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 *

136 related articles for article (PubMed ID: 12795543)

  • 1. Growing up and living with cystic fibrosis: everyday life and encounters with the health care and social services--a qualitative study.
    Gjengedal E; Rustøen T; Wahl AK; Hanesta BR
    ANS Adv Nurs Sci; 2003; 26(2):149-59. PubMed ID: 12795543
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Parents' experiences of asthma: process from chaos to coping.
    Trollvik A; Severinsson E
    Nurs Health Sci; 2004 Jun; 6(2):93-9. PubMed ID: 15130094
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Experiences of adolescents with cystic fibrosis during their transition from paediatric to adult health care: a qualitative study of young Australian adults.
    Brumfield K; Lansbury G
    Disabil Rehabil; 2004 Feb; 26(4):223-34. PubMed ID: 15164956
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Children's experiences of cystic fibrosis: a systematic review of qualitative studies.
    Jamieson N; Fitzgerald D; Singh-Grewal D; Hanson CS; Craig JC; Tong A
    Pediatrics; 2014 Jun; 133(6):e1683-97. PubMed ID: 24843053
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Through the looking glass: children's perceptions of growing up with cystic fibrosis.
    D'Auria JP; Christian BJ; Richardson LF
    Can J Nurs Res; 1997; 29(4):99-112. PubMed ID: 9697438
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Living in limbo--patients with cystic fibrosis waiting for transplant.
    Macdonald K
    Br J Nurs; 2006 May 25-Jun 7; 15(10):566-72. PubMed ID: 16835554
    [TBL] [Abstract][Full Text] [Related]  

  • 7. One breath at a time: living with cystic fibrosis.
    Rinaldi Carpenter D; Narsavage GL
    J Pediatr Nurs; 2004 Feb; 19(1):25-32. PubMed ID: 14963867
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Intercountry adoption and nursing care.
    Rykkje L
    Scand J Caring Sci; 2007 Dec; 21(4):507-14. PubMed ID: 18036014
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Isolation, motivation and balance: living with type 1 or cystic fibrosis-related diabetes.
    Tierney S; Deaton C; Webb K; Jones A; Dodd M; McKenna D; Rowe R
    J Clin Nurs; 2008 Apr; 17(7B):235-43. PubMed ID: 18578799
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Transition - how adolescents with cystic fibrosis their parents experience the change from paediatric to adult care].
    Becher C; Regamey N; Spichiger E
    Pflege; 2014 Dec; 27(6):359-68. PubMed ID: 25416483
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Development and evaluation of a multi-family psychoeducational program for cystic fibrosis.
    Goldbeck L; Babka C
    Patient Educ Couns; 2001 Aug; 44(2):187-92. PubMed ID: 11479059
    [TBL] [Abstract][Full Text] [Related]  

  • 12. International adoption families: a unique health care journey.
    Smit EM
    Pediatr Nurs; 2010; 36(5):253-8. PubMed ID: 21067077
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Increased congregational support for parents of children with cystic fibrosis.
    Szczesniak RD; Zou Y; Wetzel JD; Krause N; Grossoehme DH
    J Relig Health; 2015 Apr; 54(2):664-75. PubMed ID: 25119628
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The experiences of family members in the year following the diagnosis of a child or adolescent with cancer: a qualitative systematic review.
    Mu PF; Lee MY; Sheng CC; Tung PC; Huang LY; Chen YW
    JBI Database System Rev Implement Rep; 2015 Jun; 13(5):293-329. PubMed ID: 26455612
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Family-centred care for families living with cystic fibrosis in a rural setting: A qualitative study.
    Jessup M; Smyth W; Abernethy G; Shields L; Douglas T;
    J Clin Nurs; 2018 Feb; 27(3-4):e590-e599. PubMed ID: 29048768
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Pathways to adult diagnosis of CF: the impact of pre-diagnosis experience on post-diagnosis responses and needs.
    Widerman E
    Patient Educ Couns; 2004 Jan; 52(1):69-77. PubMed ID: 14729293
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Parents' information needs about the treatment of their chronically ill child: a qualitative study.
    Hummelinck A; Pollock K
    Patient Educ Couns; 2006 Aug; 62(2):228-34. PubMed ID: 16139981
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Continuity of care and caring: what matters to parents of children with life-threatening conditions.
    Heller KS; Solomon MZ;
    J Pediatr Nurs; 2005 Oct; 20(5):335-46. PubMed ID: 16182093
    [TBL] [Abstract][Full Text] [Related]  

  • 19. What are the experiences of the child with a brain tumour and their parents?
    Soanes L; Hargrave D; Smith L; Gibson F
    Eur J Oncol Nurs; 2009 Sep; 13(4):255-61. PubMed ID: 19423391
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Parent interview findings regarding the impact of cystic fibrosis on families.
    Phillips S; Bohannon WE; Gayton WF; Friedman SB
    J Dev Behav Pediatr; 1985 Jun; 6(3):122-7. PubMed ID: 4008656
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.