Skip to main content

Advertisement

Log in

Cognitive Impairment in Huntington Disease: Diagnosis and Treatment

  • Published:
Current Neurology and Neuroscience Reports Aims and scope Submit manuscript

Abstract

Cognition has been well characterized in the various stages of Huntington disease (HD) as well as in the prodrome before the motor diagnosis is given. Although the clinical diagnosis of HD relies on the manifestation of motor abnormalities, the associated impairments have been growing in prominence for several reasons. First, research to understand the most debilitating aspects of HD has suggested that cognitive and behavioral changes place the greatest burden on families, are most highly associated with functional decline, and can be predictive of institutionalization. Second, cognitive impairments are evident at least 15 years prior to the time at which motor diagnosis is given. Finally, cognitive decline is associated with biological markers such as brain atrophy, circulating levels of brain-derived neurotrophic factors, and insulin-like growth factor 1. Efforts are now underway to develop valid and reliable measures of cognition in the prodrome as well as in all stages of HD so that clinical trials can be conducted using cognitive outcomes.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Subscribe and save

Springer+ Basic
$34.99 /Month
  • Get 10 units per month
  • Download Article/Chapter or eBook
  • 1 Unit = 1 Article or 1 Chapter
  • Cancel anytime
Subscribe now

Buy Now

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

Papers of particular interest, published recently, have been highlighted as: •• Of major importance

  1. The Huntington’s Disease Collaborative Research Group. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington’s disease chromosomes. Cell. 1993;72(6):971–83.

    Article  Google Scholar 

  2. Ferrante RJ, Kowall NW, Beal MF, et al. Selective sparing of a class of striatal neurons in Huntington’s disease. Science. 1985;230(4725):561–3.

    Article  PubMed  CAS  Google Scholar 

  3. Hedreen JC, Peyser CE, Folstein SE, Ross CA. Neuronal loss in layers V and VI of cerebral cortex in Huntington’s disease. Neurosci Lett. 1991;133(2):257–61.

    Article  PubMed  CAS  Google Scholar 

  4. Aylward EH, Nopoulos PC, Ross CA, et al. Longitudinal change in regional brain volumes in prodromal Huntington disease. J Neurol Neurosurg Psychiatry. 2011;82:405–10.

    Article  PubMed  Google Scholar 

  5. Rosas HD, Hevelone ND, Zaleta AK, et al. Regional cortical thinning in preclinical Huntington disease and its relationship to cognition. Neurology. 2005;65(5):745–7.

    Article  PubMed  CAS  Google Scholar 

  6. Paulsen JS, Magnotta VA, Mikos AE, et al. Brain structure in preclinical Huntington’s disease. Biol Psychiatry. 2006;59(1):57–63.

    Article  PubMed  CAS  Google Scholar 

  7. Roos RA. Huntington’s disease: a clinical review. Orphanet J Rare Dis. 2010;5(1):40.

    Article  PubMed  Google Scholar 

  8. Ross CA, Tabrizi SJ. Huntington’s disease: from molecular pathogenesis to clinical treatment. Lancet Neurol. 2011;10(1):83–98.

    Article  PubMed  CAS  Google Scholar 

  9. Paulsen JS, Hayden M, Stout JC, et al. Preparing for preventive clinical trials: the Predict-HD study. Arch Neurol. 2006;63(6):883–90.

    Article  PubMed  Google Scholar 

  10. Paulsen JS, Langbehn DR, Stout JC, et al. Detection of Huntington’s disease decades before diagnosis: the Predict-HD study. J Neurol Neurosurg Psychiatry. 2008;79(8):874–80.

    Article  PubMed  CAS  Google Scholar 

  11. Nance MA, Paulsen JS, Rosenblatt A, Wheelock V. A physician’s guide to the management of Huntington's disease. 3rd ed. Huntington's Disease Society of America 2011.

  12. Paulsen JS, Zhao H, Stout JC, et al. Clinical markers of early disease in persons near onset of Huntington’s disease. Neurology. 2001;57(4):658–62.

    PubMed  CAS  Google Scholar 

  13. Langbehn DR, Paulsen JS. Predictors of diagnosis in Huntington disease. Neurology. 2007;68(20):1710–7.

    Article  PubMed  Google Scholar 

  14. Biglan KM, Ross CA, Langbehn DR, et al. Motor abnormalities in premanifest persons with Huntington’s disease: the PREDICT-HD study. Mov Disord. 2009;24(12):1763–72.

