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Journal Abstract Search

191 related items for PubMed ID: 7675749

  • 1. [The diagnostic process in spina bifida: parents perception and viewpoint of clinical specialists].
    Herb G, Streeck S.
    Prax Kinderpsychol Kinderpsychiatr; 1995; 44(5):150-8. PubMed ID: 7675749
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  • 2. 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
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  • 3. [The analysis of physicians' work: announcing the end of attempts at in vitro fertilization].
    Santiago-Delefosse M, Cahen F, Coeffin-Driol C.
    Encephale; 2003; 29(4 Pt 1):293-305. PubMed ID: 14615699
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  • 4. 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
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  • 6. 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
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  • 7. Why do we need a diagnosis? A qualitative study of parents' experiences, coping and needs, when the newborn child is severely disabled.
    Graungaard AH, Skov L.
    Child Care Health Dev; 2007 May; 33(3):296-307. PubMed ID: 17439444
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  • 9. Prospective, longitudinal evaluation of health related quality of life in the pediatric spina bifida population undergoing reconstructive urological surgery.
    Parekh AD, Trusler LA, Pietsch JB, Byrne DW, DeMarco RT, Pope JC, Adams MC, Deshpande JK, Brock JW.
    J Urol; 2006 Oct; 176(4 Pt 2):1878-82. PubMed ID: 16945679
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  • 11. Quality of life for families with spina bifida in Kenya.
    van't Veer T, Meester H, Poenaru D, Kogei A, Augenstein K, Bransford R.
    Trop Doct; 2008 Jul; 38(3):160-2. PubMed ID: 18628544
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  • 12. The experience of finding an effective bowel management program for children with spina bifida: the parent's perspective.
    Sawin KJ, Thompson NM.
    J Pediatr Nurs; 2009 Aug; 24(4):280-91. PubMed ID: 19632505
    [Abstract] [Full Text] [Related]

  • 13. Neuropathic bladder and intermittent catheterization: social and psychological impact on families.
    Borzyskowski M, Cox A, Edwards M, Owen A.
    Dev Med Child Neurol; 2004 Mar; 46(3):160-7. PubMed ID: 14995085
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  • 14. PMTS and stress response sequences in parents of children with spina bifida.
    Vermaes IP, Gerris JR, Mullaart RA, Geerdink N, Janssens JM.
    Eur J Paediatr Neurol; 2008 Nov; 12(6):446-54. PubMed ID: 18222716
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  • 17. Improving the quality of end-of-life care in the pediatric intensive care unit: parents' priorities and recommendations.
    Meyer EC, Ritholz MD, Burns JP, Truog RD.
    Pediatrics; 2006 Mar; 117(3):649-57. PubMed ID: 16510643
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  • 18. Effective nurse parent communication: a study of parents' perceptions in the NICU environment.
    Jones L, Woodhouse D, Rowe J.
    Patient Educ Couns; 2007 Dec; 69(1-3):206-12. PubMed ID: 17936549
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  • 19. Family pediatrics: report of the Task Force on the Family.
    Schor EL, American Academy of Pediatrics Task Force on the Family.
    Pediatrics; 2003 Jun; 111(6 Pt 2):1541-71. PubMed ID: 12777595
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  • 20. Love and loss. Conversations with parents of babies with spinal bifida managed without surgery, 1971-1981.
    Delight E, Goodall J.
    Dev Med Child Neurol Suppl; 1990 Aug; 61():1-58. PubMed ID: 1698678
    [Abstract] [Full Text] [Related]

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