203 related articles for article (PubMed ID: 15305903)
1. Value of professional collaboration in the care of children with cancer and their families.
Eilertsen ME; Reinfjell T; Vik T
Eur J Cancer Care (Engl); 2004 Sep; 13(4):349-55. PubMed ID: 15305903
[TBL] [Abstract][Full Text] [Related]
2. Professional collaboration - support for children with cancer and their families - focus group interview - a source of information and knowledge - professionals' perspectives.
Bradley Eilertsen ME; Kristiansen K; Reinfjell T; Rannestad T; Indredavik MS; Vik T
J Interprof Care; 2009 Jul; 23(4):355-68. PubMed ID: 19370468
[TBL] [Abstract][Full Text] [Related]
3. Meeting the needs of parents around the time of diagnosis of disability among their children: evaluation of a novel program for information, support, and liaison by key workers.
Rahi JS; Manaras I; Tuomainen H; Hundt GL
Pediatrics; 2004 Oct; 114(4):e477-82. PubMed ID: 15466074
[TBL] [Abstract][Full Text] [Related]
4. A process for developing community consensus regarding the diagnosis and management of attention-deficit/hyperactivity disorder.
Foy JM; Earls MF
Pediatrics; 2005 Jan; 115(1):e97-104. PubMed ID: 15629972
[TBL] [Abstract][Full Text] [Related]
5. Exploring the role of partnership in the home care of children with special health needs: qualitative findings from two service evaluations.
McIntosh J; Runciman P
Int J Nurs Stud; 2008 May; 45(5):714-26. PubMed ID: 17307182
[TBL] [Abstract][Full Text] [Related]
6. Parents' experiences of collaboration with community healthcare professionals.
Jakobsen ES; Severinsson E
J Psychiatr Ment Health Nurs; 2006 Oct; 13(5):498-505. PubMed ID: 16965467
[TBL] [Abstract][Full Text] [Related]
7. The supportive and palliative care needs of Australian families of children who die from cancer.
Monterosso L; Kristjanson LJ; Phillips MB
Palliat Med; 2009 Sep; 23(6):526-36. PubMed ID: 19351793
[TBL] [Abstract][Full Text] [Related]
8. An exploration of best practice in multi-agency working and the experiences of families of children with complex health needs. What works well and what needs to be done to improve practice for the future?
Carter B; Cummings J; Cooper L
J Clin Nurs; 2007 Mar; 16(3):527-39. PubMed ID: 17335529
[TBL] [Abstract][Full Text] [Related]
9. Family involvement in the care of a hospitalised child: a questionnaire survey of Mozambican family caregivers.
Söderbäck M; Christensson K
Int J Nurs Stud; 2008 Dec; 45(12):1778-88. PubMed ID: 18657810
[TBL] [Abstract][Full Text] [Related]
10. Different priorities: a comparison of parents' and health professionals' perceptions of quality of life in quadriplegic cerebral palsy.
Morrow AM; Quine S; Loughlin EV; Craig JC
Arch Dis Child; 2008 Feb; 93(2):119-25. PubMed ID: 17932123
[TBL] [Abstract][Full Text] [Related]
11. School-age children with asthma and their parents: relationships with health care providers.
Buford TA
Issues Compr Pediatr Nurs; 2005; 28(3):153-62. PubMed ID: 16251161
[TBL] [Abstract][Full Text] [Related]
12. Fathers and the well-child visit.
Garfield CF; Isacco A
Pediatrics; 2006 Apr; 117(4):e637-45. PubMed ID: 16585280
[TBL] [Abstract][Full Text] [Related]
13. Being in tune with oneself, children, and parents: meanings of being a supporter to families with children who disabilities as narrated by parent-selected professionals.
Lindblad BM; Rasmussen BH; Sandman PO
J Pediatr Nurs; 2005 Jun; 20(3):214-23. PubMed ID: 15933661
[TBL] [Abstract][Full Text] [Related]
14. Two sides of the mirror: parents' and service providers' view on the family-centredness of care for children with cerebral palsy.
Jeglinsky I; Autti-Rämö I; Brogren Carlberg E
Child Care Health Dev; 2012 Jan; 38(1):79-86. PubMed ID: 21902711
[TBL] [Abstract][Full Text] [Related]
15. Preparation for cancer care: perceptions of newly qualified health care professionals.
Copp G; Caldwell K; Atwal A; Brett-Richards M; Coleman K
Eur J Oncol Nurs; 2007 Apr; 11(2):159-67. PubMed ID: 17126078
[TBL] [Abstract][Full Text] [Related]
16. Supportive and palliative care needs of families of children with life-threatening illnesses in Western Australia: evidence to guide the development of a palliative care service.
Monterosso L; Kristjanson LJ; Aoun S; Phillips MB
Palliat Med; 2007 Dec; 21(8):689-96. PubMed ID: 18073255
[TBL] [Abstract][Full Text] [Related]
17. Children with a long-term illness: parents' experiences of care.
Nuutila L; Salanterä S
J Pediatr Nurs; 2006 Apr; 21(2):153-60. PubMed ID: 16545675
[TBL] [Abstract][Full Text] [Related]
18. Effects of a nationwide programme: interventions to reduce perceived barriers to collaboration and to increase structural one-on-one contact.
Heideman J; Laurant M; Verhaak P; Wensing M; Grol R
J Eval Clin Pract; 2007 Dec; 13(6):860-6. PubMed ID: 18070256
[TBL] [Abstract][Full Text] [Related]
19. Parents' perspective on symptoms, quality of life, characteristics of death and end-of-life decisions for children dying from cancer.
Hechler T; Blankenburg M; Friedrichsdorf SJ; Garske D; Hübner B; Menke A; Wamsler C; Wolfe J; Zernikow B
Klin Padiatr; 2008; 220(3):166-74. PubMed ID: 18478489
[TBL] [Abstract][Full Text] [Related]
20. Parents' perceptions of the quality of pediatric and perinatal end-of-life care.
Widger K; Picot C
Pediatr Nurs; 2008; 34(1):53-8. PubMed ID: 18361087
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
