✦ LIBER ✦

Self-Evaluation, Coping, and Depressive Affect in African American Adults with Sickle Cell Disease

✍ Scribed by Jennifer J. Wilson; Karen M. Gil; Lauren Raezer

Book ID: 110413222
Publisher: Springer US
Year: 1997
Tongue: English
Weight: 866 KB
Volume: 21
Category: Article
ISSN: 0147-5916
DOI: 10.1023/a:1021984310786

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Individual and Family Contributions to D

Individual and Family Contributions to Depressive Symptoms in African American Children with Sickle Cell Disease

✍ Karia Kelch-Oliver; Chaundrissa Oyeshiku Smith; Dayna Diaz; Marietta H. Collins 📂 Article 📅 2007 🏛 Springer 🌐 English ⚖ 240 KB

Body Image in a Sample of Adult African

Body Image in a Sample of Adult African American Males and Females with Sickle Cell Disease (SCD)

✍ Sheethal D. Reddy; Christopher L. Edwards; Mary Wood; Keisha O’Garo; Kai Morgan; 📂 Article 📅 2010 🏛 Springer 🌐 English ⚖ 92 KB

Functional capacity in children and youn

Functional capacity in children and young adults with sickle cell disease undergoing evaluation for cardiopulmonary disease

✍ Robert I. Liem; Mary A. Nevin; Adrienne Prestridge; Luciana T. Young; Alexis A. 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 107 KB 👁 2 views

Factor V Leiden is not responsible for s

Factor V Leiden is not responsible for stroke in patients with sickling disorders and is uncommon in African Americans with sickle cell disease

✍ Kahn, Marc J.; Scher, Charles; Rozans, Marta; Michaels, Robert K.; Leissinger, C 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 49 KB 👁 1 views

Cerebrovascular accidents in patients with sickle cell anemia are among the most devastating complications of the disease. It has recently been demonstrated that some patients have a hypercoagulable state on the basis of the presence of an abnormal factor V molecule, factor V Leiden. We undertook th