckers; Lisa Golmard; Hubert F Baars; Annette F Baas
Incomplete segregation of MYH11 variants with thoracic aortic aneurysms and dissections and patent ductus arteriosus.
European journal of human genetics : EJHG 2013;21(5):487-93.
2013: Dick Lindhout
Antiepileptic drugs during pregnancy and cognitive outcomes.
Lancet neurology 2013;12(3):219-20.
2013: J J T van Harssel; Marjan J A van Kempen; N E Verbeek; H Verhelst; R J Vermeulen; S Weckhuysen; W F M Arts; M V de Jonge; Peter De Jonghe; Carolien G F de Kovel; JF de Rijk-van Andel; A Fogarasi; W B Gunning; K Hardies; A C Jansen; A Kelemen; Bobby P C Koeleman; Dick Lindhout; Arvid Suls; Emma van Daalen; Eva H Brilstra
Clinical and genetic aspects of PCDH19-related epilepsy syndromes and the possible role of PCDH19 mutations in males with autism spectrum disorders.
Neurogenetics 2013;14(1):23-34.
2012: Anca E Rapcencu; Dick Lindhout; Saskia Bulk
Frequently asked questions on epilepsy, pregnancy and lactation: a EURAP-NL report.
Seizure : the journal of the British Epilepsy Association 2012;21(8):606-9.
2012: Marie-José van den Boogaard; Annemarie H Van Der Hout; Yvon Bronkhorst; Marijn Créton; Marco S Cune; Eric Hennekam; Dick Lindhout; Hans Kristian Ploos van Amstel
Mutations in WNT10A are present in more than half of isolated hypodontia cases.
Journal of medical genetics 2012;49(5):327-31.
2012: Sietske H G Kevelam; Dick Lindhout; Martin Poot; Nienke E Verbeek; Ellen van Binsbergen; Kees P J Braun; Floor E Jansen; Eva H Brilstra
Copy number variations in patients with electrical status epilepticus in sleep.
Journal of child neurology 2012;27(2):178-82.
2011: Linda Volkers; Paul Augustijn; Joost H G Das; Alfred L George; Kristopher M Kahlig; Bobby P C Koeleman; Dick Lindhout; Hans Stroink; Marjan J A van Kempen; Onno Van Nieuwenhuizen; Nienke E Verbeek; Martin B Rook
Nav 1.1 dysfunction in genetic epilepsy with febrile seizures-plus or Dravet syndrome.
The European journal of neuroscience 2011;34(8):1268-75.
2011: Hester Y Kroes; Dick Lindhout; Dorien T Lugtenberg; Rutger A J Nievelstein; Anneke I den Hollander; Ron Hochstenbach; Onno Van Nieuwenhuizen; Martin Poot
Chromosomal abnormalities resembling Joubert syndrome: two cases illustrating the diagnostic pitfalls.
Clinical dysmorphology 2011;20(3):136-42.
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: Hester Y Kroes; Bert G A Van Zanten; Sander A De Ru; Maartje Boon; Grazia M S Mancini; Marjo S van der Knaap; Bwee Tien Poll-The; Dick Lindhout
Is hearing loss a feature of Joubert syndrome, a ciliopathy?
International journal of pediatric otorhinolaryngology 2010;74(9):1034-8.
2010: Sarah von Spiczak; Hiltrud Muhle; Ingo Helbig; Carolien G F de Kovel; Jochen Hampe; Verena Gaus; Bobby P C Koeleman; Dick Lindhout; Stefan Schreiber; Thomas Sander; Ulrich Stephani
Association study of TRPC4 as a candidate gene for generalized epilepsy with photosensitivity.
Neuromolecular medicine 2010;12(3):292-9.
2010: Carolien G F de Kovel; Dalila Pinto; U Tauer; S Lorenz; H Muhle; C Leu; B A Neubauer; A Hempelmann; Petra M.C. Callenbach; I E Scheffer; S F Berkovic; Gabrielle Rudolf; P Striano; A Siren; B Baykan; T Sander; Dick Lindhout; Dorothée G A Kasteleijn-Nolst Trenité; U Stephani; Bobby P C Koeleman
Whole-genome linkage scan for epilepsy-related photosensitivity: a mega-analysis.
Epilepsy research 2010;89(2-3):286-94.
2010: Elisabeth Siti Herini; Marjan J A van Kempen; Surini Yusoff; SY Patria; Masafumi Matsuo; Dick Lindhout; Hisahide Nishio
Novel SCN1A mutations in Indonesian patients with severe myoclonic epilepsy in infancy.
Pediatrics international : official journal of the Japan Pediatric Society 2010;52(2):234-9.
2010: Hester van Wieringen; T G W Letteboer; Rob Rodrigues Pereira; Sanne de Ruiter; W A F Balemans; Dick Lindhout
[Diagnosis of fetal alcohol spectrum disorders].
Nederlands tijdschrift voor geneeskunde 2010;154():A331.
2009: Ilse Wegner; Peter M Edelbroek; Saskia Bulk; Dick Lindhout
Lamotrigine kinetics within the menstrual cycle, after menopause, and with oral contraceptives.
Neurology 2009;73(17):1388-93.
2009: Linda Volkers; Martin B Rook; Joost H G Das; Nienke E Verbeek; W Antoinette Groenewegen; Marjan J A van Kempen; Dick Lindhout; Bobby P C Koeleman
Functional analysis of novel KCNQ2 mutations found in patients with Benign Familial Neonatal Convulsions.
Neuroscience letters 2009;462(1):24-9.
2009: Koen L I van Gassen; Marina de Wit; Marian van Kempen; W Saskia van der Hel; Peter C van Rijen; Antony P Jackson; Dick Lindhout; Pierre N E de Graan
Hippocampal Nabeta3 expression in patients with temporal lobe epilepsy.
Epilepsia 2009;50(4):957-62.
2009: M A van Es; F P Diekstra; Jan Veldink; Frank Baas; P R Bourque; H Jurgen Schelhaas; Eric Strengman; E A M Hennekam; Dick Lindhout; Roel A Ophoff; Leonard H Van den Berg
A case of ALS-FTD in a large FALS pedigree with a K17I ANG mutation.
Neurology 2009;72(3):287-8.
2008: Marie-José H van den Boogaard; Dominique de Costa; Ingrid P C Krapels; Fan Liu; Cock van Duijn; Richard J Sinke; Dick Lindhout; Régine P M Steegers-Theunissen
The MSX1 allele 4 homozygous child exposed to smoking at periconception is most sensitive in developing nonsyndromic orofacial clefts.
Human genetics 2008;124(5):525-34.
2008: T G W Letteboer; Hans-Jurgen Mager; Repke J Snijder; Dick Lindhout; Hans-Kristian Ploos van Amstel; Pieter Zanen; Kees J J Westermann
Genotype-phenotype relationship for localization and age distribution of telangiectases in hereditary hemorrhagic telangiectasia.
American journal of medical genetics. Part A 2008;146A(21):2733-9.
2008: Koen L I van Gassen; Marina de Wit; Marian Groot Koerkamp; Marije G A Rensen; Peter C van Rijen; Frank C P Holstege; Dick Lindhout; P N E De Graan
Possible role of the innate immunity in temporal lobe epilepsy.
Epilepsia 2008;49(6):1055-65.
2008: Dick Lindhout
Somatic mosaicism as a basic epileptogenic mechanism?
Brain : a journal of neurology 2008;131(Pt 4):900-1.
2008: Hester Y Kroes; Patrick H A van Zon; Dietje Fransen van de Putte; Marcel R Nelen; Rutger-Jan Nievelstein; Dienke Wittebol-Post; Onno Van Nieuwenhuizen; Grazia M S Mancini; Marjo S van der Knaap; Mei Lan Kwee; Saskia M Maas; Jan Maarten Cobben; Jacques E E De Nef; Dick Lindhout; Richard J Sinke
DNA analysis of AHI1, NPHP1 and CYCLIN D1 in Joubert syndrome patients from the Netherlands.
European journal of medical genetics 2008;51(1):24-34.
2007: Carolien G F de Kovel; Dalila Pinto; Gerrit-Jan de Haan; Dorothée G A Kasteleijn-Nolst Trenité; Dick Lindhout; Bobby P C Koeleman
Association analysis of BRD2 (RING3) and epilepsy in a Dutch population.
Epilepsia 2007;48(11):2191-2.
2007: D Black; J M Cobben; R Didden; Dick Lindhout; R R Pereira; H van Wieringen
Low levels of prenatal alcohol exposure can cause fetal damage.
BJOG : an international journal of obstetrics and gynaecology 2007;114(6):778-9; author reply 779.
2007: Dalila Pinto; Dorothée G A Kasteleijn-Nolst Trenité; Heather J Cordell; Manuel Mattheisen; Konstantin Strauch; Dick Lindhout; Bobby P C Koeleman
Explorative two-locus linkage analysis suggests a multiplicative interaction between the 7q32 and 16p13 myoclonic seizures-related photosensitivity loci.
Genetic epidemiology 2007;31(1):42-50.
2006: Dalila Pinto; Sandrien Louwaars; Birgit Westland; Linda Volkers; Gerrit-Jan de Haan; Dorothée G A Kasteleijn-Nolst Trenité; Dick Lindhout; Bobby P C Koeleman
Heterogeneity at the JME 6p11-12 locus: absence of mutations in the EFHC1 gene in linked Dutch families.
Epilepsia 2006;47(10):1743-6.
2006: Anne Hempelmann; Kirsten P Taylor; Armin Heils; Susanne Lorenz; Jean-François Prud'homme; Rima Nabbout; Olivier Dulac; Gabrielle Rudolf; Federico Zara; Amedeo Bianchi; Robert Robinson; R Mark Gardiner; Athanasios Covanis; Dick Lindhout; Ulrich Stephani; Christian E Elger; Yvonne G Weber; Holger Lerche; Peter Nürnberg; Katherine L Kron; Ingrid E Scheffer; John C Mulley; Samuel F Berkovic; Thomas Sander
Exploration of the genetic architecture of idiopathic generalized epilepsies.
Epilepsia 2006;47(10):1682-90.
2006: Gerrit-Jan de Haan; Dalila Pinto; Dietbrandt Carton; Adri Bader; Jorine Witte; Edith Peters; Gerard van Erp; Willem Vandereyken; Eduard H J F Boezeman; Martin C Wapenaar; Paul Boon; D J J Halley; Bobby P C Koeleman; Dick Lindhout
A novel splicing mutation in KCNQ2 in a multigenerational family with BFNC followed for 25 years.
Epilepsia 2006;47(5):851-9.
2006: T G W Letteboer; Johannes J Mager; Repke J Snijder; Bobby P C Koeleman; Dick Lindhout; JK Ploos van Amstel; Cornelius J J Westermann
Genotype-phenotype relationship in hereditary haemorrhagic telangiectasia.
Journal of medical genetics 2006;43(4):371-7.
2006: Gerrit-Jan de Haan; Dalila Pinto; Ed Bertram; Dorothée G A Kasteleijn-Nolst Trenité; Bobby P C Koeleman; Dick Lindhout
Oligogenic inheritance in photosensitive juvenile myoclonic epilepsy?
Epileptic disorders : international epilepsy journal with videotape 2006;8(1):32-6.
2006: Benno Bonke; Aad Tibben; Dick Lindhout; Theo Stijnen
Calculating risk changes after negative mutation test outcomes for autosomal dominant hereditary late-onset disorders.
Heredity 2006;96(3):259-61.
2005: Gerrit-Jan de Haan; Dorothee Kasteleijn-Nolst Trenité; Hans Stroink; Jaime Parra; Rob Voskuyl; Marian van Kempen; Dick Lindhout; Ed Bertram
Monozygous twin brothers discordant for photosensitive epilepsy: first report of possible visual priming in humans.
Epilepsia 2005;46(9):1545-9.
2005: J M Cobben; Dick Lindhout
[Lithium, a potentially dangerous drug].
Nederlands tijdschrift voor geneeskunde 2005;149(28):1599.
2005: Dalila Pinto; Gerrit-Jan de Haan; D Carton; Adri Bader; Jorine Witte; E Peters; M Gerard van Erp; W Vandereyken; Eduard H J F Boezeman; P Boon; D J J Halley; Bobby P C Koeleman; Dick Lindhout
Gene symbol: KCNQ2. Disease: Benign neonatal familial convulsion.
Human genetics 2005;117(2-3):300.
2005: Klara ten Berg; E Bettina Samrén; A C C van Oppen; Martijn Engelsman; Dick Lindhout
Levetiracetam use and pregnancy outcome.
Reproductive toxicology (Elmsford, N.Y.) 2005;20(1):175-8.
2005: Benno Bonke; Aad Tibben; Dick Lindhout; Angus J Clarke; Theo Stijnen
Genetic risk estimation by healthcare professionals.
The Medical journal of Australia 2005;182(3):116-8.
2005: Klara ten Berg; A C C van Oppen; Peter Nikkels; A C Gittenberger-de Groot; G B van der Voet; E H Brilstra; Dick Lindhout
Complex cardiac defect with hypoplastic right ventricle in a fetus with valproate exposure.
Prenatal diagnosis 2005;25(2):156-8.
