Risultati della ricerca - Sameer M. Zuberi

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  1. 1
    A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy

    A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy di Sameer M. Zuberi

    Pubblicazione 1999
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  2. 2
    Dravet syndrome—From epileptic encephalopathy to channelopathy

    Dravet syndrome—From epileptic encephalopathy to channelopathy di Andreas Brunklaus, Sameer M. Zuberi

    Pubblicazione 2014
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  3. 3
    Update on diagnosis and management of childhood epilepsies

    Update on diagnosis and management of childhood epilepsies di Sameer M. Zuberi, Joseph D. Symonds

    Pubblicazione 2015
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  4. 4
    Comorbidities and predictors of health‐related quality of life in Dravet syndrome

    Comorbidities and predictors of health‐related quality of life in Dravet syndrome di Andreas Brunklaus, Liam Dorris, Sameer M. Zuberi

    Pubblicazione 2011
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  5. 5
    Phenotypic spectrum and genetics of <i> <scp>SCN</scp> 2A </i> ‐related disorders, treatment options, and outcomes in epilepsy and beyond

    Phenotypic spectrum and genetics of <i> <scp>SCN</scp> 2A </i> ‐related disorders, treatment options, and outcomes in epilepsy and beyond di Markus Wolff, Andreas Brunklaus, Sameer M. Zuberi

    Pubblicazione 2019
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  6. 6
    Dravet syndrome and its mimics: Beyond <i><scp>SCN</scp>1A</i>

    Dravet syndrome and its mimics: Beyond <i><scp>SCN</scp>1A</i> di Dora Steel, Joseph D. Symonds, Sameer M. Zuberi, Andreas Brunklaus

    Pubblicazione 2017
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  7. 7
    Prognostic, clinical and demographic features in SCN1A mutation-positive Dravet syndrome

    Prognostic, clinical and demographic features in SCN1A mutation-positive Dravet syndrome di Andreas Brunklaus, Rachael Ellis, Eleanor Reavey, GORDON FORBES, Sameer M. Zuberi

    Pubblicazione 2012
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  8. 8
    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? di Martin J. Brodie, Sameer M. Zuberi, Ingrid E. Scheffer, Robert S. Fisher

    Pubblicazione 2018
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  9. 9
    The burden of illness in Lennox–Gastaut syndrome: a systematic literature review

    The burden of illness in Lennox–Gastaut syndrome: a systematic literature review di Adam Strzelczyk, Sameer M. Zuberi, Pasquale Striano, Felix Rosenow, Susanne Schubert‐Bast

    Pubblicazione 2023
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  10. 10
    A White Paper on the medical and social needs of people with epilepsy and intellectual disability: The Task Force on Intellectual Disabilities and Epilepsy of the International League Against Epilepsy

    A White Paper on the medical and social needs of people with epilepsy and intellectual disability: The Task Force on Intellectual Disabilities and Epilepsy of the International Lea... di Mike Kerr, Christine Linehan, Rose Thompson, Marco Mula, Antonio Gil‐Nagal, Sameer M. Zuberi, Mike Glynn

    Pubblicazione 2014
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  11. 11
    The humanistic and economic burden of Dravet syndrome on caregivers and families: Implications for future research

    The humanistic and economic burden of Dravet syndrome on caregivers and families: Implications for future research di Mark P. Jensen, Andreas Brunklaus, Liam Dorris, Sameer M. Zuberi, Kelly G. Knupp, Bradley S. Galer, Arnold R. Gammaitoni

    Pubblicazione 2017
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  12. 12
    Guidance on Dravet syndrome from infant to adult care: Road map for treatment planning in Europe

    Guidance on Dravet syndrome from infant to adult care: Road map for treatment planning in Europe di Elena Cardenal‐Muñoz, Stéphane Auvin, Vicente Villanueva, J. Helen Cross, Sameer M. Zuberi, Lieven Lagae, José Ángel Aibar

