BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

96 related articles for article (PubMed ID: 26840856)

  • 1. Palliative Care Teams as Advocates for Adults with Sickle Cell Disease.
    Ajayi TA; Edmonds KP; Thornberry K; Atayee RA
    J Palliat Med; 2016 Feb; 19(2):195-201. PubMed ID: 26840856
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Transitioning Adolescents and Young Adults With Sickle Cell Disease From Pediatric to Adult Health Care: Provider Perspectives.
    Stollon NB; Paine CW; Lucas MS; Brumley LD; Poole ES; Peyton T; Grant AW; Jan S; Trachtenberg S; Zander M; Bonafide CP; Schwartz LA
    J Pediatr Hematol Oncol; 2015 Nov; 37(8):577-83. PubMed ID: 26492583
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Adolescents with sickle cell disease in a rural community: are they ready to transition to adulthood?
    Mennito S; Hletko P; Ebeling M; Amann LA; Roberts J
    South Med J; 2014 Sep; 107(9):578-82. PubMed ID: 25188623
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Primary Care Providers' Comfort Levels in Caring for Patients with Sickle Cell Disease.
    Whiteman LN; Haywood C; Lanzkron S; Strouse JJ; Feldman L; Stewart RW
    South Med J; 2015 Sep; 108(9):531-6. PubMed ID: 26332477
    [TBL] [Abstract][Full Text] [Related]  

  • 5. An Integrative Review: The Evolution of Provider Knowledge, Attitudes, Perceptions and Perceived Barriers to Caring for Patients with Sickle Cell Disease 1970-Now.
    Reich J; Cantrell MA; Smeltzer SC
    J Pediatr Hematol Oncol Nurs; 2023; 40(1):43-64. PubMed ID: 35854420
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Improving Clinician Attitudes of Respect and Trust for Persons With Sickle Cell Disease.
    Haywood C; Williams-Reade J; Rushton C; Beach MC; Geller G
    Hosp Pediatr; 2015 Jul; 5(7):377-84. PubMed ID: 26136312
    [TBL] [Abstract][Full Text] [Related]  

  • 7. How sickle cell disease patients experience, understand and explain their pain: An Interpretative Phenomenological Analysis study.
    Coleman B; Ellis-Caird H; McGowan J; Benjamin MJ
    Br J Health Psychol; 2016 Feb; 21(1):190-203. PubMed ID: 26333530
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A primary care provider's guide to preventive and acute care management of adults and children with sickle cell disease.
    Pack-Mabien A; Haynes J
    J Am Acad Nurse Pract; 2009 May; 21(5):250-7. PubMed ID: 19432908
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Adults with sickle cell disease: an interdisciplinary approach to home care and self-care management with a case study.
    Lee L; Askew R; Walker J; Stephen J; Robertson-Artwork A
    Home Healthc Nurse; 2012 Mar; 30(3):172-83; quiz 183-5. PubMed ID: 22391660
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Palliative care teams on the prairie: composition, perceived challenges & opportunities.
    Schrader SL; Nelson ML; Eidsness LM
    S D Med; 2007 Apr; 60(4):147-9, 151-3. PubMed ID: 17555150
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Sickle cell hospital unit: a disease-specific model.
    Adams-Graves P; Ostric EJ; Martin M; Richardson P; Lewis JB
    J Healthc Manag; 2008; 53(5):305-15; discussion 316-7. PubMed ID: 18856136
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Assessing the quality of life of children with sickle cell anaemia using self-, parent-proxy, and health care professional-proxy reports.
    Constantinou C; Payne N; Inusa B
    Br J Health Psychol; 2015 May; 20(2):290-304. PubMed ID: 24758574
    [TBL] [Abstract][Full Text] [Related]  

  • 13. End-of-life in adults with congenital heart disease: a call for early communication.
    Tobler D; Greutmann M; Colman JM; Greutmann-Yantiri M; Librach LS; Kovacs AH
    Int J Cardiol; 2012 Mar; 155(3):383-7. PubMed ID: 21094550
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Experiences of African Americans Living With Sickle Cell Disease.
    Wickersham KE; Dawson RM; Becker KP; Everhart KC; Miles HS; Schultz BE; Tucker CM; Wright PJ; Jenerette CM
    J Transcult Nurs; 2022 May; 33(3):334-345. PubMed ID: 35094624
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Development and evaluation of a palliative care curriculum for cystic fibrosis healthcare providers.
    Linnemann RW; O'Malley PJ; Friedman D; Georgiopoulos AM; Buxton D; Altstein LL; Sicilian L; Lapey A; Sawicki GS; Moskowitz SM
    J Cyst Fibros; 2016 Jan; 15(1):90-5. PubMed ID: 25817162
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Health related quality of life and perception of stigmatisation in adolescents living with sickle cell disease in Nigeria: A cross sectional study.
    Adeyemo TA; Ojewunmi OO; Diaku-Akinwumi IN; Ayinde OC; Akanmu AS
    Pediatr Blood Cancer; 2015 Jul; 62(7):1245-51. PubMed ID: 25810358
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Use of a depression and sleep impairment treatment guideline to improve quality of life for patients with sickle cell disease.
    Simo SM; Siela D
    Int J Palliat Nurs; 2018 May; 24(5):246-255. PubMed ID: 29792764
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Sickle cell disease patients with and without extremely high hospital use: pain, opioids, and coping.
    Brown SE; Weisberg DF; Balf-Soran G; Sledge WH
    J Pain Symptom Manage; 2015 Mar; 49(3):539-47. PubMed ID: 25057985
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Pain management in sickle cell disease: palliative care begins at birth?
    Benjamin L
    Hematology Am Soc Hematol Educ Program; 2008; ():466-74. PubMed ID: 19074128
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Pain management and quality of life in sickle cell disease.
    Howard J; Thomas VJ; Rawle HM
    Expert Rev Pharmacoecon Outcomes Res; 2009 Aug; 9(4):347-52. PubMed ID: 19670995
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.