An anthropometric assessment of Huntington's disease patients and families
β Scribed by Lindsay A. Farrer; F. John Meaney
- Publisher
- John Wiley and Sons
- Year
- 1985
- Tongue
- English
- Weight
- 794 KB
- Volume
- 67
- Category
- Article
- ISSN
- 0002-9483
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π SIMILAR VOLUMES
Assessment programs recently designed to follow-up patients with Huntington's disease (HD) in therapeutic trials have not included electrophysiological testing in the list of mandatory examinations. This omission is likely due to the current lack of data establishing a clear correlation between the
## Abstract We report the characteristics of 691 Mexican patients with Huntington's disease (HD). These patients, representing 401 families, constitute the largest series of Mexican HD cases as yet described in the literature. We found the clinical characteristics of these patients to be similar to
## Abstract Little is known about subjective perceptions of quality of life (QOL) in Huntington's disease (HD). The current study determined correlates of patient and caregiver QOL and assessed change over time. Participants were 22 patientβcaregiver dyads, who rated QOL at baseline and 6 months la
## Abstract We performed a 6βmonth openβlabel trial to evaluate the tolerability and efficacy of coenzyme Q10 (CoQ) in 10 patients with Huntington's disease (HD), Subjects were evaluated at baseline, 3 months, and 6 months using the HD Rating Scale (HDRS), the HD Functional Capacity Scale (HDFCS),
## Abstract We report on a family with comorbidity of Huntington's disease (HD) and idiopathic restless legs syndrome (RLS). All family members investigated and affected by RLS are also affected by HD, but not vice versa. The association of HD and RLS is discussed with respect to dopaminergic dysfu