Search Results - Agneta Anderzén-Carlsson

Young children's experiences of support when fearful during treatment for acute lymphoblastic leukaemia-A longitudinal interview study by Ingela Leibring, Agneta Anderzén‐Carlsson

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Patients' and radiographers' experiences of dose reducing abdominal compression in radiographic examinations-A qualitative study by Oili Piippo‐Huotari, Eva Funk, Håkan Geijer, Agneta Anderzén‐Carlsson

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Interventions for adults with deafblindness - an integrative review by Camilla Warnicke, Moa Wahlqvist, Agneta Anderzén-Carlsson, Ann-Sofie Sundqvist

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Congenital chloride diarrhea and Pendred syndrome: case report of siblings with two rare recessive disorders of SLC26 family genes by Eva Lindberg, Claes Moller, Juha Kere, Satu Wedenoja, Agneta Anderzén-Carlsson

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Community-based support for children who are next-of-kin for a parent experiencing illness or disability - a scoping review by Anne Kjersti Myhrene Steffenak, Agneta Anderzén-Carlsson, Elin Opheim, Tuva Sandsdalen

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'All for the well-being of the infant': nurses' perceptions of preterm infants' eye examinations: a phenomenographic study by Martina Carlsen Misic, Emma Olsson, Randi Dovland Andersen, Agneta Anderzén-Carlsson

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Public health nurses' experiences working with children who are next of kin: a qualitative study by Marie Dahlen Granrud, Tuva Sandsdalen, Agneta Anderzén-Carlsson, Anne Kjersti Myhrene Steffenak

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Children with Cerebral Palsy and Their Parents Have Different Experiences of Pain Management: A Qualitative Study by Elisabeth Rønning Rinde, Agneta Anderzén-Carlsson, Reidun Birgitta Jahnsen, Randi Dovland Andersen

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How paediatric departments in Sweden facilitate giving children a voice on their experiences of healthcare: A cross‐sectional study by Anna Nordlind, Ann‐Sofie Sundqvist, Agneta Anderzén‐Carlsson, Ann‐Charlotte Almblad, Karin Ängeby

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Translation and psychometric evaluation of the Swedish versions of the Nuss Questionnaire modified for Adults and the Single Step Questionnaire by Louise Norlander, Jan Karlsson, Agneta Anderzén-Carlsson, Mårten Vidlund, Mats Dreifaldt, Jesper Andreasson, Ann-Sofie Sundqvist

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Translation, cultural adaptation and validation of a patient‐reported experience measure for children by Anna Nordlind, Agneta Anderzén‐Carlsson, Ann‐Sofie Sundqvist, Karin Ängeby, Jo Wray, Geralyn Oldham, Ann‐Charlotte Almblad

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Cultural adaptation and harmonization of four Nordic translations of the revised Premature Infant Pain Profile (PIPP-R) by Emma Olsson, Agneta Anderzén-Carlsson, Sigríður María Atladóttir, Anna Axelin, Marsha Campbell-Yeo, Mats Eriksson, Guðrún Kristjánsdóttir, Emilia Peltonen, Bonnie Stevens, Bente Vederhus, Randi Dovland Andersen

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Pain burden in children with cerebral palsy (CPPain) survey: Study protocol by Randi Dovland Andersen, Lara Genik, Ann I. Alriksson‐Schmidt, Agneta Anderzen‐Carlsson, Chantel Burkitt, Sindre K. Bruflot, Christine T. Chambers, Reidun B. Jahnsen, Ira Jeglinsky‐Kankainen, Olav Aga Kildal, Kjersti Ramstad, Jordan Sheriko, Frank J. Symons, Lars Wallin, Guro L. Andersen

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