Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1966 1
1967 1
1968 1
1969 1
1970 1
1973 1
1974 4
1975 1
1976 2
1977 3
1978 1
1979 3
1980 1
1982 2
1983 1
1984 2
1985 3
1986 2
1987 1
1988 1
1989 8
1990 3
1991 3
1992 6
1993 3
1994 5
1995 13
1996 8
1997 5
1998 12
1999 4
2000 6
2001 7
2002 6
2003 6
2004 3
2005 7
2006 6
2007 3
2008 5
2009 4
2010 6
2011 3
2012 6
2013 5
2014 5
2015 4
2016 8
2017 6
2018 8
2019 12
2020 3
2021 10
2022 11
2023 6
2024 5

Text availability

Article attribute

Article type

Publication date

Search Results

240 results

Results by year

Filters applied: . Clear all
Page 1
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.
Acute hepatic porphyrias (AHP) can cause severe neurological symptoms involving the central, autonomic, and peripheral nervous system. ...AHPs are genetically inherited disorders that result from heme biosynthesis enzyme deficiencies and comprise four forms: acute …
Acute hepatic porphyrias (AHP) can cause severe neurological symptoms involving the central, autonomic, and peripheral nervous system …
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 erythropoietic porphyrias are congenital erythropoietic porphyria (CEP), and erythropoietic protoporphyria (EPP). The acute hepatic porphyrias include ALA dehydratase deficiency porphyria, acute intermittent porphyria (AIP), hereditar …
The erythropoietic porphyrias are congenital erythropoietic porphyria (CEP), and erythropoietic protoporphyria (EPP). The acute …
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.
They are caused by well-characterized enzyme defects in the complex heme biosynthetic pathway and are divided into categories of acute vs non-acute or hepatic vs erythropoietic porphyrias. Acute hepatic porphyrias (acute intermittent porphyri …
They are caused by well-characterized enzyme defects in the complex heme biosynthetic pathway and are divided into categories of acute …
Update on the Porphyrias.
Dickey AK, Leaf RK, Balwani M. Dickey AK, et al. Annu Rev Med. 2024 Jan 29;75:321-335. doi: 10.1146/annurev-med-042921-123602. Epub 2023 Aug 4. Annu Rev Med. 2024. PMID: 37540847 Free article. Review.
Antiepileptic Drugs and Liver Disease.
Vidaurre J, Gedela S, Yarosz S. Vidaurre J, et al. Pediatr Neurol. 2017 Dec;77:23-36. doi: 10.1016/j.pediatrneurol.2017.09.013. Epub 2017 Sep 22. Pediatr Neurol. 2017. PMID: 29097018 Review.
Acute, symptomatic seizures or epilepsy may complicate the course of hepatic disease. ...Medications undergoing extensive hepatic metabolism, such as valproic acid, phenytoin, and felbamate should be used as drugs of last resort. In special circumstances, as in patients af …
Acute, symptomatic seizures or epilepsy may complicate the course of hepatic disease. ...Medications undergoing extensive hepatic met …
Porphyria.
Bissell DM, Anderson KE, Bonkovsky HL. Bissell DM, et al. N Engl J Med. 2017 Aug 31;377(9):862-872. doi: 10.1056/NEJMra1608634. N Engl J Med. 2017. PMID: 28854095 Review. No abstract available.
Porphyria Diagnostics-Part 1: A Brief Overview of the Porphyrias.
Ramanujam VS, Anderson KE. Ramanujam VS, et al. Curr Protoc Hum Genet. 2015 Jul 1;86:17.20.1-17.20.26. doi: 10.1002/0471142905.hg1720s86. Curr Protoc Hum Genet. 2015. PMID: 26132003 Free PMC article. Review.
Precisely which of these chemicals builds up depends on the type of porphyria. Porphyria is not a single disease but a group of nine disorders: acute intermittent porphyria (AIP), hereditary coproporphyria (HCP), variegate porphyria (VP), …
Precisely which of these chemicals builds up depends on the type of porphyria. Porphyria is not a single disease but a group o …
AGA Clinical Practice Update on Diagnosis and Management of Acute Hepatic Porphyrias: Expert Review.
Wang B, Bonkovsky HL, Lim JK, Balwani M. Wang B, et al. Gastroenterology. 2023 Mar;164(3):484-491. doi: 10.1053/j.gastro.2022.11.034. Epub 2023 Jan 13. Gastroenterology. 2023. PMID: 36642627 Free PMC article. Review.
DESCRIPTION: The acute hepatic porphyrias (AHP) are rare, inborn errors of heme-metabolism and include acute intermittent porphyria, hereditary coproporphyria, variegate porphyria, and porphyria due to severe deficiency of 5-aminolevulini …
DESCRIPTION: The acute hepatic porphyrias (AHP) are rare, inborn errors of heme-metabolism and include acute intermittent …
Abdominal Pain Mimics.
Murali N, El Hayek SM. Murali N, et al. Emerg Med Clin North Am. 2021 Nov;39(4):839-850. doi: 10.1016/j.emc.2021.07.003. Epub 2021 Sep 10. Emerg Med Clin North Am. 2021. PMID: 34600641 Free PMC article. Review.
Acute Porphyrias.
Besur S, Schmeltzer P, Bonkovsky HL. Besur S, et al. J Emerg Med. 2015 Sep;49(3):305-12. doi: 10.1016/j.jemermed.2015.04.034. Epub 2015 Jul 7. J Emerg Med. 2015. PMID: 26159905 Review.
The acute hepatic porphyrias are further classified into acute intermittent porphyria (AIP), hereditary coproporphyria, variegate porphyria, and porphyria due to severe deficiency of delta-aminolevulinic acid (ALA) dehydratase (ALADP). DI …
The acute hepatic porphyrias are further classified into acute intermittent porphyria (AIP), hereditary copropor …
240 results