Results 1 to 10 of about 2,183 (180)

Comparison of Asymptomatic Brain Lesions Between Thalassemia Major and Sickle Cell Anemia Patients

Medicina
Background and Objectives: This study aimed to identify asymptomatic brain lesions in patients with β-thalassemia major (TM) and sickle cell anemia (SCA) and evaluate the correlation of these lesions with factors such as splenectomy, thrombocytosis, and ...
Derya Yavuz Demiray, Özge Eriş Davut, Gönül Oktay   +2 more
doaj   +1 more source

Secondary hemophagocytic lymphohistiocytosis in a child with Sickle Cell Anemia and Hepatitis A and Hepatitis E co-infection: A case report

Pediatric Hematology Oncology Journal
Background: Secondary hemophagocytic lymphohistiocytosis (HLH) is a potentially fatal condition commonly triggered by infections. HLH secondary to hepatitis E or hepatitis A and E coinfection has been scarcely reported.
Govind Choudhary, Nida Mirza, Swati Patel   +2 more
doaj   +1 more source

Soluble transferrin receptor in sickle cell diseases: correlation with spleen function

São Paulo Medical Journal
OBJECTIVE: To correlate spleen function with soluble transferrin receptor (sTfR) levels and red cell ferritin (RCF) values in patients with sickle cell diseases. DESIGN: Prospective study.
Helena Zerlotti Wolf Grotto, Elza Miyuki Kimura, Márcia Victor Carneiro   +2 more
doaj   +1 more source

Apneia obstrutiva do sono em portadores da anemia falciforme Obstructive sleep apnea in sickle cell disease carriers

Revista Brasileira de Hematologia e Hemoterapia, 2010
A Síndrome da Apneia Obstrutiva do Sono (SAOS) é definida como episódios recorrentes de obstrução completa ou parcial das vias aéreas superiores que ocorrem durante o sono.
Cristina Salles, Regina T. T. Ramos, Marcos A. Matos   +2 more
doaj  

SICKLE CELL ANEMIA

Annals of Surgery, 1950
H, WILSON, R H, PATTERSON, L W, DIGGS
openaire   +3 more sources

Sickle Cell Anemia

Postgraduate Medicine, 1952
For general practitioners, as well as specialists, this department offers the latest, proved methods of treatment of conditions encountered in an average practice. It is not, of course, intended to present these discussions as the only acceptable therapeutic procedures to be used, but rather to offer simple regimens and recommendations based on the ...
G W, JAMES, W B, PORTER
openaire   +2 more sources

Sickle cell anemia and pregnancy

American Journal of Obstetrics and Gynecology, 1949
Abstract The present study is a review of eleven cases of sickle cell anemia associated with pregnancy observed on the Obstetrical Service of the Johns Hopkins Hospital over a 20-year period (1927–1947). No deaths occurred in these eleven mothers during the period of the pregnancy or puerperium.
G W, ANDERSON, T, BUSBY
openaire   +2 more sources

Enuresis in Sickle Cell Anemia

Archives of Pediatrics & Adolescent Medicine, 1967
IT IS WELL recognized that patients with sickle cell disease have hyposthenuria. 1 This hyposthenuria results in the excretion of increased volumes of urine during a 24-hour period. It has been our impression that this polyuria results in an increased incidence of enuresis among children with sickle cell anemia.
G, Suster, F A, Oski
openaire   +2 more sources

Sickle Cell Anemia

American Journal of Diseases of Children, 1923
J. B. Herrick, 1 in 1910, reported a peculiar dyscrasia characterized by severe anemia, with the occurrence in the blood of elongated and sickle-shaped erythrocytes. Three instances of this condition have since been described, one by R. E. Washburn; 2 one by Cook and Myer, 3 and one by V. R. Mason. 4 Emmel 5 further studied the blood of Cook and Myer's
openaire   +1 more source

Sickle Cell Anemia

Annals of Internal Medicine, 1978
Excerpt To the editor: The "natural history" of sickle cell anemia in Saudi Arabs (Ann Intern Med88:1-6, 1978) is certainly different from the disease as we see it in the United States but not as d...
openaire   +2 more sources