• A 25-Hour Fast Among Quiescent Hereditary Coproporphyria and Variegate Porphyria Patients is Associated With a Low Risk of Complications
• A Case of Hereditary Coproporphyria in which the Patient's Course Improved after the Discontinuation of Givosiran
• A case of hereditary coproporphyria precipitated by efavirenz
• A case of hereditary coproporphyria with posterior reversible encephalopathy and novel coproporphyrinogen oxidase gene mutation c.863T>G (p.Leu288Trp)
• A case of hereditary coproporphyria with posterior reversible encephalopathy and novel coproporphyrinogen oxidase gene mutation c.863T>G (p.Leu288Trp)
• A case report of hereditary coproporphyria with neurological, haematological and renal involvement
• A challenging diagnosis for potential fatal diseases: recommendations for diagnosing acute porphyrias
• A mouse model of hereditary coproporphyria identified in an ENU mutagenesis screen
• A next-generation-sequencing panel for mutational analysis of dominant acute hepatic porphyrias
• A Unique Neuropsychiatric Syndrome in Variant Hereditary Coproporphyria: Case Report and Review of the Literature
• ABCB6 polymorphisms are not overly represented in patients with porphyria
• Acute exacerbation of hereditary coproporphyria mimics early surgical infection following intrathecal pump implantation for chronic abdominal pain: A case report
• Acute Hepatic Porphyria
• Acute Hepatic Porphyria
• Acute hepatic porphyria and cancer risk: a nationwide cohort study
• Acute hepatic porphyrias: Identification of 46 hydroxymethylbilane synthase, 11 coproporphyrinogen oxidase, and 20 protoporphyrinogen oxidase novel mutations
• Acute Hepatic Porphyrias: Review and Recent Progress
• Acute Intermittent Porphyria
• Acute Intermittent Porphyria
• Acute porphyria presenting as epilepsia partialis continua
• Acute Porphyrias
• Acute porphyrias - A neurological perspective
• Acute porphyrias in the USA: features of 108 subjects from porphyrias consortium
• Acute porphyrias: a German monocentric study of the biochemical, molecular genetic, and clinical data of 62 families
• AGA Clinical Practice Update on Diagnosis and Management of Acute Hepatic Porphyrias: Expert Review
• An Overview of Acute Hepatic Porphyrias: Clinical Implications, Diagnostic Approaches, and Management Strategies
• An overview of the cutaneous porphyrias
• Analysis of the mechanism underlying a mild phenotype of hereditary coproporphyria due to a homozygous missense mutation in the transcription initiation codon of the coproporphyrinogen III oxidase gene
• BALB.NCT-<em>Cpox</em> ^<em>nct</em> is a unique mouse model of hereditary coproporphyria
• BALB.NCT-Cpox (nct) is a unique mouse model of hereditary coproporphyria
• Best practice guidelines on clinical management of acute attacks of porphyria and their complications
• Case-based discussion of the acute hepatic porphyrias: Updates on pathogenesis, diagnosis and management
• Cerebral Hypoperfusion in Hereditary Coproporphyria (HCP): A Single Photon Emission Computed Tomography (SPECT) Study
• Cerebral vasospasm and anterior circulation stroke secondary to an exacerbation of hereditary corproporphyria
• Clinical features of acute attacks, chronic symptoms, and long-term complications among patients with acute hepatic porphyria in Japan: a real-world claims database study
• Clinical features of genetic cutaneous porphyrias in Israel: A nationwide survey
• Clinical Guide and Update on Porphyrias
• Co-existence of hereditary coproporphyria and porphyria cutanea tarda: The importance of genetic testing
• Cutaneous porphyrias part I: epidemiology, pathogenesis, presentation, diagnosis, and histopathology
• Cutaneous Porphyrias: Causes, Symptoms, Treatments and the Danish Incidence 1989-2013
• Delirium with delayed diagnosis of hereditary coproporphyria
• Development and validation of diagnostic algorithms for the laboratory diagnosis of porphyrias
• Drugs and acute porphyrias: reasons for a hazardous relationship
• Epidemiology of cutaneous porphyria in Israel: a nationwide cohort study
• Expert consensus statement on acute hepatic porphyria in Belgium
• Givosiran for the treatment of acute hepatic porphyria
• Greater disease burden of variegate porphyria than hereditary coproporphyria: An Israeli nationwide study of neurocutaneous porphyrias
• Heme biosynthesis and the porphyrias
• Hepatic porphyria: A narrative review
• Hepatocellular carcinoma in acute hepatic porphyrias: A Damocles Sword
