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Editorial Office, Department of Blood Disorder and Treatment, United Kingdom

Publications

  • Opinion   
    Acute intermittent porphyria
    Author(s): Andriya Collins*

    A rare autosomal dominant condition known as acute intermittent porphyria is marked by a lack of Hydroxymethylbilane Synthase (HMBS). It manifests as sickness, vomiting, seizures, peripheral neuropathy, and abdominal discomfort. Intravenous heme is used as a treatment for acute episodes. An ortho topic liver transplant is the only effective therapy... Read More»
    DOI: 10.37532/puljbdt.2022.5(5).03

 
Google Scholar citation report
Citations : 88

Journal of Blood Disorders and Treatment received 88 citations as per Google Scholar report

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