1-9 of 9
Authors: Michael S Hildebrand
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Journal Article
Stuttering associated with a pathogenic variant in the chaperone protein cyclophilin 40
Angela T Morgan and others
Brain, Volume 146, Issue 12, December 2023, Pages 5086–5097, https://doi.org/10.1093/brain/awad314
Published: 18 November 2023
Journal Article
Defective lipid signalling caused by mutations in PIK3C2B underlies focal epilepsy
Luca Gozzelino and others
Brain, Volume 145, Issue 7, July 2022, Pages 2313–2331, https://doi.org/10.1093/brain/awac082
Published: 04 July 2022
Journal Article
UNC13B and focal epilepsy
Timothy E. Green and others
Brain, Volume 145, Issue 3, March 2022, Pages e10–e12, https://doi.org/10.1093/brain/awab485
Published: 05 April 2022
Journal Article
Genome-wide association study of febrile seizures implicates fever response and neuronal excitability genes
Line Skotte and others
Brain, Volume 145, Issue 2, February 2022, Pages 555–568, https://doi.org/10.1093/brain/awab260
Published: 12 January 2022
Journal Article
Atypical development of Broca’s area in a large family with inherited stuttering
Daisy G Y Thompson-Lake and others
Brain, Volume 145, Issue 3, March 2022, Pages 1177–1188, https://doi.org/10.1093/brain/awab364
Published: 23 November 2021
Journal Article
Pathogenic WDFY3 variants cause neurodevelopmental disorders and opposing effects on brain size
Diana Le Duc and others
Brain, Volume 142, Issue 9, September 2019, Pages 2617–2630, https://doi.org/10.1093/brain/awz198
Published: 20 July 2019
Journal Article
Dorsal language stream anomalies in an inherited speech disorder
Frédérique J Liégeois and others
Brain, Volume 142, Issue 4, April 2019, Pages 966–977, https://doi.org/10.1093/brain/awz018
Published: 23 February 2019
Journal Article
Kufs disease due to mutation of CLN6: clinical, pathological and molecular genetic features
Samuel F Berkovic and others
Brain, Volume 142, Issue 1, January 2019, Pages 59–69, https://doi.org/10.1093/brain/awy297
Published: 15 December 2018
Journal Article
Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A
Dalia Kasperavičiūtė and others
Brain, Volume 136, Issue 10, October 2013, Pages 3140–3150, https://doi.org/10.1093/brain/awt233
Published: 06 September 2013
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