Sarah Heron - Dissemin

Papers authored by Sarah Heron

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2013 Sarah E. Heron

, Yeh Sze Ong, Simone C. Yendle, Jacinta M. McMahon, Samuel F. Berkovic, Ingrid E. Scheffer, Leanne M. Dibbens

Mutations in PRRT2 are not a common cause of infantile epileptic encephalopathies

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This paper is available in a repository.

2012 Ingrid E. Scheffer, Bronwyn E. Grinton, Sarah E. Heron

, Sara Kivity, Zaid Afawi, Xenia Iona, Hadassa Goldberg-Stern, Maria Kinali, Ian Andrews, Renzo Guerrini, Carla Marini, Lynette G. Sadleir, Samuel F. Berkovic, Leanne M. Dibbens

PRRT2 phenotypic spectrum includes sporadic and fever-related infantile seizures

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This paper is made freely available by the publisher.

Sarah E. Heron

, Katherine R. Smith, Melanie Bahlo, Lino Nobili

, Esther Kahana, Laura Licchetta, Karen L. Oliver

, Aziz Mazarib, Zaid Afawi, Amos Korczyn, Giuseppe Plazzi, Steven Petrou, Samuel F. Berkovic, Ingrid E. Scheffer, Leanne M. Dibbens

Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy

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Karl Martin Klein, Terence J. O'Brien, Kavita Praveen, Sarah E. Heron

, John C. Mulley, Simon Foote, Samuel F. Berkovic, Ingrid E. Scheffer

Familial focal epilepsy with variable foci mapped to chromosome 22q12: Expansion of the phenotypic spectrum

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Zaid Afawi, Haim Bassan, Sarah Heron

, Karen Oliver

, Rachel Straussberg, Ingrid Scheffer, Richard Leventer, Amos Korczyn, Samuel Berkovic

Benign Neonatal Sleep Myoclonus

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Sarah E. Heron

, Bronwyn E. Grinton, Sara Kivity, Zaid Afawi, Sameer M. Zuberi

, James N. Hughes, Clair Pridmore, Bree L. Hodgson, Xenia Iona, Lynette G. Sadleir, James Pelekanos, Eric Herlenius, Hadassa Goldberg-Stern, Haim Bassan, Eric Haan and 10 other authors

PRRT2 Mutations Cause Benign Familial Infantile Epilepsy and Infantile Convulsions with Choreoathetosis Syndrome

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Sarah Weckhuysen, Peter de Jonghe, Simone Mandelstam

, Arvid Suls, Dominique Audenaert, Tine Deconinck, Lieve Rf F. Claes, Liesbet Deprez, Katrien Smets, Dimitrina Hristova, Iglika Yordanova, Albena Jordanova, Berten Ceulemans, An Jansen, Danièle Hasaerts and 10 other authors

KCNQ2 encephalopathy: Emerging phenotype of a neonatal epileptic encephalopathy

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2011 John C. Mulley, Sarah E. Heron

, Leanne M. Dibbens

Proposed genetic classification of the "benign" familial neonatal and infantile epilepsies

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John C. Mulley, Sarah E. Heron

, Robyn H. Wallace, Jozef Gecz, Leanne M. Dibbens

"Blinders, phenotype, and fashionable genetic analysis": setting the record straight for epilepsy!

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L. M. Dibbens, R. Kneen, M. A. Bayly, S. E. Heron

, T. Arsov

, J. A. Damiano, T. Desai, J. Gibbs, F. McKenzie, J. C. Mulley, A. Ronan, I. E. Scheffer

Recurrence risk of epilepsy and mental retardation in females due to parental mosaicism of PCDH19 mutations

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John C. Mulley, Xenia Iona, Bree Hodgson, Sarah E. Heron

, Samuel F. Berkovic, Ingrid E. Scheffer, Leanne M. Dibbens

The Role of Seizure-RelatedSEZ6as a Susceptibility Gene in Febrile Seizures

Download from downloads.hindawi.com

2010 Sarah E. Heron

, Ingrid E. Scheffer, Bronwyn E. Grinton, Helen Eyre, Karen L. Oliver

, Sharon Bain, Samuel F. Berkovic, John C. Mulley

Familial neonatal seizures with intellectual disability caused by a microduplication of chromosome 2q24.3

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Sarah E. Heron

, Marta Hernandez, Caitlin Edwards, Edward Edkins, Floor E. Jansen, Ingrid E. Scheffer, Samuel F. Berkovic, John C. Mulley

Neonatal seizures and Long QT Syndrome: A cardiocerebral channelopathy?

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2009 Sarah E. Heron

, Ingrid E. Scheffer, Xenia Iona, Sameer M. Zuberi

, Rachael Birch, Jacinta M. McMahon, Carla M. Bruce, Samuel F. Berkovic, John C. Mulley

De novo SCN1A mutations in Dravet syndrome and related epileptic encephalopathies are largely of paternal origin

Download from digital.library.adelaide.edu.au

Hadassa Goldberg-Stern, Rafi Kaufmann, Sara Kivity, Zaid Afawi, Sara E. Heron

Novel mutation in KCNQ2 causing benign familial neonatal seizures

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2008 Christopher P. Derry, Sarah E. Heron

, Fiona Phillips, Stephen Howell, Jacinta MacMahon, Hilary A. Phillips, John S. Duncan, John C. Mulley, Samuel F. Berkovic, Ingrid E. Scheffer

Severe autosomal dominant nocturnal frontal lobe epilepsy associated with psychiatric disorders and intellectual disability

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2007 S. E. Heron

, K. Cox, B. E. Grinton, S. M. Zuberi

, Sara Kivity, Z. Afawi, R. Straussberg, S. F. Berkovic, I. E. Scheffer, J. C. Mulley

Deletions or duplications in KCNQ2 can cause benign familial neonatal seizures

Download from www.ncbi.nlm.nih.gov

Sarah E. Heron

, Houman Khosravani, Diego Varela, Chris Bladen, Tristiana C. Williams, Michelle R. Newman, Ingrid E. Scheffer, Samuel F. Berkovic, John C. Mulley, Gerald W. Zamponi

Extended spectrum of idiopathic generalized epilepsies associated with CACNA1H functional variants

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R. Xu, R. Xua, E. A. Thomas, E. V. Gazina, K. L. Richards, M. Quick, R. H. Wallace, L. A. Harkin, S. E. Heron

, S. F. Berkovic, I. E. Scheffer, J. C. Mulley, S. Petrou

Generalized epilepsy with febrile seizures plus–associated sodium channel β1 subunit mutations severely reduce beta subunit–mediated modulation of sodium channel function

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L. M. Dibbens, S. E. Heron

, J. C. Mulley

A polygenic heterogeneity model for common epilepsies with complex genetics

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Papers authored by Sarah Heron