Neurologic events after partial exchange transfusion for priapism in sickle cell disease

The Journal of Pediatrics

Volumn 120, Issue 6, 1992, Pages 882-885

  Rackoff, Wayne R ^a,b,c,d,e   Ohene Frempong, Kwaku ^a,b,c,d,e   Month, Stacy ^a,b,c,d,e   Scott, J Paul ^a,b,c,d,e   Neahring, Betsy ^a,b,c,d,e   Cohen, Alan R ^a,b,c,d,e  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

^b CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^c KAISER PERMANENTE MEDICAL CENTER   (United States)

^d MEDICAL COLLEGE OF WISCONSIN   (United States)

^e Children's Hospital of Wisconsin   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTERIOGRAPHY; ARTICLE; BRAIN ARTERY; CLINICAL ARTICLE; COMPLICATION; EXCHANGE BLOOD TRANSFUSION; HEADACHE; HOMOZYGOSITY; HUMAN; INTRACRANIAL PRESSURE; MALE; NEUROLOGIC DISEASE; PRIAPISM; PRIORITY JOURNAL; SCHOOL CHILD; SEIZURE; SICKLE CELL ANEMIA;

ANEMIA, SICKLE CELL; CASE REPORT; CEREBROVASCULAR DISORDERS; CHILD; EPILEPSY; EXCHANGE TRANSFUSION, WHOLE BLOOD; HEADACHE; HEMOGLOBIN, SICKLE; HOMOZYGOTE; HUMAN; INTRACRANIAL PRESSURE; MALE; PRIAPISM; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0026546545     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-3476(05)81954-7     Document Type: Article

References (18)

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4. Priapism in association with sickle hemoglobinopathies in children
5. Intensive transfusion therapy for priapism in boys with sickle cell anemia
6. Automated erythrocytopheresis for relief of priapism in sickle cell hemoglobinopathies
7. The natural history of stroke in sickle cell disease
8. Effect of transfusion therapy on arteriographic abnormalities and on recurrence of stroke in sickle cell disease
9. High risk of recurent stroke after discontinuance of five to twelve years of transfusion therapy in patients with sickle cell disease
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11. Hypertension, convulsions, and cerebral haemorrhage in sickle cell anaemia patients after blood transfusions [Letter]
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14. Beyond hemoglobin polymerization: the red blood cell membrane and sickle cell disease pathophysiology
15. Is sickle cell disease a thrombotic event?
16. Protein S deficiency in sickle cell anemia
17. Sickle cell crises