Torthaí cuardaigh - 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? de réir Bobby P.C. Koeleman

    Foilsithe / Cruthaithe 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 de réir Frank Dudbridge, Bobby P. C. Koeleman

    Foilsithe / Cruthaithe 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 de réir Frank Dudbridge, Bobby P. C. Koeleman, John A. Todd, David Clayton

    Foilsithe / Cruthaithe 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 de réir Alexandra Zhernakova, Peter Eerligh, Cisca Wijmenga, Pilar Barrera, Bart O. Roep, Bobby P. C. Koeleman

    Foilsithe / Cruthaithe 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 de réir Remi Stevelink, Bobby P.C. Koeleman, Josemir W. Sander, Floor E. Jansen, Kees P. J. Braun

    Foilsithe / Cruthaithe 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 de réir Fleur S. Kleijwegt, Sandra Laban, Gaby Duinkerken, Antoinette M. Joosten, Bobby P. C. Koeleman, Tatjana Nikolić, Bart O. Roep

    Foilsithe / Cruthaithe 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 de réir Bianca Berghuis, Job van der Palen, Gerrit‐Jan de Haan, Dick Lindhout, Bobby P.C. Koeleman, Josemir W. Sander

    Foilsithe / Cruthaithe 2017
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  8. 8
    KIR in Type 1 Diabetes

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

    Foilsithe / Cruthaithe 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 de réir Maurits Sanders, Cynthia M C Lemmens, Floor E. Jansen, Eva H. Brilstra, Bobby P.C. Koeleman, Kees P. J. Braun

    Foilsithe / Cruthaithe 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 de réir Bianca Berghuis, Gerrit‐Jan de Haan, Marcel P. H. van den Broek, Josemir W. Sander, Dick Lindhout, Bobby P.C. Koeleman

    Foilsithe / Cruthaithe 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 de réir Remi Stevelink, Maurits Sanders, Maarten P. Tuinman, Eva H. Brilstra, Bobby P.C. Koeleman, Floor E. Jansen, Kees P. J. Braun

    Foilsithe / Cruthaithe 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 de réir Mehran Firouzi, Hemanth Ramanna, Bart Kok, Habo J. Jongsma, Bobby P. C. Koeleman, Pieter A. Doevendans, W. Antoinette Groenewegen, Richard N.W. Hauer

    Foilsithe / Cruthaithe 2004
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  13. 13
    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 de réir 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

    Foilsithe / Cruthaithe 2004
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  14. 14
    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... de réir 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

    Foilsithe / Cruthaithe 2018
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  15. 15
    Outcomes and comorbidities of SCN1A-related seizure disorders

    Outcomes and comorbidities of SCN1A-related seizure disorders de réir 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

    Foilsithe / Cruthaithe 2018
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  16. 16
    Common Variation in ISL1 Confers Genetic Susceptibility for Human Congenital Heart Disease

    Common Variation in ISL1 Confers Genetic Susceptibility for Human Congenital Heart Disease de réir 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

    Foilsithe / Cruthaithe 2010
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  17. 17
    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 de réir 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

    Foilsithe / Cruthaithe 2006
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  18. 18
    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 de réir 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

    Foilsithe / Cruthaithe 2011
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  19. 19
    Abnormal islet sphingolipid metabolism in type 1 diabetes

    Abnormal islet sphingolipid metabolism in type 1 diabetes de réir 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

    Foilsithe / Cruthaithe 2018
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  20. 20
    Genetic correlation between background EEG oscillations and genetic generalized epilepsy

    Genetic correlation between background EEG oscillations and genetic generalized epilepsy de réir Remi Stevelink, Jurjen J. Luykx, Bochao Lin, Costin Leu, Dennis Lal, Alexander Smith, Dick Schijven, Johannes A. Carpay, Koen Rademaker, Roiza A. Rodrigues Baldez, Kees P. J. Braun, Floor E. Jansen, affiliations, Dirk J. A. Smit, Bobby P.C. Koeleman

    Foilsithe / Cruthaithe 2019
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