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Chris Sies Selected Research

Coproporphyria

9/2018A case of hereditary coproporphyria with posterior reversible encephalopathy and novel coproporphyrinogen oxidase gene mutation c.863T>G (p.Leu288Trp).

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Chris Sies Research Topics

Disease

1Coproporphyria
09/2018
1Brain Diseases (Brain Disorder)
09/2018
1Hypertension (High Blood Pressure)
09/2018
1Seizures (Absence Seizure)
09/2018
1Acute Intermittent Porphyria (Porphyria, Acute)
09/2018
1Hereditary Coproporphyria (Coproporphyrinogen Oxidase Deficiency)
09/2018

Drug/Important Bio-Agent (IBA)

1heme arginateIBA
09/2018
1Coproporphyrinogen Oxidase (Coproporphyrinogen III Oxidases)IBA
09/2018
1CreatinineIBA
09/2018
1PorphobilinogenIBA
09/2018
1PorphyrinsIBA
09/2018
1SodiumIBA
09/2018