Clinical Pediatrics

Sisson, Thomas R. C.

doi: 10.1177/000992287101001201pmid: 4334543

Wilson, John T.

doi: 10.1177/000992287101001202pmid: 5168664

doi: 10.1177/000992287101001203pmid: N/A

Skinner, Alfred L.

doi: 10.1177/000992287101001204pmid: 5139943

doi: 10.1177/000992287101001205pmid: N/A

doi: 10.1177/000992287101001206pmid: 5139944

doi: 10.1177/000992287101001207pmid: N/A

Livingston, Samuel

doi: 10.1177/000992287101001208pmid: 5139945

Diggs, L.W.; Flowers, Ernestine

doi: 10.1177/000992287101001209pmid: 5139946

Because the natural history of sickle cell disease and of its variant forms has not been fully studied, because the disease is associated with ma jor socioeconomic problems and with poverty, and because sickle cell anemia and related hemoglobinopathies are frequent, reports of ob servations made in the home environment seem justified and necessary.

Hoeffel, J.C.; Jacottin, G.; Bourgeois, J.M.

doi: 10.1177/000992287101001210pmid: 4334544

Primary renal cysts in children are extremely vari able. Each entity has a distinctive radiologic pattern.