
Dr Brashear Explains Alternating Hemiplegia of Childhood
Allison Brashear, MD of the Department of Neurology at Wake Forest University discusses the symptoms and genetics of Alternating Hemiplegia of Childhood.
Read MoreMedia site for AHC and related disorders
Allison Brashear, MD of the Department of Neurology at Wake Forest University discusses the symptoms and genetics of Alternating Hemiplegia of Childhood.
Read MoreDr. 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 …
Read MoreArn 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 …
Read MoreKaren 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 …
Read MoreCaroline Dion, mother of Kaya, was interviewed by AHCIM in Minneapolis, 2014 “Caroline found the diagnosis for her daughter without help from the medical community” The purpose of AHC International …
Read MoreLandis Pino, Mother of Madison and Marley, was interviewed by the AHCIM in October 2014 Landis has TWO children affected by AHC which is extremely rare. When the interview was …
Read MoreProfessor Helen Cross was interviewed by AHCIM in London, May 2015 “If we find a treatment for AHC it may well help other disorders” “the children who now are negative …
Read MoreMeg Krenn, mother of Emory, was interviewed by AHCIM in August 2015 Meg and Bill Krenn have 4 children together which is not common among AHC families. They have a …
Read MoreMallory Eastman, sister of Caroline Eastman, was interviewed by AHCIM in August 2015 Mallory shares her view as a sibling to an AHC hero. She tells us among other things …
Read MoreSho Yano was interviewed by AHCIM in Washington, DC, August 2015 Sho Yano believes that ATP1A3 mutations are much more common than we realize Some people have 1 or 2 …
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