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Similar articles for PubMed (Select 12220449)

1.

Family issues in a psychoeducation group for women with a BRCA mutation.

Speice J, McDaniel SH, Rowley PT, Loader S.

Clin Genet. 2002 Aug;62(2):121-7.

PMID:
12220449
2.

Theory development from studies with young women with breast cancer who are BRCA mutation negative.

Hamilton R, Kopin S.

ANS Adv Nurs Sci. 2013 Apr-Jun;36(2):E41-53. doi: 10.1097/ANS.0b013e3182901ff1.

PMID:
23644270
3.

Closing the loop: action research in a multimodal hereditary cancer patient conference is an effective tool to assess and address patient needs.

Espenschied CR, MacDonald DJ, Culver JO, Sand S, Hurley K, Banks KC, Weitzel JN, Blazer KR.

J Cancer Educ. 2012 Jun;27(3):467-77. doi: 10.1007/s13187-012-0373-9.

4.

Family matters: examining a multi-family group intervention for women with BRCA mutations in the scope of genetic counselling.

Mendes A, Chiquelho R, Santos TA, Sousa L.

J Community Genet. 2010 Dec;1(4):161-8. doi: 10.1007/s12687-010-0022-0. Epub 2010 Oct 5.

5.

Attitudes to reproductive genetic testing in women who had a positive BRCA test before having children: a qualitative analysis.

Ormondroyd E, Donnelly L, Moynihan C, Savona C, Bancroft E, Evans DG, Eeles R, Lavery S, Watson M.

Eur J Hum Genet. 2012 Jan;20(1):4-10. doi: 10.1038/ejhg.2011.146. Epub 2011 Aug 3.

6.

Mood state profile and coping strategies after BRCA-1/2 genetic test disclosure: a retrospective study in Italy.

Annunziata MA, Muzzatti B, Narciso D, Mella S, Viel A, Bidoli E, Dolcetti R.

Support Care Cancer. 2011 Jun;19(6):733-5. doi: 10.1007/s00520-011-1097-9. Epub 2011 Jan 27. No abstract available.

PMID:
21267604
7.
8.

Women receiving news of a family BRCA1/2 mutation: messages of fear and empowerment.

Crotser CB, Dickerson SS.

J Nurs Scholarsh. 2010 Dec;42(4):367-78. doi: 10.1111/j.1547-5069.2010.01366.x. Epub 2010 Oct 4.

PMID:
21091619
9.

Learning about a twist in the road: perspectives of at-risk relatives learning of potential for cancer.

Crotser CB, Dickerson SS.

Oncol Nurs Forum. 2010 Nov;37(6):723-33. doi: 10.1188/10.ONF.723-733.

PMID:
21059584
10.

BRCA carriers' thoughts on risk management in relation to preimplantation genetic diagnosis and childbearing: when too many choices are just as difficult as none.

Quinn GP, Vadaparampil ST, Tollin S, Miree CA, Murphy D, Bower B, Silva C.

Fertil Steril. 2010 Nov;94(6):2473-5. doi: 10.1016/j.fertnstert.2010.03.064. Epub 2010 May 5.

PMID:
20447630
11.

"Am I my genes?": Questions of identity among individuals confronting genetic disease.

Klitzman R.

Genet Med. 2009 Dec;11(12):880-9. doi: 10.1097/GIM.0b013e3181bfd212.

12.

BRCA1 and BRCA2 germline mutation analysis among Indian women from south India: identification of four novel mutations and high-frequency occurrence of 185delAG mutation.

Vaidyanathan K, Lakhotia S, Ravishankar HM, Tabassum U, Mukherjee G, Somasundaram K.

J Biosci. 2009 Sep;34(3):415-22.

13.

The effect of BRCA gene testing on family relationships: A thematic analysis of qualitative interviews.

Douglas HA, Hamilton RJ, Grubs RE.

J Genet Couns. 2009 Oct;18(5):418-35. doi: 10.1007/s10897-009-9232-1. Epub 2009 May 29.

PMID:
19479365
14.

Survey of unaffected BRCA and mismatch repair (MMR) mutation positive individuals.

McKinnon W, Banks KC, Skelly J, Kohlmann W, Bennett R, Shannon K, Larson-Haidle J, Ashakaga T, Weitzel JN, Wood M.

Fam Cancer. 2009;8(4):363-9. doi: 10.1007/s10689-009-9248-6. Epub 2009 May 24.

15.

Identification of patients at high risk of psychological distress after BRCA1 genetic testing.

Ertmański S, Metcalfe K, Trempała J, Głowacka MD, Lubiński J, Narod SA, Gronwald J.

Genet Test Mol Biomarkers. 2009 Jun;13(3):325-30. doi: 10.1089/gtmb.2008.0126.

PMID:
19405874
16.

Prevalence of BRCA1 and BRCA2 gene mutations in families with medium and high risk of breast and ovarian cancer in Brazil.

Esteves VF, Thuler LC, Amêndola LC, Koifman RJ, Koifman S, Frankel PP, Vieira RJ; Brazilian Network of Breast and Ovarian Familial Cancer Aggregation.

Braz J Med Biol Res. 2009 May;42(5):453-7.

17.

Coping with genetic testing for breast cancer susceptibility.

Dougall AL, Smith AW, Somers TJ, Posluszny DM, Rubinstein WS, Baum A.

Psychosom Med. 2009 Jan;71(1):98-105. doi: 10.1097/PSY.0b013e318190d7b4. Epub 2009 Jan 5.

PMID:
19124622
18.

The trajectory of psychological impact in BRCA1/2 genetic testing: does time heal?

Beran TM, Stanton AL, Kwan L, Seldon J, Bower JE, Vodermaier A, Ganz PA.

Ann Behav Med. 2008 Oct;36(2):107-16. doi: 10.1007/s12160-008-9060-9. Epub 2008 Sep 12.

PMID:
18787910
19.

Five recurrent BRCA1/2 mutations are responsible for cancer predisposition in the majority of Slovenian breast cancer families.

Krajc M, Teugels E, Zgajnar J, Goelen G, Besic N, Novakovic S, Hocevar M, De Grève J.

BMC Med Genet. 2008 Sep 10;9:83. doi: 10.1186/1471-2350-9-83.

20.

BRCA1/2 in high-risk African American women with breast cancer: providing genetic testing through various recruitment strategies.

Pal T, Vadaparampil S, Betts J, Miree C, Li S, Narod SA.

Genet Test. 2008 Sep;12(3):401-7. doi: 10.1089/gte.2007.0108.

PMID:
18752448
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