2005: Kirsi Alakurtti; Ekkehard Weber; Riitta Rinne; Gerit Theil; Gerrit-Jan de Haan; Dick Lindhout; Paula Salmikangas; Pekka Saukko; Ulla Lahtinen; Anna-Elina Lehesjoki
Loss of lysosomal association of cystatin B proteins representing progressive myoclonus epilepsy, EPM1, mutations.
European journal of human genetics : EJHG 2005;13(2):208-15.
2005: Mark Nellist; Ozgur Sancak; Miriam A Goedbloed; M van Veghel-Plandsoen; anneke maat-kievit; Dick Lindhout; Bert H J Eussen; Annelies de Klein; D J J Halley; Ans M W van den Ouweland
Large deletion at the TSC1 locus in a family with tuberous sclerosis complex.
Genetic testing 2005;9(3):226-30.
2005: Dalila Pinto; Birgit Westland; Gerrit-Jan de Haan; Gabrielle Rudolf; Berta Martins da Silva; Edouard Hirsch; Dick Lindhout; Dorothée G A Kasteleijn-Nolst Trenité; Bobby P C Koeleman
Genome-wide linkage scan of epilepsy-related photoparoxysmal electroencephalographic response: evidence for linkage on chromosomes 7q32 and 16p13.
Human molecular genetics 2005;14(1):171-8.
2005: T G W Letteboer; Richard Zewald; E J Kamping; G de Haas; Johannes J Mager; Repke J Snijder; Dick Lindhout; F A M Hennekam; Cornelius J J Westermann; JK Ploos van Amstel
Hereditary hemorrhagic telangiectasia: ENG and ALK-1 mutations in Dutch patients.
Human genetics 2005;116(1-2):8-16.
2004: Torbjörn Tomson; Dina Battino; Erminio Bonizzoni; John Craig; Dick Lindhout; Emilio Perucca; Anne Sabers; Frank Vajda
EURAP: an international registry of antiepileptic drugs and pregnancy.
Epilepsia 2004;45(11):1463-4.
2004: Gerrit-Jan de Haan; D J J Halley; Jan C Doelman; Huibert H Geesink; Paul B Augustijn; Anke D Jager-Jongkind; Marianne Majoie; Adri J Bader; Lian A W M Leliefeld-Ten Doeschate; Wout Deelen; Ed Bertram; Anna E Lehesjoki; Dick Lindhout
Univerricht-Lundborg disease: underdiagnosed in the Netherlands.
Epilepsia 2004;45(9):1061-3.
2004: Gerrit-Jan de Haan; Peter M Edelbroek; J Segers; Martijn Engelsman; Dick Lindhout; M Dévilé-Notschaele; Paul B Augustijn
Gestation-induced changes in lamotrigine pharmacokinetics: a monotherapy study.
Neurology 2004;63(3):571-3.
2004: Dalila Pinto; Gerrit-Jan de Haan; Guus A M A J Janssen; Eduard H J F Boezeman; M Gerard van Erp; Birgit Westland; Jorine Witte; Adri Bader; D J J Halley; Dorothée G A Kasteleijn-Nolst Trenité; Dick Lindhout; Bobby P C Koeleman
Evidence for linkage between juvenile myoclonic epilepsy-related idiopathic generalized epilepsy and 6p11-12 in Dutch families.
Epilepsia 2004;45(3):211-7.
2004: Ulrich Stephani; Ulrike Tauer; Bobby Koeleman; Dalila Pinto; Bernd A Neubauer; Dick Lindhout
Genetics of photosensitivity (photoparoxysmal response): a review.
Epilepsia 2004;45 Suppl 1():19-23.
2003: Petra M.C. Callenbach; Arn van den Maagdenberg; Jouke-Jan Hottenga; Eelke H van den Boogerd; René F M de Coo; Dick Lindhout; Rune R Frants; Lodewijk A Sandkuijl; Oebele F Brouwer
Familial partial epilepsy with variable foci in a Dutch family: clinical characteristics and confirmation of linkage to chromosome 22q.
Epilepsia 2003;44(10):1298-305.
2003: AK Mostert; PF Dijkstra; B R H Jansen; JR van Horn; Bianca de Graaf; Peter Heutink; Dick Lindhout
Familial multiple epiphyseal dysplasia due to a matrilin-3 mutation: further delineation of the phenotype including 40 years follow-up.
American journal of medical genetics. Part A 2003;120A(4):490-7.
2003: Johannes M W van ven Ouweland; Kim Cryns; Ronald Pennings; Inge Walraven; George M C Janssen; J Antonie Maassen; Bernard F E Veldhuijzen; Alexander B Arntzenius; Dick Lindhout; Cor W R J Cremers; Guy Van Camp; Lambert D Dikkeschei
Molecular characterization of WFS1 in patients with Wolfram syndrome.
The Journal of molecular diagnostics : JMD 2003;5(2):88-95.
2003: Thomas Sander; Christine Windemuth; Herbert Schulz; Kathrin Saar; Elena Gennaro; Concetta Riggio; Amedeo Bianchi; Federico Zara; Gabrielle Rudolf; Fabienne Picard; Christine Bulteau; Anna Kaminska; Cécile Cieuta; Jean-François Prud'homme; Olivier Dulac; Louise Bate; Robert Robinson; R Mark Gardiner; Athanasios Covanis; Gerrit-Jan de Haan; Guus A M A J Janssen; M Gerard van Erp; Eduard H J F Boezeman; Dick Lindhout; Armin Heils; Peter Nürnberg; Dieter Janz
Exploration of a putative susceptibility locus for idiopathic generalized epilepsy on chromosome 8p12.
Epilepsia 2003;44(1):32-9.
2002: E Anderson; S Berkovic; O Dulac; M Gardiner; S Jain; M Laue Friis; Dick Lindhout; Jeffrey L Noebels; R Ottman; A Scaramelli; J Serratosa; Ortrud K Steinlein; G Avanzini; J Bailey-Wilson; L Cardon; R Fischbach; Katrina Gwinn-Hardy; Mark Leppert; J Ott; K Lindblad-Toh; K Weiss; M Laue-Friis
ILAE genetics commission conference report: molecular analysis of complex genetic epilepsies.
Epilepsia 2002;43(10):1262-7.
2002: Christine Windemuth; Herbert Schulz; Kathrin Saar; Elena Gennaro; Amedeo Bianchi; Federico Zara; Christine Bulteau; Anna Kaminska; Dorothée Ville; Cécile Cieuta; R Nabbout-Tarantino; Jean-François Prud'homme; Olivier Dulac; Louise Bate; R Mark Gardiner; Dick Lindhout; Thomas F Wienker; Dieter Janz; Thomas Sander
No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 5 in families with typical absence seizures.
Epilepsy research 2002;51(1-2):23-9.
