Aceruloplasminemia: a case report

Antonio Pinto, Antonino Tuttolomondo, Giuseppe Licata, Domenico Di Raimondo, Clara Camaschella, Domenico Di Raimondo, Paola Fernandez

Risultato della ricerca: Articlepeer review

8 Citazioni (Scopus)


Hereditary aceruloplasminemia is a rare autosomal recessivedisease, firstly identified by Miyajima et al. in Japan in1987. The disease is caused by the absence of an a2-glycoprotein, the ceruloplasmin (Cp), a copper-containingferroxidase, mainly synthesized in hepatocytes and widelyexpressed, including the central nervous system, whichcatalyses the oxidation of ferrous to ferric iron, a changerequired for release of iron to plasma transferrin.
Lingua originaleEnglish
pagine (da-a)395-399
Numero di pagine5
RivistaInternal and Emergency Medicine
Stato di pubblicazionePublished - 2008

All Science Journal Classification (ASJC) codes

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  • ???subjectarea.asjc.2700.2711???


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