Results 291 to 300 of about 1,975,307 (342)

Homozygous hemoglobin C disease

Blood, 2013
![Figure][1] A 44-year-old African American female presented with a pain crisis and a history of hemoglobinopathy, menometrorrhagia secondary to acquired von Willebrand factor (vWF) deficiency, and a history of multiple vaso-occlusive events necessitating lifelong warfarin therapy ...
Samir, Dalia, Ling, Zhang
openaire   +2 more sources

Homozygous hemoglobin C disease

The American Journal of Medicine, 1955
E.D. Thomas, A.G. Motulsky, D.H. Walters
openaire   +2 more sources

Vasoocclusion with Homozygous Hemoglobin-C Disease

Journal of Pediatric Hematology/Oncology, 1988
Hemoglobin-CC is a relatively uncommon hemoglobinopathy, seen primarily in the black population. These patients usually have a mild clinical course, without significant risk of vasoocclusive crises. There are no routine recommendations for preparation prior to surgery.
J A, Fort, J R, Graham-Pole, J, Chopik
openaire   +2 more sources

Hemoglobin C disease in infancy and childhood☆☆☆★★★

The Journal of Pediatrics, 1994
We reviewed the clinical course, physical findings, and hematologic values in 16 pediatric patients with hemoglobin C disease, all but one identified by a newborn hemoglobinopathy screening program. The patients had a few symptoms or physical findings. Height and weight percentiles were normal.
J F, Olson, R E, Ware, W H, Schultz, T R, Kinney   +3 more
openaire   +2 more sources

Homozygous hemoglobin C disease.

Blood, 2005
  +6 more sources

Angiography in Hemoglobin S-C Disease

Annals of Internal Medicine, 1986
Excerpt To the editor: Radiographic contrast media have been reported to cause morphologic "sickling" in vitro of erythrocytes containing hemoglobin S (1).
openaire   +1 more source

The effects of exchange transfusion for prevention of complications during pregnancy of sickle hemoglobin C disease patients

Transfusion, 2016
B. Benites, Thais Celi Lopes Benevides, Isabella Salvetti Valente, J. F. Marques, S. Gilli, Sara Teresinha Olalla Saad   +5 more
semanticscholar   +1 more source

Fatal Hemoglobin S-C Disease Crises Following Tonsillectomy

Archives of Otolaryngology - Head and Neck Surgery, 1965
WHILE many improvements in surgical and anesthetic techniques have made the tonsillectomy and adenoidectomy an even safer procedure than in previous years, fatal complications still occur. Each year in the United States, about 300 persons die during the operation or as a direct result of it.1Many of these deaths are preventable.
openaire   +2 more sources

Splenic infarction in sickle cell-hemoglobin C disease. Demonstration by selective splenic arteriogram and scintillation scan.

Archives of Internal Medicine, 1976
K. Yeung, L. Lessin
semanticscholar   +1 more source

Outcome of pregnancy in sickle cell anemia and sickle cell-hemoglobin C disease. An analysis of 181 pregnancies in 98 patients, and a review of the literature.

American Journal of Obstetrics and Gynecology, 1980
P. Milner, B. Jones, J. Döbler
semanticscholar   +1 more source