Huntington’s disease
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Nance MA: Clinical aspects of CAG repeat diseases. Brain Pathol 1997, 7:881–900. A recent review of the clinical and genetic features of this newly recognized category of diseases.
Nance MA: Huntington disease—another chapter rewritten. Am J Hum Genet 1996, 59:1–6.
Leroi I, Michalon M: Treatment of the psychiatric manifestations of Huntington’s: a review of the literature. Can J Psychiatry 1998, 43(9):933–940. A recent clinically oriented review of the literature.
Schoenfeld M, Myers RN, Cupples LA, et al.: Increased rate of suicide among patients with Huntington’s disease. J Neurol Neurosurg Psychiatry 1984, 47:1283–1287.
Farrer LA: Suicide and attempted suicide in Huntington disease: implications for preclinical testing of persons at risk. Am J Med Genet 1986, 2:305–311.
Almqvist EW, Block M, Brinkman R, et al.: A worldwide assessment of the frequency of suicide, suicide attempts, or psychiatric hospitalization after predictive testing for Huntington disease. Am J Hum Genet 1999, 64:1293–1304. Large sample size helps allay physicians’ fears about patient suicide after confirmation of carrier status. Good testing protocols and screening are essential to continued success.
Rothlind JC, Bylsma FW, Peyser C, et al.: Cognitive and motor correlates of everyday functioning in early Huntington’s disease. J Nerv Ment Dis 1993, 181:194–199.
Bamford KA, Caine ED, Kido DK, et al.: A prospective evaluation of cognitive decline in early Huntington’s disease: functional and radiographic correlates. Neurology 1995, 45:1867–1873.
Wichmann T, DeLong MR: Functional and pathophysiological models of the basal ganglia. Curr Opin Neurobiol 1996, 6:751–758.
Storey E, Beal MF: Neurochemical substrates of rigidity and chorea in Huntington’s disease. Brain 1993, 116:1201–1222.
Lauterbach EC, Cummings JL, Duffy J: Neuropsychiatric correlates and treatment of lenticulostriatal diseases. J Neuropsychiatry Clin Neurosci 1998, 10(3):249–266.
Rosenblatt A, Ranen NG, Nance MA, Paulsen JS: A Physician’s Guide to the Management of Huntington’s Disease, edn 2. New York: Huntington’s Disease Society of America; 1999:41. The management of Huntington’s disease is reviewed by a group of experienced clinicians who address the full range of issues encountered by patients and families. Very useful sections on behavioral and environmental strategies for caregivers are included.
Jenson P, Fenge K, Bolwig TG, et al.: Crime in Huntington’s disease: a study of more registered offences among patients, relatives, and controls. J Neurol Neurosurg Psychiatry 1998, 65:467–471. The only systematic look in the literature at crime rates for patients with Huntington’s disease.
Sanberg PR, Fibiger HC, Mark RF: Body weight and dietary factors in Huntington’s disease patients compared with matched controls. Med J Aust 1981, 1:407–409.
Chase TN: Rational approaches to the pharmacotherapy of chorea. In Basal Ganglia. Edited by Yahr MD. New York: Raven Press; 1976:337–350.
Shale H, Tanner C: Pharmacological options for the management of dyskinesias. Drugs 1996, 52:849–860.
van Vugt JPP, van Hilten BJ, Roos RAC: Hypokinesia in Huntington’s disease. Mov Disord 1996, 11(4):384–388.
Richelson E: Preclinical pharmacology of neuroleptics: focus on new generation compounds. J Clin Psychiatry 1996, 57(suppl 11):4–11.
Casey DE: The relationship of pharmacology to side effects. J Clin Psychiatry 1997, 58(suppl 10):55–62.
Goff DC, Baldessarini RJ: Drug interactions with antipsychotic agents. J Clin Psychopharmacol 1993, 13:57–67.
Collaborative Working Group on Clinical Trial Evaluation: Assessment of EPS and tardive dyskinesia in clinical trials. J Clin Psychiatry 1998, 59(suppl 12):23–27.
Reveley MA, Dursun SM, Andrews H: A comparative trial of use of sulpiride and risperidone in Huntington’s disease: a pilot study. J Psychopharmacol 1996, 10:162–165.
Dallocchio C, Buffa C, Tinelli C, Mazzarello P: Effectiveness of risperidone in Huntington chorea patients. J Clin Psychopharmacol 1999, 19:101–103.
Chouinard G, Jones B, Remington G, et al.: A Canadian multicenter placebo-controlled study of fixed doses of risperidone and haloperidol in the treatment of chronic schizophrenic patients. J Clin Psychopharmacol 1993, 13:25–40.
Factor SA, Friedman JH: The emerging role of clozapine in the treatment of movement disorders. Mov Disord 1997, 12:483–496.
Bonuccelli U, Ceravolo R, Maremmani C, et al.: Clozapine in Huntington’s chorea. Neurology 1994, 44:821–823.
van Vugt JPP, Siesling S, Vergeer M, et al.: Clozapine versus placebo in Huntington’s disease: a double blind randomised comparative study. J Neurol Neurosurg Psychiatry 1997, 63:35–39.
Ereshefsky L: Pharmacokinetics and drug interactions: update for new antipsychotics. J Clin Psychiatry 1996, 57(suppl 11):12–25.
Leszczyszyn D, Nohria V, Anderson S: Sustained improvement of juvenile Huntington disease with levodopa/carbidopa [abstract]. Mov Disord 1997, 12:846.
Racette BA, Perlmutter JS: Levodopa responsive parkinsonism in an adult with Huntington’s disease. J Neurol Neurosurg Psychiatry 1998, 64:557–579.
Folstein SE, Chase GA, Wahl WE, et al.: Huntington’s disease in Maryland: clinical aspects of racial variation. Am J Hum Genet 1987, 41:168–179.
Burns A, Folstein S, Brandt J, et al.: Clinical assessment of irritability, aggression, and apathy in Huntington and Alzheimer disease. J Nerv Ment Dis 1999, 178(1):20–26.
Mendez MF: Huntington’s disease: update and review of neuropsychiatric aspects. Int J Psychiatry Med 1994, 24(3):189–208.
Silvestri R, Raffaele M, De Domenico P, et al.: Sleep features in Tourette’s syndrome, neuroacanthocytosis and Huntington’s chorea. Neurophysiol Clin 1995, 25(2):66–77.
Aldrich MS: Insomnia in neurological diseases. J Psychosom Res 1993, 17(suppl 1):1–11.
Taylor N, Bramble D: Sleep disturbance and Huntington’s disease [letter]. Br J Psychiatry 1997, 171:393.
Fedoroff JP, Peyser C, Franz ML, et al.: Sexual disorders in Huntington’s disease. J Neuropsychiatry 1994, 6:147–153.
Rich SS, Ovsiew F: Leuprolide acetate for exhibitionism in Huntington’s disease. Mov Disord 1994, 9(3):353–357.
Ranen NG, Peyser CE, Folstein SE: ECT as a treatment for depression in Huntington’s disease. J Neuropsychiatry 1994, 6(2):154–159.
International Huntington Association (IHA) and the World Federation of Neurology (WFN) Research Group on Huntington’s Chorea: Guidelines for the molecular genetics predictive test in Huntington’s disease. Neurology 1994, 44:1533–1536.
Hersch S, Jones R, Koroshetz W, Quaid K: The neurogenetics genie: testing for the Huntington’s disease mutation. Neurology 1994, 44:1369–1373. Discussion of the recommended protocol for genetic testing in Huntington’s disease. Outlines the rationale and reviews the issues that should be considered by all clinicians recommending such testing.
The American College of Medical Genetics/American Society of Human Genetics Huntington Disease Genetic Testing Working Group: Laboratory guidelines for Huntington disease genetic testing. Am J Hum Genet 1998, 62:1243–1247.
Feigin A: Advances in Huntington’s disease: implications for experimental therapeutics. Curr Opin Neurol 1998, 11:357–362. Review of the clinical implications of recent basic science advances in understanding the molecular pathology of Huntington’s disease.
Rosas HD, Koroshetz WJ, Jenkins BG, et al.: Riluzole therapy in Huntington’s disease (HD). Mov Disord 1999, 14:326–330.
Kieburtz K, Feigin A, McDermott M, et al.: A controlled trial of remacemide hydrochloride in Huntington’s disease. Mov Disord 1996, 11:273–277.
Kieburtz K: Antiglutamate therapies in Huntington’s disease. J Neural Transm Suppl 1999, 55:97–102.
Koroshetz WJ, Jenkins BG, Rosen BR, Beal MF: Energy metabolism defects in Huntington’s disease and effects of coenzyme Q10. Ann Neurol 1997, 41:160–165.
Peyser CE, Folstein M, Chase GA, et al.: Trial of d-alphatocopherol in Huntington’s disease. Am J Psychiatry 1995, 152:1771–1775.
Ranen NG, Peyser CE, Coyle JT, et al.: A controlled trial of idebenone in Huntington’s disease. Mov Disord 1996, 11:549–554.
Shannon KM, Kordower JH: Neural transplantation for Huntington’s disease: experimental rationale and recommendations for clinical trials. Cell Transplant 1996, 5:339–352.
Kopyov OV, Jacques S, Lieberman A, et al.: Safety of intrastriatal neurotransplantation for Huntington’s disease patients. Exp Neurol 1998, 149:97–108.
University of Kansas Department of Neurology Huntington’s disease Web page: http://www.kumc.edu/ hospital/huntingtons/HSGFTrans.html.