    Article  PubMed  Google Scholar 

  15. Paulsen JS, Nopoulos PC, Aylward E, et al. Striatal and white matter predictors of estimated diagnosis for Huntington disease. Brain Res Bull. 2010;82(3–4):201–7.

    Article  PubMed  Google Scholar 

  16. Aylward EH, Sparks BF, Field KM, et al. Onset and rate of striatal atrophy in preclinical Huntington disease. Neurology. 2004;63(1):66–72.

    PubMed  CAS  Google Scholar 

  17. Unified Huntington’s disease rating scale: reliability and consistency. Huntington Study Group. Mov Disord. 1996;11(2):136–142.

    Google Scholar 

  18. Carlozzi NE, Stout JC, Mills JA, et al. Estimating premorbid IQ in the prodromal phase of a neurodegenerative disease. Clin Neuropsychol. 2011;25(5):757–77.

    Google Scholar 

  19. O’Rourke JJ, Adams WH, Duff K, et al. Estimating premorbid functioning in huntington’s disease: the relationship between disease progression and the wide range achievement test reading subtest. Arch Clin Neuropsychol. 2011;26(1):59–66.

    Article  PubMed  Google Scholar 

  20. Petersen RC. Conversion. Neurology. 2006;67(9 Suppl 3):S12–13.

    PubMed  Google Scholar 

  21. Duff K, Beglinger LJ, Theriault D, et al. Cognitive deficits in Huntington’s disease on the Repeatable Battery for the Assessment of Neuropsychological Status. J Clin Exp Neuropsychol. 2009;1–9.

  22. Paulsen JS, Duff K. Extending MCI beyond Alzheimer disease. Neurology. 2009;72(13):1116–7.

    Article  PubMed  Google Scholar 

  23. •• Peavy GM, Jacobson MW, Goldstein JL, et al. Cognitive and functional decline in Huntington’s disease: Dementia criteria revisited. Move Disord. 2010;25(9):1163–1169. This is the first paper to explicitly criticize current dementia criteria and propose appropriate criteria specific to HD.

    Article  Google Scholar 

  24. Mickes L, Jacobson M, Peavy G, et al. A comparison of two brief screening measures of cognitive impairment in Huntington’s disease. Mov Disord. 2010;25(13):2229–33.

    Article  PubMed  Google Scholar 

  25. Hamilton JM, Salmon DP, Corey-Bloom J, et al. Behavioural abnormalities contribute to functional decline in Huntington’s disease. J Neurol Neurosurg Psychiatry. 2003;74(1):120–2.

    Article  PubMed  CAS  Google Scholar 

  26. Nehl C, Paulsen JS. Huntington Study Group: cognitive and psychiatric aspects of Huntington disease contribute to functional capacity. J Nerv Ment Dis. 2004;192(1):72–4.

    Article  PubMed  Google Scholar 

  27. Williams JK, Barnette JJ, Reed D, et al. Development of the Huntington disease family concerns and strategies survey from focus group data. J Nurs Meas. 2010;18(2):83–99.

    Article  PubMed  Google Scholar 

  28. Paulsen JS, Zimbelman JL, Hinton SC, et al. fMRI biomarker of early neuronal dysfunction in presymptomatic Huntington’s Disease. AJNR Am J Neuroradiol. 2004;25(10):1715–21.

    PubMed  Google Scholar 

  29. Nopoulos PC, Aylward EH, Ross CA, et al. Smaller intracranial volume in prodromal Huntington’s disease: evidence for abnormal neurodevelopment. Brain. 2011;134(Pt 1):137–42.

    Article  PubMed  Google Scholar 

  30. Lemay M, Fimbel E, Beuter A, et al. Sensorimotor mapping affects movement correction deficits in early Huntington’s disease. Exp Brain Res. 2005;165(4):454–60.

    Article  PubMed  CAS  Google Scholar 

  31. •• Say MJ, Jones R, Scahill RI, et al. Visuomotor integration deficits precede clinical onset in Huntington’s disease. Neuropsychologia 2011;49(2):264–270. This discusses a new task with potential for usage in clinical trials for HD.

