Studies of catecholamine metabolism in two hereditary forms of dystonia.
作者信息
Wotten G F, Eldridge R, Gordon E K, Axelrod J
出版信息
Trans Am Neurol Assoc. 1973;98:245-7.
PMID:4784942
Abstract
摘要
相似文献
1
Studies of catecholamine metabolism in two hereditary forms of dystonia.
Trans Am Neurol Assoc. 1973;98:245-7.
2
[Role of catecholamines in the biochemical mechanisms of the pathogenesis of hepatocerebral dystrophy].
Zh Nevropatol Psikhiatr Im S S Korsakova. 1982;82(7):78-84.
3
[Pathogenesis and treatment of torsion dystonia].
Zh Nevropatol Psikhiatr Im S S Korsakova. 1978;78(8):1121-8.
4
Excretion of catecholamines in relatives of patients with familial neuroblastoma.
Cancer Res. 1976 Jan;36(1):10-12.
5
Effect of supplemental ascorbic acid in a case of torsion dystonia.
Adv Neurol. 1976;14:319-27.
6
[Catecholamine excretion in torsion dystonia].
Zh Nevropatol Psikhiatr Im S S Korsakova. 1978;78(4):495-503.
7
[Catecholamines metabolism in extrapyramidal disorders in children].
Zh Nevropatol Psikhiatr Im S S Korsakova. 1977;77(10):1466-9.
8
Catecholaminergic activity in idiopathic torsion dystonia.
Neurology. 1987 May;37(5):779-83. doi: 10.1212/wnl.37.5.779.
9
10
Catecholamine measurements in pheochromocytoma and neuroblastoma.
Ann Clin Lab Sci. 1974 May-Jun;4(3):174-7.
Zotero 插件