The genetic basis of porphyria cutanea tarda

Author:

Enriquez de Salamanca R.,Olmos A.,Pe�a M. L.,Berges L.,Perpi�� J.

Publisher

Springer Science and Business Media LLC

Subject

Dermatology,General Medicine

Reference30 articles.

1. Benedetto AV, Kushner JP, Taylor JS (1978) Porphyria cutanea tarda in three generations of a single family. N Engl J Med 298:358?362

2. Blekkenhorst G, Pimstone NR, Eales L (1976) Porphyria cutanea tarda in South Africa. Metabolic basis of disordered haem biosynthesis. In: Doss M (ed) Porphyrins in human disease. Karger, Basel, pp 229?311

3. Brodie MJ, Thompson GG, Moore MR, McColl KEL, Goldberg A, Hardie RA, Hunter JAA (1979) Maem biosynthesis in cutaneous hepatic porphyria: comparison with alcoholism and liver disease. Acta Hepato-Gastroenterol 26:122?128

4. Day RS, De Salamanca RE, Eales L (1978) Quantitation of red cell porphyrins by fluorescence scanning after thin layer chromatography. Clin Chim Acta 89:25?33

5. Dehlin O, Enerbäck L, Lundvall O (1973) Porphyria cutanea tarda: a genetic disease? A biochemical and fluorescence microscopical study in four families. Acta Med Scand 194:265?270

Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Die chronische hepatische Porphyrie (Porphyria cutanea tarda);Ergebnisse der Inneren Medizin und Kinderheilkunde / Advances in Internal Medicine and Pediatrics;1993

2. Genetics and pathogenesis of human uroporphyrinogen decarboxylase defects;Clinical Biochemistry;1989-06

3. References;Disorders of Porphyrin Metabolism;1987

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