Huntington's disease
Explore this paper's citation graph
Summary
Your contributions to the investigation of this tragic disorder are presented and a review of current ideas about the disease is reviewed.
- Type
- review
- Published
- 1984-08-01
- Cited by
- 3,102
- References
- 92
- OpenAlex
- https://openalex.org/W2039776384
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:1536080
Keywords
Choreiform movement, Huntington's disease, Disease, Dementia, Psychology
References
- Two models for a maternal factor in the inheritance of Huntington disease.
- Fluorescence spectroscopic studies of Huntington fibroblast membranes.
- Depletion of somatostatin-like immunoreactivity in the rat central nervous system by cysteamine
- Factors related to onset age of Huntington disease.
- Somatostatin regulates dopamine release in rat striatal slices and cat caudate nuclei
- Huntington disease and Tourette syndrome. II. Uptake of glutamic acid and other amino acids by fibroblasts.
- Ultrastructural features of immunoreactive somatostatin neurons in the rat caudate nucleus
- Monoamines in the human neostriatum: topographic distribution in normals and in Parkinson's disease and their role in akinesia, rigidity, chorea, and tremor.
- Effects of lesions on somatostatin-like immunoreactivity in the rat striatum.
- Central cholinergic‐anticholinergic antagonism in Huntington's chorea
- Kainic acid and the glutamate receptor
- Physostigmine in choreiform movement disorders
- Maternal transmission in Huntington's disease.
- The high frequency of juvenile Huntington's chorea in South Africa
- The relation of type of initial symptoms and line of transmission to ages at onset and death in Huntington's disease
- Huntington chorea is not associated with hyperactivity of nigrostriatal dopaminergic neurons
- Huntington's disease: regional alteration in muscarinic cholinergic receptor binding in human brain.
- Decreased muscarinic receptor concentration in post-mortem brain in Huntington's chorea.
- Regional distribution of methionine-enkephalin and substance P-like immunoreactivity in normal human brain and in Huntington's disease.
- Electron spin resonance, hematological, and deformability studies of erythrocytes from patients with Huntington's disease.
Cited by
- Adenosine-dopamine interactions in the brain.
- Graft-induced Recovery of Inhibitory Avoidance Conditioning in Striatal Lesioned Rats is Related to Choline Acetyltransferase Activity
- Infantile Huntington’s Disease
- Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation.
- Cognitive deficits in Huntington's disease are predicted by dopaminergic PET markers and brain volumes.
- An intangible reality: the experience of uncertainty among intimate partners of persons with prodromal huntington disease
- Awareness of involuntary movements in Huntington disease.
- Nonparticipation in Huntington's Disease Predictive Testing: Reasons for Caution in Interpreting Findings
- High suicidal ideation in persons testing for Huntington's disease
- Comparison of huntingtin proteolytic fragments in human lymphoblast cell lines and human brain
- Impaired glutamate transport and glutamate-glutamine cycling: downstream effects of the Huntington mutation.
- ETUDE DE L'AMPLIFICATION DE LA NEURODEGENERESCENCE EXCITOTOXIQUE PAR UNE DYSFONCTION MITOCHONDRIALE : IMPLICATIONS POUR LA MALADIE DE HUNTINGTON
- Reproductive decision making before and after predictive testing for Huntington's disease: an Australian perspective
- Prevalence of Huntington disease in New South Wales in 1996
- Therapeutic RNA interference for neurodegenerative diseases: From promise to progress.
- Wheel running from a juvenile age delays onset of specific motor deficits but does not alter protein aggregate density in a mouse model of Huntington's disease
- Inhibition of specific HDACs and sirtuins suppresses pathogenesis in a Drosophila model of Huntington's disease.
- Sorting out the Dementias
- Sleep Patterns in Patients With Huntington's Disease and Their Unaffected First-Degree Relatives: A Brief Report
- Using systemic approaches, methods and techniques in rehabilitation medicine
Related papers
- Behavioral pathology induced by repeated systemic injections of 3-nitropropionic acid mimics the motoric symptoms of Huntington's disease.
- Designing primate models to assess the prodromal phase of Huntington's disease.
- Huntington's disease: review and anesthetic case management.
- Pridopidine in treatment of Huntington's disease: beyond chorea?
- Symptomatic Treatment and Management of Huntington's Disease: An Overview
- Non-choreic movement disorders as initial manifestations of Huntington's disease.
- Vertical saccades in Huntington's disease and non-degenerative choreoathetoid disorders