Socioeconomic distress and health status: the urban-rural dichotomy of services utilization for people with sickle cell disorder in North Carolina

scientific article published on January 2000

Socioeconomic distress and health status: the urban-rural dichotomy of services utilization for people with sickle cell disorder in North Carolina is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1111/J.1748-0361.2000.TB00435.X
P698PubMed publication ID10916314
P5875ResearchGate publication ID227608885

P2093author name stringHaque A
Telfair J
P2860cites workGeographic information systems (GIS): new perspectives in understanding human health and environmental relationshipsQ39434167
Adaptation and coping: a look at a sickle cell patient population over age 30--an integral phase of the life long developmental processQ44906631
Social factors and infant mortality: identifying high-risk groups and proximate causesQ46160385
Stress, coping, and psychological adjustment of adults with sickle cell diseaseQ46313429
How does the prevalence of specific morbidities compare with measures of socio-economic status at small area level?Q50108789
P433issue1
P921main subjecturbanizationQ161078
sickle-cell diseaseQ185034
socioeconomicsQ1643441
dichotomyQ10361123
P304page(s)43-55
P577publication date2000-01-01
P1433published inJournal of Rural HealthQ15764712
P1476titleSocioeconomic distress and health status: the urban-rural dichotomy of services utilization for people with sickle cell disorder in North Carolina
P478volume16

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cites work (P2860)
Q37379248A biopsychosocial-spiritual model of chronic pain in adults with sickle cell disease
Q37622209A systematic review of barriers and interventions to improve appropriate use of therapies for sickle cell disease
Q38022571Adherence to transcranial Doppler screening guidelines among children with sickle cell disease
Q44349172Daily Opioid Use Fluctuates as a Function of Pain, Catastrophizing, and Affect in Patients with Sickle Cell Disease: an Electronic Daily Diary Analysis
Q35593843Experiences of Pediatric Patients With Sickle Cell Disease in Rural Emergency Departments
Q38266305Implementation of transcranial Doppler ultrasonography screening and primary stroke prevention in urban and rural sickle cell disease populations
Q64966819Knowledge, beliefs and practices regarding sickle cell eye disease of patients at the sickle cell unit, Jamaica.
Q37607927Maintaining High Level of Care at Satellite Sickle Cell Clinics
Q39642809Rural/urban differences in access to and utilization of services among people in Alabama with sickle cell disease
Q35735978Sickle cell disease in California: sociodemographic predictors of emergency department utilization
Q35778071Sickle-cell disease in California: a population-based description of emergency department utilization
Q36338160Socio-environmental exposures and health outcomes among persons with sickle cell disease
Q40052245The Association between Educational Attainment and Patterns of Emergency Department Utilization among Adults with Sickle Cell Disease
Q34655911The rural context of health care provision
Q37624297Transition from pediatric to adult care in sickle cell disease: establishing evidence-based practice and directions for research
Q36100590USING LIVED EXPERIENCES OF ADULTS TO UNDERSTAND CHRONIC PAIN: SICKLE CELL DISEASE, AN EXEMPLAR.

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