2002: Benno Bonke; Aad Tibben; Dick Lindhout; Theo Stijnen
Favourable mutation test outcomes for individuals at risk for Huntington disease change the perspectives of first-degree relatives.
Human genetics 2002;111(3):297-8.
2002: Thomas Sander; Christine Windemuth; Herbert Schulz; Kathrin Saar; Elena Gennaro; Amedeo Bianchi; Federico Zara; Christine Bulteau; Anna Kaminska; Dorothée Ville; Cécile Cieuta; Jean-François Prud'homme; Olivier Dulac; Louise Bate; R Mark Gardiner; Gerrit-Jan de Haan; Guus A M A J Janssen; Jorine Witte; D J J Halley; Dick Lindhout; Thomas F Wienker; Dieter Janz
No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 18q21.1.
American journal of medical genetics 2002;114(6):673-8.
2002: Mieke M van Haelst; H J F M M Eussen; F Visscher; J L M de Ruijter; Stenvert L S Drop; Dick Lindhout; Cokkie H Wouters; L C P Govaerts
Silver-Russell phenotype in a patient with pure trisomy 1q32.1-q42.1: further delineation of the pure 1q trisomy syndrome.
Journal of medical genetics 2002;39(8):582-5.
2002: AK Mostert; PF Dijkstra; JR van Horn; B R H Jansen; Peter Heutink; Dick Lindhout
[Radiologische Besonderheiten einer bilateral vererblichen Mikro-Epiphysendysplasie - deutliche Entität einer Skelettdysplasie].
RöFo : Fortschritte auf dem Gebiete der Röntgenstrahlen und der Nuklearmedizin 2002;174(7):887-92.
2002: Klara ten Berg; Dick Lindhout
Concordance as well as discordance for congenital malformations in valproate-exposed half-siblings with parental consanguinity may indicate a specific gene-teratogen interaction.
Clinical dysmorphology 2002;11(3):227-8; author reply 229-30.
2002: Gerrit-Jan de Haan; D J J Halley; Wout Deelen; Dick Lindhout
[From gene to disease; progressive myoclonus epilepsy of Unverricht-Lundborg and mutations in the cystatin B gene].
Nederlands tijdschrift voor geneeskunde 2002;146(18):846-8.
2002: Bart P C van de Warrenburg; Richard J Sinke; C C Verschuuren-Bemelmans; Hans Scheffer; Ewout R Brunt; PF Ippel; JA Maat-Kievit; Dennis Dooijes; Nicolette C Notermans; Dick Lindhout; Nine V A M Knoers; H P H Kremer
Spinocerebellar ataxias in the Netherlands: prevalence and age at onset variance analysis.
Neurology 2002;58(5):702-8.
2002: Klara ten Berg; Dick Lindhout
Antiepileptic drugs in pregnancy: options for the prevention of congenital abnormalities.
Community genetics 2002;5(1):40-9.
2002: Petra M.C. Callenbach; René F M de Coo; Alla A Vein; W F M Arts; Jan C Oosterwijk; Gerard Hageman; Robert ten Houten; Gisela M Terwindt; Dick Lindhout; Rune R Frants; Oebele F Brouwer
Benign familial infantile convulsions: a clinical study of seven Dutch families.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2002;6(5):269-83.
2002: AK Mostert; B R H Jansen; PF Dijkstra; E Wesby-van Swaay; JR van Horn; Peter Heutink; Dick Lindhout
Bilateral hereditary micro-epiphyseal dysplasia: further delineation of the phenotype with 40 years follow-up.
International orthopaedics 2002;26(3):188-93.
2001: Mieke M van Haelst; Diane Van Opstal; Dick Lindhout; Frans J Los
Management of prenatally detected trisomy 8 mosaicism.
Prenatal diagnosis 2001;21(12):1075-8.
2001: Miriam A Goedbloed; Mark Nellist; Brenda Verhaaf; Arnold J J Reuser; Dick Lindhout; Lone Sunde; Senno Verhoef; D J J Halley; Ans M W van den Ouweland
Analysis of TSC2 stop codon variants found in tuberous sclerosis patients.
European journal of human genetics : EJHG 2001;9(11):823-8.
2001: Senno Verhoef; Dick Lindhout; D J J Halley; Ans M W van den Ouweland
[From gene to disease; TSC1 and TSC2 genes and tuberous sclerosis complex].
Nederlands tijdschrift voor geneeskunde 2001;145(40):1928-30.
2001: Paul B Augustijn; J Parra; C H Wouters; P Joosten; Dick Lindhout; W van Emde Boas
Ring chromosome 20 epilepsy syndrome in children: electroclinical features.
Neurology 2001;57(6):1108-11.
2001: Anja Wagner; Yvonne M C Hendriks; E Johanna Meijers-Heijboer; Wiljo J F De Leeuw; Hans Morreau; Robert M W Hofstra; Carli Tops; E Bik; Annette H J T Bröcker-Vriends; Conny A van der Meer; Dick Lindhout; H F A Vasen; Martijn H Breuning; Cees J Cornelisse; C van Krimpen; Martinus F Niermeijer; A H Zwinderman; Juul Wijnen; Riccardo Fodde
Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigree.
Journal of medical genetics 2001;38(5):318-22.
2001: Carla Rosenberg; Cokkie H Wouters; Karoly Szuhai; R Dorland; Peter Pearson; B T Poll-The; R M Colombijn; Martijn H Breuning; Dick Lindhout
A Rett syndrome patient with a ring X chromosome: further evidence for skewing of X inactivation and heterogeneity in the aetiology of the disease.
European journal of human genetics : EJHG 2001;9(3):171-7.
2000: Thomas Sander; Herbert Schulz; Kathrin Saar; Elena Gennaro; M C Riggio; Amedeo Bianchi; Federico Zara; D Luna; Christine Bulteau; Anna Kaminska; Dorothée Ville; Cécile Cieuta; F Picard; Jean-François Prud'homme; Louise Bate; A Sundquist; R Mark Gardiner; Guus A M A J Janssen; Gerrit-Jan de Haan; Dorothée G A Kasteleijn-Nolst Trenité; Adri Bader; Dick Lindhout; Olaf Riess; Thomas F Wienker; Dieter Janz; A Reis
Genome search for susceptibility loci of common idiopathic generalised epilepsies.
Human molecular genetics 2000;9(10):1465-72.
1999: Bert B A de Vries; Bert H J Eussen; Otto P van Diggelen; A van Der Heide; Wout Deelen; L C P Govaerts; Dick Lindhout; Cokkie H Wouters; JO van Hemel
Submicroscopic Xpter deletion in a boy with growth and mental retardation caused by a familial t(X;14).
American journal of medical genetics 1999;87(2):189-94.
