Nathan - Living with Hereditary Coproporphyria (HCP)
This video was created for U.S. audiences. Nathan is living with hereditary coproporphyria (HCP), a type of acute hepatic porphyria (AHP). In this video, he shares his experience living with this rare disease. AHP refers to a family of rare, genetic diseases characterized by potentially life-threatening attacks and, for many patients, chronic debilitating symptoms that negatively impact daily functioning and quality of life. Learn more: www.PinpointAHP.com AS1-USA-00401
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Megan - Living with acute hepatic porphyria (AHP)
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Patients Talk About the Pain of Acute Hepatic Porphyria (AHP)
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Acute Hepatic Porphyria: What happens in the body?
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Acute Hepatic Porphyria: What happens in the body?
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Marc – Living with Wild-Type ATTR Amyloidosis with Cardiomyopathy
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Ania (UK) - Living with Acute Intermittent Porphyria
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Pathophysiology of Acute Hepatic Porphyria (AHP)
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Alnylam & RNAi Therapeutics: Making our Medicines
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Physiopathologie de la PHA
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Acute Hepatic Porphyria: What happens in the body?
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Diagnosing AHP
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Ania - Living with Acute Intermittent Porphyria
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Alnylam & RNAi Therapeutics: Making our Medicines
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Ben, Lebt Mit AHP
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Alnylam Announces $250 Million Expansion of U.S. RNAi Therapeutics Manufacturing Facility
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Alnylam & RNAi Therapeutics: Silencing Disease. Amplifying Life.
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Stephanie, Atteinte de PHA
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