1.
Haematologica
; 69(2): 127-32, 1984.
Article
in English
| MEDLINE
| ID: mdl-6428999
Subject(s)
Intestinal Absorption , Thalassemia/metabolism , Vitamin E/metabolism , Child , Child, Preschool , Female , Homozygote , Humans , Male , Thalassemia/genetics
2.
Pediatr Med Chir
; 3(6): 555-7, 1981.
Article
in Italian
| MEDLINE
| ID: mdl-7343954
ABSTRACT
The authors describe six subjects with Reye's syndrome. All subjects died nevertheless the treatment (exchange-transfusions infusions of citrulline and ornithine). The autoptical studies showed cerebral oedema and fatty degeneration of the liver. Hepatic and seric OTC activity was measured in three patients: enzyme activity was virtually absent in one patient and normal in the other two. Instead in one patient was found partial CPS deficiency. However, Reye's syndrome is not only correlated with enzymatic deficiency of urea's cycle but sometimes also with toxic and metabolic causes.