1999: E Bettina Samrén; C.M. Duijn; G C Christiaens; Albert Hofman; Dick Lindhout
Antiepileptic drug regimens and major congenital abnormalities in the offspring.
Annals of neurology 1999;46(5):739-46.
1999: Juul Wijnen; Wiljo J F De Leeuw; H F A Vasen; Heleen van der Klift; Pål Møller; Astrid T Stormorken; Hanne Meijers-Heijboer; Dick Lindhout; Fred H Menko; Sandra Vossen; Gabriela Möslein; Carli Tops; Annette H J T Bröcker-Vriends; Y Wu; Robert M W Hofstra; Rolf Sijmons; Cees J Cornelisse; Hans Morreau; Riccardo Fodde
Familial endometrial cancer in female carriers of MSH6 germline mutations.
Nature genetics 1999;23(2):142-4.
1999: Senno Verhoef; L Bakker; AM Tempelaars; AL Hesseling-Janssen; T Mazurczak; S Jozwiak; A Fois; Gabriella Bartalini; B A Zonnenberg; A J van Essen; Dick Lindhout; D J J Halley; Ans M W van den Ouweland
High rate of mosaicism in tuberous sclerosis complex.
American journal of human genetics 1999;64(6):1632-7.
1999: Brage S Andresen; Simon E Olpin; E A Kvittingen; Persefoni Augoustides-Savvopoulou; Dick Lindhout; D J Halley; Christine Vianey-Saban; Ronald J A Wanders; Lodewijk IJlst; Lisbeth Dahl Schroeder; Lars Bolund; Niels Gregersen
DNA-based prenatal diagnosis for very-long-chain acyl-CoA dehydrogenase deficiency.
Journal of inherited metabolic disease 1999;22(3):281-5.
1999: Anne Marie Westerman; MM Entius; E de Baar; P P Boor; R Koole; Marie-Louise F Van Velthuysen; G Johan A Offerhaus; Dick Lindhout; Felix W M de Rooij; J H Paul Wilson
Peutz-Jeghers syndrome: 78-year follow-up of the original family.
Lancet 1999;353(9160):1211-5.
1999: Marjon van Slegtenhorst; Senno Verhoef; AM Tempelaars; L Bakker; Q Wang; Marja W Wessels; R Bakker; Mark Nellist; Dick Lindhout; D J J Halley; Ans M W van den Ouweland
Mutational spectrum of the TSC1 gene in a cohort of 225 tuberous sclerosis complex patients: no evidence for genotype-phenotype correlation.
Journal of medical genetics 1999;36(4):285-9.
1999: Senno Verhoef; R van Diemen-Steenvoorde; W L Akkersdijk; N M Bax; Y Ariyurek; C J Hermans; Onno Van Nieuwenhuizen; Peter Nikkels; Dick Lindhout; D J J Halley; K Lips; Ans M W van den Ouweland
Malignant pancreatic tumour within the spectrum of tuberous sclerosis complex in childhood.
European journal of pediatrics 1999;158(4):284-7.
1999: I E Knol; Margreet G E M Ausems; Dick Lindhout; Otto P van Diggelen; H Verwey; J Davies; JK Ploos van Amstel; Bwee Tien Poll-The
Different phenotypic expression in relatives with fabry disease caused by a W226X mutation.
American journal of medical genetics 1999;82(5):436-9.
1999: José M Serratosa; Pilar Gómez-Garre; M E Gallardo; B Anta; DB de Bernabé; Dick Lindhout; Paul B Augustijn; Carlo Alberto Tassinari; R M Malafosse; M Topcu; Djamel Grid; Charlotte Dravet; Samuel F Berkovic; Santiago Rodríguez de Córdoba
A novel protein tyrosine phosphatase gene is mutated in progressive myoclonus epilepsy of the Lafora type (EPM2).
Human molecular genetics 1999;8(2):345-52.
1999: Anne Marie Westerman; MM Entius; P P Boor; R Koole; E de Baar; G Johan A Offerhaus; J Lubinski; Dick Lindhout; D J Halley; Felix W M de Rooij; J H Paul Wilson
Novel mutations in the LKB1/STK11 gene in Dutch Peutz-Jeghers families.
Human mutation 1999;13(6):476-81.
1998: Juul Wijnen; Heleen van der Klift; H F A Vasen; PM Khan; Fred H Menko; Carli Tops; Hanne Meijers-Heijboer; Dick Lindhout; Pål Møller; Riccardo Fodde
MSH2 genomic deletions are a frequent cause of HNPCC.
Nature genetics 1998;20(4):326-8.
1998: Senno Verhoef; C T Schrander-Stumpel; VD Vuzevski; AM Tempelaars; L A Jansen; G A Malfeyt; T L Ceelen; Dick Lindhout; D J J Halley; Ans M W van den Ouweland
Familial cylindromatosis mimicking tuberous sclerosis complex and confirmation of the cylindromatosis locus, CYLD1, in a large family.
Journal of medical genetics 1998;35(10):841-5.
1998: J Zguricas; D M de Raeymaecker; P J Snijders; A Hoekstra; Dick Lindhout; Steven E R Hovius
Psychomotor development in children with triphalangeal thumbs. A preliminary study.
Journal of hand surgery (Edinburgh, Scotland) 1998;23(4):526-9.
1998: J Zguricas; W F Bakker; HC Heus; Dick Lindhout; Peter Heutink; Steven E R Hovius
Genetics of limb development and congenital hand malformations.
Plastic and reconstructive surgery 1998;101(4):1126-35.
1998: Q Wang; Senno Verhoef; AM Tempelaars; P L Bakker; R Vrtel; AL Hesseling-Janssen; Mark Nellist; Arnold P Oranje; Hans Stroink; Dick Lindhout; D J J Halley; Ans M W van den Ouweland
Identification of a large insertion and two novel point mutations (3671del8 and S1221X) in tuberous sclerosis complex (TSC) patients. Mutations in brief no. 119. Online.
Human mutation 1998;11(4):331-2.
1998: Senno Verhoef; R Vrtel; L Bakker; I Stolte-Dijkstra; Mark Nellist; J H Begeer; J Zaremba; S Jozwiak; AM Tempelaars; Dick Lindhout; D J J Halley; Ans M W van den Ouweland
Recurrent mutation 4882delTT in the GAP-related domain of the tuberous sclerosis TSC2 gene.
Human mutation 1998;Suppl 1():S85-7.
1997: E Bettina Samrén; C.M. Duijn; S Koch; Vilho Hiilesmaa; H Klepel; A H Bardy; G B Mannagetta; A W Deichl; Eija Gaily; Marja-Liisa Granström; H Meinardi; Diederick Grobbee; Albert Hofman; Dieter Janz; Dick Lindhout
Maternal use of antiepileptic drugs and the risk of major congenital malformations: a joint European prospective study of human teratogenesis associated with maternal epilepsy.
