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Transthyretin-related hereditary amyloidosis with recurrent vomiting and renal insufficiency as the initial presentation: A case report

RATIONALE: Hereditary amyloidosis is diagnosed worldwidely with an increasing incidence. As the most common form, transthyretin-related hereditary amyloidosis (ATTR amyloidosis) is an autosomal dominant inherited disease due to mutations of TTR. Over the past several decades, more than 130 mutations...

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שמור ב:
מידע ביבליוגרפי
הוצא לאור ב:Medicine (Baltimore)
Main Authors: Xu, Jing, Yang, Meng, Pan, Xiaoxia, Yu, Xialian, Xie, Jingyuan, Ren, Hong, Li, Xiao, Chen, Nan
פורמט: Artigo
שפה:Inglês
יצא לאור: Wolters Kluwer Health 2017
נושאים:
גישה מקוונת:https://ncbi.nlm.nih.gov/pmc/articles/PMC5348144/
https://ncbi.nlm.nih.gov/pubmed/28272196
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000005737
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