Movement Disorders Update [LIBRARY OF GENETIC Movement Disorders ► NEW TOPIC PAGE]

Movement Disorders: MedlinePlus

[LIBRARY OF GENETIC  Movement Disorders ► NEW TOPIC PAGE]

Movement Disorders Update

MedlinePlus sent this bulletin at 04/14/2016 01:10 PM EDT

New on the MedlinePlus Movement Disorders page:

Genetics Home Reference: fragile X-associated tremor/ataxia syndrome

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: spinocerebellar ataxia type 2

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: spinocerebellar ataxia type 1

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: familial paroxysmal kinesigenic dyskinesia

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: familial paroxysmal nonkinesigenic dyskinesia

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: spinocerebellar ataxia type 3

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: triosephosphate isomerase deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: infantile-onset spinocerebellar ataxia

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: essential tremor

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: succinic semialdehyde dehydrogenase deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: hypermanganesemia with dystonia, polycythemia, and cirrhosis

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: pantothenate kinase-associated neurodegeneration

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: mitochondrial membrane protein-associated neurodegeneration

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: spinocerebellar ataxia type 6

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: rapid-onset dystonia parkinsonism

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: sepiapterin reductase deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: myoclonic epilepsy myopathy sensory ataxia

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: myoclonus-dystonia

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: autosomal recessive spastic ataxia of Charlevoix-Saguenay

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: congenital mirror movement disorder

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: dilated cardiomyopathy with ataxia syndrome

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: chorea-acanthocytosis

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: deafness-dystonia-optic neuronopathy syndrome

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: autosomal recessive cerebellar ataxia type 1

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: dentatorubral-pallidoluysian atrophy

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: ataxia with vitamin E deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: biotin-thiamine-responsive basal ganglia disease

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: ataxia neuropathy spectrum

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Movement Disorders Update