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Fear, coping and support- from the perspective of children aged 10-17-year old having acute lymphoblastic leukemia

International journal of qualitative studies on health and well-being, 2024-12, Vol.19 (1), p.2310147-2310147

2024

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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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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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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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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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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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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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'All for the well-being of the infant': nurses' perceptions of preterm infants' eye examinations: a phenomenographic study

BMC pediatrics, 2024-09, Vol.24 (1), p.579-11, Article 579

2024

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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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Children with Cerebral Palsy and Their Parents Have Different Experiences of Pain Management: A Qualitative Study

Children (Basel), 2024-08, Vol.11 (9), p.1055

2024

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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

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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Experiences of living with funnel chest prior to corrective surgery: An interview study

PloS one, 2024-07, Vol.19 (7), p.e0304968

2024

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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

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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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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Fear, coping and support- from the perspective of children aged 10-17-year old having acute lymphoblastic leukemia

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

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

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

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

Interventions for adults with deafblindness - an integrative review

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

'All for the well-being of the infant': nurses' perceptions of preterm infants' eye examinations: a phenomenographic study

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

Children with Cerebral Palsy and Their Parents Have Different Experiences of Pain Management: A Qualitative Study

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

Experiences of living with funnel chest prior to corrective surgery: An interview 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

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

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