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Ацерулоплазминемия Клинические признаки и патофизиологические механизмы

Ацерулоплазминемия Клинические признаки и патофизиологические механизмы

Емна Еллоуз / Имен Кетата

54,51 €
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Editorial:
KS OmniScriptum Publishing
Año de edición:
2024
Materia
Medicina: cuestiones generales
ISBN:
9786207624379
54,51 €
IVA incluido
Disponible

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Sobre IBD

Ацерулоплазминемия, редкое генетическое заболевание, характеризуется разнообразными клиническими симптомами и накоплением железа в тканях, механизмы, лежащие в основе этого заболевания, во многом неизвестны. Наш мета-анализ 110 пациентов, проведенный в соответствии с рекомендациями PRISMA 2020, показал, что у мужчин с уровнем ферритина >700 нг/мл заболевание начинается с диабета, а у женщин или тех, у кого уровень ферритина

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