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Last Updated: 01/07/2026
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Found 342 publications
Stability of plasma and erythrocyte porphyrins: implications for diagnosis and monitoring of erythropoietic protoporphyria.
Journal: Journal of clinical pathology
Published: August 08, 2025
Primary adrenal insufficiency associated with homozygous hereditary coproporphyria.
Journal: European journal of endocrinology
Published: June 03, 2025
Novel Biallelic Variants in CPOX Gene in a Case of Hereditary Coproporphyria With Antenatal Onset and Adverse Neonatal Outcome: A Potential Diagnostic Clue of Harderoporphyria?
Journal: Prenatal diagnosis
Published: April 09, 2025
Coproporphyrinogen oxidase deficiency causes primary adrenal insufficiency and 46,XY DSD.
Journal: The Journal of clinical endocrinology and metabolism
Published: January 13, 2025
Diagnosing Porphyria in a Female Patient With Diffuse Pelvic Pain: A Case Study.
Journal: Cureus
Published: November 30, 2024
Psychiatric Presentation of Hereditary Coproporphyria with Coproporphyrinogen Oxidase Gene Mutation c.734 C>T: A Case Report.
Journal: Noro psikiyatri arsivi
Published: November 05, 2024
Hepatocellular Carcinoma in Acute Hepatic Porphyria: A Meta-Analysis of Observational Studies.
Journal: Digestive diseases and sciences
Published: August 29, 2024
Acute hepatic porphyria in Denmark; a retrospective study.
Journal: Orphanet journal of rare diseases
Published: August 05, 2024
Therapeutic approach to acute crises of hepatic porphyrias.
Journal: Revista clinica espanola
Published: June 22, 2024
Understanding Hepatic Porphyrias: Symptoms, Treatments, and Unmet Needs.
Journal: Seminars in liver disease
Published: May 21, 2024
Preimplantation diagnosis and embryo selection in a patient with severe hereditary coproporphyria.
Journal: The New Zealand medical journal
Published: May 02, 2024
Last Updated: 01/07/2026