Sickle Cell Disease—Pathophysiology and Treatment

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Bibliographic Details
Published inCurrent problems in pediatric and adolescent health care Vol. 36; no. 10; pp. 346 - 376
Main Authors Redding-Lallinger, Rupa, Knoll, Christine
Format Journal Article
LanguageEnglish
Published United States Mosby, Inc 01.11.2006
Subjects
Acute Disease
Adolescent
Adult
Age Factors
Analgesics, Non-Narcotic - administration & dosage
Analgesics, Non-Narcotic - therapeutic use
Analgesics, Opioid - administration & dosage
Analgesics, Opioid - therapeutic use
Anemia, Sickle Cell - complications
Anemia, Sickle Cell - diagnosis
Anemia, Sickle Cell - drug therapy
Anemia, Sickle Cell - epidemiology
Anemia, Sickle Cell - genetics
Anemia, Sickle Cell - physiopathology
Anemia, Sickle Cell - therapy
Antibiotic Prophylaxis
Antisickling Agents - administration & dosage
Antisickling Agents - therapeutic use
Blood Transfusion
Child
Child, Preschool
Diagnosis, Differential
Female
Genotype
Hematopoietic Stem Cell Transplantation
Hospitalization
Humans
Hydroxyurea - administration & dosage
Hydroxyurea - therapeutic use
Ibuprofen - administration & dosage
Ibuprofen - therapeutic use
Immunization
Infant
Infant, Newborn
Male
Morphine - administration & dosage
Morphine - therapeutic use
Pain - diagnosis
Pain - drug therapy
Pain - etiology
Pain Measurement
Penicillins - administration & dosage
Penicillins - therapeutic use
Risk Factors
Stroke - epidemiology
Stroke - prevention & control
Time Factors
Treatment Outcome
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Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-3
content type line 23
ObjectType-Review-1
ISSN:1538-5442
1538-3199
DOI:10.1016/j.cppeds.2006.07.002