590 results on '"Treadwell, Marsha"'
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52. Stepping Systematically Forward Toward Health Equity in Sickle Cell Disease
53. Quality of care in sickle cell disease
54. Community engagement to inform the development of a sickle cell counselor training and certification program in Ghana
55. Proceedings of a Sickle Cell Disease Ontology workshop — Towards the first comprehensive ontology for Sickle Cell Disease
56. Optimizing Acute Sickle Cell Care at Community Health Partners Medical Center
57. Looking ahead: ethical and social challenges of somatic gene therapy for sickle cell disease in Africa
58. Safety and physiological effects of two different doses of elosulfase alfa in patients with morquio a syndrome: A randomized, double‐blind, pilot study
59. Sickle cell disease and H3Africa: enhancing genomic research on cardiovascular diseases in African patients
60. Using Formative Research to Develop a Counselor Training Program for Newborn Screening in Ghana
61. Patient reports of health outcome for adults living with sickle cell disease: development and testing of the ASCQ-Me item banks
62. Adult Sickle Cell Quality-of-Life Measurement Information System (ASCQ-Me)
63. A Quality Improvement Initiative to Improve Emergency Department Care for Pediatric Patients with Sickle Cell Disease.
64. Caught between pity, explicit bias, and discrimination: a qualitative study on the impact of stigma on the quality of life of persons living with sickle cell disease in three African countries
65. Pediatric sickle cell disease
66. Contributors
67. The Effect of an Adapted Digital Mental Health Intervention for Sickle Cell Disease on Engagement: A Pilot Randomized Controlled Trial
68. Mental health and psychological resilience in sickle cell disease
69. Quality of Life in Sickle Cell Disease
70. Mortality in Adults with Sickle Cell Disease: Results from the Sickle Cell Disease Implementation Consortium (SCDIC) Registry
71. Optimizing Shared Decision Making about Hydroxyurea in Young Children with Sickle Cell Anemia
72. Baseline Patient and Provider Reports of Quality of Care and Confidence Providing ED Management of Vaso-Occlusive Episodes
73. A New Phen X Collection: Sickle Cell Disease Psychosocial and Social Determinants of Health Protocols
74. Barriers to hydroxyurea use from the perspectives of providers, individuals with sickle cell disease, and families: Report from a U.S. regional collaborative
75. A Biopsychosocial-Spiritual Model of Chronic Pain in Adults with Sickle Cell Disease
76. Transitioning Adolescents With Sickle Cell Disease From Pediatric to Adult Care: Results From a New Survey of Health Care Professionals
77. Early Evaluation of the Use of Crizanlizumab in Sickle Cell Disease: A National Alliance of Sickle Cell Centers Study
78. Improving Completion Rates of Transcranial Doppler Ultrasounds in Children with Sickle Cell Disease Using Quality Improvement Efforts: In-Clinic Vs. Population-Based Assessments
79. Using quality improvement strategies to enhance pediatric pain assessment
80. Grndad and Disease Modifying Therapy (DMT): Shifts in Dmt Are Seen at the Adolescent/Young Adult Transition in Sickle Cell Disease in a Multi-Site Prospective Registry
81. Population based surveillance in sickle cell disease: Methods, findings and implications from the California registry and surveillance system in hemoglobinopathies project (RuSH)
82. Chapter 8 - Pediatric sickle cell disease
83. Psychosocial and behavioral outcomes in children with sickle cell disease and their healthy siblings
84. Engaging Caregivers and Providers of Children With Sickle Cell Anemia in Shared Decision Making for Hydroxyurea: Protocol for a Multicenter Randomized Controlled Trial (Preprint)
85. Autonomic reactivity and clinical severity in children with sickle cell disease
86. Improving Preventive Care for Children With Sickle Cell Anemia: A Quality Improvement Initiative
87. Electronic Health Record–Embedded Individualized Pain Plans for Emergency Department Treatment of Vaso-occlusive Episodes in Adults With Sickle Cell Disease: Protocol for a Preimplementation and Postimplementation Study (Preprint)
88. Predictors of Maternal Morbidity Among Participants Enrolled in the Sickle Cell Disease Implementation Consortium Registry
89. Sex Based Differences in Sickle Cell Disease
90. Hydroxyurea Use and Outcomes of Pregnancy in Sickle Cell Disease
91. The mediating effects of family functioning on psychosocial outcomes in healthy siblings of children with sickle cell disease
92. Clinical Vignette - Avascular Necrosis of the Femoral Head in a 7 year old with Sickle Cell Disease: 090
93. Patient Navigation: Effectiveness of a Model for Sickle Cell Disease: 057
94. Development of a Measure to Assess Barriers to Care in Sickle Cell Disease: 056
95. Genetic Counseling for Everyone: Increasing Availability in a Sickle Cell Network: 042
96. Transition from pediatric to adult care in sickle cell disease: Establishing evidence-based practice and directions for research
97. Perceptions of US Adolescents and Adults With Sickle Cell Disease on Their Quality of Care
98. Education and employment status of children and adults with thalassemia in North America†‡
99. Social and Psychological Factors Associated With Health Care Transition for Young Adults Living With Sickle Cell Disease
100. A Pilot Adult Sickle Cell Hematology Clinic in California's Inland Empire Improves Patient Outcome
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