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Journal Abstract Search

361 related items for PubMed ID: 28577358

  • 1. Sensitivity of alternative measures of functioning and wellbeing for adults with sickle cell disease: comparison of PROMIS® to ASCQ-Me℠.
    Keller S, Yang M, Treadwell MJ, Hassell KL.
    Health Qual Life Outcomes; 2017 Jun 02; 15(1):117. PubMed ID: 28577358
    [Abstract] [Full Text] [Related]

  • 2. Patient reports of health outcome for adults living with sickle cell disease: development and testing of the ASCQ-Me item banks.
    Keller SD, Yang M, Treadwell MJ, Werner EM, Hassell KL.
    Health Qual Life Outcomes; 2014 Aug 22; 12():125. PubMed ID: 25146160
    [Abstract] [Full Text] [Related]

  • 3. Psychometric analysis of the adult sickle cell quality of life measurement information system (ACSQ-Me) in a UK population.
    Cooper O, McBain H, Tangayi S, Telfer P, Tsitsikas D, Yardumian A, Mulligan K.
    Health Qual Life Outcomes; 2019 Apr 29; 17(1):74. PubMed ID: 31036017
    [Abstract] [Full Text] [Related]

  • 4. Preliminary construct validity of patient-reported outcomes to assess chronic pain in adults with sickle cell disease.
    Mucalo L, Field JJ, Highland J, Khan H, Hankins JS, Singh A, Brandow AM.
    Blood Adv; 2023 Jul 25; 7(14):3658-3665. PubMed ID: 37058480
    [Abstract] [Full Text] [Related]

  • 5. The relationship between frequency and severity of vaso-occlusive crises and health-related quality of life and work productivity in adults with sickle cell disease.
    Rizio AA, Bhor M, Lin X, McCausland KL, White MK, Paulose J, Nandal S, Halloway RI, Bronté-Hall L.
    Qual Life Res; 2020 Jun 25; 29(6):1533-1547. PubMed ID: 31933113
    [Abstract] [Full Text] [Related]

  • 6. Patient-reported outcomes in sickle cell disease and association with clinical and psychosocial factors: Report from the sickle cell disease implementation consortium.
    Knisely MR, Pugh N, Kroner B, Masese R, Gordeuk V, King AA, Smith SM, Gurney JG, Adams R, Wun T, Snyder A, Glassberg J, Shah N, Treadwell M, Sickle Cell Disease Implementation Consortium.
    Am J Hematol; 2020 Sep 25; 95(9):1066-1074. PubMed ID: 32449965
    [Abstract] [Full Text] [Related]

  • 7. Health-related quality of life and neuropathic pain in sickle cell disease in Jamaica.
    Bartlett R, Ramsay Z, Ali A, Grant J, Rankine-Mullings A, Gordon-Strachan G, Asnani M.
    Disabil Health J; 2021 Oct 25; 14(4):101107. PubMed ID: 33867318
    [Abstract] [Full Text] [Related]

  • 8. Assessment of health-related quality of life among adults hospitalized with sickle cell disease vaso-occlusive crisis.
    Esham KS, Rodday AM, Smith HP, Noubary F, Weidner RA, Buchsbaum RJ, Parsons SK.
    Blood Adv; 2020 Jan 14; 4(1):19-27. PubMed ID: 31891655
    [Abstract] [Full Text] [Related]

  • 9. A pilot test of the Adult Sickle Cell Quality of Life Measurement Information System (ASCQ-Me) and the Jenerette Self-Care Assessment (J-SAT) Tools in adults with sickle cell disease.
    Bulgin D, Douglas C, Tanabe P.
    Pilot Feasibility Stud; 2019 Jan 14; 5():85. PubMed ID: 31312513
    [Abstract] [Full Text] [Related]

  • 10. A preliminary investigation of the psychometric properties of PROMIS® scales in emerging adults with sickle cell disease.
    Hildenbrand AK, Quinn CT, Mara CA, Peugh JL, McTate EA, Britto MT, Crosby LE.
    Health Psychol; 2019 May 14; 38(5):386-390. PubMed ID: 31045421
    [Abstract] [Full Text] [Related]