    Article  PubMed  Google Scholar 

  32. •• Tabrizi SJ, Scahill RI, Durr A, et al. Biological and clinical changes in premanifest and early stage Huntington’s disease in the TRACK-HD study: the 12-month longitudinal analysis. Lancet Neurol. 2011;10(1):31–42. This is one of few papers showing longitudinal data useful for clinical trial design.

    Article  PubMed  Google Scholar 

  33. Solomon AC, Stout JC, Weaver M, et al. Ten-year rate of longitudinal change in neurocognitive and motor function in prediagnosis Huntington disease. Mov Disord. 2008;23(13):1830–6.

    Article  PubMed  Google Scholar 

  34. Rupp J, Blekher T, Jackson J, et al. Progression in Prediagnostic Huntington Disease. J Neurol Neurosurg Psychiatry. 2010;81(4):379–84.

    Google Scholar 

  35. Paulsen J. Early detection of Huntington’s disease. Future Neurology. 2010;5(1):85–104.

    Article  Google Scholar 

  36. Hinton SC, Paulsen JS, Hoffmann RG, et al. Motor timing variability increases in preclinical Huntington’s disease patients as estimated onset of motor symptoms approaches. J Int Neuropsychol Soc. 2007;13(3):539–43.

    Article  PubMed  Google Scholar 

  37. Zimbelman JL, Paulsen JS, Mikos A, et al. fMRI detection of early neural dysfunction in preclinical Huntington’s disease. J Int Neuropsychol Soc. 2007;13(5):758–69.

    Article  PubMed  Google Scholar 

  38. •• Rowe KC, Paulsen JS, Langbehn DR, et al. Self-paced timing detects and tracks change in prodromal Huntington disease. Neuropsychology 2010;24(4):435–442. This is a most comprehensive study of timing impairments in HD. Cross-sectional and longitudinal effects sizes are excellent supporting usage of this test in clinical trials.

    Article  PubMed  Google Scholar 

  39. Jin X, Costa RM. Start/stop signals emerge in nigrostriatal circuits during sequence learning. Nature. 2010;466(7305):457–62.

    Article  PubMed  CAS  Google Scholar 

  40. •• Stout JC, Paulsen JS, Queller S, et al. Neurocognitive signs in prodromal huntington disease. Neuropsychology 2011;25(1):1–14. This is a most comprehensive summary of cross-sectional effect sizes in prodromal HD using a proximity index to estimate stage of HD prodrome. All new tests published should be compared against these effect sizes for inclusion in HD clinical trials.

    Article  PubMed  Google Scholar 

  41. Bechtel N, Scahill RI, Rosas HD, et al. Tapping linked to function and structure in premanifest and symptomatic Huntington disease. Neurology. 2010;75(24):2150–60.

    Article  PubMed  CAS  Google Scholar 

  42. Johnson SA, Stout JC, Solomon AC, et al. Beyond disgust: impaired recognition of negative emotions prior to diagnosis in Huntington’s disease. Brain. 2007;130(Pt 7):1732–44.

    Article  PubMed  Google Scholar 

  43. Snowden JS, Austin NA, Sembi S, et al. Emotion recognition in Huntington’s disease and frontotemporal dementia. Neuropsychologia. 2008;46(11):2638–49.

    Article  PubMed  CAS  Google Scholar 

  44. Henley SMD, Wild EJ, Hobbs NZ, et al. Defective emotion recognition in early HD is neuropsychologically and anatomically generic. Neuropsychologia. 2008;46(8):2152–60.

    Article  PubMed  Google Scholar 

  45. de Gelder B, Van den Stock J, Balaguer RdD, Bachoud-Lévi A-C. Huntington’s disease impairs recognition of angry and instrumental body language. Neuropsychologia. 2008;46(1):369–73.

    Article  PubMed  Google Scholar 

  46. •• Calder AJ, Keane J, Young AW, et al. The relation between anger and different forms of disgust: Implications for emotion recognition impairments in Huntington's disease. Neuropsychologia 2010;48(9):2719–2729. This is a most comprehensive review of findings of emotional recognition in HD and an excellent study dissecting components of emotional recognition.

    Article  PubMed  Google Scholar 

  47. Hamilton JM, Murphy C, Paulsen JS. Odor detection, learning, and memory in Huntington’s disease. J Int Neuropsychol Soc. 1999;5(7):609–15.

