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Original Articles

Functional disability of children with spina bifida: Its impact on parents’ psychological status and family functioning

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Pages 322-328 | Received 10 Apr 2012, Accepted 02 May 2012, Published online: 19 Jun 2012

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Monique M. Ridosh, Kathleen J. Sawin, Bonita P. Klein-Tasman & Grayson N. Holmbeck. (2017) Depressive Symptoms in Parents of Children with Spina Bifida: A Review of the Literature. Comprehensive Child and Adolescent Nursing 40:2, pages 71-110.
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Articles from other publishers (12)

Eun Kyoung Choi, Hyeseon Yun & Eunjeong Bae. (2022) An Online-Based Transition Care Program for Adolescents with Spina Bifida Using Intervention Mapping: A Protocol for Program Development. International Journal of Environmental Research and Public Health 19:3, pages 1056.
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Frederik Booysen, Ferdi Botha & Edwin Wouters. (2021) Conceptual causal models of socioeconomic status, family structure, family functioning and their role in public health. BMC Public Health 21:1.
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Eun Kyoung Choi, Eunyoung Jung, Eunjeong Bae, Yoonhye Ji & Anna Lee. (2020) Two-Step Integrative Education Program and mHealth for Korean Children with Spina Bifida: A Quasi-Experimental Pre-Post Study. Journal of Pediatric Nursing 51, pages e92-e99.
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Angela Schulz, Mohit Jain, Thomas Butt, Rachel Ballinger, Lina Eliasson, Jake Macey, Tessa Peasgood, Andrew Olaye, Irini-Alexia Terzakis-Snyder, Iris Dyck & Andrea West. (2020) The Challenges of Living with and Caring for a Child or Children Affected by Neuronal Ceroid Lipofuscinosis Type 2 Disease: In-Depth Family Surveys in the United Kingdom and Germany. Journal of Inborn Errors of Metabolism and Screening 8.
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Maha Sudki Nahal, Åsa B. Axelsson, Asma Imam & Helena Wigert. (2018) Palestinian children's narratives about living with spina bifida: Stigma, vulnerability, and social exclusion. Child: Care, Health and Development 45:1, pages 54-62.
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Idunn Brekke, Elena Albertini Früh, Lisbeth Gravdal Kvarme & Henrik Holmstrøm. (2017) Long-time sickness absence among parents of pre-school children with cerebral palsy, spina bifida and down syndrome: a longitudinal study. BMC Pediatrics 17:1.
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Myles Maxey & Troy E. Beckert. (2016) Adolescents with Disabilities. Adolescent Research Review 2:2, pages 59-75.
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Maha Sudki Hmeidan Nahal, Helena Wigert, Asma Imam & Åsa B. Axelsson. (2017) From Feeling Broken to Looking Beyond Broken: Palestinian Mothers’ Experiences of Having a Child With Spina Bifida. Journal of Family Nursing 23:2, pages 226-251.
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Monique M. Ridosh, Kathleen J. Sawin, Rachel F. Schiffman & Bonnie P. Klein-Tasman. (2016) Factors associated with parent depressive symptoms and family quality of life in parents of adolescents and young adults with and without Spina Bifida. Journal of Pediatric Rehabilitation Medicine 9:4, pages 287-302.
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Femke Bannink, Richard Idro & Geert Van Hove. (2016) Parental stress and support of parents of children with spina bifida in Uganda. African Journal of Disability 5:1.
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Aashish T. Kabra, Paul J. Feustel & Barry A. Kogan. (2015) Screening for depression and anxiety in childhood neurogenic bladder dysfunction. Journal of Pediatric Urology 11:2, pages 75.e1-75.e7.
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Rosa M. Limiñana-Gras, María del Pilar Sánchez-López, María Teresa Calvo-Llena & Francisco Javier Corbalán. (2015) Personality Styles, Psychological Adjustment and Gender Differences in Parents of Children with Congenital Disabilities. Health 07:11, pages 1492-1505.
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