Langbehn, D.R., Hayden, M.R. and Paulsen, J.S. (2010) CAG-Repeat Length and the Age of Onset in Huntington Disease (HD): A Review and Validation Study of Statistical Approaches. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 9999B, 397-408.
http://dx.doi.org/10.1002/ajmg.b.30992

has been cited by the following article:

• TITLE: Episodic Learning and Memory in Prodromal Huntington’s Disease: The Role of Multimodal Encoding and Selective Reminding

  AUTHORS: Tarja-Brita Robins Wahlin, Åke Wahlin, Gerard J. Byrne

  KEYWORDS: Prodromal Huntington’s Disease, Fuld Object Memory Evaluation, Episodic Memory, Short-Term Memory, Neurodegenerative Diseases

  JOURNAL NAME: International Journal of Clinical Medicine, Vol.6 No.11, November 30, 2015

  ABSTRACT: This study investigated episodic memory in prodromal HD. Three groups were compared (N = 70): mutation carriers with less than 12.5 years to disease onset (n = 16), mutation carriers with 12.5 or more years to disease onset (n = 16), and noncarriers (n = 38). Episodic memory was assessed using the Fuld Object Memory Evaluation, which included multimodal presentation and selective reminding, and the Claeson-Dahl Learning Test which included verbal repeated presentation and recall trials. Both carrier groups demonstrated deficient episodic memory compared to noncarriers. The results suggest deficient episodic memory in prodromal HD, and that inconsistent retrieval contributes to these deficits. Multimodal presentation attenuates the deficits.