Search Results - Dick Lindhout

Refine Results
  1. 1
    EURAP: An International Registry of Antiepileptic Drugs and Pregnancy

    EURAP: An International Registry of Antiepileptic Drugs and Pregnancy by Torbjörn Tomson, Dina Battino, Erminio Bonizzoni, John Craig, Dick Lindhout, Emilio Perucca, Anne Sabers, Frank Vajda

    Published 2004
    Get full text Get full text
    Carta
    Save to List
    Saved in:
  2. 2
    Seizure control and treatment changes in pregnancy: Observations from the <scp>EURAP</scp> epilepsy pregnancy registry

    Seizure control and treatment changes in pregnancy: Observations from the <scp>EURAP</scp> epilepsy pregnancy registry by Dina Battino, Torbjörn Tomson, Erminio Bonizzoni, John Craig, Dick Lindhout, Anne Sabers, Emilio Perucca, Frank Vajda

    Published 2013
    Get full text
    Artigo
    Save to List
    Saved in:
  3. 3
    Fetal methotrexate syndrome: A systematic review of case reports

    Fetal methotrexate syndrome: A systematic review of case reports by Eline A. Verberne, Emma de Haan, J. Peter van Tintelen, Dick Lindhout, Mieke M. van Haelst

    Published 2019
    Get full text
    Revisão
    Save to List
    Saved in:
  4. 4
    Pregnancy registries: Differences, similarities, and possible harmonization

    Pregnancy registries: Differences, similarities, and possible harmonization by Torbjörn Tomson, Dina Battino, John Craig, Sonia Hernández–Dı́az, Lewis B. Holmes, Dick Lindhout, Jim Morrow, Jacqueline A. French

    Published 2010
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  5. 5
    Antiepileptic drugs and intrauterine death

    Antiepileptic drugs and intrauterine death by Torbjörn Tomson, Dina Battino, Erminio Bonizzoni, John Craig, Dick Lindhout, Emilio Perucca, Anne Sabers, Sanjeev V. Thomas, Frank Vajda

    Published 2015
    Get full text
    Artigo
    Save to List
    Saved in:
  6. 6
    Carbamazepine‐ and oxcarbazepine‐induced hyponatremia in people with epilepsy

    Carbamazepine‐ and oxcarbazepine‐induced hyponatremia in people with epilepsy by Bianca Berghuis, Job van der Palen, Gerrit‐Jan de Haan, Dick Lindhout, Bobby P.C. Koeleman, Josemir W. Sander

    Published 2017
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  7. 7
    Prevalence of SCN1A-Related Dravet Syndrome among Children Reported with Seizures following Vaccination: A Population-Based Ten-Year Cohort Study

    Prevalence of SCN1A-Related Dravet Syndrome among Children Reported with Seizures following Vaccination: A Population-Based Ten-Year Cohort Study by Nienke E. Verbeek, Nicoline van der Maas, Floor E. Jansen, Marjan J. A. van Kempen, Dick Lindhout, Eva H. Brilstra

    Published 2013
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  8. 8
    Epidemiology, pathophysiology and putative genetic basis of carbamazepine‐ and oxcarbazepine‐induced hyponatremia

    Epidemiology, pathophysiology and putative genetic basis of carbamazepine‐ and oxcarbazepine‐induced hyponatremia by Bianca Berghuis, Gerrit‐Jan de Haan, Marcel P. H. van den Broek, Josemir W. Sander, Dick Lindhout, Bobby P.C. Koeleman

    Published 2016
    Get full text
    Revisão
    Save to List
    Saved in:
  9. 9
    Loss of lysosomal association of cystatin B proteins representing progressive myoclonus epilepsy, EPM1, mutations

    Loss of lysosomal association of cystatin B proteins representing progressive myoclonus epilepsy, EPM1, mutations by Kirsi Alakurtti, Ekkehard Weber, Riitta Rinne, Gerit Theil, Gerrit‐Jan de Haan, Dick Lindhout, Paula Salmikangas, Pekka Saukko, Ulla Lahtinen, Anna‐Elina Lehesjoki

    Published 2004
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  10. 10
    A leucine-to-proline mutation in the insulin receptor in a family with insulin resistance.

    A leucine-to-proline mutation in the insulin receptor in a family with insulin resistance. by M. P. Klinkhamer, Nicole A. Groen, Gerard C. van der Zon, Dick Lindhout, L. A. Sandkuyl, H. M. J. Krans, W. Möller, J. A. Maassen

    Published 1989
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  11. 11
    Genome-wide linkage scan of epilepsy-related photoparoxysmal electroencephalographic response: evidence for linkage on chromosomes 7q32 and 16p13

    Genome-wide linkage scan of epilepsy-related photoparoxysmal electroencephalographic response: evidence for linkage on chromosomes 7q32 and 16p13 by Dalila Pinto, Birgit Westland, Gerrit‐Jan de Haan, Gabrielle Rudolf, Berta Martins da Silva, Édouard Hirsch, Dick Lindhout, Dorothee Kasteleijn‐Nolst Trenité, Bobby P.C. Koeleman

    Published 2004
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  12. 12
    Mutational spectrum of the TSC1 gene in a cohort of 225 tuberous sclerosis complex patients: no evidence for genotype-phenotype correlation

