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Aceruloplasminemia Clinical signs and pathophysiological mechanisms

Aceruloplasminemia Clinical signs and pathophysiological mechanisms

EMNA ELLOUZ / Imen Ketata

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Editorial:
KS OmniScriptum Publishing
Año de edición:
2024
Materia
Medicina: cuestiones generales
ISBN:
9786207624348
54,38 €
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Aceruloplasminemia, a rare genetic disease, is characterized by a variety of clinical symptoms and tissue iron accumulation, with the underlying mechanisms largely unknown. Our meta-analysis of 110 patients, performed according to PRISMA 2020 guidelines, revealed that males with ferritin levels >700 ng/ml, start the disease with diabetes, while females or those with ferritin

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Otros libros del autor

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