Dystonia in Ashkenazi Jews: clinical characterization of a founder mutation. Read more about Dystonia in Ashkenazi Jews: clinical characterization of a founder mutation.
Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32-34. Read more about Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32-34.
Idiopathic dystonia among Ashkenazi Jews: evidence for autosomal dominant inheritance. Read more about Idiopathic dystonia among Ashkenazi Jews: evidence for autosomal dominant inheritance.
AIDS-related vacuolar myelopathy is not associated with coinfection by human T-lymphotropic virus type I. Read more about AIDS-related vacuolar myelopathy is not associated with coinfection by human T-lymphotropic virus type I.
McArdle's disease: biochemical and molecular genetic studies. Read more about McArdle's disease: biochemical and molecular genetic studies.
Status epilepticus: divergence of sympathetic activity and cardiovascular response. Read more about Status epilepticus: divergence of sympathetic activity and cardiovascular response.
Intermittent ataxia and immunodeficiency with multiple carboxylase deficiencies: a biotin-responsive disorder. Read more about Intermittent ataxia and immunodeficiency with multiple carboxylase deficiencies: a biotin-responsive disorder.
