Phenotypic Heterogeneity in Huntington Disease

References

• Bracketiridge C. J. The relation of sex of affected parent to the age at onset of HD. J. Med. Genet. 1973; 4: 333
   Google Scholar
• Brackenridge C. J. Familial correlations for age at onset and age at death in Huntington's Disease. J. Med. Genet. 1972; 9: 23
   Google Scholar
• Brackenridge C. J. Parental factors associated with rigidity in Huntington's Disease. J. Med Genet. 1980; 17: 112–114
   Google Scholar
• Bickford J. A. R., Ellison R. M. The high incidence of Huntington's Chorea in the Duchy of Cornwall. J. Ment. Sci. 1953; 99: 291–294
   Google Scholar
• Boehnke M., Conneally P. M., Lange K. Two models for a maternal factor in the inheritance of Huntington Disease. Am. J. Hum. Genet. 1983; 35: 845–860
   PubMed Web of Science ®Google Scholar
• Brandt J., et al. Clinical correlates of dementia and disability in Huntington disease, Submitted
   Google Scholar
• Bruyn G. W. Huntington's Chorea, historical, clinical and laboratory synopsis. Handbook of Clinical Neurology, P. J. Vinken, G. W. Bruyn. North-Holland, Amsterdam 1968; Vol. 6: 298–378
   Google Scholar
• Carson N. A. J., Cusworth D. C., Dent C. E., Field C. M. B., Neill D. W., Westall R. G. Homocystinuria. A new inborn error of metabolism associated with mental difficiency. Arch. Dis. Child. 1963; 38: 425–436
   Google Scholar
• Davenport C. B. Huntington's Chorea in relation to heredity and eugenics. Am. J. Insanity 1916; 73: 195–222
   Google Scholar
• Delhanty J. D. A., Parrington J. M., Casey G., et al. Growth, DNA repair, sister chromatid exchange and chromosome studies in fibroblasts from Huntington's disease patients. Ann. Hum. Genet. 1981; 45: 181–198
   Google Scholar
• Folstein M. F., Folstein S., McHugh P. R. Mini-Mental State. A practical method for grading the cognitive state of patients for the clinician. J. Psychiatr. Res. 1975; 12: 189–198
   PubMed Web of Science ®Google Scholar
• Folstein S. E., Jensen B., Folstein M. F. The measurement of abnormal movement: methods developed for Huntington's disease. Neurobehav. Toxicol. Teratol. 1983; 5: 605–609
   PubMedGoogle Scholar
• Folstein S. E., Abbott M. H., Chase G. A., Jensen B. A., Folstein M. F. The association of affective disorder with Huntington's Disease in a case series and in families. Psychol. Med. 1983; 13: 537–542
   PubMedGoogle Scholar
• Folstein S. E., Folstein M. F. Psychiatric features of Huntington's Disease: recent approaches and findings. Psychiatr. Dev. 1983; 2: 193–206
   Google Scholar
• Gusella J. F., et al. A polymorphic DNA marker genetically linked to Huntington's Disease. Nature (London) 1983; 306: 234–238
   PubMed Web of Science ®Google Scholar
• Hamilton A. S. A report of 27 cases of chronic progressive chorea. Am. J. Insanity 1908; 64: 403–475
   Google Scholar
• Harper P. S., Samuel P., et al. A Genetic Linkage Study of Huntington's Chorea. Presented at Edinburgh Conference on Gene Mapping. 1979
   Google Scholar
• Harding A. E. The clinical features and classification of the late onset autosomal dominant cerebellar ataxias. Brain 1982; 105: 1–28
   PubMed Web of Science ®Google Scholar
• Human Genetic Mutant Cell Repository8th edn. The National Institute of General Medical Sciences, U.S. Department of Health and Human Services. 1981
   Google Scholar
• Huntington G. On chorea. Medical and Surgical Reporter (Philadelphia) 1872; 26: 317
