These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

161 related articles for article (PubMed ID: 27320470)

  • 21. Attitudes toward clinical trials among patients with sickle cell disease.
    Haywood C; Lanzkron S; Diener-West M; Haythornthwaite J; Strouse JJ; Bediako S; Onojobi G; Beach MC;
    Clin Trials; 2014 Jun; 11(3):275-283. PubMed ID: 24532686
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A longitudinal examination predicting emergency room use in children with sickle cell disease and their caregivers.
    Brown RT; Connelly M; Rittle C; Clouse B
    J Pediatr Psychol; 2006 Mar; 31(2):163-73. PubMed ID: 16467316
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Family Resilience From the Perspective of Caregivers of Youth With Sickle Cell Disease.
    Reader SK; Pantaleao A; Keeler CN; Ruppe NM; Kazak AE; Rash-Ellis DL; Wadman J; Miller RE; Deatrick JA
    J Pediatr Hematol Oncol; 2020 Mar; 42(2):100-106. PubMed ID: 31815887
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Correlates of pain-rating concordance for adolescents with sickle cell disease and their caregivers.
    Barakat LP; Simon K; Schwartz LA; Radcliffe J
    Clin J Pain; 2008 Jun; 24(5):438-46. PubMed ID: 18496309
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Sensitivity of alternative measures of functioning and wellbeing for adults with sickle cell disease: comparison of PROMIS® to ASCQ-Me℠.
    Keller S; Yang M; Treadwell MJ; Hassell KL
    Health Qual Life Outcomes; 2017 Jun; 15(1):117. PubMed ID: 28577358
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Stakeholder Views of Clinical Trials in Low- and Middle-Income Countries: A Systematic Review.
    Joseph PD; Caldwell PH; Tong A; Hanson CS; Craig JC
    Pediatrics; 2016 Feb; 137(2):e20152800. PubMed ID: 26812926
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Disease management, coping, and functional disability in pediatric sickle cell disease.
    Oliver-Carpenter G; Barach I; Crosby LE; Valenzuela J; Mitchell MJ
    J Natl Med Assoc; 2011 Feb; 103(2):131-7. PubMed ID: 21443065
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Family pediatrics: report of the Task Force on the Family.
    Schor EL;
    Pediatrics; 2003 Jun; 111(6 Pt 2):1541-71. PubMed ID: 12777595
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Desire for parenthood and reproductive health knowledge in adolescents and young adults with sickle cell disease and their caregivers.
    Nahata L; Caltabellotta NM; Ball K; O'Brien SH; Creary SE
    Pediatr Blood Cancer; 2018 Feb; 65(2):. PubMed ID: 28944997
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Initial Evaluation of the Pediatric PROMIS® Health Domains in Children and Adolescents With Sickle Cell Disease.
    Dampier C; Barry V; Gross HE; Lui Y; Thornburg CD; DeWalt DA; Reeve BB
    Pediatr Blood Cancer; 2016 Jun; 63(6):1031-7. PubMed ID: 26895143
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Health-related quality of life after allogeneic hematopoietic stem cell transplantation for sickle cell disease.
    Bhatia M; Kolva E; Cimini L; Jin Z; Satwani P; Savone M; George D; Garvin J; Paz ML; Briamonte C; Cruz-Arrieta E; Sands S
    Biol Blood Marrow Transplant; 2015 Apr; 21(4):666-72. PubMed ID: 25559691
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Knowledge, attitudes and beliefs of primary caretakers towards sickle cell anaemia in children.
    Macharia WM; Shiroya A; Njeru EK
    East Afr Med J; 1997 Jul; 74(7):416-9. PubMed ID: 9491171
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Decision-making by adolescents and parents of children with cancer regarding health research participation.
    Read K; Fernandez CV; Gao J; Strahlendorf C; Moghrabi A; Pentz RD; Barfield RC; Baker JN; Santor D; Weijer C; Kodish E
    Pediatrics; 2009 Sep; 124(3):959-65. PubMed ID: 19706586
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Medical mistrust, perceived discrimination, and satisfaction with health care among young-adult rural latinos.
    López-Cevallos DF; Harvey SM; Warren JT
    J Rural Health; 2014; 30(4):344-51. PubMed ID: 24576017
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The Kennedy Krieger Independence Scales-Sickle Cell Disease: Executive components of transition readiness.
    Jones KE; Jacobson LA; Tarazi RA
    Rehabil Psychol; 2017 Aug; 62(3):249-257. PubMed ID: 28836806
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Fatigue in Children With Sickle Cell Disease: Association With Neurocognitive and Social-Emotional Functioning and Quality of Life.
    Anderson LM; Allen TM; Thornburg CD; Bonner MJ
    J Pediatr Hematol Oncol; 2015 Nov; 37(8):584-9. PubMed ID: 26479993
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Comprehensive, integrative management of pain for patients with sickle-cell disease.
    Yoon SL; Black S
    J Altern Complement Med; 2006 Dec; 12(10):995-1001. PubMed ID: 17212571
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The flip-side of social capital: the distinctive influences of trust and mistrust on health in rural China.
    Wang H; Schlesinger M; Wang H; Hsiao WC
    Soc Sci Med; 2009 Jan; 68(1):133-42. PubMed ID: 18986744
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Perceived Racial Bias and Health-Related Stigma Among Youth with Sickle Cell Disease.
    Wakefield EO; Popp JM; Dale LP; Santanelli JP; Pantaleao A; Zempsky WT
    J Dev Behav Pediatr; 2017; 38(2):129-134. PubMed ID: 28059954
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Risk-resistance adaptation model for caregivers and their children with sickle cell syndromes.
    Brown RT; Lambert R; Devine D; Baldwin K; Casey R; Doepke K; Ievers CE; Hsu L; Buchanan I; Eckman J
    Ann Behav Med; 2000; 22(2):158-69. PubMed ID: 10962709
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.