检索结果 - Bobby P.C. Koeleman

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  1. 1
    What do genetic studies tell us about the heritable basis of common epilepsy? Polygenic or complex epilepsy?

    What do genetic studies tell us about the heritable basis of common epilepsy? Polygenic or complex epilepsy? 由 Bobby P.C. Koeleman

    出版 2017
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  2. 2
    Efficient Computation of Significance Levels for Multiple Associations in Large Studies of Correlated Data, Including Genomewide Association Studies

    Efficient Computation of Significance Levels for Multiple Associations in Large Studies of Correlated Data, Including Genomewide Association Studies 由 Frank Dudbridge, Bobby P. C. Koeleman

    出版 2004
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  3. 3
    Unbiased Application of the Transmission/Disequilibrium Test to Multilocus Haplotypes

    Unbiased Application of the Transmission/Disequilibrium Test to Multilocus Haplotypes 由 Frank Dudbridge, Bobby P. C. Koeleman, John A. Todd, David Clayton

    出版 2000
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  4. 4
    Differential association of the PTPN22 coding variant with autoimmune diseases in a Dutch population

    Differential association of the PTPN22 coding variant with autoimmune diseases in a Dutch population 由 Alexandra Zhernakova, Peter Eerligh, Cisca Wijmenga, Pilar Barrera, Bart O. Roep, Bobby P. C. Koeleman

    出版 2005
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  5. 5
    Refractory juvenile myoclonic epilepsy: a meta‐analysis of prevalence and risk factors

    Refractory juvenile myoclonic epilepsy: a meta‐analysis of prevalence and risk factors 由 Remi Stevelink, Bobby P.C. Koeleman, Josemir W. Sander, Floor E. Jansen, Kees P. J. Braun

    出版 2018
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  6. 6
    Transfer of Regulatory Properties from Tolerogenic to Proinflammatory Dendritic Cells via Induced Autoreactive Regulatory T Cells

    Transfer of Regulatory Properties from Tolerogenic to Proinflammatory Dendritic Cells via Induced Autoreactive Regulatory T Cells 由 Fleur S. Kleijwegt, Sandra Laban, Gaby Duinkerken, Antoinette M. Joosten, Bobby P. C. Koeleman, Tatjana Nikolić, Bart O. Roep

    出版 2011
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  7. 7
    Carbamazepine‐ and oxcarbazepine‐induced hyponatremia in people with epilepsy

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

    出版 2017
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  8. 8
    KIR in Type 1 Diabetes

    KIR in Type 1 Diabetes 由 Arno R. van der Slik, Bobby P. C. Koeleman, Willem Verduijn, G.J. Bruining, Bart O. Roep, Marius J. Giphart

    出版 2003
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  9. 9
    Implications of genetic diagnostics in epilepsy surgery candidates: A single‐center cohort study

    Implications of genetic diagnostics in epilepsy surgery candidates: A single‐center cohort study 由 Maurits Sanders, Cynthia M C Lemmens, Floor E. Jansen, Eva H. Brilstra, Bobby P.C. Koeleman, Kees P. J. Braun

    出版 2019
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  10. 10
    Epidemiology, pathophysiology and putative genetic basis of carbamazepine‐ and oxcarbazepine‐induced hyponatremia

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

    出版 2016
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  11. 11
    Epilepsy surgery for patients with genetic refractory epilepsy: a systematic review

    Epilepsy surgery for patients with genetic refractory epilepsy: a systematic review 由 Remi Stevelink, Maurits Sanders, Maarten P. Tuinman, Eva H. Brilstra, Bobby P.C. Koeleman, Floor E. Jansen, Kees P. J. Braun

    出版 2018
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  12. 12
    Association of Human Connexin40 Gene Polymorphisms With Atrial Vulnerability as a Risk Factor for Idiopathic Atrial Fibrillation

