Aceruloplasminemia: a case report

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

Aceruloplasminemia: a case report

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

Promozione della Salute, Materno-Infantile, di Medicina Interna e Specialistica di Eccellenza “G. D’Alessandro”

Risultato della ricerca: Article › peer review

8 Citazioni (Scopus)

Abstract

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 originale	English
pagine (da-a)	395-399
Numero di pagine	5
Rivista	Internal and Emergency Medicine
Volume	3
Stato di pubblicazione	Published - 2008

All Science Journal Classification (ASJC) codes

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title = "Aceruloplasminemia: a case report",

abstract = "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.",

author = "Antonio Pinto and Antonino Tuttolomondo and Giuseppe Licata and {Di Raimondo}, Domenico and Clara Camaschella and {Di Raimondo}, Domenico and Paola Fernandez",

year = "2008",

language = "English",

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pages = "395--399",

journal = "Internal and Emergency Medicine",

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T1 - Aceruloplasminemia: a case report

AU - Pinto, Antonio

AU - Tuttolomondo, Antonino

AU - Licata, Giuseppe

AU - Di Raimondo, Domenico

AU - Camaschella, Clara

AU - Di Raimondo, Domenico

AU - Fernandez, Paola

PY - 2008

Y1 - 2008

N2 - 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.

AB - 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.

UR - http://hdl.handle.net/10447/34044

M3 - Article

VL - 3

SP - 395

EP - 399

JO - Internal and Emergency Medicine

JF - Internal and Emergency Medicine

SN - 1828-0447

ER -

Aceruloplasminemia: a case report

Abstract

All Science Journal Classification (ASJC) codes

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