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Article
Hepatic Ganglioside Abnormalities in a Patient with Familial Erythrophagocytic Lymphohistiocytosis
Summary: Familial erythrophagocytic lymphohistiocytosis (FEL) is an autosomal recessive disease of unknown pathogenesis. Because of evidence of increased circulating and hepatic lipids in FEL, we performed a c...
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Article
941 PLASMA INHIBITION OF LYMPHOCYTE BLASTOGENESIS IN NEPHROTIC SYNDROME: CORRELATION WITH HYPERLIPIDEMIA
The plasma of patients with Nephrotic Syndrome suppresses in vitro lymphocyte blastogenesis, but the mechanism of this effect has not been defined. The frequent association of Nephrotic Syndrome with hypertriglyc...
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Article
IMMUNODEFICIENCY IN LYMPHOHISTIOCYTOSIS: DEFECTIVE CELLULAR IMMUNITY IN ASSOCIATION WITH HYPERLIPIDEMIA
Lymphohistiocytosis (LH) is a familial syndrome characterized by abnormal accumulation of non-malignant histiocytes in lymph nodes, liver, and spleen, erythrophagocytosis, hepatoaplenomegaly, recurrent fever, ...