    Article  PubMed  CAS  Google Scholar 

  48. Bacon Moore AS, Paulsen JS, Murphy C. A test of odor fluency in patients with Alzheimer’s and Huntington’s disease. J Clin Exp Neuropsychol. 1999;21(3):341–51.

    Article  PubMed  CAS  Google Scholar 

  49. Nordin S, Paulsen JS, Murphy C. Sensory- and memory-mediated olfactory dysfunction in Huntington’s disease. J Int Neuropsychol Soc. 1995;1(3):281–90.

    Article  PubMed  CAS  Google Scholar 

  50. Montoya A, Pelletier M, Menear M, et al. Episodic memory impairment in Huntington’s disease: a meta-analysis. Neuropsychologia. 2006;44(10):1984–94.

    Article  PubMed  Google Scholar 

  51. Solomon AC, Stout JC, Johnson SA, et al. Verbal episodic memory declines prior to diagnosis in Huntington’s disease. Neuropsychologia. 2007;45(8):1767–76.

    Article  PubMed  Google Scholar 

  52. Sadek JR, White DA, Taylor KI, et al. Retrograde amnesia in dementia: comparison of HIV-associated dementia, Alzheimer’s disease, and Huntington’s disease. Neuropsychology. 2004;18(4):692–9.

    Article  PubMed  Google Scholar 

  53. Paulsen JS, Butters N, Sadek JR, et al. Distinct cognitive profiles of cortical and subcortical dementia in advanced illness. Neurology. 1995;45(5):951–6.

    PubMed  CAS  Google Scholar 

  54. Paulsen JS, Butters N, Salmon DP, et al. Prism adaptation in Alzheimer’s and Huntington’s Disease. Neuropsychology. 1993;7(1):73–81.

    Article  Google Scholar 

  55. Carella F, Bressanelli M, Piacentini S, et al. A study of arm movements in Huntington’s disease under visually controlled and blindfolded conditions. Neurol Sci. 2003;23(6):287–93.

    Article  PubMed  CAS  Google Scholar 

  56. Montoya A, Price BH, Menear M, Lepage M. Brain imaging and cognitive dysfunctions in Huntington’s disease. J Psychiatry Neurosci. 2006;31(1):21–9.

    PubMed  Google Scholar 

  57. Filoteo JV, Delis DC, Roman MJ, et al. Visual attention and perception in patients with Huntington’s disease: comparisons with other subcortical and cortical dementias. J Clin Exp Neuropsychol. 1995;17(5):654–67.

    Article  PubMed  CAS  Google Scholar 

  58. Nehl C, Ready RE, Hamilton J, Paulsen JS. Effects of depression on working memory in presymptomatic Huntington’s disease. J Neuropsychiatry Clin Neurosci. 2001;13(3):342–6.

    Article  PubMed  CAS  Google Scholar 

  59. •• Thompson JC, Poliakoff E, Sollom AC, et al. Automaticity and attention in Huntington's disease: when two hands are not better than one. Neuropsychologia 2010;48(1):171–178. This is an excellent overview and dissection of attentional impairments in HD.

    Article  PubMed  Google Scholar 

  60. Smith MM, Long JD. Cognitive changes in prodromal Huntington Disease. Unpublished manuscript 2011, The University of Iowa Department of Psychiatry.

  61. Duff K, Beglinger LJ, Schultz SK, et al. Practice effects in the prediction of long-term cognitive outcome in three patient samples: a novel prognostic index. Arch Clin Neuropsychol. 2007;22(1):15–24.

    Article  PubMed  Google Scholar 

  62. Dutilh G, Krypotos AM, Wagenmakers EJ. Task-related versus stimulus-specific practice. Exp Psychol. 2011;1–9.

  63. Rosenblatt A, Kumar BV, Margolis RL, et al. Factors contributing to institutionalization in patients with Huntington’s disease. Mov Disord. 2011;Epub ahead of print. doi:10.1002/mds.23716.

  64. •• O’Rourke JJ, Beglinger LJ, Smith MM, et al. The trail making test in prodromal Huntington disease: Contributions of disease progression to test performance. J Clin Exp Neuropsychol. 2011;33(5):567–579. This is a most comprehensive paper on the dissection of this common task and its utility in HD.