Epilepsia 1997;38(9):981-90.
1997: M van Slegtenhorst; R de Hoogt; C Hermans; M Nellist; Bart Janssen; S Verhoef; Dick Lindhout; A van den Ouweland; D Halley; J Young; M Burley; S Jeremiah; K Woodward; J Nahmias; M Fox; R Ekong; J Osborne; J Wolfe; S Povey; R G Snell; J P Cheadle; A C Jones; M Tachataki; D Ravine; J R Sampson; Mary Reeve; P Richardson; F Wilmer; C Munro; T L Hawkins; T Sepp; J B Ali; S Ward; A J Green; J R Yates; J Kwiatkowska; E P Henske; M P Short; J H Haines; S Jozwiak; D J Kwiatkowski
Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34.
Science (New York, N.Y.) 1997;277(5327):805-8.
1997: Gisela M Terwindt; Roel A Ophoff; Dick Lindhout; Joost Haan; D J J Halley; Lodewijk A Sandkuijl; Oebele F Brouwer; Rune R Frants; Michel D Ferrari
Partial cosegregation of familial hemiplegic migraine and a benign familial infantile epileptic syndrome.
Epilepsia 1997;38(8):915-21.
1997: A M Zwamborn-Hanssen; J B Bijlsma; E F Hennekam; Dick Lindhout; Frits A Beemer; E Bakker; W J Kleijer; HF de France; C E M de Die-Smulders; M Duran; A H van Gennip; J T van Mens; P L Pearson; G Mantel; R E Verhage; Joep P M Geraedts
The Dutch Uniform Multicenter Registration system for genetic disorders and malformation syndromes.
American journal of medical genetics 1997;70(4):444-7.
1997: Stefan Mundlos; Florian Otto; C Mundlos; J B Mulliken; Arthur S Aylsworth; S Albright; Dick Lindhout; W G Cole; W Henn; J H Knoll; M J Owen; R Mertelsmann; B U Zabel; B R Olsen
Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia.
Cell 1997;89(5):773-9.
1997: J Zguricas; PF Dijkstra; ES Gelsema; P J Snijders; H P Wüstefeld; H W Venema; Steven E R Hovius; Dick Lindhout
Metacarpophalangeal pattern (MCPP) profile analysis in a family with triphalangeal thumb.
Journal of medical genetics 1997;34(1):55-62.
1996: Roel A Ophoff; Gisela M Terwindt; Monique N Vergouwe; Ronald van Eijk; P J Oefner; S M Hoffman; Jane Lamerdin; Harvey W Mohrenweiser; D E Bulman; M Ferrari; Joost Haan; Dick Lindhout; Gert-Jan B van Ommen; M H Hofker; Michel D Ferrari; Rune R Frants
Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4.
Cell 1996;87(3):543-52.
1996: LM Hart; Dick Lindhout; Gerard C M van der Zon; H Kayserilli; M Y Apak; Wim J Kleijer; E R Van der Vorm; J Antonie Maassen
An insulin receptor mutant (Asp707 --> Ala), involved in leprechaunism, is processed and transported to the cell surface but unable to bind insulin.
The Journal of biological chemistry 1996;271(31):18719-24.
1996: J Seppen; E Steenken; Dick Lindhout; Piter J Bosma; Ronald P J Oude Elferink
A mutation which disrupts the hydrophobic core of the signal peptide of bilirubin UDP-glucuronosyltransferase, an endoplasmic reticulum membrane protein, causes Crigler-Najjar type II.
FEBS letters 1996;390(3):294-8.
1996: J Zguricas; Peter Heutink; L Heredero; J Deurloo; Ben A Oostra; P J Snijders; Dick Lindhout; Steven E R Hovius
Genetic aspects of polydactyly.
Handchirurgie, Mikrochirurgie, plastische Chirurgie : Organ der Deutschsprachigen Arbeitsgemeinschaft für Handchirurgie : Organ der Deutschsprachigen Arbeitsgemeinschaft für Mikrochirurgie der Peripheren Nerven und Gefässe : Organ der Vereinigung der Deutschen Plastischen Chirurgen 1996;28(4):171-5.
1996: Juul Wijnen; PM Khan; H F A Vasen; Fred H Menko; Heleen van der Klift; M van den Broek; I van Leeuwen-Cornelisse; F Nagengast; E J Meijers-Heijboer; Dick Lindhout; Gerrit Griffioen; A Cats; J Kleibeuker; Liliana Varesco; Lucio Bertario; M L Bisgaard; J Mohr; R Kolodner; Riccardo Fodde
Majority of hMLH1 mutations responsible for hereditary nonpolyposis colorectal cancer cluster at the exonic region 15-16.
American journal of human genetics 1996;58(2):300-7.
1996: Dick Lindhout
Epileptogenesis: clinical genetic and genetic epidemiologic aspects.
Epilepsy research. Supplement 1996;12():21-30.
1996: R Vrtel; Senno Verhoef; Katelijne Bouman; MM Maheshwar; Mark Nellist; Anthonie J van Essen; P L Bakker; C J Hermans; M T Bink-Boelkens; R M van Elburg; M Hoff; Dick Lindhout; J Sampson; D J J Halley; Ans M W van den Ouweland
Identification of a nonsense mutation at the 5' end of the TSC2 gene in a family with a presumptive diagnosis of tuberous sclerosis complex.
Journal of medical genetics 1996;33(1):47-51.
1995: Joost Haan; Gisela M Terwindt; Roel A Ophoff; P L Bos; Rune R Frants; Michel D Ferrari; T Krommenhoek; Dick Lindhout; L A Sandkuyl; Ronald van Eijk
Is familial hemiplegic migraine a hereditary form of basilar migraine?
Cephalalgia : an international journal of headache 1995;15(6):477-81.
1995: Piter J Bosma; Jayanta Roy-Chowdhury; C Bakker; S Gantla; A de Boer; B A Oostra; Dick Lindhout; G N Tytgat; Peter L M Jansen; Ronald P J Oude Elferink
The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome.
The New England journal of medicine 1995;333(18):1171-5.
1995: A May; Roel A Ophoff; Gisela M Terwindt; C Urban; Ronald van Eijk; Joost Haan; H C Diener; Dick Lindhout; Rune R Frants; Lodewijk A Sandkuijl
Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without aura.
Human genetics 1995;96(5):604-8.
1995: Peter E M Taschner; NM de Vos; Coriene E Catsman-Berrevoets; Sjoerd G van Duinen; Dick Lindhout; Martijn H Breuning
Application of chromosome 16 markers in the differential diagnosis of neuronal ceroid-lipofuscinosis.
