A brief review of the pathophysiology, associated pain, and psychosocial issues in sickle cell disease. - Wikidata - wikimedia - TriplyDB

A brief review of the pathophysiology, associated pain, and psychosocial issues in sickle cell disease.

A brief review of the pathophysiology, associated pain, and psychosocial issues in sickle cell disease.

http://www.wikidata.org/entity/Q36219628

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Treatment of dental complications in sickle cell disease Treatment of dental complications in sickle cell disease Changes in coping, pain, and activity after cognitive-behavioral training: a randomized clinical trial for pediatric sickle cell disease using smartphones.Adult sickle cell quality-of-life measurement information system (ASCQ-Me): conceptual model based on review of the literature and formative research.A pilot study: the effect of healing touch on anxiety, stress, pain, pain medication usage, and physiological measures in hospitalized sickle cell disease adults experiencing a vaso-occlusive pain episode.A telephonic mindfulness-based intervention for persons with sickle cell disease: study protocol for a randomized controlled trial Dental infections increase the likelihood of hospital admissions among adult patients with sickle cell disease.Health-related stigma in young adults with sickle cell disease.Genomics and pain research in sickle cell disease: an explanation of heterogeneity?Self-care recommendations of middle-aged and older adults with sickle cell disease Emotional reactions to pain predict psychological distress in adult patients with Sickle Cell Disease (SCD).Integrating interactive web-based technology to assess adherence and clinical outcomes in pediatric sickle cell disease.Responsiveness of the PedsQL to pain-related changes in health-related quality of life in pediatric sickle cell disease.Sickle Cell Disease: A Review of Nonpharmacological Approaches for Pain.Asymptomatic bacteriuria in Nigerian children with sickle cell anemia.The association of optimism and perceived discrimination with health care utilization in adults with sickle cell disease.Understanding the social networks of parents of children with sickle cell disease.Mistrust of Pediatric Sickle Cell Disease Clinical Trials Research.Successful Aging with Sickle Cell Disease: Using Qualitative Methods to Inform Theory Neuropsychological assessment, neuroimaging, and neuropsychiatric evaluation in pediatric and adult patients with sickle cell disease (SCD).Social competence in children with brain disorders: a meta-analytic review.Examining Biopsychosocial Factors in Relation to Multiple Pain Features in Pediatric Sickle Cell Disease.Traumatic Exposure History as a Risk Factor for Chronic Pain in Adult Patients with Sickle Cell Disease.A systematic review of the association between depression and health care utilization in children and adults with sickle cell disease.Preliminary validity and reliability of the Sickle Cell Disease Health-Related Stigma Scale.The Association between Educational Attainment and Patterns of Emergency Department Utilization among Adults with Sickle Cell Disease.How sickle cell disease patients experience, understand and explain their pain: An Interpretative Phenomenological Analysis study.Behavioral impact of sickle cell disease in young children with repeated hospitalization.Opioid management and dependency among adult patients with sickle cell disease.The mediating effects of family functioning on psychosocial outcomes in healthy siblings of children with sickle cell disease.Interpersonal Violence Exposure and Chronic Pain in Adult Sickle Cell Patients.Validation of the SF-36 in Jamaicans with sickle-cell disease.Locus of control, depression and quality of life among persons with sickle cell disease in Jamaica.Depressive symptoms and sickle cell pain: The moderating role of internalized stigma.The Challenges and Opportunities Associated with Sickle Cell Disease Prevention, Education, and Management.Vesiculation of healthy and defective red blood cells.Neurocognitive testing and functioning in adults sickle cell disease.Psychosocial burden of sickle cell disease on the family, Nigeria.Use of a National Electronic Health Record Network to Describe Characteristics and Healing Patterns of Sickle Cell Ulcers Plasma Membrane Lipid Domains as Platforms for Vesicle Biogenesis and Shedding?

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P2860

A brief review of the pathophysiology, associated pain, and psychosocial issues in sickle cell disease.

http://www.wikidata.org/entity/Q36219628

description

2005 nî lūn-bûn

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2005年の論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年论文

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2005年论文

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2005年论文

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name

A brief review of the pathophy ...... issues in sickle cell disease.

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A brief review of the pathophy ...... issues in sickle cell disease.

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type

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A brief review of the pathophy ...... issues in sickle cell disease.

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A brief review of the pathophy ...... issues in sickle cell disease.

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A brief review of the pathophy ...... issues in sickle cell disease.

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A brief review of the pathophy ...... issues in sickle cell disease.

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International Journal of Behavioral Medicine

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A brief review of the pathophy ...... issues in sickle cell disease.

@en

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Alvin Killough

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Charles Loughlin

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Christopher L Edwards

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Elaine Whitworth

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Gary G Bennett

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Laura M De Castro

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Mary Abrams

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Mary Wood

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Miriam Feliu

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Mischca T Scales

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P2860

Psychosocial aspects of sickle cell disease (SCD) in childhood and adolescence: a review.

Ethnic differences in thermal pain responses.

Psychopathology in patients with sickle cell disease.

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s15327558ijbm1203_6

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pathophysiology

sickle-cell disease