    Article  PubMed  Google Scholar 

  65. Paulsen JS, Salmon DP, Monsch AU, et al. Discrimination of cortical from subcortical dementias on the basis of memory and problem-solving tests. J Clin Psychol. 1995;51(1):48–58.

    Article  PubMed  CAS  Google Scholar 

  66. Beglinger LJ, Nopoulos PC, Jorge RE, et al. White matter volume and cognitive dysfunction in early Huntington’s disease. Cogn Behav Neurol. 2005;18(2):102–7.

    Article  PubMed  Google Scholar 

  67. Monsch AU, Bondi MW, Butters N, et al. A comparison of category and letter fluency in Alzheimer’s disease and Huntington’s disease. Neuropsychology. 1994;8(1):25–30.

    Article  Google Scholar 

  68. Duff K, Paulsen JS, Beglinger LJ, et al. “Frontal” behaviors before the diagnosis of Huntington’s disease and their relationship to markers of disease progression: evidence of early lack of awareness. J Neuropsychiatry Clin Neurosci. 2010;22(2):196–207.

    Article  PubMed  Google Scholar 

  69. Paulsen JS, Stout JC, DeLaPena JH, et al. Frontal behavioral syndromes in cortical and subcortical dementia. Assessment. 1996;3(3):327–37.

    Article  Google Scholar 

  70. Paulsen JS, Stout JC, Tawfik-Reedy Z, et al. (editors). The utility of the Frontal Lobe Personality Scale (FLOPS) for characterizing behavior in dementia of the Alzheimer’s type (DAT) and Huntington’s disease (HD). Arch Clin Neuropsychol. 1996.

  71. Hartelius L, Jonsson M, Rickeberg A, Laakso K. Communication and Huntington’s disease: qualitative interviews and focus groups with persons with Huntington’s disease, family members, and carers. Int J Lang Commun Disord. 2010;45(3):381–93.

    Article  PubMed  Google Scholar 

  72. Rohrer D, Salmon DP, Wixted JT, Paulsen JS. The disparate effects of Alzheimer’s disease and Huntington’s disease on semantic memory. Neuropsychology. 1999;13(3):381–8.

    Article  PubMed  CAS  Google Scholar 

  73. Chenery HJ, Copland DA, Murdoch BE. Complex language functions and subcortical mechanisms: evidence from Huntington’s disease and patients with non-thalamic subcortical lesions. Int J Lang Commun Disord. 2002;37(4):459–74.

    Article  PubMed  Google Scholar 

  74. Saldert C, Fors A, Ströberg S, Hartelius L. Comprehension of complex discourse in different stages of Huntington’s disease. Int J Lang Commun Disord. 2010;45(6):656–69.

    Article  PubMed  Google Scholar 

  75. Ferm U, Sahlin A, Sundin L, Hartelius L. Using talking mats to support communication in persons with Huntington’s disease. Int J Lang Commun Disord. 2010;45(5):523–36.

    Article  PubMed  Google Scholar 

  76. Deckel AW, Morrison D. Evidence of a neurologically based “denial of illness” in patients with Huntington’s disease. Arch Clin Neuropsychol. 1996;11(4):295–302.

    Article  PubMed  CAS  Google Scholar 

  77. McGlynn SM. Behavioral approaches to neuropsychological rehabilitation. Psychol Bull. 1990;108(3):420–41.

    Article  PubMed  CAS  Google Scholar 

  78. Snowden JS, Craufurd D, Griffiths HL, Neary D. Awareness of involuntary movements in Huntington disease. Arch Neurol. 1998;55(6):801–5.

    Article  PubMed  CAS  Google Scholar 

  79. Vitale C, Pellecchia MT, Grossi D, et al. Unawareness of dyskinesias in Parkinson’s and Huntington’s diseases. Neurol Sci. 2001;22(1):105–6.

    Article  PubMed  CAS  Google Scholar 

  80. Ho AK, Robbins AO, Barker RA. Huntington’s disease patients have selective problems with insight. Mov Disord. 2006;21(3):385–9.

    Article  PubMed  Google Scholar 

  81. Hoth KF, Paulsen JS, Moser DJ, et al. Patients with Huntington’s disease have impaired awareness of cognitive, emotional, and functional abilities. J Clin Exp Neuropsychol. 2007;29(4):365–76.

