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Results: 1 to 20 of 96

Similar articles for PubMed (Select 19816167)

1.

Initial report of a family registry of multiple myeloma.

Coleman EA, Lynch H, Enderlin C, Stewart B, Thomé SD, Kennedy R, Richardson-Nelson T, Barlogie B.

Cancer Nurs. 2009 Nov-Dec;32(6):456-64. doi: 10.1097/NCC.0b013e3181a90168.

PMID:
19816167
3.

Family history of hematopoietic malignancy and risk of lymphoma.

Chang ET, Smedby KE, Hjalgrim H, Porwit-MacDonald A, Roos G, Glimelius B, Adami HO.

J Natl Cancer Inst. 2005 Oct 5;97(19):1466-74.

4.

Familial risks and temporal incidence trends of multiple myeloma.

Altieri A, Chen B, Bermejo JL, Castro F, Hemminki K.

Eur J Cancer. 2006 Jul;42(11):1661-70. Epub 2006 Jun 6. Review.

PMID:
16753294
5.

Assessment of "gene-environment" interaction in cases of familial and sporadic pancreatic cancer.

Yeo TP, Hruban RH, Brody J, Brune K, Fitzgerald S, Yeo CJ.

J Gastrointest Surg. 2009 Aug;13(8):1487-94. doi: 10.1007/s11605-009-0923-6. Epub 2009 May 21.

PMID:
19459017
6.

Familial myeloma and monoclonal gammopathy: a report of eight African American families.

Jain M, Ascensao J, Schechter GP.

Am J Hematol. 2009 Jan;84(1):34-8. doi: 10.1002/ajh.21325.

PMID:
19037864
7.

Scoping the family history: assessment of Lynch syndrome (hereditary nonpolyposis colorectal cancer) in primary care settings--a primer for nurse practitioners.

Maradiegue A, Jasperson K, Edwards QT, Lowstuter K, Weitzel J.

J Am Acad Nurse Pract. 2008 Feb;20(2):76-84. doi: 10.1111/j.1745-7599.2007.00282.x. Review.

PMID:
18271762
8.

Familial multiple myeloma: a family study and review of the literature.

Lynch HT, Sanger WG, Pirruccello S, Quinn-Laquer B, Weisenburger DD.

J Natl Cancer Inst. 2001 Oct 3;93(19):1479-83. Review.

9.

Phenotypic heterogeneity in multiple myeloma families.

Lynch HT, Watson P, Tarantolo S, Wiernik PH, Quinn-Laquer B, Isgur Bergsagel K, Huiart L, Olopade OI, Sobol H, Sanger W, Hogg D, Weisenburger D.

J Clin Oncol. 2005 Feb 1;23(4):685-93.

10.

Prospective results of surveillance colonoscopy in dominant familial colorectal cancer with and without Lynch syndrome.

Dove-Edwin I, de Jong AE, Adams J, Mesher D, Lipton L, Sasieni P, Vasen HF, Thomas HJ.

Gastroenterology. 2006 Jun;130(7):1995-2000.

PMID:
16762622
11.

A review of genetic mutation in familial Hirschsprung's disease in South Africa: towards genetic counseling.

Moore SW, Zaahl MG.

J Pediatr Surg. 2008 Feb;43(2):325-9. doi: 10.1016/j.jpedsurg.2007.10.021.

PMID:
18280283
12.
13.

BRCA1 and BRCA2 mutations in breast and ovarian cancer syndrome: reflection on the Creighton University historical series of high risk families.

Sinilnikova OM, Mazoyer S, Bonnardel C, Lynch HT, Narod SA, Lenoir GM.

Fam Cancer. 2006;5(1):15-20. Review.

PMID:
16528604
14.

Multiple myeloma and family history of cancer. A case-control study.

Bourguet CC, Grufferman S, Delzell E, DeLong ER, Cohen HJ.

Cancer. 1985 Oct 15;56(8):2133-9.

PMID:
4027940
15.

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
16.

[Risk assessment for familial occurrence of breast cancer].

Chang-Claude J, Becher H, Hamann U, Schroeder-Kurth T.

Zentralbl Gynakol. 1995;117(8):423-34. German.

PMID:
7571905
17.

Multiple myeloma in north east Scotland: a review of incidence and survival over three decades.

Soutar RL, Dawson AA, Wilson BJ.

Health Bull (Edinb). 1996 May;54(3):232-40.

PMID:
8707567
18.

Risk patterns of multiple myeloma in Los Angeles County, 1972-1999 (United States).

Gebregziabher M, Bernstein L, Wang Y, Cozen W.

Cancer Causes Control. 2006 Sep;17(7):931-8.

PMID:
16841260
19.

Cancer incidence in the rural community of Tecumseh, Michigan: a pattern of increased lymphopoietic neoplasms.

Waterhouse D, Carman WJ, Schottenfeld D, Gridley G, McLean S.

Cancer. 1996 Feb 15;77(4):763-70.

PMID:
8616770
20.

Impact of a cancer registry-based genealogy service to support clinical genetics services.

Brewster DH, Fordyce A, Black RJ; Scottish Clinical Geneticists.

Fam Cancer. 2004;3(2):139-41.

PMID:
15340265
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