Health related quality of life in sickle cell patients: the PiSCES project - Wikidata - awgldk - TriplyDB

Health related quality of life in sickle cell patients: the PiSCES project

Health related quality of life in sickle cell patients: the PiSCES project

http://www.wikidata.org/entity/Q24810691

about

Systematic review: Hydroxyurea for the treatment of adults with sickle cell disease Wheezing in children with sickle cell disease Adult sickle cell quality-of-life measurement information system (ASCQ-Me): conceptual model based on review of the literature and formative research.Comorbidity, Pain, Utilization, and Psychosocial Outcomes in Older versus Younger Sickle Cell Adults: The PiSCES Project Hematopoietic stem cell transplantation in thalassemia major and sickle cell disease: indications and management recommendations from an international expert panel.Quality of life in patients with thalassemia major.Neuropsychological dysfunction and neuroimaging abnormalities in neurologically intact adults with sickle cell anemia.Poor health related quality of life among patients of sickle cell disease.A review of the literature on the multiple dimensions of chronic pain in adults with sickle cell disease Hydroxyurea and acute painful crises in sickle cell anemia: effects on hospital length of stay and opioid utilization during hospitalization, outpatient acute care contacts, and at home Perceived discrimination, patient trust, and adherence to medical recommendations among persons with sickle cell disease Emerging biobehavioral factors of fatigue in sickle cell disease Hydroxyurea and sickle cell anemia: effect on quality of life.Health-related quality of life in children and adolescents with sickle cell disease Spirituality, Self-Efficacy, and Quality of Life among Adults with Sickle Cell Disease.Genomics and pain research in sickle cell disease: an explanation of heterogeneity?Health related quality of life among adolescents with sickle cell disease in Saudi Arabia Pattern of referral of noncancer patients to palliative care in the eastern province of saudi arabia.Health-related quality of life in young adults with congenital central hypoventilation syndrome due to PHOX2B mutations: a cross-sectional study.Health-related quality of life (HRQL) in children with sickle cell disease and thalassemia following hematopoietic stem cell transplant (HSCT).Patient self-assessment of hospital pain, mood and health-related quality of life in adults with sickle cell disease.Saudi SCD patients' symptoms and quality of life relative to the number of ED visits.Overactive bladder in adults with sickle cell disease.Health-related quality of life in patients with sickle cell disease in Saudi Arabia.Sickle Cell Disease: A Review of Nonpharmacological Approaches for Pain.Quality of life of individuals with sickle cell disease followed at referral centers in Alagoas, Brazil.Health-related quality of life in adults with sickle cell disease (SCD): a report from the comprehensive sickle cell centers clinical trial consortium.Reproductive Health CHOICES for Young Adults with Sickle Cell Disease or Trait: Randomized Controlled Trial Outcomes over Two Years.Community Health Workers as Support for Sickle Cell Care Hematopoietic cell transplantation: a curative option for sickle cell disease.Sociodemographic aspects and quality of life of patients with sickle cell anemia Morphine stimulates platelet-derived growth factor receptor-β signalling in mesangial cells in vitro and transgenic sickle mouse kidney in vivo.Sickle Cell Disease: quality of life in patients with hemoglobin SS and SC disorders Utility of WHOQOL-BREF in measuring quality of life in sickle cell disease Pain over time and its effects on life in thalassemia.Pain management and quality of life in sickle cell disease.Severe sickle cell disease--pathophysiology and therapy.Socio-demographic characteristics and psychosocial consequences of sickle cell disease: the case of patients in a public hospital in Ghana Fatigue in adolescents and young adults with sickle cell disease: biological and behavioral correlates and health-related quality of life.Factors associated with survival in a contemporary adult sickle cell disease cohort.

P2860

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P2860

Health related quality of life in sickle cell patients: the PiSCES project

http://www.wikidata.org/entity/Q24810691

description

2005 nî lūn-bûn

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2005 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

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2005 թվականի օգոստոսին հրատարակված գիտական հոդված

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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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Health and Quality of Life Outcomes

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Donna K McClish

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Imoigele P Aisiku

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James L Levenson

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John D Roberts

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Lynne T Penberthy

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Viktor E Bovbjerg

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Wally R Smith

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P2860

Toward a theoretical model of quality-of-life appraisal: Implications of findings from studies of response shift

“Mini-mental state”

Quality of life in children with sickle cell disease in Amsterdam area

The SF-36 Health Survey as a generic outcome measure in clinical trials of patients with osteoarthritis and rheumatoid arthritis: tests of data quality, scaling assumptions and score reliability.

Experiences of hospital care and treatment seeking for pain from sickle cell disease: qualitative study.

Pain, quality of life, and coping in sickle cell disease.

Three decades of innovation in the management of sickle cell disease: the road to understanding the sickle cell disease clinical phenotype.

Quality of life in persons with human immunodeficiency virus infection: measurement by the Medical Outcomes Study instrument.

Integrating response shift into health-related quality of life research: a theoretical model.

Design of the multicenter study of hydroxyurea in sickle cell anemia. Investigators of the Multicenter Study of Hydroxyurea.

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10.1186/1477-7525-3-50

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quality of life

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