Dick Lindhout - Dissemin

Papers authored by Dick Lindhout

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2009 S. von Spiczak, F. Zara, C. G. F. de Kovel, Z. Yapici, Leanne M. Dibbens, Saul Mullen, Heather C. Mefford, Holger Trucks, Tanja Obermeier, Michael Wittig, P. De Jonghe, Zuhal Yapici, H. Hjalgrim, Thomas Sander, J. M. Madsen and 59 other authors

Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance

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Linda Volkers, Martin B. Rook, Joost H. G. Das, Nienke E. Verbeek, W. Antoinette Groenewegen, 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

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Koen L. I. Van Gassen, Marina de Wit, Marian van Kempen, Peter C. van Rijen, Pierre N. E. de Graan, W. Saskia van der Hel, Antony P. Jackson

, Dick Lindhout

Hippocampal Navβ3 expression in patients with temporal lobe epilepsy

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Ingo Helbig, Heather C. Mefford, Andrew J. Sharp, Michel Guipponi, Marco Fichera, Andre Franke, Hiltrud Muhle, Carolien de Kovel

, Carl Baker, Sarah von Spiczak, Katherine L. Kron, Ines Steinich, Verena Gaus, Costin Leu

, Bettina Schmitz and 29 other authors

15q13.3 microdeletions increase risk of idiopathic generalized epilepsy

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This paper was not found in any repository, but could be made available legally by the author.

M. A. van Es, M. A. van Es, F. P. Diekstra, J. H. Veldink, F. Baas, P. R. Bourque, H. J. Schelhaas, E. Strengman, E. A. M. Hennekam, D. Lindhout

, R. A. Ophoff, L. H. van den Berg, L. H. van den Berg

A case of ALS-FTD in a large FALS pedigree with a K17I ANG mutation.

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Dalila Pinto, Dorothée Kasteleijn-Nolst Trenité, Dick Lindhout

Endophenotype Strategy in Epilepsy Genetics

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Ilse Wegner, Peter M. Edelbroek, Saskia Bulk, Dick Lindhout

Lamotrigine kinetics within the menstrual cycle, after menopause, and with oral contraceptives.

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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

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N. Dekker, M. J. A. van Kempen, D. Lindhout

, O. van Nieuwenhuizen, E. H. Brilstra

Epilepsie en het SCN1A-gen

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Tom 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

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K. Flipsen-Ten Berg, A. C. C. van Oppen, J. M. L. Wentges-Van Holthe, S. Bulk, D. Lindhout

Retrospective case series of birth defects can predict malformation patterns associated with prenatal antiepileptic drug exposure

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M. L. Kwee, D. Lindhout

Craniofrontonasal dysplasia: Genetic heterogeneity?

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D. Lindhout

Somatic mosaicism as a basic epileptogenic mechanism?

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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

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Dick Lindhout

Genetic Counseling in a Woman with a Family History of Refractory Myoclonic Epilepsy

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This paper was not found in any repository; the policy of its publisher is unknown or unclear.

N. Dekker, M. J. A. Van Kempen, D. Lindhout

, O. Van Nieuwenhuizen, E. H. Brilstra

Epilepsy and the SCN1A gene | Epilepsie en het SCN1A-gen

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2007 Koen L. I. van Gassen, Marina de Wit, Peter C. van Rijen, Pierre N. E. de Graan, Marian J. A. Groot Koerkamp, Marian J. A. Groot Koerkamp, Marije G. A. Rensen, Frank C. P. Holstege, Dick Lindhout

Possible role of the innate immunity in temporal lobe epilepsy

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Carolien G. F. de Kovel

, Dalila Pinto, Gerrit J. de Haan, Dorothée G. Kasteleijn-Nolst Trenité, Dick Lindhout

, Bobby P. C. Koeleman

Association Analysis of BRD2 (RING3) and Epilepsy in a Dutch Population

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D. E. Fransen van de Putte, D. Lindhout

, H. Y. Kroes

Het syndroom van Joubert: beschrijving, diagnostiek en begeleiding

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D. Black, Jm M. Cobben, R. Gray, R. Didden, D. Lindhout

, Rr R. Pereira, J. Henderson, H. van Wieringen, P. Brocklehurst

Low levels of prenatal alcohol exposure can cause fetal damage

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Papers authored by Dick Lindhout