Creutzfeldt-Jakob disease--alteration in ganglioside sphingosine in the brain of a patient.

Abstract:

:Gangliosides isolated from the brain of patients with Creutzfelt-Jakob (C-J) disease were analyzed. The ganglioside current was abnormally low, and the percentage distributions of individual gangliosides and the long-chain base compositions were abnormal. The C20-sphingosine contents of all the ganglioside fractions were low. Abnormalities in ganglioside long-chain bases in adult human brain have been reported previously only in patients with inherited metabolic disorders. These abnormalities in C-J disease seem to be closely related to the cause of the disease.

journal_name

Neurosci Lett

journal_title

Neuroscience letters

authors

Tamai Y,Ohtani Y,Miura S,Narita Y,Iwata T,Kaiya H,Namba M

doi

10.1016/0304-3940(79)90060-0

subject

Has Abstract

pub_date

1979-01-01 00:00:00

pages

81-6

issue

1

eissn

0304-3940

issn

1872-7972

pii

0304-3940(79)90060-0

journal_volume

11

pub_type

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