Improving an Administrative Case Definition for Longitudinal Surveillance of Sickle Cell Disease von Snyder, Angela B., Zhou, Mei, Theodore, Rodney, Quarmyne, Maa-Ohui, Eckman, James, Lane, Peter A.

Volltext

A proposed algorithm for evaluation and management of pediatric hemophilia patients who present to the emergency department with head trauma von Kracht, M. Jensen, Stein, Amy, Knoll, Christine, Badia Alonso, Priscila, Gomez, Esteban, Quarmyne, Maa‐Ohui, Shah, Sanjay, Gendreau, Joanna

Volltext

Contribution of alternative complement pathway to delayed hemolytic transfusion reaction in sickle cell disease von Chonat, Satheesh, Quarmyne, Maa-Ohui, Bennett, Caroline M, Dean, Christina L, Joiner, Clinton H, Fasano, Ross M, Stowell, Sean R

Volltext

Eculizumab for complement mediated thrombotic microangiopathy in sickle cell disease von Chonat, Satheesh, Graciaa, Sara, Shin, H Stella, Newton, Joanna G, Quarmyne, Maa-Ohui, Boudreaux, Jeanne, Tang, Amy, Zerra, Patricia E, Rollins, Margo R, Josephson, Cassandra D, Brown, Clark, Joiner, Clinton H, Fasano, Ross M, Stowell, Sean R

Volltext

T Cell-Epstein-Barr Virus–Associated Hemophagocytic Lymphohistiocytosis (HLH) Occurs in Non-Asians and Is Associated with a T Cell Activation State that Is Comparable to Primary HL... von Shamriz, Oded, Kumar, Deepak, Shim, Jenny, Briones, Michael, Quarmyne, Maa-Ohui, Chonat, Satheesh, Lucas, Laura, Edington, Holly, White, Michael H., Mahajan, Advay, Park, Sunita, Chandrakasan, Shanmuganathan

Volltext

Decision-making about gene therapy in transfusion dependent thalassemia von Quarmyne, Maa-Ohui, Ross, Diana, Sinha, Cynthia, Bakshi, Nitya, Boudreaux, Jeanne, Krishnamurti, Lakshmanan

Volltext

Correction to: T Cell‑Epstein‑Barr Virus–Associated Hemophagocytic Lymphohistiocytosis (HLH) Occurs in Non‑Asians and Is Associated with a T Cell Activation State that Is Comparabl... von Shamriz, Oded, Kumar, Deepak, Shim, Jenny, Briones, Michael, Quarmyne, Maa‑Ohui, Chonat, Satheesh, Lucas, Laura, Edington, Holly, White, Michael H., Mahajan, Advay, Park, Sunita, Chandrakasan, Shanmuganathan

Volltext

Assessment of Patient and Caregiver Attitudes and Approaches to Decision-Making Regarding Bone Marrow Transplant for Sickle Cell Disease: A Qualitative Study von Bakshi, Nitya, Katoch, Deeksha, Sinha, Cynthia B, Ross, Diana, Quarmyne, Maa-Ohui, Loewenstein, George, Krishnamurti, Lakshmanan

Volltext

Hydroxyurea effectiveness in children and adolescents with sickle cell anemia: A large retrospective, population‐based cohort von Quarmyne, Maa‐Ohui, Dong, Wei, Theodore, Rodney, Anand, Sonia, Barry, Vaughn, Adisa, Olufolake, Buchanan, Iris D., Bost, James, Brown, Robert C., Joiner, Clinton H., Lane, Peter A.

