Note: the following are taken directly from CrossRef
Citations:
Sarah Wadman & Klaus Hoeyer (2018). Dangers of the digital fit: Rethinking seamlessness and social sustainability in data-intensive healthcare. Big Data & Society, 5(1): . DOI: 10.1177/2053951717752964
Karine Wendric & Lotte Krabbenborg (2024). Negotiating with digital self-monitoring: A qualitative study on how patients with multiple sclerosis use and experience digital self-monitoring within a scientific study. Health: An Interdisciplinary Journal for the Social Study of Health, Illness and Medicine, 28(3): 333. DOI: 10.1177/13634593231175321
Christina Buse, Daryl Marti & Sarah Nettleton (2018). Conceptualising ‘materialities of care’: making visible mundane material culture in health and social care contexts. Sociology of Health & Illness, 40(2): 243. DOI: 10.1111/1467-9566.12663
Daryl Martin, Dara Ivanov & Thorben Peter Høj Simonsen (2024). Moving Beyond Clinical Imaginaries: Technogeographies of the Everyday Urban. Journal of Medical Humanities, : . DOI: 10.1007/s10912-024-09872-y
Dara Ivanova (2020). Post‐place care: disrupting place‐care ontologies. Sociology of Health & Illness, 42(6): 1296. DOI: 10.1111/1467-9566.13100
Sarah Wadmann, Anna Brueckner Johansen, Alfred Peter Bor & Line Kessel (2024). Infrastructuring precision medicine: Making gene therapies for rare diseases workable in practice. Social Science & Medicine, 351: 116966. DOI: 10.1016/j.socscimed.2024.116966
Catherine M. Will, Flis Henwood, Kate Weine & Rosalind Williams (2020). Negotiating the practical ethics of ‘self-tracking’ in intimate relationships: Looking for care in healthy living. Social Science & Medicine, 266: 113301. DOI: 10.1016/j.socscimed.2020.113301
Meng L & Corrina Laughlin (2023). Care as infrastructure: Rethinking working mothers' childcare crisis during the COVID‐19 pandemic. Gender, Work & Organization, : . DOI: 10.1111/gwao.13107
Gideon Lasco, Alicia Renedo, Jhaki Mendoza, Maureen L. Seguin, Benjamin Palafox, Lia M. Palileo‐Villanueva, Dina Balabanov & Martin McKee (2022). ‘Doing’ hypertension: Experiential knowledge and practice in the self‐management of ‘high blood’ in the Philippines. Sociology of Health & Illness, 44(7): 1167. DOI: 10.1111/1467-9566.13503
Holly Symonds-Brown, Christine Ceci, Wendy Duggleb & Mary Ellen Purkis (2021). Re-thinking the nature of day programs for people with dementia: Implications for research. Dementia, 20(1): 326. DOI: 10.1177/1471301219884429
Hélène Mialet (2022). Bodies in Balance: Tracking Type 1 Diabetes. Body & Society, 28(3): 89. DOI: 10.1177/1357034X221109140
Maja Klause & Elisabeth Assing Hvidt (2024). E‐consultation as existential media: Exploring doctor‐patient ‘digital thrownness’ in Danish general practice. Sociology of Health & Illness, 46(8): 1849. DOI: 10.1111/1467-9566.13823
Alberto Ardissone (2022). Selective adoption of therapeutic devices among people with type 1 diabetes. Health Sociology Review, 31(3): 278. DOI: 10.1080/14461242.2021.2007160
Emma R. Powe & Kathleen J. Mee (2020). Housing: an infrastructure of care. Housing Studies, 35(3): 484. DOI: 10.1080/02673037.2019.1612038
Stefanie Puszka (2023). The Circulation of Blood and Care: Value and Kidney Disease Amongst Yolŋu in Northern Australia. Medical Anthropology, 42(5): 451. DOI: 10.1080/01459740.2023.2213391
Francisco Nunes, Tariq Anderse & Geraldine Fitzpatrick (2019). The agency of patients and carers in medical care and self-care technologies for interacting with doctors. Health Informatics Journal, 25(2): 330. DOI: 10.1177/1460458217712054
Dara Ivanova, Iris Wallenbur & Roland Bal (2020). Place-by-proxy: Care infrastructures in a foundling room. The Sociological Review, 68(1): 144. DOI: 10.1177/0038026119868642
Gillian Prater-Lee (2022). Beyond efficiency in low-income housing provision: Everyday negotiations of nonprofit staff and the limits to caring through marketized housing in Buffalo, New York. Radical Housing Journal, 4(2): 89. DOI: 10.54825/JPXY7030
Kate Weine & Catherine Will (2018). Thinking with care infrastructures: people, devices and the home in home blood pressure monitoring. Sociology of Health & Illness, 40(2): 270. DOI: 10.1111/1467-9566.12590
Holly Symonds‐Brown, Christine Cec & Harkeert Judge (2022). ‘Sand in the works?’ Infrastructural affordances and life with dementia in the community. Sociology of Health & Illness, 44(9): 1517. DOI: 10.1111/1467-9566.13532
Susanna Trnka (2021). Multi-sited therapeutic assemblages: Virtual and real-life emplacement of youth mental health support. Social Science & Medicine, 278: 113960. DOI: 10.1016/j.socscimed.2021.113960
Stine Lomborg, Camilla Morin & Finn Kensing (2021). Communication as Ongoing Care. Conjunctions, 8(1): 1. DOI: 10.7146/tjcp.v8i1.123037
Peter Mørck, Tue Odd Langhoff, Mads Christophersen, Anne Kirstine Mølle & Pernille Bjørn (2018). Variations in Oncology Consultations: How Dictation Allows Variations to be Documented in Standardized Ways. Computer Supported Cooperative Work (CSCW), 27(3-6): 539. DOI: 10.1007/s10606-018-9332-2
C.M. Bagge-Petersen, M. Skovda & H. Langstrup (2020). The socio-material self-care practices of children living with hemophilia or juvenile idiopathic arthritis in Denmark. Social Science & Medicine, 255: 113022. DOI: 10.1016/j.socscimed.2020.113022
Ceres Víctora, Patrice Schuc & Monalisa Dias de Siqueira (2021). “ALMOST NOTHING HAS CHANGED”: ORDINARY ETHICS AND FORMS OF LIFE IN PANDEMIC TIMES. Sociologia & Antropologia, 11(3): 843. DOI: 10.1590/2238-38752021v1135
Elizabeth Kaziunas, Michael S. Klinkma & Mark S. Ackerman (2019). Precarious Interventions. Proceedings of the ACM on Human-Computer Interaction, 3(CSCW): 1. DOI: 10.1145/3359215
Helena Patini Lancellott & Claudia Lee Williams Fonseca (2023). Resgatando o cuidado num terreno tóxico. Anuário Antropológico, v.48 n.1: 134. DOI: 10.4000/aa.10544
Sofie á Rogvi, Ann Dorrit Guassora, Nina Tvistholm, Gitte Win & Ulla Christensen (2021). “It Is a Full-time Job to Be Ill”: Patient Work Involved in Attending Formal Diabetes Care Among Socially Vulnerable Danish Type 2 Diabetes Patients. Qualitative Health Research, 31(14): 2629. DOI: 10.1177/10497323211041590
Thelma Wang (2024). Sex reconfigured: DIY hormone therapy and vernacular endocrinology in transfeminine communities in China. Social Science & Medicine, 353: 116956. DOI: 10.1016/j.socscimed.2024.116956
Emma R Power, Ilan Wiesel, Emma Mitchel & Kathleen J Mee (2022). Shadow care infrastructures: Sustaining life in post-welfare cities. Progress in Human Geography, 46(5): 1165. DOI: 10.1177/03091325221109837
Solène Gouilhers, Delphine Garde & Raphaël Albospeyre-Thibeau (2023). De la stérilisation imposée à la préservation de la fertilité des personnes trans : les médecins au travail. Travail, genre et sociétés, n° 50(2): 61. DOI: 10.3917/tgs.050.0061
Ayse G. Buyuktur, Pei-Yao Hung, Mark W. Newma & Mark S. Ackerman (2018). Supporting Collaboratively Constructed Independence. Proceedings of the ACM on Human-Computer Interaction, 2(CSCW): 1. DOI: 10.1145/3274295
Joan Moyà-Köhler, Andrea García-Santesmase & Lluvi Farré (2023). Tensions and Escapes in Independent Living Infrastructures for People With Disabilities Under COVID-19. Space and Culture, 26(3): 420. DOI: 10.1177/12063312231161187
Madeleine Renyi, Petra Gaugisch, Alexandra Hunck, Stefan Strunck, Christophe Kunz & Frank Teuteberg (2022). Uncovering the Complexity of Care Networks – Towards a Taxonomy of Collaboration Complexity in Homecare. Computer Supported Cooperative Work (CSCW), 31(3): 517. DOI: 10.1007/s10606-022-09433-8
Malene N. Bødker, Ulla Christense & Henriette Langstrup (2019). Home care as reablement or enabling arrangements? An exploration of the precarious dependencies in living with functional decline. Sociology of Health & Illness, 41(7): 1358. DOI: 10.1111/1467-9566.12946
Rebecca Lync & Simon Cohn (2016). In the loop: Practices of self-monitoring from accounts by trial participants. Health: An Interdisciplinary Journal for the Social Study of Health, Illness and Medicine, 20(5): 523. DOI: 10.1177/1363459315611939
Stine Lomborg, Henriette Langstru & Tariq Osman Andersen (2020). Interpretation as luxury: Heart patients living with data doubt, hope, and anxiety. Big Data & Society, 7(1): 205395172092443. DOI: 10.1177/2053951720924436
Kristin Bjornsdotti & Christine Ceci (2023). Home care nursing practice for older persons with heart failure living at home. Journal of Clinical Nursing, 32(13-14): 4103. DOI: 10.1111/jocn.16575
ASKE JUUL LASSEN (2015). Keeping disease at arm's length – how older Danish people distance disease through active ageing. Ageing and Society, 35(7): 1364. DOI: 10.1017/S0144686X14000245
Tomohiro Ujikawa (2024). CONVENIENCE STORES AS CARE INFRASTRUCTURE FOR OLDER ADULTS: The Crisis of Care in Tokyo, Japan. International Journal of Urban and Regional Research, : . DOI: 10.1111/1468-2427.13292
Sarah Wadman & Lia E. Bang (2015). Rationalising prescribing: Evidence, marketing and practice-relevant knowledge. Social Science & Medicine, 135: 109. DOI: 10.1016/j.socscimed.2015.04.032
Attila Bruni, Francesco Miel & Enrico Maria Piras (2017). Organizzare network socio-sanitari: il lavoro di pazienti e familiari nell'orchestrazione dei servizi di cura. STUDI ORGANIZZATIVI, (1): 67. DOI: 10.3280/SO2017-001003
Francesco Miele (2023). On care infrastructures and health practices: How people in health promotion programmes try to change their everyday life. Health: An Interdisciplinary Journal for the Social Study of Health, Illness and Medicine, 27(6): 980. DOI: 10.1177/13634593221093503
Jeannette Pols, Brigitte Althof & Els Bransen (2017). The Limits of Autonomy: Ideals in Care for People with Learning Disabilities. Medical Anthropology, 36(8): 772. DOI: 10.1080/01459740.2017.1367776
Milena D. Bister (2018). The concept of chronicity in action: everyday classification practices and the shaping of mental health care. Sociology of Health & Illness, 40(1): 38. DOI: 10.1111/1467-9566.12623
Giada Danesi, Mélody Pralong, Francesco Panese, Bernard Burnan & Michèle Grossen (2020). Techno-social reconfigurations in diabetes (self-) care. Social Studies of Science, 50(2): 198. DOI: 10.1177/0306312720903493