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Article title matches
- Category:Congenital erythropoietic porphyria (66 bytes)
1: ... pages with the keyword Congenital erythropoietic porphyria - Category:Porphyria (40 bytes)
1: List of pages with the keyword Porphyria - Category:Heme biosynthesis. porphyria (59 bytes)
1: List of pages with the keyword Heme biosynthesis. porphyria - Category:Variegate porphyria disease (58 bytes)
1: List of pages with the keyword Variegate porphyria disease - Category:Acute intermittent porphyria (59 bytes)
1: List of pages with the keyword Acute intermittent porphyria
Page text matches
- 1e51 (3,777 bytes)
11: ...im.org/entry/612740 612740]. A form of porphyria. Porphyrias are inherited defects in the biosynthesis of hem... - 2ivd (4,904 bytes)
24: ...n relation to a number of South African variegate porphyria-causing mutations in the human enzyme. - 2ive (4,786 bytes)
24: ...n relation to a number of South African variegate porphyria-causing mutations in the human enzyme. - 1de4 (6,655 bytes)
11: ...precipitating or exacerbating factor in variegate porphyria. Defects in HFE are associated with susceptibili... - 1hrk (3,645 bytes)
11: ...red blood cells or in the liver. EPP is a form of porphyria marked by excessive protoporphyrin in erythrocyte... - 1jph (4,189 bytes)
10: ..., suggesting that HEP is the homozygous state for porphyria cutanea tarda.<ref>PMID:8896428</ref> <ref>PMID:8... - 1jpi (5,979 bytes)
10: ..., suggesting that HEP is the homozygous state for porphyria cutanea tarda.<ref>PMID:8896428</ref> <ref>PMID:8...
25: ...URO-D) gene found in Utah pedigrees with familial porphyria cutanea tarda (F-PCT). All but one mutation alter... - 1jpk (5,979 bytes)
10: ..., suggesting that HEP is the homozygous state for porphyria cutanea tarda.<ref>PMID:8896428</ref> <ref>PMID:8...
25: ...URO-D) gene found in Utah pedigrees with familial porphyria cutanea tarda (F-PCT). All but one mutation alter... - 1jr2 (4,282 bytes)
10: ...154</ref> Note=Severe congenital erythropoietic porphyria is associated with non-immune hydrops fetalis, a ... - 1pv8 (5,281 bytes)
11: ...im.org/entry/612740 612740]. A form of porphyria. Porphyrias are inherited defects in the biosynthesis of hem... - 1r3q (6,070 bytes)
11: ..., suggesting that HEP is the homozygous state for porphyria cutanea tarda.<ref>PMID:8896428</ref> <ref>PMID:8... - 1r3r (5,820 bytes)
10: ..., suggesting that HEP is the homozygous state for porphyria cutanea tarda.<ref>PMID:8896428</ref> <ref>PMID:8... - 1r3s (6,034 bytes)
11: ..., suggesting that HEP is the homozygous state for porphyria cutanea tarda.<ref>PMID:8896428</ref> <ref>PMID:8... - 1r3t (6,037 bytes)
11: ..., suggesting that HEP is the homozygous state for porphyria cutanea tarda.<ref>PMID:8896428</ref> <ref>PMID:8... - 1r3v (6,095 bytes)
11: ..., suggesting that HEP is the homozygous state for porphyria cutanea tarda.<ref>PMID:8896428</ref> <ref>PMID:8... - 1r3w (6,031 bytes)
11: ..., suggesting that HEP is the homozygous state for porphyria cutanea tarda.<ref>PMID:8896428</ref> <ref>PMID:8... - 1r3y (6,020 bytes)
11: ..., suggesting that HEP is the homozygous state for porphyria cutanea tarda.<ref>PMID:8896428</ref> <ref>PMID:8... - 1uro (4,274 bytes)
11: ..., suggesting that HEP is the homozygous state for porphyria cutanea tarda.<ref>PMID:8896428</ref> <ref>PMID:8... - 2aex (3,826 bytes)
2: ...e Reveals the Structural Basis of Hereditary Coproporphyria==
11: ...actors or stress. A severe variant form is harderoporphyria, which is characterized by earlier onset attacks,... - 2hrc (5,479 bytes)
11: ...red blood cells or in the liver. EPP is a form of porphyria marked by excessive protoporphyrin in erythrocyte...
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