108 results on '"Lanzkron, Sophie"'
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2. Silent cerebral infarction during immune TTP remission - prevalence, predictors, and impact on cognition
3. Evidence-Based Minireview: How to utilize new therapies for sickle cell disease
4. "Buprenorphine, It Works So Differently:" Adults with Sickle Cell Disease Describe Their Experiences Transitioning to Buprenorphine for Treatment of Chronic Pain
5. Pain Attitudes in Adults with Sickle Cell Disease: A Mixed Methods Study
6. Similar Patient-Reported Quality of Life in the US and UK in Patients with Sickle Cell: A Comparative Grndad/Cousin Study
7. Silent Cerebral Infarction during Immune TTP Remission - Prevalence, Predictors and Impact on Cognition
8. Assessing the Recovery Process after a Vaso Occlusive Crisis
9. Longitudinal Outcomes of Chronically Transfused Adults with Sickle Cell Anemia and a History of Childhood Stroke
10. Self-Efficacy and Stigma in Adults with Sickle Cell Disease: An Import Study Analysis
11. Pain without gain: steroids and sickle crisis
12. Diminished ovarian reserve in young women with sickle cell anemia
13. GRNDaD: big data and sickle cell disease
14. A community-centered approach to sickle cell disease and clinical trial participation: an evaluation of perceptions, facilitators, and barriers
15. Blood Conservation Strategies in Adult Sickle Cell Patients on Chronic Transfusion Therapy: A Single Center Experience
16. The Telemedicine Experience for Individuals with Sickle Cell Disease
17. Risk of Pregnancy-Related Venous Thromboembolism in Black Women with Sickle Cell Trait
18. Sickle Cell Disease and Vestibular Dysfunction
19. Sickle Cell Disease and Cystic Fibrosis Are Associated with Increased Non-Administration of VTE Prophylaxis in Adult Patients
20. Early Evaluation of the Use of Crizanlizumab in Sickle Cell Disease: A National Alliance of Sickle Cell Centers Study
21. Silent Cerebral Infarction on Brain MRI Is Associated with Cognitive Impairment in Ittp Survivors in Hematological Remission
22. Functional Connectivity in Pediatric Sickle Cell Disease
23. Knowledge of Fertility and Perception of Fertility Treatment Among Adults with Sickle Cell Disease (KNOW FERTILITY)
24. COVID-19 in Hospitalized Patients with Sickle Cell Disease
25. Telemedicine Has Acceptable Usability and High Satisfaction in Patients with Sickle Cell Disease
26. Hydroxyurea Is a Potential Risk Factor for Diminished Ovarian Reserve in Young Adults with Sickle Cell Anemia
27. The Grndad Registry: Contemporary Natural History Data and an Analysis of Real-World Patterns of Use and Limitations of Disease Modifying Therapy in Adults with SCD
28. Young Adults with Sickle Cell Disease (SCD) Have Low Interest in Genetic Counseling and Sickle Cell Trait Testing for Sexual Partners
29. Building access to care in adult sickle cell disease: defining models of care, essential components, and economic aspects
30. 2019 sickle cell disease guidelines by the American Society of Hematology: methodology, challenges, and innovations
31. American Society of Hematology 2019 guidelines for sickle cell disease: cardiopulmonary and kidney disease
32. Quality Improvement Initiative: Improving Time to First Dose in a Sickle Cell Infusion Center
33. Economic Burden of End Organ Damage Among Patients with Sickle Cell Disease in the US
34. Anti-Mullerian Hormone, a Measure of Ovarian Reserve, Is Low in Female Subjects in the Multi-Center Study of Hydroxyurea
35. Chronic Kidney Disease Is Under-Screened in SCD and Mild Albuminuria Is Associated with a Drop in Hemoglobin: A Report from the Grndad Sickle Cell Registry
36. Standard Definitions of Pneumococcal Immunity May Not Accurately Predict Protection in Adults with Sickle Cell Disease
37. A Five Fold Decrease in Admissions for Uncomplicated Vaso-Occlusive Crisis and Other Benefits from Care in Infusion Clinics: Results from the Escaped Trial
38. Iron Overload Is Under-Recognized and Under-Treated in SCD: A Report from the Grndad Registry
39. Modifiable Cardiovascular Risk Factors in Adults with Sickle Cell Disease
40. Patient Satisfaction of Care in the Treatment of Vaso-Occlusive Crises: A Comparison of Emergency Department and Infusion Centers in the Escaped Study
41. Societal Costs of Sickle Cell Disease in the United States
42. Assessing the Safety and Efficacy of Converting Adults with Sickle Cell Disease from Full Agonist Opioids to Buprenorphine
43. Increased acute care utilization in a prospective cohort of adults with sickle cell disease
44. Developmental Outcomes of Children Exposed to Maternal Sickle Cell Disease (SCD)
45. Negative studies shape the state of sickle trait
46. Acute Care Utilization Is More Common in Patients with Sickle Cell Disease Who Have Chronic Complications and Chronic Pain: A Preliminary Report from the Escaped Trial
47. Hospitalization for Acute Pain in Sickle Cell Disease: Changes in Clinical Parameters and Factors Predicting Hospital Discharge and Re-Admission
48. The five key things you need to know to manage adult patients with sickle cell disease
49. Metabolic Syndrome Risk Among Adults Living with Sickle Cell Disease
50. Contraceptive in Women with Sickle Cell Disease: A Survey Study
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