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1947 1
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1957 3
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1961 2
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1970 2
1971 2
1973 1
1975 3
1976 1
1977 13
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1988 2
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1990 8
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1992 4
1993 9
1994 14
1995 7
1996 6
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1999 8
2000 7
2001 2
2002 6
2003 7
2004 7
2005 9
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2007 4
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2013 11
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337 results

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Page 1
Hereditary Coproporphyria.
Wang B, Bissell DM. Wang B, et al. 2012 Dec 13 [updated 2022 May 19]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2012 Dec 13 [updated 2022 May 19]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 23236641 Free Books & Documents. Review.
CLINICAL CHARACTERISTICS: Hereditary coproporphyria (HCP) is an acute (hepatic) porphyria in which the acute symptoms are neurovisceral and occur in discrete episodes. ...
CLINICAL CHARACTERISTICS: Hereditary coproporphyria (HCP) is an acute (hepatic) porphyria in which the acute symptoms are neur …
Hereditary coproporphyria.
Martásek P. Martásek P. Semin Liver Dis. 1998;18(1):25-32. doi: 10.1055/s-2007-1007137. Semin Liver Dis. 1998. PMID: 9516675 Review.
Hereditary coproporphyria (HC) is a rare acute hepatic porphyria. Attacks may be precipitated by certain drugs, alcohol, infections, or low caloric intake. ...
Hereditary coproporphyria (HC) is a rare acute hepatic porphyria. Attacks may be precipitated by certain drugs, alcohol, infec …
[Porphyria].
Stölzel U, Stauch T, Kubisch I. Stölzel U, et al. Internist (Berl). 2021 Sep;62(9):937-951. doi: 10.1007/s00108-021-01066-1. Epub 2021 Jun 29. Internist (Berl). 2021. PMID: 34185109 Free PMC article. German.
Patients with symptomatic (clinically active) acute hepatic porphyria, e.g. acute intermittent porphyria, porphyria variegata, hereditary coproporphyria, and aminolevulinic acid dehydratase deficiency porphyria, display accumulation of porphyrin precursors, 5-aminol …
Patients with symptomatic (clinically active) acute hepatic porphyria, e.g. acute intermittent porphyria, porphyria variegata, hereditary …
Acute porphyrias - A neurological perspective.
Gerischer LM, Scheibe F, Nümann A, Köhnlein M, Stölzel U, Meisel A. Gerischer LM, et al. Brain Behav. 2021 Nov;11(11):e2389. doi: 10.1002/brb3.2389. Epub 2021 Oct 17. Brain Behav. 2021. PMID: 34661997 Free PMC article. Review.
AHPs are genetically inherited disorders that result from heme biosynthesis enzyme deficiencies and comprise four forms: acute intermittent porphyria (AIP), variegate porphyria (VP), hereditary coproporphyria (HCP), and ALA-dehydratase porphyria (ALADP). ...
AHPs are genetically inherited disorders that result from heme biosynthesis enzyme deficiencies and comprise four forms: acute intermittent …
Clinical Guide and Update on Porphyrias.
Stölzel U, Doss MO, Schuppan D. Stölzel U, et al. Gastroenterology. 2019 Aug;157(2):365-381.e4. doi: 10.1053/j.gastro.2019.04.050. Epub 2019 May 11. Gastroenterology. 2019. PMID: 31085196 Review.
Acute hepatic porphyrias (acute intermittent porphyria, variegate porphyria, hereditary coproporphyria, and aminolevulinic acid dehydratase deficient porphyria) manifest in attacks and are characterized by overproduction of porphyrin precursors, producing often seri …
Acute hepatic porphyrias (acute intermittent porphyria, variegate porphyria, hereditary coproporphyria, and aminolevulinic aci …
Hereditary coproporphyria.
BERGER H, GOLDBERG A. BERGER H, et al. Br Med J. 1955 Jul 9;2(4931):85-8. doi: 10.1136/bmj.2.4931.85. Br Med J. 1955. PMID: 14378650 Free PMC article. No abstract available.
Heme biosynthesis and the porphyrias.
Phillips JD. Phillips JD. Mol Genet Metab. 2019 Nov;128(3):164-177. doi: 10.1016/j.ymgme.2019.04.008. Epub 2019 Apr 22. Mol Genet Metab. 2019. PMID: 31326287 Free PMC article. Review.
The acute hepatic porphyrias include ALA dehydratase deficiency porphyria, acute intermittent porphyria (AIP), hereditary coproporphyria (HCP) and variegate porphyria (VP). Porphyria cutanea tarda (PCT) is the only porphyria that has both genetic and/or environmenta …
The acute hepatic porphyrias include ALA dehydratase deficiency porphyria, acute intermittent porphyria (AIP), hereditary copropor …
Hereditary coproporphyria.
Goldberg A, Rimington C, Lochhead AC. Goldberg A, et al. Lancet. 1967 Mar 25;1(7491):632-6. doi: 10.1016/s0140-6736(67)92538-x. Lancet. 1967. PMID: 4163920 No abstract available.
Hereditary coproporphyria.
Connon JJ, Turkington V. Connon JJ, et al. Lancet. 1968 Aug 3;2(7562):263-4. doi: 10.1016/s0140-6736(68)92359-3. Lancet. 1968. PMID: 4173691 No abstract available.
Hereditary Coproporphyria Mimicking Guillain-Barre Syndrome After COVID-19 Infection.
Upchurch M, Donnelly JP, Deremiah E, Barthol C, Hafeez S, Anderson KE, Seifi A. Upchurch M, et al. Cureus. 2022 Jan 25;14(1):e21586. doi: 10.7759/cureus.21586. eCollection 2022 Jan. Cureus. 2022. PMID: 35228944 Free PMC article.
Hereditary coproporphyria (HCP) is a rare disorder caused by a deficiency of an enzyme, coproporphyrinogen oxidase, in the heme synthetic pathway. ...
Hereditary coproporphyria (HCP) is a rare disorder caused by a deficiency of an enzyme, coproporphyrinogen oxidase, in the hem …
337 results