    Mutational spectrum of the TSC1 gene in a cohort of 225 tuberous sclerosis complex patients: no evidence for genotype-phenotype correlation by Marjon van Slegtenhorst, Senno Verhoef, A.M.P. Tempelaars, Lida Bakker, Qi Wang, Marja W. Wessels, Remco Bakker, Mark Nellist, Dick Lindhout, Dicky Halley, Ans van den Ouweland

    Published 1999
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  13. 13
    Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without aura

    Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without aura by Arne May, Roel A. Ophoff, Gisela M. Terwindt, Christine Urban, Ronald van Eijk, Joost Haan, H.-C. Diener, Dick Lindhout, Rune R. Frants, Lodewijk A. Sandkuijl, Michel D. Ferrari

    Published 1995
    Get full text
    Artigo
    Save to List
    Saved in:
  14. 14
    The gene for triphalangeal thumb maps to the subtelomeric region of chromosome 7q

    The gene for triphalangeal thumb maps to the subtelomeric region of chromosome 7q by Peter Heutink, Julia Zguricas, Linda van Oosterhout, Guido J. Breedveld, Leon Testers, Lodewijk A. Sandkuijl, Pieter J.L.M. Snijders, Jean Weissenbach, Dick Lindhout, Steven E.R. Hovius, Ben A. Oostra

    Published 1994
    Get full text
    Artigo
    Save to List
    Saved in:
  15. 15
    Novel mutations in theLKB1/STK11 gene in Dutch Peutz-Jeghers families

    Novel mutations in theLKB1/STK11 gene in Dutch Peutz-Jeghers families by Anne Marie Westerman, Mark M. Entius, Patrick P.C. Boor, Rita Koole, Ellen de Baar, G. Johan A. Offerhaus, Jan Lubiński, Dick Lindhout, Dicky Halley, Felix W.M. de Rooij, J. H. P. Wilson

    Published 1999
    Get full text
    Artigo
    Save to List
    Saved in:
  16. 16
    A CASE OF ALS-FTD IN A LARGE FALS PEDIGREE WITH A K17I <i>ANG</i> MUTATION

    A CASE OF ALS-FTD IN A LARGE FALS PEDIGREE WITH A K17I <i>ANG</i> MUTATION by Michael A. van Es, Frank P. Diekstra, Jan H. Veldink, Frank Baas, Pierre R. Bourque, Helenius J. Schelhaas, E Strengman, Eric A. M. Hennekam, Dick Lindhout, Roel A. Ophoff, Leonard H. van den Berg

    Published 2009
    Get full text
    Artigo
    Save to List
    Saved in:
  17. 17
    The Genetic Basis of the Reduced Expression of Bilirubin UDP-Glucuronosyltransferase 1 in Gilbert's Syndrome

    The Genetic Basis of the Reduced Expression of Bilirubin UDP-Glucuronosyltransferase 1 in Gilbert's Syndrome by Piter J. Bosma, Jayanta Roy Chowdhury, Conny Bakker, Shailaja Gantla, Anita de Boer, Ben A. Oostra, Dick Lindhout, Guido N.J. Tytgat, Peter L. M. Jansen, Ronald P.J. Oude Elferink, Namita Roy Chowdhury

    Published 1995
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  18. 18
    Mutations Involving the Transcription Factor CBFA1 Cause Cleidocranial Dysplasia

    Mutations Involving the Transcription Factor CBFA1 Cause Cleidocranial Dysplasia by Stefan Mundlos, F Otto, C Mundlos, John B. Mulliken, A.S Aylsworth, Susan G. Albright, Dick Lindhout, William G. Cole, Wolfram Henn, Joan H.M. Knoll, Michael J. Owen, Roland Mertelsmann, Bernhard Zabel, Bjørn R. Olsen

    Published 1997
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  19. 19
    Maternal Use of Antiepileptic Drugs and the Risk of Major Congenital Malformations: A Joint European Prospective Study of Human Teratogenesis Associated with Maternal Epilepsy

    Maternal Use of Antiepileptic Drugs and the Risk of Major Congenital Malformations: A Joint European Prospective Study of Human Teratogenesis Associated with Maternal Epilepsy by E. Bettina Samrén, Cornelia M. van Duijn, S. Koch, V. Hiilesmaa, H Klepel, A. Bardy, G. Beck Mannagetta, A Deichl, Eija Gaily, I. L. Granström, H. Meinardi, Diederick E. Grobbee, A. Hofman, Diéter Janz, Dick Lindhout

    Published 1997
    Get full text Get full text
    Revisão
    Save to List
    Saved in:
  20. 20
    Nav1.1 dysfunction in genetic epilepsy with febrile seizures-plus or Dravet syndrome

    Nav1.1 dysfunction in genetic epilepsy with febrile seizures-plus or Dravet syndrome by Linda Volkers, Kristopher M. Kahlig, Nienke E. Verbeek, Joost H.G. Das, Marjan J. A. van Kempen, Hans Stroink, Paul B. Augustijn, Onno van Nieuwenhuizen, Dick Lindhout, Alfred L. George, Bobby P.C. Koeleman, Martin B. Rook

    Published 2011
    Get full text
    Artigo
    Save to List
    Saved in:

Search Tools: