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Results: 1 to 20 of 96

Similar articles for PubMed (Select 16055464)

1.

Collecting genetic information in primary care: evaluating a new family history tool.

Qureshi N, Bethea J, Modell B, Brennan P, Papageorgiou A, Raeburn S, Hapgood R, Modell M.

Fam Pract. 2005 Dec;22(6):663-9. Epub 2005 Jul 29.

2.

Family history in pediatric primary care.

Trotter TL, Martin HM.

Pediatrics. 2007 Sep;120 Suppl 2:S60-5. Review.

PMID:
17767006
3.

Collection and use of cancer family history in primary care.

Qureshi N, Wilson B, Santaguida P, Carroll J, Allanson J, Culebro CR, Brouwers M, Raina P.

Evid Rep Technol Assess (Full Rep). 2007 Oct;(159):1-84. Review.

4.

Assessing family history of heart disease in primary care consultations: a qualitative study.

Hall R, Saukko PM, Evans PH, Qureshi N, Humphries SE.

Fam Pract. 2007 Oct;24(5):435-42. Epub 2007 Aug 28.

5.

The relative accuracy of a questionnaire compared with pedigree analysis in genetic risk assessment for infertility.

Kaplan KD, Brown M, Croughan MS, Turek PJ.

J Urol. 2008 Apr;179(4):1499-505. doi: 10.1016/j.juro.2007.11.056. Epub 2008 Mar 4.

PMID:
18295272
6.

The use of family history questionnaires: an examination of genetic risk estimates and genetic testing eligibility in the non-responder population.

Armel SR, Hitchman K, Millar K, Zahavich L, Demsky R, Murphy J, Rosen B.

J Genet Couns. 2011 Aug;20(4):355-64. doi: 10.1007/s10897-011-9359-8. Epub 2011 Mar 30.

PMID:
21448763
7.

An overview of ethnicity and assessment of family history in primary care settings.

Maradiegue A, Edwards QT.

J Am Acad Nurse Pract. 2006 Oct;18(10):447-56. Review.

PMID:
16999709
8.

Development and evaluation of a brief self-completed family history screening tool for common chronic disease prevention in primary care.

Walter FM, Prevost AT, Birt L, Grehan N, Restarick K, Morris HC, Sutton S, Rose P, Downing S, Emery JD.

Br J Gen Pract. 2013 Jun;63(611):e393-400. doi: 10.3399/bjgp13X668186.

9.

Family history screening: use of the three generation pedigree in clinical practice.

Brock JA, Allen VM, Keiser K, Langlois S.

J Obstet Gynaecol Can. 2010 Jul;32(7):663-72. Review.

PMID:
20707955
10.

Family history questionnaires designed for clinical use: a systematic review.

Reid GT, Walter FM, Brisbane JM, Emery JD.

Public Health Genomics. 2009;12(2):73-83. doi: 10.1159/000160667. Epub 2008 Oct 2. Review.

PMID:
19039251
11.

A pilot study of a family history risk assessment tool for cardiovascular disease.

MacLeod HM, McNally EM.

J Genet Couns. 2008 Oct;17(5):499-507. doi: 10.1007/s10897-008-9174-z. Epub 2008 Sep 13.

PMID:
18791812
12.

Hereditary nonpolyposis colorectal cancer: diagnostic strategies and their implications.

Bonis PA, Trikalinos TA, Chung M, Chew P, Ip S, DeVine DA, Lau J.

Evid Rep Technol Assess (Full Rep). 2007 May;(150):1-180. Review.

13.

Reading between the lines: a comparison of responders and non-responders to a family history questionnaire and implications for cancer genetic counselling.

Appleby-Tagoe JH, Foulkes WD, Palma L.

J Genet Couns. 2012 Apr;21(2):273-91. doi: 10.1007/s10897-011-9399-0. Epub 2011 Aug 16.

PMID:
21845493
14.

Validation of a self-administered, computerized tool for collecting and displaying the family history of cancer.

Acheson LS, Zyzanski SJ, Stange KC, Deptowicz A, Wiesner GL.

J Clin Oncol. 2006 Dec 1;24(34):5395-402. Epub 2006 Nov 6.

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17.

Family history taking and genetic counselling in primary care.

Rose P, Humm E, Hey K, Jones L, Huson SM.

Fam Pract. 1999 Feb;16(1):78-83.

18.

The accuracy of ethnicity data in primary care and its impact on cardiovascular risk assessment and management--PREDICT CVD-8.

Riddell T, Lindsay G, Kenealy T, Jackson R, Crengle S, Bramley D, Wells S, Marshall R.

N Z Med J. 2008 Sep 5;121(1281):40-8.

PMID:
18797483
19.

Cancer family history reporting: impact of method and psychosocial factors.

Kelly KM, Shedlosky-Shoemaker R, Porter K, Remy A, DeSimone P, Andrykowski MA.

J Genet Couns. 2007 Jun;16(3):373-82. Epub 2007 Feb 23.

PMID:
17318453
20.

The genetic family history as a risk assessment tool in internal medicine.

Frezzo TM, Rubinstein WS, Dunham D, Ormond KE.

Genet Med. 2003 Mar-Apr;5(2):84-91.

PMID:
12644777
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