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Authors: Mary D King
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Journal Article

KMT2B-related disorders: expansion of the phenotypic spectrum and long-term efficacy of deep brain stimulation

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Laura Cif and others
Brain, Volume 143, Issue 11, November 2020, Pages 3242–3261, https://doi.org/10.1093/brain/awaa304
Published: 05 November 2020
Journal Article

Clinical spectrum and genotype–phenotype associations of KCNA2-related encephalopathies

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Silvia Masnada and others
Brain, Volume 140, Issue 9, September 2017, Pages 2337–2354, https://doi.org/10.1093/brain/awx184
Published: 24 August 2017
Journal Article

Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2

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A. Reghan Foley and others
Brain, Volume 137, Issue 1, January 2014, Pages 44–56, https://doi.org/10.1093/brain/awt315
Published: 15 November 2013
Journal Article

Migrating partial seizures of infancy: expansion of the electroclinical, radiological and pathological disease spectrum Get access

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Amy McTague and others
Brain, Volume 136, Issue 5, May 2013, Pages 1578–1591, https://doi.org/10.1093/brain/awt073
Published: 18 April 2013
Journal Article

SGCE mutations cause psychiatric disorders: clinical and genetic characterization Get access

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Kathryn J. Peall and others
Brain, Volume 136, Issue 1, January 2013, Pages 294–303, https://doi.org/10.1093/brain/aws308
Published: 28 January 2013