[慢性肝卟啉症的遗传性和非遗传性形式：肝脏和红细胞中尿卟啉原脱羧酶的不同表现（作者译）] - Suppr

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超能文献

[Hereditary and non-hereditary form of chronic hepatic porphyria: different behaviour of uroporphyrinogen decarboxylase in liver and erythrocytes (author's transl)].

作者信息

Doss M, von Tiepermann R, Look D, Henning H, Nikolowski J, Ryckmanns F, Braun-Falco O

出版信息

Klin Wochenschr. 1980 Dec 15;58(24):1347-56. doi: 10.1007/BF01477732.

DOI:10.1007/BF01477732

PMID:7206594

Abstract

摘要

相似文献

[Hereditary and non-hereditary form of chronic hepatic porphyria: different behaviour of uroporphyrinogen decarboxylase in liver and erythrocytes (author's transl)].[慢性肝卟啉症的遗传性和非遗传性形式：肝脏和红细胞中尿卟啉原脱羧酶的不同表现（作者译）]

Klin Wochenschr. 1980 Dec 15;58(24):1347-56. doi: 10.1007/BF01477732.

[Uroporphyrinogen decarboxylase in erythrocytes: studies on the primary genetic enzyme defect in chronic hepatic porphyria (author's transl)].红细胞中的尿卟啉原脱羧酶：慢性肝性卟啉症原发性遗传酶缺陷的研究（作者译）

J Clin Chem Clin Biochem. 1978 Sep;16(9):513-7.

Is hepatoerythropoietic porphyria a homozygous form of porphyria cutanea tarda? Inheritance of uroporphyrinogen decarboxylase deficiency in a Spanish family.肝红细胞生成性卟啉症是迟发性皮肤卟啉症的纯合子形式吗？一个西班牙家庭中尿卟啉原脱羧酶缺乏症的遗传情况。

Br J Dermatol. 1984 May;110(5):613-7. doi: 10.1111/j.1365-2133.1984.tb04687.x.

Uroporphyrinogen decarboxylase activity of human tissues [proceedings].人体组织的尿卟啉原脱羧酶活性[会议论文集]

Biochem Soc Trans. 1977;5(5):1470-2. doi: 10.1042/bst0051470.

Decreased activity of hepatic uroporphyrinogen decarboxylase in sporadic porphyria cutanea tarda.迟发性皮肤卟啉症偶发病例中肝尿卟啉原脱羧酶活性降低。

N Engl J Med. 1978 Aug 10;299(6):274-8. doi: 10.1056/NEJM197808102990603.

Immunochemical study of uroporphyrinogen decarboxylase in a patient with mild hepatoerythropoietic porphyria.一名轻度肝红细胞生成性卟啉症患者的尿卟啉原脱羧酶免疫化学研究。

J Clin Invest. 1987 May;79(5):1533-7. doi: 10.1172/JCI112985.

Uroporphyrinogen decarboxylase deficiency in experimental chronic hepatic porphyria.实验性慢性肝性卟啉病中的尿卟啉原脱羧酶缺乏症

Hoppe Seylers Z Physiol Chem. 1980 Aug;361(8):1217-22. doi: 10.1515/bchm2.1980.361.2.1217.

An inherited enzymatic defect in porphyria cutanea tarda: decreased uroporphyrinogen decarboxylase activity.迟发性皮肤卟啉症中的一种遗传性酶缺陷：尿卟啉原脱羧酶活性降低。

J Clin Invest. 1976 Nov;58(5):1089-97. doi: 10.1172/JCI108560.

Erythrocyte uroporphyrinogen decarboxylase activity in porphyria cutanea tarda: a study of 40 consecutive patients.迟发性皮肤卟啉症患者的红细胞尿卟啉原脱羧酶活性：40例连续患者的研究

J Invest Dermatol. 1989 Sep;93(3):332-4.

Familial porphyria cutanea tarda with normal erythrocytic urodecarboxylase: an exception to the rule?红细胞尿卟啉脱羧酶正常的家族性迟发性皮肤卟啉症：规则的例外？

Dermatologica. 1989;178(4):206-8. doi: 10.1159/000248428.

