The primary objective of the Scholar Program at our Center is to prepare the candidate for a career inacademic medicine and biomedical research and to assist in the development of individuals (either MD, PhD,or MD. PhD) into productive independent investigators in the field of sickle cell disease. This program will addto the critical mass of such 'Scholars' over time. Most important is that it is this cadre of individuals who will,we hope, become the Clinical Program Directors and NIH Principal Investigators of tomorrow. The resourcesfor this individual will include patients receiving state-of-the-art clinical care at St. Christopher's Hospital forChildren and Thomas Jefferson University Hospital, the clinical research staff of the Marian AndersonComprehensive Sickle Cell Center, the MAC Research Laboratory Facilities in the Department of Pediatrics atThomas Jefferson University, and the Laboratory Facilities and Education Program of the Cardeza Program forHematology Research also at Jefferson Medical School. Dr. Marie Stuart, the Principal Investigator of theProgram, will serve as one of the Mentors for this Scholar, with dual mentorship as appropriate, dependent onthe area of research activities identified by the Scholar in pursuit of his/her academic and scholarly activities. Itis anticipated that this individual will develop a research program that will complement the ongoing basicscience, translational, and clinical research of the Marian Anderson Center's investigators.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Specialized Center--Cooperative Agreements (U54)
Project #
2U54HL070585-06
Application #
7458499
Study Section
Special Emphasis Panel (ZHL1-CSR-O (F1))
Project Start
2008-04-01
Project End
2012-03-31
Budget Start
2008-04-01
Budget End
2009-03-31
Support Year
6
Fiscal Year
2008
Total Cost
$164,002
Indirect Cost
Name
Thomas Jefferson University
Department
Type
DUNS #
053284659
City
Philadelphia
State
PA
Country
United States
Zip Code
19107
Goligher, Ewan C; Ely, E Wesley; Sulmasy, Daniel P et al. (2017) Physician-Assisted Suicide and Euthanasia in the ICU: A Dialogue on Core Ethical Issues. Crit Care Med 45:149-155
Daniel, Lauren C; Li, Yimei; Smith, Kelsey et al. (2015) Lessons Learned From a Randomized Controlled Trial of a Family-Based Intervention to Promote School Functioning for School-Age Children With Sickle Cell Disease. J Pediatr Psychol 40:1085-94
Dampier, Carlton; Ely, Beth; Brodecki, Darcy et al. (2014) Pain characteristics and age-related pain trajectories in infants and young children with sickle cell disease. Pediatr Blood Cancer 61:291-6
Robinson, M Renee; Daniel, Lauren C; O'Hara, Emily A et al. (2014) Insurance status as a sociodemographic risk factor for functional outcomes and health-related quality of life among youth with sickle cell disease. J Pediatr Hematol Oncol 36:51-6
Barakat, Lamia P; Daniel, Lauren C; Smith, Kelsey et al. (2014) Parental problem-solving abilities and the association of sickle cell disease complications with health-related quality of life for school-age children. J Clin Psychol Med Settings 21:56-65
Smith, Kelsey E; Patterson, Chavis A; Szabo, Margo M et al. (2013) Predictors of Academic Achievement for School Age Children with Sickle Cell Disease. Adv Sch Ment Health Promot 6:5-20
Setty, B N Yamaja; Key, Nigel S; Rao, A Koneti et al. (2012) Tissue factor-positive monocytes in children with sickle cell disease: correlation with biomarkers of haemolysis. Br J Haematol 157:370-80
McQuaid, Elizabeth L; Barakat, Lamia P (2012) Introduction to special section: advancing research on the intersection of families, culture, and health outcomes. J Pediatr Psychol 37:827-31
Dampier, Carlton; LeBeau, Petra; Rhee, Seungshin et al. (2011) Health-related quality of life in adults with sickle cell disease (SCD): a report from the comprehensive sickle cell centers clinical trial consortium. Am J Hematol 86:203-5
Quinn, Charles T; Stuart, Marie J; Kesler, Karen et al. (2011) Tapered oral dexamethasone for the acute chest syndrome of sickle cell disease. Br J Haematol 155:263-7

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