Amyloidosis, Inflammation, and Oxidative Stress in the Heart of an Alkaptonuric Patient

Background. Alkaptonuria, a rare autosomal recessive metabolic disorder caused by deficiency in homogentisate 1,2-dioxygenase activity, leads to accumulation of oxidised homogentisic acid in cartilage and collagenous structures present in all organs and tissues, especially joints and heart, causing...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Millucci, Lia, Ghezzi, Lorenzo, Paccagnini, Eugenio, Giorgetti, Giovanna, Viti, Cecilia, Braconi, Daniela, Laschi, Marcella, Geminiani, Michela, Soldani, Patrizia, Lupetti, Pietro, Orlandini, Maurizio, Benvenuti, Chiara, Perfetto, Federico, Spreafico, Adriano, Bernardini, Giulia, Santucci, Annalisa
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi Publishing Corporation 2014
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4020161/
https://ncbi.nlm.nih.gov/pubmed/24876668
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2014/258471
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados