Hereditary coproporphyria. A family with unusually few and mild symptoms.
作者信息
Lomholt J C, With T K
出版信息
Acta Med Scand. 1969 Jul-Aug;186(1-2):83-5.
PMID:5807649
Abstract
摘要
相似文献
1
Hereditary coproporphyria. A family with unusually few and mild symptoms.
Acta Med Scand. 1969 Jul-Aug;186(1-2):83-5.
2
[Role of hereditary predisposition in the development of late cutaneous porphyria].
Klin Med (Mosk). 1972 Jan;50(1):101-10.
3
[Hereditary coproporphyria in 2 Dutch families].
Ned Tijdschr Geneeskd. 1984 May 12;128(19):892-5.
4
[A new variety of porphyria, mixed or variegate hereditary coproporphyria].
Rev Fr Etud Clin Biol. 1969 Mar;14(3):279-82.
5
[Hereditary coproporphyria].
Rev Clin Esp. 1968 Jul 15;110(1):81-2.
6
Hereditary coproporphyria.
Panminerva Med. 1966 Jul-Aug;8(7):288-9.
7
Clinical aspects of importance in the porphyrias.
Br J Clin Pract. 1968 Dec 12;22(12):505-15.
8
[Hereditary coproporphyria].
Ugeskr Laeger. 1973 Nov 19;135(47):2571.
9
[Hereditary coproporphyria in the Federal Republic of Germany (author's transl)].
J Clin Chem Clin Biochem. 1978 Sep;16(9):519-24.
10
Hepatic delta-aminolaevulinic acid synthetase in an attack of hereditary coproporphyria and during remission.
Lancet. 1971 Mar 20;1(7699):560-4. doi: 10.1016/s0140-6736(71)91161-5.
引用本文的文献
1
Hereditary coproporphyria: incidence in a large English family.
J Med Genet. 1984 Oct;21(5):341-9. doi: 10.1136/jmg.21.5.341.
2
Coexistence of hereditary coproporphyria and epilepsy: coproporphyrinogen oxidase deficiency in liver and kidney.
J Neurol. 1981;226(1):25-33. doi: 10.1007/BF00313315.
3
The porphyrias: a review.
J Clin Pathol. 1972 Dec;25(12):1013-33. doi: 10.1136/jcp.25.12.1013.
4
Hereditary coproporphyria and epilepsy.
Arch Dis Child. 1977 Aug;52(8):646-50. doi: 10.1136/adc.52.8.646.
5
Catecholamine uptake, accumulation, and release in acute porphyria.
J Clin Invest. 1977 Nov;60(5):1141-8. doi: 10.1172/JCI108866.
Zotero 插件