American journal of medical genetics 1995;57(2):338-43.
1995: Senno Verhoef; R Vrtel; T van Essen; L Bakker; E Sikkens; D J J Halley; Dick Lindhout; Ans M W van den Ouweland
Somatic mosaicism and clinical variation in tuberous sclerosis complex.
Lancet 1995;345(8943):202.
1994: A P Bos; A M Pattenier; R E Grobbee; Dick Lindhout; Dick Tibboel; Jan C Molenaar
Etiological aspects of congenital diaphragmatic hernia: results of a case comparison study.
Human genetics 1994;94(4):445-6.
1994: Bart Janssen; J Sampson; M van der Est; Wout Deelen; Senno Verhoef; I Daniels; A Hesseling; P Brook-Carter; Mark Nellist; Dick Lindhout
Refined localization of TSC1 by combined analysis of 9q34 and 16p13 data in 14 tuberous sclerosis families.
Human genetics 1994;94(4):437-40.
1994: J G van Baal; N J Smits; J N Keeman; Dick Lindhout; Senno Verhoef
The evolution of renal angiomyolipomas in patients with tuberous sclerosis.
The Journal of urology 1994;152(1):35-8.
1994: Roel A Ophoff; Ronald van Eijk; Lodewijk A Sandkuijl; Gisela M Terwindt; C P Grubben; Joost Haan; Dick Lindhout; Michel D Ferrari; Rune R Frants
Genetic heterogeneity of familial hemiplegic migraine.
Genomics 1994;22(1):21-6.
1994: J Zguricas; P J Snijders; Steven E R Hovius; Peter Heutink; Ben A Oostra; Dick Lindhout
Phenotypic analysis of triphalangeal thumb and associated hand malformations.
Journal of medical genetics 1994;31(6):462-7.
1994: Dick Lindhout
Waardenburg syndrome and neural tube defects.
American journal of medical genetics 1994;50(4):387.
1994: Peter Heutink; J Zguricas; L van Oosterhout; G J Breedveld; L Testers; Lodewijk A Sandkuijl; P J Snijders; J Weissenbach; Dick Lindhout; Steven E R Hovius
The gene for triphalangeal thumb maps to the subtelomeric region of chromosome 7q.
Nature genetics 1994;6(3):287-92.
1994: Dick Lindhout; J G Omtzigt
Teratogenic effects of antiepileptic drugs: implications for the management of epilepsy in women of childbearing age.
Epilepsia 1994;35 Suppl 4():S19-28.
1993: C C Rietberg; Dick Lindhout
Adult patients with spina bifida cystica: genetic counselling, pregnancy and delivery.
European journal of obstetrics, gynecology, and reproductive biology 1993;52(1):63-70.
1993: Peter Devilee; R S Cornelis; A Bootsma; A Bardoel; Marcel van Vliet; Inge van Leeuwen; F J Cleton; A de Klein; Dick Lindhout; H F A Vasen
Linkage to markers for the chromosome region 17q12-q21 in 13 Dutch breast cancer kindreds.
American journal of human genetics 1993;52(4):730-5.
1993: J N van den Anker; E E van Vught; G R Zandwijken; Titia E Cohen-Overbeek; Dick Lindhout
Severe limb abnormalities: analysis of a cluster of five cases born during a period of 45 days.
American journal of medical genetics 1993;45(5):659-67.
1993: J G Omtzigt; Frans J Los; J W Meijer; Dick Lindhout
The 10,11-epoxide-10,11-diol pathway of carbamazepine in early pregnancy in maternal serum, urine, and amniotic fluid: effect of dose, comedication, and relation to outcome of pregnancy.
Therapeutic drug monitoring 1993;15(1):1-10.
1992: J G Omtzigt; Frans J Los; A M Hagenaars; P A Stewart; E S Sachs; Dick Lindhout
Prenatal diagnosis of spina bifida aperta after first-trimester valproate exposure.
Prenatal diagnosis 1992;12(11):893-7.
1992: Dick Lindhout; H Meinardi; J W Meijer; H Nau
Antiepileptic drugs and teratogenesis in two consecutive cohorts: changes in prescription policy paralleled by changes in pattern of malformations.
Neurology 1992;42(4 Suppl 5):94-110.
1992: Dick Lindhout
Pharmacogenetics and drug interactions: role in antiepileptic-drug-induced teratogenesis.
Neurology 1992;42(4 Suppl 5):43-7.
1992: Dick Lindhout; J G Omtzigt; M C Cornel
Spectrum of neural-tube defects in 34 infants prenatally exposed to antiepileptic drugs.
Neurology 1992;42(4 Suppl 5):111-8.
1992: J M W van den Ouweland; G Jan Bruining; Dick Lindhout; J M Wit; B F Veldhuyzen; J Antonie Maassen
Mutations in mitochondrial tRNA genes: non-linkage with syndromes of Wolfram and chronic progressive external ophthalmoplegia.
Nucleic acids research 1992;20(4):679-82.
1992: E R van der Vorm; Gerard C M van der Zon; W Möller; H Michiel J Krans; Dick Lindhout; J Antonie Maassen
An Arg for Gly substitution at position 31 in the insulin receptor, linked to insulin resistance, inhibits receptor processing and transport.
The Journal of biological chemistry 1992;267(1):66-71.
1992: J G Omtzigt; H Nau; Frans J Los; L Pijpers; Dick Lindhout
The disposition of valproate and its metabolites in the late first trimester and early second trimester of pregnancy in maternal serum, urine, and amniotic fluid: effect of dose, co-medication, and the presence of spina bifida.
European journal of clinical pharmacology 1992;43(4):381-8.
1992: Dick Lindhout; J G Omtzigt
Pregnancy and the risk of teratogenicity.
Epilepsia 1992;33 Suppl 4():S41-8.
1992: Dick Lindhout; T Sander; D J Halley; D G Kasteleijn-Nolst Trenité
In search for genes predisposing to epilepsy: motives and methods.
Acta neurologica Scandinavica. Supplementum 1992;140():51-8.
1991: E R van der Vorm; Dick Lindhout; J M Wit; R J Odink; H Michiel J Krans; J Antonie Maassen
[Molecular heterogeneity of congenital forms of insulin resistance].
Nederlands tijdschrift voor geneeskunde 1991;135(26):1165-70.
1991: L A Janssen; Sue Povey; J Attwood; L A Sandkuyl; Dick Lindhout; P Flodman; M Smith; Julian R Sampson; Jonathan L Haines; E C Merkens
A comparative study on genetic heterogeneity in tuberous sclerosis: evidence for one gene on 9q34 and a second gene on 11q22-23.
Annals of the New York Academy of Sciences 1991;615():306-15.
1991: Dick Lindhout; P G Frets; M F Niermeijer
Approaches to genetic counseling.
Annals of the New York Academy of Sciences 1991;630():223-9.
1990: Helen Brandenburg; M G Jahoda; J W Wladimiroff; Frans J Los; Dick Lindhout
Convulsions in epileptic women after administration of prostaglandin E2 derivative.
Lancet 1990;336(8723):1138.
1990: L A Janssen; L A Sandkuyl; E C Merkens; anneke maat-kievit; Julian R Sampson; P Fleury; R C Hennekam; G C Grosveld; Dick Lindhout; D J J Halley
Genetic heterogeneity in tuberous sclerosis.
Genomics 1990;8(2):237-42.
1990: Hans Stroink; Arnold P Oranje; M Hoff; Dick Lindhout; M H Willems; P Fleury
[Tuberous sclerosis].
Nederlands tijdschrift voor geneeskunde 1990;134(32):1535-40.
1990: J T Brons; HJ van der Harten; Herman P van Geijn; Juriy W Wladimiroff; M F Niermeijer; Dick Lindhout; P A Stuart; Chris J L M Meijer; N F Arts
Prenatal ultrasonographic diagnosis of radial-ray reduction malformations.
Prenatal diagnosis 1990;10(5):279-88.
1990: J Antonie Maassen; Dick Lindhout; A Reuss; Wim J Kleijer
Prenatal analysis of insulin receptor autophosphorylation in a family with leprechaunism.
Prenatal diagnosis 1990;10(1):13-6.
1989: R H Lekanne Deprez; B J Potter van Loon; Gerard C M van der Zon; W Möller; Dick Lindhout; M P Klinkhamer; H Michiel J Krans; J Antonie Maassen
Individuals with only one allele for a functional insulin receptor have a tendency to hyperinsulinaemia but not to hyperglycaemia.
Diabetologia 1989;32(10):740-4.
1989: M P Klinkhamer; N A Groen; Gerard C M van der Zon; Dick Lindhout; L A Sandkuyl; H Michiel J Krans; W Möller; J Antonie Maassen
A leucine-to-proline mutation in the insulin receptor in a family with insulin resistance.
The EMBO journal 1989;8(9):2503-7.
1989: A Reuss; J C den Hollander; Martinus F Niermeijer; Juriy W Wladimiroff; Otto P van Diggelen; Dick Lindhout; Frans J Los
Prenatal diagnosis of cystic kidney disease with ventriculomegaly: a report of six cases in two related sibships.
American journal of medical genetics 1989;33(3):385-9.
1988: J W Wladimiroff; P A Stewart; A Reuss; E van Swaay; Dick Lindhout; E S Sachs
[Pregnancy and antiepileptic agents; the value of prenatal ultrasonography studies for the detection of congenital malformations].
Nederlands tijdschrift voor geneeskunde 1988;132(32):1486-9.
1988: Gerard Hageman; E P Ippel; F A Beemer; J M de Pater; Dick Lindhout; J Willemse
The diagnostic management of newborns with congenital contractures: a nosologic study of 75 cases.
American journal of medical genetics 1988;30(4):883-904.
1988: J Antonie Maassen; M P Klinkhamer; Gerard C M van der Zon; H Sips; W Möller; H Michiel J Krans; Dick Lindhout; F A Beemer
Fibroblasts from a leprechaun patient have defects in insulin binding and insulin receptor autophosphorylation.
Diabetologia 1988;31(8):612-7.
1988: M L Kwee; Dick Lindhout
Inheritance of cranio-fronto-nasal syndrome.
American journal of medical genetics 1988;30(3):841-2.
1988: R J Moene; M Sobotka-Plojhar; A Oppenheimer-Dekker; Dick Lindhout
Ventricular septal defect with overriding aorta in trisomy-18.
European journal of pediatrics 1988;147(5):556-7.
1988: Dick Lindhout
Valproic acid and congenital malformations.
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 1988;15(2):167.
1988: Juriy W Wladimiroff; P A Stewart; A Reuss; E van Swaay; Dick Lindhout; E S Sachs
The role of ultrasound in the early diagnosis of fetal structural defects following maternal anticonvulsant therapy.
Ultrasound in medicine & biology 1988;14(8):657-60.
1987: Kamlesh Madan; Dick Lindhout; A Palan
Premature centromere division (PCD): a dominantly inherited cytogenetic anomaly.
Human genetics 1987;77(2):193-6.
1987: Dick Lindhout; G Hageman
Amyoplasia congenita-like condition and maternal malathion exposure.
Teratology 1987;36(1):7-9.
1986: Dick Lindhout; D Schmidt
In-utero exposure to valproate and neural tube defects.
Lancet 1986;1(8494):1392-3.
1986: N C Roelvink; Wouter Kamphorst; Dick Lindhout; H Ponssen
Concordant cerebral oligodendroglioma in identical twins.
Journal of neurology, neurosurgery, and psychiatry 1986;49(6):706-8.
1985: Dick Lindhout; Gerard Hageman; F A Beemer; P F Ippel; L Breslau-Siderius; J Willemse
The Pena-Shokeir syndrome: report of nine Dutch cases.
American journal of medical genetics 1985;21(4):655-68.
1985: Dick Lindhout; R P Golding; A H Taets van Amerongen
Fibrodysplasia ossificans progressiva: current concepts and the role of CT in acute changes.
Pediatric radiology 1985;15(3):211-3.
1984: Dick Lindhout; H Meinardi
[Use of valproic acid in pregnancy: an indication for prenatal diagnosis of spina bifida].
Nederlands tijdschrift voor geneeskunde 1984;128(52):2438-40.
1984: Dick Lindhout; H Meinardi
Spina bifida and in-utero exposure to valproate.
Lancet 1984;2(8399):396.
1984: M L Kwee; Dick Lindhout
Craniofrontonasal dysplasia: genetic heterogeneity?
Clinical genetics 1984;26(1):80.
1984: Dick Lindhout; R J Höppener; H Meinardi
Teratogenicity of antiepileptic drug combinations with special emphasis on epoxidation (of carbamazepine).
Epilepsia 1984;25(1):77-83.
1983: M L Kwee; Dick Lindhout
Frontonasal dysplasia, coronal craniosynostosis, pre- and postaxial polydactyly and split nails: a new autosomal dominant mutant with reduced penetrance and variable expression?
Clinical genetics 1983;24(3):200-5.
1983: J J Heimans; Dick Lindhout
Charcot-Marie-Tooth disease.
Journal of medical genetics 1983;20(1):77-8.
1982: Dick Lindhout; H Meinardi
False-negative pregnancy test women taking carbamazepine.
Lancet 1982;2(8296):505.