HLA and porphyria cutanea tarda-Reference-Cited by-同舟云学术

HLA and porphyria cutanea tarda

Published:1980-11 Issue:2 Volume:269 Page:209-210
ISSN:0340-3696
Container-title:Archives of Dermatological Research
language:en
Short-container-title:Arch Dermatol Res

Author:

Llorente L.,Enr�quez R.,Campillo F.,Pe�a M. L.

Publisher

Springer Science and Business Media LLC

Subject

Dermatology,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/BF00406542.pdf

Reference4 articles.

1. Kushner JP, Barbuto AJ, Lee GR (1976) An inherited enzymatic defect in porphyria cutanea tarda: Decreased uroporphyrinogen decarboxylase activity. J Clin Invest 58:1089?1097

2. Benedetto AV, Kushner JP, Taylor JS (1978) Porphyria cutanea tarda in three generations of a single family. N Engl J Med 298:858?862

3. De Verneuil H, Aitken G, Nordmann Y (1978) Familial and sporadic porphyria cutanea: Two different diseases. Hum Genet 44:145?151

4. Elder GH, Sheppard DM, Enríquez de Salamanca R, Olmos A (1980) Identification of two types of porphyria cutanea tarda by measurement of erythrocyte uroporphyrinogen decarboxylase. Clin Sci Mol Med 59:1?8

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1. Porphyria Cutanea Tarda and Related Disorders;The Porphyrin Handbook;2003

2. C282Y and H63D mutations in the HFE gene are not associated with porphyria cutanea tarda in bulgaria;Hepatology;1999-12

3. Mutations in the hemochromatosis gene, porphyria cutanea tarda, and iron overload;Hepatology;1998-01

4. Increased frequency of the haemochromatosis Cys282Tyr mutation in sporadic porphyria cutanea tarda;The Lancet;1997-02

5. The frequency of hemochromatosis-associated alleles is increased in British patients with sporadic porphyria cutanea tarda;Hepatology;1997-01