Parkinsonian Disorders

A group of disorders which feature impaired motor control characterized by bradykinesia, MUSCLE RIGIDITY; TREMOR; and postural instability. Parkinsonian diseases are generally divided into primary parkinsonism (see PARKINSON DISEASE), secondary parkinsonism (see PARKINSON DISEASE, SECONDARY) and inherited forms. These conditions are associated with dysfunction of dopaminergic or closely related motor integration neuronal pathways in the BASAL GANGLIA.

Also Known As:

Parkinsonism; Ramsay Hunt Paralysis Syndrome; Autosomal Dominant Juvenile Parkinson Disease; Autosomal Dominant Juvenile Parkinsonism; Autosomal Dominant Parkinsonism; Autosomal Recessive Juvenile Parkinson Disease; Autosomal Recessive Parkinsonism; Chromosome 6-Linked Autosomal Recessive Parkinsonism; Experimental Parkinson Disease; Experimental Parkinsonism; Experimental Parkinsonism, MPTP-Induced; Familial Parkinson Disease, Autosomal Recessive; Juvenile Parkinson Disease; Juvenile Parkinson Disease, Autosomal Dominant; Juvenile Parkinson Disease, Autosomal Recessive; Juvenile Parkinsonism, Autosomal Dominant; Juvenile Parkinsonism, Autosomal Recessive; MPTP-Induced Experimental Parkinsonism; Parkinson Disease 2; Parkinson Disease 2, Autosomal Recessive Juvenile; Parkinson Disease Autosomal Recessive, Early Onset; Parkinson Disease, Autosomal Dominant. Juvenile; Parkinson Disease, Experimental; Parkinson Disease, Familial, Autosomal Recessive; Parkinson Disease, Juvenile; Parkinson Disease, Juvenile, Autosomal Dominant; Parkinson Disease, Juvenile, Autosomal Recessive; Parkinsonian Diseases; Parkinsonian Syndromes; Parkinsonism, Early Onset, with Diurnal Fluctuation; Parkinsonism, Early-Onset, With Diurnal Fluctuation; Parkinsonism, Juvenile, Autosomal Dominant; Parkinsonism, Juvenile, Autosomal Recessive; Chromosome 6 Linked Autosomal Recessive Parkinsonism; Diseases, Experimental Parkinson; Dominant Parkinsonism, Autosomal; Experimental Parkinson Diseases; Experimental Parkinsonism, MPTP Induced; Experimental Parkinsonisms; Juvenile Parkinsonism; Juvenile Parkinsonism, Familial; Juvenile Parkinsonisms; MPTP Induced Experimental Parkinsonism; Parkinson Diseases, Experimental; Parkinsonism, Autosomal Dominant; Parkinsonism, Autosomal Recessive; Parkinsonism, Familial Juvenile; Parkinsonism, MPTP-Induced Experimental; Parkinsonisms, Experimental; Parkinsonisms, Juvenile; Recessive Parkinsonism, Autosomal; Autosomal Recessive Juvenile Parkinsonism; Familial Juvenile Parkinsonism; Parkinsonian Syndrome; Parkinsonism, Experimental; Parkinsonism, Juvenile

Nervous System Diseases: 14737
- Central Nervous System Diseases: 4371
  - Brain Diseases: 16141
    - Basal Ganglia Diseases: 350
      - Parkinsonian Disorders: 9322
  - Movement Disorders: 4780
    - Parkinsonian Disorders: 9322

C M Hendrix Selected Research

C M Hendrix Research Topics

Disease

Drug/Important Bio-Agent (IBA)