Diagnosis of secondary amyloidosis in alkaptonuria

BACKGROUND: Alkaptonuria (AKU) is an inborn error of catabolism due to a deficient activity of homogentisate 1,2-dioxygenase. Patients suffer from a severe arthropathy, cardiovascular and kidney disease but other organs are affected, too. We found secondary amyloidosis as a life-threatening complica...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Asıl Yazarlar: Millucci, Lia, Ghezzi, Lorenzo, Bernardini, Giulia, Braconi, Daniela, Lupetti, Pietro, Perfetto, Federico, Orlandini, Maurizio, Santucci, Annalisa
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2014
Konular:
Research
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4189149/
https://ncbi.nlm.nih.gov/pubmed/25567001
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13000-014-0185-9
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!

Benzer Materyaller