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Items: 1 to 20 of 83

1.

DNA testing and genetic counseling: truth or consequences.

Reynolds NC, Lebel RR, Hamsher Kde S, Blackwell B, Elejalde BR, Winter GR.

Wis Med J. 1994 Feb;93(2):51-4. Review.

PMID:
8191778
2.

American Society of Clinical Oncology policy statement update: genetic testing for cancer susceptibility.

American Society of Clinical Oncology.

J Clin Oncol. 2003 Jun 15;21(12):2397-406. Epub 2003 Apr 11.

PMID:
12692171
3.

Psychological aspects of genetic counselling: a review of the experience with Huntington's disease.

van 't Spijker A, ten Kroode HF.

Patient Educ Couns. 1997 Sep-Oct;32(1-2):33-40. Review.

PMID:
9355570
4.

To know or not to know: a review of behaviour and suicidal ideation in preclinical Huntington's disease.

Robins Wahlin TB.

Patient Educ Couns. 2007 Mar;65(3):279-87. Epub 2006 Sep 26. Review.

PMID:
17000074
5.

Psychological aspects of genetic counseling: a legal perspective.

Sharpe NF.

Am J Med Genet. 1994 Apr 15;50(3):234-8. Review.

PMID:
8042666
6.

Genetic jeopardy and the new clairvoyance.

Wexler NS.

Prog Med Genet. 1985;6:277-304. Review. No abstract available.

PMID:
2941821
7.

Adults seeking presymptomatic gene testing for Huntington disease.

Williams JK, Schutte DL, Evers CA, Forcucci C.

Image J Nurs Sch. 1999;31(2):109-14.

PMID:
10380384
8.

Attitudes of Dutch general practitioners towards presymptomatic DNA-testing for Huntington disease.

Thomassen R, Tibben A, Niermeijer MF, van der Does E, van de Kamp JJ, Verhage F.

Clin Genet. 1993 Feb;43(2):63-8.

PMID:
8448902
9.

Genetic testing and mental health: the model of Huntington disease.

Williams JK, Schutte DL.

Online J Issues Nurs. 2000;5(3):3. Review.

PMID:
11380269
10.

[Analysis of 14 individuals who requested predictive genetic testing for hereditary neuromuscular diseases].

Yoshida K, Tamai M, Kubota T, Kawame H, Amano N, Ikeda S, Fukushima Y.

Rinsho Shinkeigaku. 2002 Feb;42(2):113-7. Japanese.

PMID:
12424959
11.

A hereditary disorder in the family and the family life cycle: Huntington disease as a paradigm.

Brouwer-Dudokdewit AC, Savenije A, Zoeteweij MW, Maat-Kievit A, Tibben A.

Fam Process. 2002 Winter;41(4):677-92.

PMID:
12613124
12.

Informed consent and Huntington disease: a model for communication.

Sharpe NF.

Am J Med Genet. 1994 Apr 15;50(3):239-46. Review.

PMID:
8042667
13.

Testing for the Huntington gene: a right to know, a right not to know, or a duty to know.

Shaw MW.

Am J Med Genet. 1987 Feb;26(2):243-6. No abstract available.

PMID:
2949608
14.

Disclosures of Huntington disease risk within families: patterns of decision-making and implications.

Klitzman R, Thorne D, Williamson J, Chung W, Marder K.

Am J Med Genet A. 2007 Aug 15;143A(16):1835-49.

PMID:
17632780
15.

The whole truth and nothing but the truth, but what is the truth?

van den Boer-van den Berg HM, Maat-Kievit AA.

J Med Genet. 2001 Jan;38(1):39-42.

16.

Predictive testing for Huntington's disease: risk perception, reasons for testing and psychological profile of test applicants.

Decruyenaere M, Evers-Kiebooms G, Boogaerts A, Cassiman JJ, Cloostermans T, Demyttenaere K, Dom R, Fryns JP, Van den Berghe H.

Genet Couns. 1995;6(1):1-13.

PMID:
7794556
17.

High suicidal ideation in persons testing for Huntington's disease.

Robins Wahlin TB, Bäckman L, Lundin A, Haegermark A, Winblad B, Anvret M.

Acta Neurol Scand. 2000 Sep;102(3):150-61.

PMID:
10987374
18.

Pitfalls in counseling for predictive testing in Huntington disease.

Demyttenaere K, Evers-Kiebooms G, Decruyenaere M.

Birth Defects Orig Artic Ser. 1992;28(1):105-11. No abstract available.

PMID:
1340218
19.

[About Huntington's disease: role of families and health professionals in information transmission].

Delliaux M, Delval A, Krystkowiak P, Destée A, Defebvre L, Dujardin K.

Rev Neurol (Paris). 2008 Feb;164(2):148-55. doi: 10.1016/j.neurol.2007.08.002. Epub 2008 Feb 4. French.

PMID:
18358873
20.

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