    Article  PubMed  Google Scholar 

  82. Mestre T, Ferreira J, Coelho MM, et al. Therapeutic interventions for disease progression in Huntington’s disease. Cochrane Database Syst Rev. 2009;(3):CD006455.

  83. Adam OR, Jankovic J. Symptomatic treatment of Huntington disease. Neurotherapeutics. 2008;5(2):181–97.

    Article  PubMed  CAS  Google Scholar 

  84. Beglinger LJ, Adams WH, Paulson H, et al. Randomized controlled trial of atomoxetine for cognitive dysfunction in early Huntington disease. J Clin Psychopharmacol. 2009;29(5):484–7.

    Article  PubMed  CAS  Google Scholar 

  85. Vaccarino AL, Anderson K, Borowsky B, et al. An item response analysis of the motor and behavioral subscales of the unified Huntington’s disease rating scale in huntington disease gene expansion carriers. Mov Disord. 2011;26(5):877–84.

    Article  PubMed  Google Scholar 

  86. Vaccarino AL, Sills T, Borowsky B, et al. Assessment of cognitive symptoms in prodromal and early huntington disease. PLoS Currents: Huntington Disease [Internet Knol] 2011 Jun 21, Version 101: http://knol.google.com/k/anthony-l-vaccarino/assessment-of-cognitive-symptoms-in/19jerwgzmryar/16.

  87. Vaccarino AL, Sills T, Anderson KE, et al. Assessing behavioural manifestations prior to clinical diagnosis of huntington disease: “anger and irritability” and “obsessions and compulsions”. PLoS Currents: Huntington Disease [Internet] 2011 Mar 30 [revised 2011 Jun 13] Version 141: http://knol.google.com/k/anthony-l-vaccarino/assessing-behavioural-manifestations/19jerwgzmryar/19.

  88. Vaccarino AL, Sills T, Anderson KE, et al. Assessment of depression, anxiety and apathy in prodromal and early huntington disease. PLoS Currents: Huntington Disease [Internet] 2011 Apr 7 [revised 2011 Jun 17] Version 94: http://knol.google.com/k/anthony-l-vaccarino/assessment-of-depression-anxiety-and/19jerwgzmryar/11.

  89. Vaccarino AL, Sills T, Anderson KE, et al. Assessment of motor symptoms and functional impact in prodromal and early huntington disease. PLoS Currents: Huntington Disease [Internet] 2011 Jun 14, Version 209: http://knol.google.com/k/anthony-l-vaccarino/assessment-of-motor-symptoms-and/19jerwgzmryar/11.

  90. Teixeira AL, Barbosa IG, Diniz BS, Kummer A. Circulating levels of brain-derived neurotrophic factor: correlation with mood, cognition and motor function. Biomarkers of Medicine. 2010;4(6):871–87.

    Article  CAS  Google Scholar 

  91. Saleh N, Moutereau S, Azulay JP, et al. High insulinlike growth factor I is associate with cognitive decline in Huntington disease. Neurology. 2010;75(1):57–63.

    Article  PubMed  CAS  Google Scholar 

  92. Rowe KC, Paulsen JS, Langbehn DR, et al. Patterns of serotonergic antidepressant usage in prodromal Huntington disease. Psychiatry Res. 2011;In press.

Download references

Acknowledgment

J.S. Paulsen and the PREDICT–HD study are supported by the National Institutes for Health, National Institute of Neurological Disorders and Stroke (R01 NS040068-11), CHDI Foundation, Inc., and the National Institute of Neurological Disorders & Stroke, (R01 NS054893) Cognitive and Functional Brain Changes in Preclinical HD.

Disclosure

Conflicts of interest: J.S. Paulsen: has received a consulting fee or honoraria from Schlesinger Associates; and has received support for travel to meetings for a study from the National Institutes of Health, the CHDI Foundation, the Huntington’s Disease Society of America, and the Huntington’s Study Group.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Jane S. Paulsen.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Paulsen, J.S. Cognitive Impairment in Huntington Disease: Diagnosis and Treatment. Curr Neurol Neurosci Rep 11, 474–483 (2011). https://doi.org/10.1007/s11910-011-0215-x

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11910-011-0215-x

Keywords

Navigation