[Inborn errors of catecholamine metabolism].
作者信息
Suzuki T
机构信息
Department of Clinical Genetics, Medical Institute of Bioregulation, Kyushu University.
出版信息
Ryoikibetsu Shokogun Shirizu. 1998(19 Pt 2):640-4.
PMID:9645154
Abstract
摘要
相似文献
1
[Inborn errors of catecholamine metabolism].[儿茶酚胺代谢的先天性缺陷]
Ryoikibetsu Shokogun Shirizu. 1998(19 Pt 2):640-4.
2
[Inborn errors of catecholamine metabolism].[儿茶酚胺代谢的先天性缺陷]
Ryoikibetsu Shokogun Shirizu. 2000(29 Pt 4):527-31.
3
Abnormalities of biogenic amines affecting the metabolism of serotonin and catecholamines.影响血清素和儿茶酚胺代谢的生物胺异常。
Mult Scler. 1998 Feb;4(1):37-8. doi: 10.1177/135245859800400109.
4
Genetics and molecular biology of hypotension.低血压的遗传学与分子生物学
Curr Opin Nephrol Hypertens. 1994 Jan;3(1):13-24. doi: 10.1097/00041552-199401000-00002.
5
Aromatic L-amino acid decarboxylase deficiency with hyperdopaminuria. Clinical and laboratory findings in response to different therapies.芳香族L-氨基酸脱羧酶缺乏症伴高多巴胺尿症。不同治疗方法的临床和实验室结果。
Neuropediatrics. 2002 Aug;33(4):203-8. doi: 10.1055/s-2002-34497.
6
Monoamine neurotransmitter deficiencies.单胺神经递质缺乏症。
Handb Clin Neurol. 2013;113:1819-25. doi: 10.1016/B978-0-444-59565-2.00051-4.
7
[A deficiency of dihydrobiopterin synthesis. The effects of L-dopa, 5HTP and BH4].[二氢生物蝶呤合成缺陷。左旋多巴、5-羟色氨酸和四氢生物蝶呤的作用]
Rinsho Shinkeigaku. 1988 Apr;28(4):376-81.
8
Catecholamine phenotyping: clues to the diagnosis, treatment, and pathophysiology of neurogenetic disorders.儿茶酚胺表型分析：神经遗传性疾病诊断、治疗及病理生理学的线索
J Neurochem. 1996 Nov;67(5):1781-90. doi: 10.1046/j.1471-4159.1996.67051781.x.
9
[Disorders of tetrahydrobiopterin homeostasis].[四氢生物蝶呤稳态紊乱]
Ryoikibetsu Shokogun Shirizu. 1998(18 Pt 1):125-9.
10
Aromatic L-amino acid decarboxylase deficiency: clinical features, diagnosis, and treatment of a second family.
J Child Neurol. 1997 Sep;12(6):349-54. doi: 10.1177/088307389701200602.
Zotero 插件