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Family Practice|March 1, 1991
Attitudes towards predictive testing in Huntington's disease--a deep interview study in SwedenB Mattsson, E W AlmqvistClinical Genetics|September 17, 2003
Psychological consequences and predictors of adverse events in the first 5 years after predictive testing for Huntington's diseaseE W Almqvist, R R Brinkman, S Wiggins, et al.Clinical Genetics|October 12, 2001
High incidence rate and absent family histories in one quarter of patients newly diagnosed with Huntington disease in British ColumbiaE W Almqvist, D S Elterman, P M MacLeod, et al.American Journal of Human Genetics|April 17, 1999
A worldwide assessment of the frequency of suicide, suicide attempts, or psychiatric hospitalization after predictive testing for Huntington diseaseE W Almqvist, M Bloch, R Brinkman, et al.American Journal of Human Genetics|February 28, 2001
Measurement of mutational flow implies both a high new-mutation rate for Huntington disease and substantial underascertainment of late-onset casesD Falush, E W Almqvist, R R Brinkmann, et al.Clinical Genetics|May 20, 1999
Accurate determination of the number of CAG repeats in the Huntington disease gene using a sequence-specific internal DNA standardO Bruland, E W Almqvist, Y P Goldberg, et al.American Journal of Human Genetics|October 30, 1998
A Huntington disease-like neurodegenerative disorder maps to chromosome 20pF Xiang, E W Almqvist, M Huq, et al.Clinical Genetics|November 1, 1987
Linkage of G8 (D4S10) in two Swedish families with Huntington's diseaseG Holmgren, E W Almqvist, M Anvret, et al.The American Journal of Psychiatry|December 1, 2000
Familial aggregation of psychotic symptoms in Huntington's diseaseD Tsuang, E W Almqvist, H Lipe, et al.Brain Research Bulletin|November 26, 2003
Caudate volume as an outcome measure in clinical trials for Huntington's disease: a pilot studyE H Aylward, A Rosenblatt, K Field, et al.Pageof 2