We don't wear it on our sleeve
Sickle cell disease and the (in)visible body in parts
Dados Bibliográficos
| ID | 4588946 |
|---|---|
| Autores | Rebekah Ciribassi (0000-0003-4905-3173, Cornell University), Rebekah M Ciribassi, Crystal L Patil (0000-0003-4536-4599, University of Illinois Chicago, autor correspondente) |
| Ano | 2016 |
| Volume | 148 |
| Páginas | 131-138 |
| Data de publicação | 2016-01-01 |
| Peer Reviewed | Sim |
| Open Access | Sim |
| Tipo | ARTICLE |
| Periódico | Social Science & Medicine (JOURNAL) |
| Identificadores do periódico | ISSN: 0277-9536 • E-ISSN: 1873-5347 |
| Editora | Elsevier BV (PUBLISHER) |
| DOI | 10.1016/j.socscimed.2015.11.033 |
| PMID | 26692094 |
| OpenAlex | W2175674667 |
| Idioma | EN |
| Citações recebidas | 22 |
| Referências citadas | 43 |
Bioinformatics · Biomedicine · Disease · Ethnography · Ideology · Invisibility · Pathology · Political science · Politics · Sociology · Variety (cybernetics · Anthropological Studies and Insights · Anthropology · Computer Science · Gender Studies · Hemoglobinopathies and Related Disorders · Law · Medicine · Race, Genetics, and Society
Ecological approach to sickle cell disease and environmental quality assessment in Guadeloupe (French West Indies)
Who Deserves Access to Care in Children's Hospitals
Effects of Experienced Discrimination in Pediatric Sickle Cell Disease
Our Blood Itself Is Disabled
Centering PrEP
Invisible women
Obstacles to use of patient expertise to improve care
I want to become someone!” gender, reproduction and the moral career of motherhood for women with sickle cell disorders
Douleurs et souffrances de jeunes drépanocytaires en Île-de-France
The indignities of shielding during the Covid-19 pandemic for people with sickle cell disorders
Law, Morality, and Health Care Professionals
Intersectionality and employment in the United Kingdom
Provider Perspectives on Group PrEP Care for Sex Workers
Politics of diversity in the framing of blood donation
Communicating and understanding pain
"Can you bury him before he dies?" Sickle cell disease and social sites of suffering in Malawi and Uganda
Sci-fi chips and sickled cells
Epidemiological placism in public health emergencies
Assessing Latour
Pain Management
Vaccine Hesitancy and the Accumulation of Distrust
Negotiated Discretion
Qualitative Data Analysis with Atlas.ti
The Birth of the Clinic
Racism Without Racists
Sickle cell and thalassaemia
Black/Female/Body Hypervisibility and Invisibility
Dying in the City of the Blues
Race and social attitudes about sickle cell disease
Navigating the African Diaspora
Healthcare injustice in patients with sickle cell disease
The Body, the Ghetto and the Penal State
Living a 'normal' life
Talcott Parsons, the Sick Role and Chronic Illness
The American dominative medical system as a reflection of social relations in the larger society
Pain management and symptoms of substance dependence among patients with sickle cell disease
Witnessing and the Medical Gaze
The Commodification of the Body and its Parts
Talking with Me or Talking at Me? The Impact of Status Characteristics on Doctor-Patient Interaction
Territory, Ancestry and Descent
Visibility
Cultivating the Body
Missing Bodies
Our Neo-Cartesian Bodies in Parts
Critical realism, agency and sickle cell
| Obras citantes distintas | 22 |
|---|---|
| Citações por ano | 2,44 |
| Intervalo de citações | 2017 - 2026 (10) |
| Velocidade de citação | current |
| Altamente citado | Não |
| Tipos de citação | Neutras: 22 |