Volltext

Patient and family experience with chronic transfusion therapy for sickle cell disease: A qualitative study von Hawkins, Lauren M, Sinha, Cynthia B, Ross, Diana, Yee, Marianne E M, Quarmyne, Maa-Ohui, Krishnamurti, Lakshmanan, Bakshi, Nitya

Volltext

Hydroxyurea Optimization through Precision Study (HOPS): study protocol for a randomized, multicenter trial in children with sickle cell anemia von Meier, Emily R, Creary, Susan E, Heeney, Matthew M, Dong, Min, Appiah-Kubi, Abena O, Nelson, Stephen C, Niss, Omar, Piccone, Connie, Quarmyne, Maa-Ohui, Quinn, Charles T, Saving, Kay L, Scott, John P, Talati, Ravi, Latham, Teresa S, Pfeiffer, Amanda, Shook, Lisa M, Vinks, Alexander A, Lane, Adam, McGann, Patrick T

Volltext

Genotype-phenotype correlations in hereditary elliptocytosis and hereditary pyropoikilocytosis von Niss, Omar, Chonat, Satheesh, Dagaonkar, Neha, Almansoori, Marya O., Kerr, Karol, Rogers, Zora R., McGann, Patrick T., Quarmyne, Maa-Ohui, Risinger, Mary, Zhang, Kejian, Kalfa, Theodosia A.

Volltext

Lymphangiosarcoma of the thorax and thoracic vertebrae in a 16-year-old girl von Quarmyne, Maa-Ohui, Gupta, Anita, Adams, Denise M

Volltext

Volume regulation and KCl cotransport in reticulocyte populations of sickle and normal red blood cells von Quarmyne, Maa-Ohui, Risinger, Mary, Linkugel, Andrew, Frazier, Anna, Joiner, Clinton

Volltext

Hemoglobin F Only Syndrome at Birth: A Case of Maternal HbA2' Complicating the Diagnosis of β-Thalassemia von Yee, Marianne E M, Quarmyne, Maa-Ohui, Segbefia, Catherine, Young, Andrew N, Zhuang, Lina, Kutlar, Ferdane

Volltext

10-Year Mortality in Patients with Sickle Cell Disease from a Large Population-Based Cohort von Lai, Kristina, Yee, Marianne McPherson, Gee, Beatrice, Quarmyne, Maa-Ohui, Fasano, Ross M., Maillis, Alexander, Lane, Peter A.

Volltext

Trends in Hospital Utilization for Acute Illness in a Large Population-Based Cohort of Children and Adolescents with Sickle Cell Disease (SCD): 2010–2017 von Lai, Kristina, Anand, Sonia, Quarmyne, Maa-Ohui, Dampier, Carlton, Lane, Peter A., Ibrahim, Amenah

Volltext

Individualized, PK-Guided Dosing of Hydroxyurea Is Not Associated with Increased Hematologic Toxicity Compared to Weight-Based Initial Dosing: Interim Results from the Hops Trial von Appiah-Kubi, Abena, Jacob, Seethal A, Heeney, Matthew M., Brown, Clark, Creary, Susan E., Hollenkamp, Christine R, Meier, Emily Riehm, Niss, Omar, Piccone, Connie M., Quarmyne, Maa-Ohui, Quinn, Charles T., Remiker, Allison, Saving, Kay L, Dong, Min, McGann, Patrick T.

Volltext

Role of Menstrual Bleeding Assessments in Sickle Cell Clinics in Improving Quality of Care for Women- a Multicenter Approach von Bhasin, Neha, Rush, Gillian, Strouse, John J, Moffatt-Bazile, Kim, E Mohamed, Rania, Jacob, Seethal A, Sathi, Bindu Kanathezhath, Smink, Gayle M, Schultz, Corinna L., DiVirgilio, Nicole, Vichinsky, Elliott P., Velez, Maria C, Hagar, Robert, Quarmyne, Maa-Ohui, Ogu, Ugochi, Treadwell, Marsha

Volltext

Effect of Acute Transfusion on Cerebral Oxygenation in Patients with Sickle Cell Disease von Quarmyne, Maa-Ohui, Figueroa, Janet, McCracken, Courtney, Quinn, Charles T., Brown, Clark, Joiner, Clinton H.

Volltext