Myoclonus, Epilepsy, and Ataxia Resulting From Potassium Channel Gene Mutation: Expanding the Spectrum Underlying Ramsay Hunt Syndrome

समान संसाधन

• Progressive myoclonus and epilepsy with dentatorubral degeneration: a clinicopathological study of the Ramsay Hunt syndrome.
  द्वारा: Bird, T D, और अन्य
  प्रकाशित: (1978)
• Ataxia with Oculomotor Apraxia Type 1—New Mutation, Characteristic Phenotype
  द्वारा: Balint, Bettina, और अन्य
  प्रकाशित: (2019)
• Genetic Dystonia‐ataxia Syndromes: Clinical Spectrum, Diagnostic Approach, and Treatment Options
  द्वारा: Rossi, Malco, और अन्य
  प्रकाशित: (2018)
• Mitochondrial myopathy and lactic acidaemia with myoclonic epilepsy, ataxia and hypothalamic infertility: a variant of Ramsay-Hunt syndrome?
  द्वारा: Fitzsimons, R B, और अन्य
  प्रकाशित: (1981)
• Mutation of the nuclear lamin gene LMNB2 in progressive myoclonus epilepsy with early ataxia
  द्वारा: Damiano, John A., और अन्य
  प्रकाशित: (2015)