## Communicated by Peter Byers Hereditary coproporphyria (HC) is an acute hepatic porphyria with autosomal dominant inheritance caused by deficient activity of coproporphyrinogen III oxidase (CPO). Clinical manifestations of the disease are characterized by acute attacks of neurological dysfunctio
✦ LIBER ✦
Coexistence of hereditary coproporphyria and epilepsy: Coproporphyrinogen oxidase deficiency in liver and kidney
✍ Scribed by M. Doss; R. Tiepermann; K. -H. Pflüger
- Book ID
- 104717698
- Publisher
- Springer
- Year
- 1981
- Tongue
- English
- Weight
- 516 KB
- Volume
- 226
- Category
- Article
- ISSN
- 0340-5354
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Systematic analysis of coproporphyrinoge
✍
R. Rosipal; J. Lamoril; H. Puy; V. Da Silva; L. Gouya; F.W.M. De Rooij; K. Te Ve
📂
Article
📅
1999
🏛
John Wiley and Sons
🌐
English
⚖ 478 KB
👁 2 views
Hereditary coproporphyria: Exon screenin
✍
William E. Schreiber; Xian Zhang; Janine Senz; Azim Jamani
📂
Article
📅
1997
🏛
John Wiley and Sons
🌐
English
⚖ 171 KB
👁 2 views
Hereditary coproporphyria is a dominantly inherited disorder of porphyrin metabolism caused by a partial deficiency of coproporphyrinogen oxidase, the sixth enzyme in the heme synthetic pathway. We investigated the molecular basis of hereditary coproporphyria in three unrelated patients, amplifying
Two novel mutations and coexistence of t
✍
Å. Wiman; Y. Floderus; P. Harper
📂
Article
📅
2002
🏛
Nature Publishing Group
🌐
English
⚖ 73 KB
Metabolism of pyrazinamide and allopurin
✍
Tetsuya Yamamoto; Kazuya Higashino; Norio Kono; Masanori Kawachi; Masahisa Nanah
📂
Article
📅
1989
🏛
Elsevier Science
🌐
English
⚖ 505 KB
Studies on the etiology of trace metal-i
✍
James S. Woods; Michelle R. Southern
📂
Article
📅
1989
🏛
Elsevier Science
🌐
English
⚖ 744 KB
Xanthine oxidase and arginase in the liv
✍
Khalil, Fouad ;Haggag, Gaber
📂
Article
📅
1960
🏛
Springer-Verlag
⚖ 530 KB