   Google Scholar
• Mattsson B. Huntington's Chorea in Sweden. II. Social and clinical data. Acta Psychiatr. Scand. 1974, Suppl. 255: 221–235
   Google Scholar
• McKusick V. A. Mendelian Inheritance in Man6th edn. Johns Hopkins University Press, Baltimore 1983
   Google Scholar
• Meyers R. H., Madden J. J., Teague J. L., Falek A. Factors related to onset of Huntington Disease. Am. J. Hum. Genet. 1982; 34: 481–488
   Google Scholar
• Minski L., Guttmann E. Huntington's Chorea: a study of 34 families. J. Ment. Sci. 1938; 84: 21–96
   Google Scholar
• Murphy E. A., Chase G. A. Principles of Genetic Counseling. Chicago Yearbook Medical Publishers. 1975
   Google Scholar
• National roster of HD families established (news). Ann. Neurol. 1980; 7(2)195
   Google Scholar
• Newcombe R. G., Walker D. A., Harper P. S. Factors influencing age at onset and duration of survival in Huntington's chorea. Ann. Hum. Genet. 1981; 45: 387–396
   PubMed Web of Science ®Google Scholar
• Paterson M. C., Bech-Hansen N. T., Blattner W. A., et al (1982) Survey of human hereditary and familial disorders for gamma ray response in vitro: occurrence of both cellular radio-sensitivity and radio resistence in cancer-prone families. Proc. 1st Conf. Radio Protectors and Anticarcinogens, Gaithersburg, Md, 1982. Academic Press, NewYork
   Google Scholar
• Pericak-Vance M. A., Elston R. C., Conneally P. M., Dawson D. V. Age-of-onset heterogeneity in Huntington Disease families. Am. J. Med. Genet. 1983; 14: 49–59
   PubMed Web of Science ®Google Scholar
• Pericak-Vance M. A., Conneally P. M., et al. Linkage in Huntington's Disease. Presented at: Edinburgh Conference on Gene Mapping. 1979
   Google Scholar
• Pyeritz R. E., Murphy E. A., McKusick V. A. Clinical variability in the Marfan Syndrome(s). Birth Defects: Original Article Series 1979; 15(58)155–178
   Google Scholar
• Reed F. E., Neel J. V. Huntington Chorea in Michigan. 2. Selection and Mutation. Am. J. Hum. Genet. 1959; 11: 107
   PubMed Web of Science ®Google Scholar
• Rosenberg R. N., Nyhan W. L., Coutinho P., Bay C. Joseph's disease in the United States and the Azores Islands. Adv. Neurol. 1978; 21: 33–57
   Google Scholar
• Thompson W. D., Orvaschel H., Prusoff B. A., Kidd K. K. An evaluation of the family history method for ascertaining psychiatric disorders. Arch. Gen. Psychiatr. 1982; 39: 53–58
   PubMed Web of Science ®Google Scholar
• Valle D., Pai G. S., Thomas G. H., Pyeritz E. E. Homocystinuria due to cystathionine b-synthase deficiency: clinical manifestations and therapy. Johns Hopkins Med. J. 1980; 146: 110–117
   Google Scholar
• Wallace D. C., Hall A. C. Evidence of genetic heterogeneity in Huntington's Chorea. J. Neurol., Neurosurg. Psychiatr. 1972; 35: 789–800
   Google Scholar
• Wendt G. G., Drohn D. Die Huntingtonische Chorea: Eine Populationsgenetische Studie. Fortschr. Allgemeinen und Klinischen Humangenetik, Band IV. Georg Thieme, Stuttgart 1972
   Google Scholar
• Went L. N., Vegter-Van der Vlis M., Bruyn G. W., Volkers W. S. Huntington's Chorea in the Netherlands. The problem of genetic heterogeneity. Ann. Hum. Genet. 1983; 47: 205–214
   Google Scholar
• Went L. N., Vegter-Van Der Vlis M., Volkers W., Collewijn H. Huntington's Chorea. Early Diagnosis and Prevention of Genetic Diseases, L. N. Went, Chr Vermeij-Keers, G. J. M. van der Linden. Leiden University Press. 1975; 13–25
   Google Scholar