    Association of Human Connexin40 Gene Polymorphisms With Atrial Vulnerability as a Risk Factor for Idiopathic Atrial Fibrillation 由 Mehran Firouzi, Hemanth Ramanna, Bart Kok, Habo J. Jongsma, Bobby P. C. Koeleman, Pieter A. Doevendans, W. Antoinette Groenewegen, Richard N.W. Hauer

    出版 2004
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  13. 13
    Survival of autoreactive T lymphocytes by microRNA-mediated regulation of apoptosis through TRAIL and Fas in type 1 diabetes

    Survival of autoreactive T lymphocytes by microRNA-mediated regulation of apoptosis through TRAIL and Fas in type 1 diabetes 由 Vincent M. de Jong, Arno R. van der Slik, Sandra Laban, Ruben van ‘t Slot, Bobby P. C. Koeleman, Arnaud Zaldumbide, Bart O. Roep

    出版 2016
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  14. 14
    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 由 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

    出版 2004
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  15. 15
    Influence of contraindicated medication use on cognitive outcome in Dravet syndrome and age at first afebrile seizure as a clinical predictor in <i><scp>SCN</scp>1A</i>‐related seizure phenotypes

    Influence of contraindicated medication use on cognitive outcome in Dravet syndrome and age at first afebrile seizure as a clinical predictor in <i><scp>SCN</scp>1A</i>‐related sei... 由 Iris Lange, Boudewijn Gunning, Anja C. M. Sonsma, Lisette van Gemert, Marjan van Kempen, Nienke E. Verbeek, Joost Nicolai, Nine Knoers, Bobby P.C. Koeleman, Eva H. Brilstra

    出版 2018
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  16. 16
    Outcomes and comorbidities of SCN1A-related seizure disorders

    Outcomes and comorbidities of SCN1A-related seizure disorders 由 Iris Lange, Boudewijn Gunning, Anja C. M. Sonsma, Lisette van Gemert, Marjan van Kempen, Nienke E. Verbeek, Claudia Sinoo, Joost Nicolai, Nine Knoers, Bobby P.C. Koeleman, Eva H. Brilstra

    出版 2018
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  17. 17
    Common Variation in ISL1 Confers Genetic Susceptibility for Human Congenital Heart Disease

    Common Variation in ISL1 Confers Genetic Susceptibility for Human Congenital Heart Disease 由 Kristen N. Stevens, Hákon Hákonarson, Chong Ae Kim, Pieter A. Doevendans, Bobby P. C. Koeleman, Seema Mital, Jennifer Raue, Joseph Glessner, John G. Coles, Vı́ctor Moreno, Anne Granger, Stephen B. Gruber, Peter J. Gruber

    出版 2010
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  18. 18
    Evidence of association of macrophage migration inhibitory factor gene polymorphisms with systemic lupus erythematosus

    Evidence of association of macrophage migration inhibitory factor gene polymorphisms with systemic lupus erythematosus 由 Elena Sánchez, Luis Miguel Gómez, Miguel Ángel López‐Nevot, Miguel Á. González‐Gay, José Mario Sabio, Norberto Ortego‐Centeno, Enrique de Ramón, Juan‐Manuel Anaya, M.F. González‐Escribano, Bobby P. C. Koeleman, Javier Martı́n

    出版 2006
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  19. 19
    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 由 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

    出版 2011
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  20. 20
    Abnormal islet sphingolipid metabolism in type 1 diabetes

    Abnormal islet sphingolipid metabolism in type 1 diabetes 由 Laurits J. Holm, Lars Krogvold, Jane P. Hasselby, Simranjeet Kaur, Laura A. Claessens, Mark A. Russell, Clayton E. Mathews, Kristian F. Hanssen, Noel G. Morgan, Bobby P. C. Koeleman, Bart O. Roep, Ivan Gerling, Flemming Pociot, Knut Dahl‐Jørgensen, Karsten Buschard

    出版 2018
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