scholarly article | Q13442814 |
P2093 | author name string | Haque A | |
Telfair J | |||
P2860 | cites work | Geographic information systems (GIS): new perspectives in understanding human health and environmental relationships | Q39434167 |
Adaptation and coping: a look at a sickle cell patient population over age 30--an integral phase of the life long developmental process | Q44906631 | ||
Social factors and infant mortality: identifying high-risk groups and proximate causes | Q46160385 | ||
Stress, coping, and psychological adjustment of adults with sickle cell disease | Q46313429 | ||
How does the prevalence of specific morbidities compare with measures of socio-economic status at small area level? | Q50108789 | ||
P433 | issue | 1 | |
P921 | main subject | urbanization | Q161078 |
sickle-cell disease | Q185034 | ||
socioeconomics | Q1643441 | ||
dichotomy | Q10361123 | ||
P304 | page(s) | 43-55 | |
P577 | publication date | 2000-01-01 | |
P1433 | published in | Journal of Rural Health | Q15764712 |
P1476 | title | Socioeconomic distress and health status: the urban-rural dichotomy of services utilization for people with sickle cell disorder in North Carolina | |
P478 | volume | 16 |
Q37379248 | A biopsychosocial-spiritual model of chronic pain in adults with sickle cell disease |
Q37622209 | A systematic review of barriers and interventions to improve appropriate use of therapies for sickle cell disease |
Q38022571 | Adherence to transcranial Doppler screening guidelines among children with sickle cell disease |
Q44349172 | Daily Opioid Use Fluctuates as a Function of Pain, Catastrophizing, and Affect in Patients with Sickle Cell Disease: an Electronic Daily Diary Analysis |
Q35593843 | Experiences of Pediatric Patients With Sickle Cell Disease in Rural Emergency Departments |
Q38266305 | Implementation of transcranial Doppler ultrasonography screening and primary stroke prevention in urban and rural sickle cell disease populations |
Q64966819 | Knowledge, beliefs and practices regarding sickle cell eye disease of patients at the sickle cell unit, Jamaica. |
Q37607927 | Maintaining High Level of Care at Satellite Sickle Cell Clinics |
Q39642809 | Rural/urban differences in access to and utilization of services among people in Alabama with sickle cell disease |
Q35735978 | Sickle cell disease in California: sociodemographic predictors of emergency department utilization |
Q35778071 | Sickle-cell disease in California: a population-based description of emergency department utilization |
Q36338160 | Socio-environmental exposures and health outcomes among persons with sickle cell disease |
Q40052245 | The Association between Educational Attainment and Patterns of Emergency Department Utilization among Adults with Sickle Cell Disease |
Q34655911 | The rural context of health care provision |
Q37624297 | Transition from pediatric to adult care in sickle cell disease: establishing evidence-based practice and directions for research |
Q36100590 | USING LIVED EXPERIENCES OF ADULTS TO UNDERSTAND CHRONIC PAIN: SICKLE CELL DISEASE, AN EXEMPLAR. |
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