Torthaí cuardaigh - Ingrid E. Scheffer

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  1. 1
    Generalized epilepsy with febrile seizures plus. A genetic disorder with heterogeneous clinical phenotypes

    Generalized epilepsy with febrile seizures plus. A genetic disorder with heterogeneous clinical phenotypes de réir Ingrid E. Scheffer

    Foilsithe / Cruthaithe 1997
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  2. 2
    Epilepsy Genetics Revolutionizes Clinical Practice

    Epilepsy Genetics Revolutionizes Clinical Practice de réir Ingrid E. Scheffer

    Foilsithe / Cruthaithe 2014
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  3. 3
    SCN1A‐related phenotypes: Epilepsy and beyond

    SCN1A‐related phenotypes: Epilepsy and beyond de réir Ingrid E. Scheffer, Rima Nabbout

    Foilsithe / Cruthaithe 2019
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  4. 4
    Febrile seizures

    Febrile seizures de réir Lynette G. Sadleir, Ingrid E. Scheffer

    Foilsithe / Cruthaithe 2007
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  5. 5
    The new definition and classification of seizures and epilepsy

    The new definition and classification of seizures and epilepsy de réir Jessica Falco-Walter, Ingrid E. Scheffer, Robert S. Fisher

    Foilsithe / Cruthaithe 2017
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  6. 6
    Defining Dravet syndrome: An essential pre‐requisite for precision medicine trials

    Defining Dravet syndrome: An essential pre‐requisite for precision medicine trials de réir Wenhui Li, Amy L. Schneider, Ingrid E. Scheffer

    Foilsithe / Cruthaithe 2021
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  7. 7
    Genetic literacy series: genetic epilepsy with febrile seizures <i>plus</i>

    Genetic literacy series: genetic epilepsy with febrile seizures <i>plus</i> de réir Kenneth A. Myers, Ingrid E. Scheffer, Samuel F. Berkovic

    Foilsithe / Cruthaithe 2018
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  8. 8
    Natural History Studies and Clinical Trial Readiness for Genetic Developmental and Epileptic Encephalopathies

    Natural History Studies and Clinical Trial Readiness for Genetic Developmental and Epileptic Encephalopathies de réir Elizabeth E. Palmer, Katherine B. Howell, Ingrid E. Scheffer

    Foilsithe / Cruthaithe 2021
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  9. 9
    Benign occipital epilepsies of childhood: clinical features and genetics

    Benign occipital epilepsies of childhood: clinical features and genetics de réir Isabella Taylor, Samuel F. Berkovic, Sara Kivity, Ingrid E. Scheffer

    Foilsithe / Cruthaithe 2008
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  10. 10
    Epidemiology of Developmental and Epileptic Encephalopathy and of Intellectual Disability and Epilepsy in Children

    Epidemiology of Developmental and Epileptic Encephalopathy and of Intellectual Disability and Epilepsy in Children de réir Gemma Poke, James Stanley, Ingrid E. Scheffer, Lynette G. Sadleir

    Foilsithe / Cruthaithe 2022
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  11. 11
    The 2017 ILAE classification of seizure types and the epilepsies: what do people with epilepsy and their caregivers need to know?

    The 2017 ILAE classification of seizure types and the epilepsies: what do people with epilepsy and their caregivers need to know? de réir Martin J. Brodie, Sameer M. Zuberi, Ingrid E. Scheffer, Robert S. Fisher

    Foilsithe / Cruthaithe 2018
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  12. 12
    Lamotrigine can be beneficial in patients with Dravet syndrome

    Lamotrigine can be beneficial in patients with Dravet syndrome de réir Linda J. Dalic, Saul A. Mullen, Eliane Roulet Perez, Ingrid E. Scheffer

    Foilsithe / Cruthaithe 2014
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  13. 13
    Idiopathic Generalized Epilepsy

    Idiopathic Generalized Epilepsy de réir Orrin Devinsky, Christopher Elder, Shobi Sivathamboo, Ingrid E. Scheffer, Matthias J. Koepp

    Foilsithe / Cruthaithe 2023
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  14. 14
    Genetic architecture of childhood speech disorder: a review

    Genetic architecture of childhood speech disorder: a review de réir Angela Morgan, David J. Amor, Miya St John, Ingrid E. Scheffer, Michael S. Hildebrand

    Foilsithe / Cruthaithe 2024
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  15. 15
    EEG features of absence seizures in idiopathic generalized epilepsy: Impact of syndrome, age, and state

    EEG features of absence seizures in idiopathic generalized epilepsy: Impact of syndrome, age, and state de réir Lynette G. Sadleir, Ingrid E. Scheffer, Sherry Smith, Bendix Carstensen, K Farrell, Mary Connolly

    Foilsithe / Cruthaithe 2009
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  16. 16
    <i>GRIN2A</i>

    <i>GRIN2A</i> de réir Samantha J. Turner, Angela Mayes, Andrea Verhoeven, Simone Mandelstam, Angela Morgan, Ingrid E. Scheffer

    Foilsithe / Cruthaithe 2015
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  17. 17
    Stiripentol efficacy and safety in Dravet syndrome: a 12‐year observational study

    Stiripentol efficacy and safety in Dravet syndrome: a 12‐year observational study de réir Kenneth A. Myers, Paul Lightfoot, Shekhar G. Patil, J. Helen Cross, Ingrid E. Scheffer

    Foilsithe / Cruthaithe 2018
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  18. 18
    Practical considerations for the use of fenfluramine to manage patients with Dravet syndrome or Lennox–Gastaut syndrome in clinical practice

    Practical considerations for the use of fenfluramine to manage patients with Dravet syndrome or Lennox–Gastaut syndrome in clinical practice de réir Elaine Wirrell, Lieven Lagae, Ingrid E. Scheffer, J. Helen Cross, Nicola Specchio, Adam Strzelczyk

    Foilsithe / Cruthaithe 2024
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  19. 19
    Channelopathies in Idiopathic Epilepsy

    Channelopathies in Idiopathic Epilepsy de réir Sarah E. Heron, Ingrid E. Scheffer, Samuel F. Berkovic, Leanne M. Dibbens, John C. Mulley

    Foilsithe / Cruthaithe 2007
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  20. 20
    Susceptibility genes for complex epilepsy

    Susceptibility genes for complex epilepsy de réir John C. Mulley, Ingrid E. Scheffer, Louise A. Harkin, Samuel F. Berkovic, Leanne M. Dibbens

    Foilsithe / Cruthaithe 2005
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