ATP1A3 Mutation in Adult Rapid-Onset Ataxia. Kathleen J. Sweadner et al (2016), PLoS ONE http://dx.doi.org/10.1371/journal.pon… A 21-year old male presented with ataxia and dysarthria that had appeared over a period …
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Heterozygous mutations of the ATP1A3 gene cause rapid-onset dystonia-parkinsonism (RDP)1,2 and alternating hemiplegia of childhood (AHC).3,4 Intermediate AHC/RDP presentations and phenotypic diversity emerge.5 Aiming at identification of ATP1A3-related conditions beyond …
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Dr. Mohamad Mikati was interviewed by AHCIM in Washington 2016 “CBD can possibly prevent the toxicity of the gene mutation that causes AHC” The purpose of AHC International Library is …
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Dr. Kenneth Silver was interviewed by AHCIM in July 2014 The purpose of AHC International Library is to collect information about AHC and related disorders and make them visible for …
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Allison Brashear, Professor of neurology, was interviewed by AHCIM in London 2016 Allison is looking to teens or young adults that have the ATP1A3 mutation to participate in a study …
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Erin Heinzen, Assistant professor, was interviewed by AHCIM in London 2016 The purpose of AHC International Media is to collect information about AHC and related disorders and make them visible …
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Arn M.J.M van den Maagdenberg, professor of neurogenetics, was interviewed by AHCIM in London 2016 The purpose of AHC International Media is to collect information about AHC and related disorders …
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Karen Lykke-Hartmann, associate professor, was interviewed by AHCIM in London 2016 The purpose of AHC International Media is to collect information about AHC and related disorders and make them visible …
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Vicky Platt, mother of Emma, was interviewed by AHCIM in London 2016 The purpose of AHC International Library is to collect information about AHC and related disorders and make them …
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Helen Cross, Professor of Paediatric neurology, was interviewed by AHCIM in London 2016 “We are moving forward with research on AHC” The purpose of AHC International Library is to collect …
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