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Results 1 - 6 of 6 for gaba
  1. GABA-transaminase deficiency 
    GABA-transaminase deficiency is a brain disease (encephalopathy) that begins in infancy. Babies with this disorder have recurrent seizures (epilepsy), uncontrolled ...
    https://medlineplus.gov/.../condition/gaba-transaminase-deficiency - Genetics
  2. Succinic semialdehyde dehydrogenase deficiency 
    ... the brain (neurotransmitter) called gamma-amino butyric acid (GABA). The primary role of GABA is to prevent the brain from being overloaded ... results in an increase in the amount of GABA and a related molecule called gamma-hydroxybutyrate (GHB) ...
    https://medlineplus.gov/...nic-semialdehyde-dehydrogenase-deficiency - Genetics
  3. Juvenile myoclonic epilepsy 
    ... Macdonald RL, Botzolakis EJ, Hu N, Gallagher MJ. GABA(A) receptor alpha1 subunit mutation A322D associated with ... expression and alters the composition of wild type GABA(A) receptors. J Biol Chem. 2010 Aug 20; ...
    https://medlineplus.gov/.../condition/juvenile-myoclonic-epilepsy - Genetics
  4. Schizoaffective disorder 
    ... of a receptor for gamma-amino butyric acid (GABA), a chemical called a neurotransmitter that sends signals in the brain. GABA's primary role is to prevent the brain ...
    https://medlineplus.gov/genetics/condition/schizoaffective-disorder - Genetics
  5. Genetic epilepsy with febrile seizures plus 
    ... the SCN1A voltage-gated sodium channel leads to gamma-aminobutyric acid-ergic (GABAergic) interneuron abnormalities. J Biol Chem. 2010 ...
    https://medlineplus.gov/...netic-epilepsy-with-febrile-seizures-plus - Genetics
  6. Childhood absence epilepsy 
    ... 1038/nrn811. Citation on PubMed Hirose S. Mutant GABA(A) receptor subunits in genetic (idiopathic) epilepsy. Prog ...
    https://medlineplus.gov/.../condition/childhood-absence-epilepsy - Genetics