BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

107 related articles for article (PubMed ID: 15681516)

  • 1. 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; 23(4):685-93. PubMed ID: 15681516
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 32(6):456-64. PubMed ID: 19816167
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Familiality of benign and malignant paraproteinemias. A population-based cancer-registry study of multiple myeloma families.
    Ogmundsdóttir HM; Haraldsdóttirm V; Jóhannesson GM; Olafsdóttir G; Bjarnadóttir K; Sigvaldason H; Tulinius H
    Haematologica; 2005 Jan; 90(1):66-71. PubMed ID: 15642671
    [TBL] [Abstract][Full Text] [Related]  

  • 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. PubMed ID: 16753294
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Familial occurrence of complex regional pain syndrome.
    de Rooij AM; de Mos M; Sturkenboom MC; Marinus J; van den Maagdenberg AM; van Hilten JJ
    Eur J Pain; 2009 Feb; 13(2):171-7. PubMed ID: 18514555
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Family study of the inheritance of pectus excavatum.
    Creswick HA; Stacey MW; Kelly RE; Gustin T; Nuss D; Harvey H; Goretsky MJ; Vasser E; Welch JC; Mitchell K; Proud VK
    J Pediatr Surg; 2006 Oct; 41(10):1699-703. PubMed ID: 17011272
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Febrile convulsions in selected large families: a single-major-locus mode of inheritance?
    Maher J; McLachlan RS
    Dev Med Child Neurol; 1997 Feb; 39(2):79-84. PubMed ID: 9062421
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Study of inheritance of diabetes mellitus in Western Indian population by pedigree analysis.
    Deo SS; Gore SD; Deobagkar DN; Deobagkar DD
    J Assoc Physicians India; 2006 Jun; 54():441-4. PubMed ID: 16909690
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Heterogeneity of the genetic risk in age-related macular disease: a population-based familial risk study.
    Assink JJ; Klaver CC; Houwing-Duistermaat JJ; Wolfs RC; van Duijn CM; Hofman A; de Jong PT
    Ophthalmology; 2005 Mar; 112(3):482-7. PubMed ID: 15745778
    [TBL] [Abstract][Full Text] [Related]  

  • 10. CARD15 mutations in Dutch familial and sporadic inflammatory bowel disease and an overview of European studies.
    van der Linde K; Boor PP; Houwing-Duistermaat JJ; Crusius BJ; Wilson PJ; Kuipers EJ; de Rooij FW
    Eur J Gastroenterol Hepatol; 2007 Jun; 19(6):449-59. PubMed ID: 17489054
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Familial Ménière's disease in five generations.
    Frykholm C; Larsen HC; Dahl N; Klar J; Rask-Andersen H; Friberg U
    Otol Neurotol; 2006 Aug; 27(5):681-6. PubMed ID: 16868516
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Familial testicular torsion.
    Cubillos J; Palmer JS; Friedman SC; Freyle J; Lowe FC; Palmer LS
    J Urol; 2011 Jun; 185(6 Suppl):2469-72. PubMed ID: 21555017
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The genetic spectrum of a population-based sample of familial hemiplegic migraine.
    Thomsen LL; Kirchmann M; Bjornsson A; Stefansson H; Jensen RM; Fasquel AC; Petursson H; Stefansson M; Frigge ML; Kong A; Gulcher J; Stefansson K; Olesen J
    Brain; 2007 Feb; 130(Pt 2):346-56. PubMed ID: 17142831
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Alport syndrome. Molecular genetic aspects.
    Hertz JM
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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; 97(19):1466-74. PubMed ID: 16204696
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Multiplex families with multiple system atrophy.
    Hara K; Momose Y; Tokiguchi S; Shimohata M; Terajima K; Onodera O; Kakita A; Yamada M; Takahashi H; Hirasawa M; Mizuno Y; Ogata K; Goto J; Kanazawa I; Nishizawa M; Tsuji S
    Arch Neurol; 2007 Apr; 64(4):545-51. PubMed ID: 17420317
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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. PubMed ID: 18271762
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Familial aggregation of age-related macular degeneration in the Utah population.
    Luo L; Harmon J; Yang X; Chen H; Patel S; Mineau G; Yang Z; Constantine R; Buehler J; Kaminoh Y; Ma X; Wong TY; Zhang M; Zhang K
    Vision Res; 2008 Feb; 48(3):494-500. PubMed ID: 18252239
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Quantitative method to describe the inner characteristics of hereditary nonpolyposis colorectal cancer family].
    Zhang YZ; Sheng JQ; Li XM; Zhang H; Li SR; Li N
    Zhonghua Yi Xue Za Zhi; 2006 Oct; 86(40):2863-7. PubMed ID: 17200025
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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. PubMed ID: 19037864
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.