Search Results - Scheffer, Ingrid E

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  1. 1
    Genetic Testing in Epilepsy: What Should You Be Doing?

    Genetic Testing in Epilepsy: What Should You Be Doing? by Scheffer, Ingrid E.

    Published 2011
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  2. 2
    The Key to FAME: Intronic Repeat Expansions Cause Human Epilepsies

    The Key to FAME: Intronic Repeat Expansions Cause Human Epilepsies by Scheffer, Ingrid E.

    Published 2018
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  3. 3
    Solving the Molecular Basis of the Developmental and Epileptic Encephalopathies: Are We there Yet?

    Solving the Molecular Basis of the Developmental and Epileptic Encephalopathies: Are We there Yet? by Scheffer, Ingrid E.

    Published 2021
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  4. 4
    When Monogenic Isn’t Monogenic—Unravelling the Oligogenic Architecture of the Developmental and Epileptic Encephalopathies

    When Monogenic Isn’t Monogenic—Unravelling the Oligogenic Architecture of the Developmental and Epileptic Encephalopathies by Scheffer, Ingrid E., Liao, Jianxiang

    Published 2019
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  5. 5
    Genetic Contributions to Acquired Epilepsies

    Genetic Contributions to Acquired Epilepsies by Perucca, Piero, Scheffer, Ingrid E.

    Published 2020
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  6. 6
    Febrile seizures

    Febrile seizures by Sadleir, Lynette G, Scheffer, Ingrid E

    Published 2007
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  7. 7
    Therapeutic use of medicinal cannabis in difficult to manage epilepsy

    Therapeutic use of medicinal cannabis in difficult to manage epilepsy by Lawson, John A., Scheffer, Ingrid E.

    Published 2018
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  8. 8
    Reply

    Reply by Mitchell, L. Anne, Scheffer, Ingrid E.

    Published 2007
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  9. 9
    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 by Palmer, Elizabeth E., Howell, Katherine, Scheffer, Ingrid E.

    Published 2021
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  10. 10
    Defining Dravet syndrome: An essential pre‐requisite for precision medicine trials

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

    Published 2021
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  11. 11
    Ectopic Posterior Pituitary Lobe and Periventricular Heterotopia: Cerebral Malformations with the Same Underlying Mechanism?

    Ectopic Posterior Pituitary Lobe and Periventricular Heterotopia: Cerebral Malformations with the Same Underlying Mechanism? by Mitchell, L. Anne, Thomas, Paul Q., Zacharin, Margaret R., Scheffer, Ingrid E.

    Published 2002
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  12. 12
    Dysarthria and broader motor speech deficits in Dravet syndrome

    Dysarthria and broader motor speech deficits in Dravet syndrome by Turner, Samantha J., Brown, Amy, Arpone, Marta, Anderson, Vicki, Morgan, Angela T., Scheffer, Ingrid E.

    Published 2017
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  13. 13
    In silico prioritization based on coexpression can aid epileptic encephalopathy gene discovery

    In silico prioritization based on coexpression can aid epileptic encephalopathy gene discovery by Oliver, Karen L., Lukic, Vesna, Freytag, Saskia, Scheffer, Ingrid E., Berkovic, Samuel F., Bahlo, Melanie

    Published 2016
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  14. 14
    Ion Channels in Genetic Epilepsy: From Genes and Mechanisms to Disease-Targeted Therapies

    Ion Channels in Genetic Epilepsy: From Genes and Mechanisms to Disease-Targeted Therapies by Oyrer, Julia, Maljevic, Snezana, Scheffer, Ingrid E., Berkovic, Samuel F., Petrou, Steven, Reid, Christopher A.

    Published 2018
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  15. 15
    Harnessing Gene Expression Networks to Prioritize Candidate Epileptic Encephalopathy Genes

    Harnessing Gene Expression Networks to Prioritize Candidate Epileptic Encephalopathy Genes by Oliver, Karen L., Lukic, Vesna, Thorne, Natalie P., Berkovic, Samuel F., Scheffer, Ingrid E., Bahlo, Melanie

    Published 2014
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  16. 16
    GRIN2A: An aptly named gene for speech dysfunction

    GRIN2A: An aptly named gene for speech dysfunction by Turner, Samantha J., Mayes, Angela K., Verhoeven, Andrea, Mandelstam, Simone A., Morgan, Angela T., Scheffer, Ingrid E.

    Published 2015
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  17. 17
    Is a microRNA‐328 binding site in PAX6 associated with Rolandic epilepsy?

    Is a microRNA‐328 binding site in PAX6 associated with Rolandic epilepsy? by McGlade, Amelia, Myers, Kenneth A., Berkovic, Samuel F., Scheffer, Ingrid E., Petrovski, Slavé, Hildebrand, Michael S.

    Published 2017
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  18. 18
    Medullary tyrosine hydroxylase catecholaminergic neuronal populations in sudden unexpected death in epilepsy

    Medullary tyrosine hydroxylase catecholaminergic neuronal populations in sudden unexpected death in epilepsy by Patodia, Smriti, Tan, Ian, Ellis, Matthew, Somani, Alyma, Scheffer, Ingrid E., Sisodiya, Sanjay M., Thom, Maria

    Published 2020
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  19. 19
    Familial Clustering of Seizure Types within the Idiopathic Generalized Epilepsies

    Familial Clustering of Seizure Types within the Idiopathic Generalized Epilepsies by Winawer, Melodie R., Marini, Carla, Grinton, Bronwyn E, Rabinowitz, Daniel, Berkovic, Samuel F., Scheffer, Ingrid E., Ottman, Ruth

    Published 2005
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  20. 20
    A systematic review and meta-analysis of 271 PCDH19-variant individuals identifies psychiatric comorbidities, and association of seizure onset and disease severity

    A systematic review and meta-analysis of 271 PCDH19-variant individuals identifies psychiatric comorbidities, and association of seizure onset and disease severity by Kolc, Kristy L, Sadleir, Lynette G, Scheffer, Ingrid E, Ivancevic, Atma, Roberts, Rachel, Pham, Duyen H, Gecz, Jozef

    Published 2018
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