  • 11. Use of the new pediatric PROMIS measures of pain and physical experiences for children with sickle cell disease.
    Singh A, DasGupta M, Simpson PM, Panepinto JA.
    Pediatr Blood Cancer; 2019 May 14; 66(5):e27633. PubMed ID: 30688017
    [Abstract] [Full Text] [Related]

  • 12. Adult sickle cell quality-of-life measurement information system (ASCQ-Me): conceptual model based on review of the literature and formative research.
    Treadwell MJ, Hassell K, Levine R, Keller S.
    Clin J Pain; 2014 Oct 14; 30(10):902-14. PubMed ID: 24300219
    [Abstract] [Full Text] [Related]

  • 13. Poor Sleep Quality in Jamaican Adults With Sickle Cell Disease: Prevalence, Risk Factors, and Association With Quality of Life.
    Chin N, Asnani M.
    Hemoglobin; 2024 Mar 14; 48(2):87-93. PubMed ID: 38616298
    [Abstract] [Full Text] [Related]

  • 14. Assessing sleep and pain among adults with myalgic encephalomyelitis/chronic fatigue syndrome: psychometric evaluation of the PROMIS® sleep and pain short forms.
    Yang M, Keller S, Lin JS.
    Qual Life Res; 2022 Dec 14; 31(12):3483-3499. PubMed ID: 35896905
    [Abstract] [Full Text] [Related]

  • 15. Initial Evaluation of the Pediatric PROMIS® Health Domains in Children and Adolescents With Sickle Cell Disease.
    Dampier C, Barry V, Gross HE, Lui Y, Thornburg CD, DeWalt DA, Reeve BB.
    Pediatr Blood Cancer; 2016 Jun 14; 63(6):1031-7. PubMed ID: 26895143
    [Abstract] [Full Text] [Related]

  • 16. Adherence to hydroxyurea, health-related quality of life domains, and patients' perceptions of sickle cell disease and hydroxyurea: a cross-sectional study in adolescents and young adults.
    Badawy SM, Thompson AA, Lai JS, Penedo FJ, Rychlik K, Liem RI.
    Health Qual Life Outcomes; 2017 Jul 05; 15(1):136. PubMed ID: 28679417
    [Abstract] [Full Text] [Related]

  • 17. Qualitative and Psychometric Evaluation of 29-Item Patient-Reported Outcomes Measurement Information System® to Assess General Health-Related Quality of Life in Patients With Moderately to Severely Active Inflammatory Bowel Disease.
    Sands BE, Panés J, Feagan BG, Zhang H, Vetter ML, Mathias SD, Huang KG, Johanns J, Germinaro M, Sahoo A, Terry NA, Han C.
    Value Health; 2024 Sep 05; 27(9):1225-1234. PubMed ID: 38843977
    [Abstract] [Full Text] [Related]

  • 18. PROMIS® Adult Health Profiles: Efficient Short-Form Measures of Seven Health Domains.
    Cella D, Choi SW, Condon DM, Schalet B, Hays RD, Rothrock NE, Yount S, Cook KF, Gershon RC, Amtmann D, DeWalt DA, Pilkonis PA, Stone AA, Weinfurt K, Reeve BB.
    Value Health; 2019 May 05; 22(5):537-544. PubMed ID: 31104731
    [Abstract] [Full Text] [Related]

  • 19. Patient-Reported Outcomes of Quality of Life, Functioning, and GI/Psychiatric Symptom Severity in Patients with Inflammatory Bowel Disease (IBD).
    IsHak WW, Pan D, Steiner AJ, Feldman E, Mann A, Mirocha J, Danovitch I, Melmed GY.
    Inflamm Bowel Dis; 2017 May 05; 23(5):798-803. PubMed ID: 28301432
    [Abstract] [Full Text] [Related]

  • 20. What is the future of patient-reported outcomes in sickle-cell disease?
    Singh SA, Bakshi N, Mahajan P, Morris CR.
    Expert Rev Hematol; 2020 Nov 05; 13(11):1165-1173. PubMed ID: 33034214
    [Abstract] [Full Text] [Related]

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