BIOMAT Database Logo BIOMAT Database Logo

The patient with sickle cell anemia. 1972

R W Davis

UI MeSH Term Description Entries
D000755 Anemia, Sickle Cell A disease characterized by chronic hemolytic anemia, episodic painful crises, and pathologic involvement of many organs. It is the clinical expression of homozygosity for hemoglobin S. Hemoglobin S Disease,HbS Disease,Sickle Cell Anemia,Sickle Cell Disease,Sickle Cell Disorders,Sickling Disorder Due to Hemoglobin S,Anemias, Sickle Cell,Cell Disease, Sickle,Cell Diseases, Sickle,Cell Disorder, Sickle,Cell Disorders, Sickle,Disease, Hemoglobin S,Hemoglobin S Diseases,Sickle Cell Anemias,Sickle Cell Diseases,Sickle Cell Disorder

Related Publications

R W Davis
A trauma patient with sickle cell anemia.
June 1997, Journal of emergency nursing,
R W Davis
Pancytopenia in a patient with sickle cell anemia.
October 1975, American journal of diseases of children (1960),
R W Davis
Babesiosis in a patient with sickle cell anemia.
April 1997, The American journal of medicine,
R W Davis
The sickle cell anemia patient in surgery.
December 1979, AORN journal,
R W Davis
Sickle cell anemia in the female patient.
May 2006, Obstetrical & gynecological survey,
R W Davis
Sickle cell anemia and the dental patient.
January 1974, Journal of the Louisiana Dental Association,
R W Davis
JAMA Patient Page: sickle cell anemia.
May 1999, JAMA,
R W Davis
The dental management of the patient with sickle cell anemia.
August 1960, Archives of pediatrics,
R W Davis
Legionnaires' disease in a patient with sickle cell anemia.
November 1981, Maryland state medical journal,
R W Davis
Malignant hyperthermia in a patient with sickle cell anemia.
January 1989, The Turkish journal of pediatrics,
Copied contents to your clipboard!