    Pubblicazione 2021
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  13. 13
    Comorbidities and predictors of health‐related quality of life in Dravet syndrome: A 10‐year, prospective follow‐up study

    Comorbidities and predictors of health‐related quality of life in Dravet syndrome: A 10‐year, prospective follow‐up study di Phoebe Makiello, Tony Feng, Benjamin Dunwoody, Felix Steckler, Joseph D. Symonds, Sameer M. Zuberi, Liam Dorris, Andreas Brunklaus

    Pubblicazione 2023
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  14. 14
    Trauma, Coping, and Adjustment when Parenting a Child with Dravet Syndrome

    Trauma, Coping, and Adjustment when Parenting a Child with Dravet Syndrome di Anthony Mercier, Liam Dorris, Andreas Brunklaus, Joseph D. Symonds, Sameer M. Zuberi, Teresa Finch, Galia Wilson, Claire Eldred

    Pubblicazione 2025
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  15. 15
    <i>SCN9A</i> should not be considered an epilepsy gene; Refuting a gene–disease association

    <i>SCN9A</i> should not be considered an epilepsy gene; Refuting a gene–disease association di Ismael Ghanty, Eduardo Pérez‐Palma, Camilo Villamán, Daniel Stobo, Joseph D. Symonds, Sameer M. Zuberi, Dennis Lal, Andreas Brunklaus

    Pubblicazione 2025
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  16. 16
    Two cases of sudden unexpected death in epilepsy in a GEFS+ family with an <i>SCN1A</i> mutation

    Two cases of sudden unexpected death in epilepsy in a GEFS+ family with an <i>SCN1A</i> mutation di Neeti Hindocha, Lina Nashef, Frances Elmslie, Rachael Birch, Sameer M. Zuberi, Ammar Al‐Chalabi, Lia Crotti, Peter J. Schwartz, Andrew Makoff

    Pubblicazione 2008
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  17. 17
    The clinical, economic, and humanistic burden of Dravet syndrome – A systematic literature review

    The clinical, economic, and humanistic burden of Dravet syndrome – A systematic literature review di Joseph Sullivan, Alison Deighton, Maria Candida Vila, Shelagh M. Szabo, B. Maru, Jacqueline S. Gofshteyn, Emma James, Salvador Rico, Sameer M. Zuberi

    Pubblicazione 2022
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  18. 18
    Heart rate variability in epilepsy: A potential biomarker of <scp>sudden unexpected death in epilepsy</scp> risk

    Heart rate variability in epilepsy: A potential biomarker of <scp>sudden unexpected death in epilepsy</scp> risk di Kenneth A. Myers, Luis Bello‐Espinosa, Joseph D. Symonds, Sameer M. Zuberi, Robin Clegg, Lynette G. Sadleir, Jeffrey Buchhalter, Ingrid E. Scheffer

    Pubblicazione 2018
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  19. 19
    Neonatal seizures: Is there a relationship between ictal electroclinical features and etiology? A critical appraisal based on a systematic literature review

    Neonatal seizures: Is there a relationship between ictal electroclinical features and etiology? A critical appraisal based on a systematic literature review di Magda Lahorgue Nunes, Elissa Yozawitz, Sameer M. Zuberi, Eli M. Mizrahi, Maria Roberta Cilio, Solomon L. Moshé, Perrine Plouin, Sampsa Vanhatalo, Ronit Pressler

    Pubblicazione 2018
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  20. 20
    Gene variant effects across sodium channelopathies predict function and guide precision therapy

    Gene variant effects across sodium channelopathies predict function and guide precision therapy di Andreas Brunklaus, Tony Feng, Tobias Brünger, Eduardo Pérez‐Palma, Henrike Heyne, Emma Matthews, Christopher Semsarian, Joseph D. Symonds, Sameer M. Zuberi, Dennis Lal, Stéphanie Schorge

    Pubblicazione 2022
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