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Journal Abstract Search

244 related items for PubMed ID: 29047145

  • 21. Impact of arginine therapy on mitochondrial function in children with sickle cell disease during vaso-occlusive pain.
    Morris CR, Brown LAS, Reynolds M, Dampier CD, Lane PA, Watt A, Kumari P, Harris F, Manoranjithan S, Mendis RD, Figueroa J, Shiva S.
    Blood; 2020 Sep 17; 136(12):1402-1406. PubMed ID: 32384147
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  • 25. Pain management in adults with sickle cell disease in a medical center emergency department.
    Solomon LR.
    J Natl Med Assoc; 2010 Nov 17; 102(11):1025-32. PubMed ID: 21141290
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  • 26. Impact of an individualized pain plan to treat sickle cell disease vaso-occlusive episodes in the emergency department.
    Siewny L, King A, Melvin CL, Carpenter CR, Hankins JS, Colla JS, Preiss L, Luo L, Cox L, Treadwell M, Davila N, Masese RV, McCuskee S, Gollan SS, Tanabe P.
    Blood Adv; 2024 Oct 22; 8(20):5330-5338. PubMed ID: 38815230
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  • 27. Opioid doses and acute care utilization outcomes for adults with sickle cell disease: ED versus acute care unit.
    Molokie RE, Montminy C, Dionisio C, Farooqui MA, Gowhari M, Yao Y, Suarez ML, Ezenwa MO, Schlaeger JM, Wang ZJ, Wilkie DJ.
    Am J Emerg Med; 2018 Jan 22; 36(1):88-92. PubMed ID: 28802541
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  • 30. Low dose ketamine versus morphine for acute severe vaso occlusive pain in children: a randomized controlled trial.
    Lubega FA, DeSilva MS, Munube D, Nkwine R, Tumukunde J, Agaba PK, Nabukenya MT, Bulamba F, Luggya TS.
    Scand J Pain; 2018 Jan 26; 18(1):19-27. PubMed ID: 29794277
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  • 33. Clinical practice guideline improves the treatment of sickle cell disease vasoocclusive pain.
    Morrissey LK, Shea JO, Kalish LA, Weiner DL, Branowicki P, Heeney MM.
    Pediatr Blood Cancer; 2009 Mar 26; 52(3):369-72. PubMed ID: 19023890
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  • 35. Barriers and facilitators to care for individuals with sickle cell disease in central North Carolina: The emergency department providers' perspective.
    Masese RV, Bulgin D, Douglas C, Shah N, Tanabe P.
    PLoS One; 2019 Mar 26; 14(5):e0216414. PubMed ID: 31063506
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  • 38. Patient characteristics affect the response to ketamine and opioids during the treatment of vaso-occlusive episode-related pain in sickle cell disease.
    Nobrega R, Sheehy KA, Lippold C, Rice AL, Finkel JC, Quezado ZMN.
    Pediatr Res; 2018 Feb 26; 83(2):445-454. PubMed ID: 28902183
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  • 39. A randomized, placebo-controlled trial of arginine therapy for the treatment of children with sickle cell disease hospitalized with vaso-occlusive pain episodes.
    Morris CR, Kuypers FA, Lavrisha L, Ansari M, Sweeters N, Stewart M, Gildengorin G, Neumayr L, Vichinsky EP.
    Haematologica; 2013 Sep 26; 98(9):1375-82. PubMed ID: 23645695
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  • 40. Timing of opioid administration as a quality indicator for pain crises in sickle cell disease.
    Mathias MD, McCavit TL.
    Pediatrics; 2015 Mar 26; 135(3):475-82. PubMed ID: 25667245
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