引用本文的文献

Different types of porphyria cutanea tarda.迟发性皮肤卟啉症的不同类型。

Arch Dermatol Res. 1984;276(3):207-8. doi: 10.1007/BF00414024.

Hereditary uroporphyrinogen-decarboxylase deficiency predisposing porphyria cutanea tarda (chronic hepatic porphyria) in females after oral contraceptive medication.遗传性尿卟啉原脱羧酶缺乏症使女性在口服避孕药后易患迟发性皮肤卟啉症（慢性肝性卟啉症）。

Arch Dermatol Res. 1985;278(1):13-6. doi: 10.1007/BF00412489.

Effects of polyhalogenated aromatic compounds on porphyrin metabolism.多卤代芳香化合物对卟啉代谢的影响。

Environ Health Perspect. 1985 May;60:139-43. doi: 10.1289/ehp.8560139.

The genetic basis of porphyria cutanea tarda.迟发性皮肤卟啉症的遗传基础。

Arch Dermatol Res. 1985;277(1):8-12. doi: 10.1007/BF00406473.

Erythrocytapheresis. A method for rapid extracorporeal elimination of erythrocytes. Results in 65 patients.

Klin Wochenschr. 1988 May 2;66(9):404-9. doi: 10.1007/BF01737944.

Professor Dr. Dr. h. c. Otto Braun-Falco.奥托·布劳恩-法尔科教授，医学博士、荣誉博士

Arch Dermatol Res. 1987;279 Suppl:S4-23. doi: 10.1007/BF00585915.

Heterogeneity of familial porphyria cutanea tarda.迟发性皮肤卟啉症家族性的异质性

J Med Genet. 1988 Oct;25(10):669-76. doi: 10.1136/jmg.25.10.669.

Incidence of hereditary porphyria cutanea tarda (PCT) in a sample of the Italian population.意大利人群样本中迟发性皮肤卟啉病（PCT）的发病率。

Arch Dermatol Res. 1992;284(4):212-4. doi: 10.1007/BF00375795.

本文引用的文献

Acquired toxic porphyria cutanea tarda due to hexachlorobenzene. Report of 348 cases caused by this fungicide.由六氯苯引起的获得性迟发性皮肤卟啉病。关于这种杀菌剂所致348例病例的报告。

JAMA. 1963 Jan 12;183:88-91.

Different patterns of human porphyria.人类卟啉症的不同类型。

Br Med J. 1963 Aug 3;2(5352):272-6. doi: 10.1136/bmj.2.5352.272.

[General symptoms of late skin porphyria (porphyria cutanea tarda) as an indication for its treatment].

Dtsch Med Wochenschr. 1961 Jan 20;86:127-33. doi: 10.1055/s-0028-1112755.

Uroporphyrinogen decarboxylase deficiency in experimental chronic hepatic porphyria.实验性慢性肝性卟啉病中的尿卟啉原脱羧酶缺乏症

Hoppe Seylers Z Physiol Chem. 1980 Aug;361(8):1217-22. doi: 10.1515/bchm2.1980.361.2.1217.

Pathobiochemical transition of secondary coproporphyrinuria to chronic hepatic porphyria in humans.人类继发性粪卟啉尿症向慢性肝卟啉症的病理生化转变。

Klin Wochenschr. 1980 Feb 1;58(3):141-8. doi: 10.1007/BF01477271.

The effect of griseofulvin in hereditary porphyria cutanea tarda. Investigation of porphyrins and blood lipids.灰黄霉素对迟发性皮肤卟啉症的疗效。卟啉与血脂的研究。

Arch Dermatol. 1966 Jan;93(1):21-7.

Porphyria cutanea tarda in an 8-year-old boy.一名8岁男孩患迟发性皮肤卟啉病。

Arch Dermatol. 1969 Apr;99(4):451-4.

Klin Wochenschr. 1971 Aug 15;49(16):941-2. doi: 10.1007/BF01485221.

[Porphyria cutanea tarda in 3 successive generations].[迟发性皮肤卟啉症连续三代发病]

Med Welt. 1970 Mar 21;12:508-10.

[Chronic hepatic porphyrias (author's transl)].

Z Klin Chem Klin Biochem. 1971 Nov;9(6):471-7.

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