Literature DB >> 7914682

The neurogenetics genie: testing for the Huntington's disease mutation.

S Hersch1, R Jones, W Koroshetz, K Quaid.   

Abstract

Even though the discovery of the HD gene will make genetic testing much easier to perform, until there is an effective treatment, it will be no easier for HD families to learn who among them carries the mutation. We believe that the standard of care for obtaining genetic testing for HD, as well as for other inherited neurodegenerative disorders, must continue to include extensive counseling, psychological assessment and support, a neurologic examination, and post-test follow-up. We advocate a flexible approach consistent with the individual's particular needs, but we emphasize that it is essential that these basic elements be adequately addressed.

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Year:  1994        PMID: 7914682     DOI: 10.1212/wnl.44.8.1369

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  5 in total

1.  Huntington's Disease.

Authors: 
Journal:  Curr Treat Options Neurol       Date:  2000-05       Impact factor: 3.598

Review 2.  Huntington's disease genetics.

Authors:  Richard H Myers
Journal:  NeuroRx       Date:  2004-04

Review 3.  An overview of psychiatric symptoms in Huntington's disease.

Authors:  K E Anderson; K S Marder
Journal:  Curr Psychiatry Rep       Date:  2001-10       Impact factor: 5.285

4.  PRECREST: a phase II prevention and biomarker trial of creatine in at-risk Huntington disease.

Authors:  Herminia D Rosas; Gheorghe Doros; Sona Gevorkian; Keith Malarick; Martin Reuter; Jean-Philippe Coutu; Tyler D Triggs; Paul J Wilkens; Wayne Matson; David H Salat; Steven M Hersch
Journal:  Neurology       Date:  2014-02-07       Impact factor: 9.910

5.  Emotional and functional impact of DNA testing on patients with symptoms of Huntington's disease.

Authors:  J Jankovic; J Beach; T Ashizawa
Journal:  J Med Genet       Date:  1995-07       Impact factor: 6.318

  5 in total

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