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A lifelong struggle for a lighter tomorrow: A qualitative study on experiences of obesity in primary healthcare patients

Journal of clinical nursing, 2023-03, Vol.32 (5-6), p.834-846

2023

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Interventions for children with deafblindness—An integrative review

Child : care, health & development, 2023-05, Vol.49 (3), p.407-430

2023

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Healthcare‐professional patients’ conceptions of being ill and hospitalised – a phenomenographic study

Journal of clinical nursing, 2017-06, Vol.26 (11-12), p.1725-1736

2017

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Interventions for adults with deafblindness - an integrative review

BMC health services research, 2022-12, Vol.22 (1), p.1594-1594, Article 1594

2022

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Translation, cultural adaptation and validation of a patient‐reported experience measure for children

Health expectations : an international journal of public participation in health care and health policy, 2024-02, Vol.27 (1), p.e13924-n/a

2024

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Public health nurses’ experiences working with children who are next of kin: a qualitative study

BMC health services research, 2022-11, Vol.22 (1), p.1-1427, Article 1427

2022

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Young children’s experiences of support when fearful during treatment for acute lymphoblastic leukaemia—A longitudinal interview study

Nursing open, 2022-01, Vol.9 (1), p.527-540

2022

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Skin-to-Skin Contact Facilitates More Equal Parenthood - A Qualitative Study From Fathers' Perspective

Journal of pediatric nursing, 2017-05, Vol.34 (May-Jun 2017), p.e2-e9

2017

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Community-based support for children who are next-of-kin for a parent experiencing illness or disability – a scoping review

BMC health services research, 2021-11, Vol.21 (1), p.1-1250, Article 1250

2021

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Promoting person‐centred care in the perioperative setting through patient advocacy: An observational study

Journal of clinical nursing, 2018-06, Vol.27 (11-12), p.2403-2415

2018

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How paediatric departments in Sweden facilitate giving children a voice on their experiences of healthcare: A cross‐sectional study

Health expectations : an international journal of public participation in health care and health policy, 2022-02, Vol.25 (1), p.384-393

2022

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Living an ordinary life - yet not: the everyday life of children and adolescents living with a parent with deafblindness

International journal of qualitative studies on health and well-being, 2022-12, Vol.17 (1), p.2064049-2064049

2022

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Congenital chloride diarrhea and Pendred syndrome: case report of siblings with two rare recessive disorders of SLC26 family genes

BMC medical genetics, 2020-04, Vol.21 (1), p.79-79, Article 79

2020

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Life strategies of people with deafblindness due to Usher syndrome type 2a - a qualitative study

International journal of qualitative studies on health and well-being, 2019-01, Vol.14 (1), p.1656790-1656790

2019

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Experiences of rehabilitation services from the perspective of older adults with dual sensory loss - a qualitative study

International journal of qualitative studies on health and well-being, 2022-12, Vol.17 (1), p.2052559-2052559

2022

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"I can manage the challenge" - a qualitative study describing experiences of living with balance limitations after first-ever stroke

International journal of qualitative studies on health and well-being, 2021-01, Vol.16 (1), p.1857044-1857044

2021

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A qualitative evaluation of the National Expert Team regarding the assessment and diagnosis of deafblindness in Sweden

Scandinavian journal of disability research : SJDR, 2017-10, Vol.19 (4), p.362-374

Anderzén-Carlsson, Agneta

2017

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The lived experiences of work and health of people living with deaf-blindness due to Usher syndrome type 2

International journal of qualitative studies on health and well-being, 2020-01, Vol.15 (1), p.1846671-1846671

2020

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Adaptation, Translation, and Validation of a Patient-Reported Experience Measure for Children and Young People for the Canadian Context

Journal of pediatric surgery, 2024-05, Vol.59 (5), p.810-817

2024

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Parental experiences of providing skin-to-skin care to their newborn infant-Part 1: A qualitative systematic review

International journal of qualitative studies on health and well-being, 2014-01, Vol.9 (1), p.24906-24906

2014

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Life is back to normal and yet not - partners' and patient's experiences of life of the first year after colorectal cancer surgery

Journal of clinical nursing, 2012-02, Vol.21 (3-4), p.555-563

2012

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Translation and psychometric evaluation of the Swedish versions of the Nuss Questionnaire modified for Adults and the Single Step Questionnaire

Journal of patient-reported outcomes, 2021-02, Vol.5 (1), p.21-21, Article 21

2021

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Patients' and radiographers' experiences of dose reducing abdominal compression in radiographic examinations—A qualitative study

Nursing open, 2020-05, Vol.7 (3), p.680-689

2020

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Health-Related Quality of Life, Family Climate and Sense of Coherence of Families in Which a Parent Has Deafblindness

Frontiers in education (Lausanne), 2020-08, Vol.5

2020

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Fear and Coping in Children 5–9 years old Treated for Acute Lymphoblastic Leukemia - A Longitudinal Interview Study

Journal of pediatric nursing, 2019-05, Vol.46, p.e29-e36

2019

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A lifelong struggle for a lighter tomorrow: A qualitative study on experiences of obesity in primary healthcare patients

Interventions for children with deafblindness—An integrative review

Healthcare‐professional patients’ conceptions of being ill and hospitalised – a phenomenographic study

Interventions for adults with deafblindness - an integrative review

Translation, cultural adaptation and validation of a patient‐reported experience measure for children

Public health nurses’ experiences working with children who are next of kin: a qualitative study

Young children’s experiences of support when fearful during treatment for acute lymphoblastic leukaemia—A longitudinal interview study

Skin-to-Skin Contact Facilitates More Equal Parenthood - A Qualitative Study From Fathers' Perspective

Community-based support for children who are next-of-kin for a parent experiencing illness or disability – a scoping review

Promoting person‐centred care in the perioperative setting through patient advocacy: An observational study

How paediatric departments in Sweden facilitate giving children a voice on their experiences of healthcare: A cross‐sectional study

Living an ordinary life - yet not: the everyday life of children and adolescents living with a parent with deafblindness

Congenital chloride diarrhea and Pendred syndrome: case report of siblings with two rare recessive disorders of SLC26 family genes

Life strategies of people with deafblindness due to Usher syndrome type 2a - a qualitative study

Experiences of rehabilitation services from the perspective of older adults with dual sensory loss - a qualitative study

"I can manage the challenge" - a qualitative study describing experiences of living with balance limitations after first-ever stroke

A qualitative evaluation of the National Expert Team regarding the assessment and diagnosis of deafblindness in Sweden

The lived experiences of work and health of people living with deaf-blindness due to Usher syndrome type 2

Adaptation, Translation, and Validation of a Patient-Reported Experience Measure for Children and Young People for the Canadian Context

Parental experiences of providing skin-to-skin care to their newborn infant-Part 1: A qualitative systematic review

Life is back to normal and yet not - partners' and patient's experiences of life of the first year after colorectal cancer surgery

Translation and psychometric evaluation of the Swedish versions of the Nuss Questionnaire modified for Adults and the Single Step Questionnaire

Patients' and radiographers' experiences of dose reducing abdominal compression in radiographic examinations—A qualitative study

Health-Related Quality of Life, Family Climate and Sense of Coherence of Families in Which a Parent Has Deafblindness

Fear and Coping in Children 5–9 years old Treated for Acute Lymphoblastic Leukemia - A Longitudinal Interview Study

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