• Hereditary Coproporphyria Associated with the Q306X Mutation in the Coproporphyrin Oxidase Gene Presenting with Acute Ataxia
• Hereditary coproporphyria from clinician's point of view--a case report
• Hereditary Coproporphyria Mimicking Guillain-Barre Syndrome After COVID-19 Infection
• High penetrance, recurrent attacks and thrombus formation in a family with hereditary coproporphyria
• International Porphyria Molecular Diagnostic Collaborative: an evidence-based database of verified pathogenic and benign variants for the porphyrias
• Key terms and definitions in acute porphyrias: Results of an international Delphi consensus led by the European porphyria network
• Kidney Involvement in Acute Hepatic Porphyrias: Pathophysiology and Diagnostic Implications
• Kidney transplantation in hereditary coproporphyria using tacrolimus and mycophenolate mofetil: a case report
• Lamotrigine in the treatment of psychotic depression associated with hereditary coproporphyria -- case report and a brief review of the literature
• Liver failure after Hydroxycut use in a patient with undiagnosed hereditary coproporphyria
• Liver failure after Hydroxycut™ use in a patient with undiagnosed hereditary coproporphyria
• Liver transplantation in the management of porphyria
• Long-term follow-up of acute porphyria in female patients: Update of clinical outcome and life expectancy
• Management of a patient with colon cancer and rotor syndrome: A case report
• Molecular analysis of 19 Spanish patients with mixed porphyrias
• Murine models of the human porphyrias: Contributions toward understanding disease pathogenesis and the development of new therapies
• Neonatal-Onset Hereditary Coproporphyria: A New Variant of Hereditary Coproporphyria
• Neurocutaneous porphyrias
• Neurological and neuropsychiatric manifestations of porphyria
• Neurological Manifestations of Acute Porphyrias
• Neuropathic pain in hereditary coproporphyria
• Opioid dependence with successful transition to suboxone (buprenorphine/naloxone) in a young woman with hereditary coproporphyria
• Pathogenesis and clinical features of the acute hepatic porphyrias (AHPs)
• PICO questions and DELPHI methodology for improving the management of patients with acute hepatic porphyria
• Pilot study of mitochondrial bioenergetics in subjects with acute porphyrias
• Porphyria
• Porphyria and its neurologic manifestations
• Porphyria Diagnostics-Part 1: A Brief Overview of the Porphyrias
• Porphyria-induced posterior reversible encephalopathy syndrome and central nervous system dysfunction
• Porphyria: What Is It and Who Should Be Evaluated?
• Porphyrias-what is verified?
• Preimplantation diagnosis and embryo selection in a patient with severe hereditary coproporphyria
• Quantification of Urine and Plasma Porphyrin Precursors Using LC-MS in Acute Hepatic Porphyrias: Improvement in Routine Diagnosis and in the Monitoring of Kidney Failure Patients
• Recent advances on porphyria genetics: Inheritance, penetrance &amp; molecular heterogeneity, including new modifying/causative genes
• Risk for incident comorbidities, nonhepatic cancer and mortality in acute hepatic porphyria: A matched cohort study in 1244 individuals
• Risk of primary liver cancer in acute hepatic porphyria patients: A matched cohort study of 1244 individuals
• Role of genetic testing in the management of patients with inherited porphyria and their families
• Seven Novel Mutations in Bulgarian Patients with Acute Hepatic Porphyrias (AHP)
• Sick leave, disability, and mortality in acute hepatic porphyria: a nationwide cohort study
• Successful Radiation Therapy for Breast Cancer in a Patient With Hereditary Coproporphyria
• Systemic Lupus Erythematosus and Hereditary Coproporphyria: Two Different Entities Diagnosed by WES in the Same Patient
• The cutaneous porphyrias
• The cutaneous porphyrias
• The enzyme engineering of mutant homodimer and heterodimer of coproporphyinogen oxidase contributes to new insight into hereditary coproporphyria and harderoporphyria
• The incidence of inherited porphyrias in Europe
• Understanding Hepatic Porphyrias: Symptoms, Treatments, and Unmet Needs
• Unusual Case of Severe Hypertension in a 20-Year-Old Woman
• Update on the diagnosis and management of the autosomal dominant acute hepatic porphyrias
• Update review of the acute porphyrias
• X-linked dominant protoporphyria: response to "Cutaneous porphyrias part 1"