Amiloidosis renal hereditaria por depósito de apolipoproteína AI: un reto diagnóstico-Reference-Cited by-同舟云学术

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Amiloidosis renal hereditaria por depósito de apolipoproteína AI: un reto diagnóstico

Published:2015-05 Issue:3 Volume:35 Page:322-327
ISSN:0211-6995
Container-title:Nefrología
language:es
Short-container-title:Nefrología

Author:

Samillán-Sosa Kelly del Rocío,Sención-Martínez Gloria,Lopes-Martín Vanessa,Martínez-González Miguel Angel,Solé Manel,Arostegui Jose Luis,Mesa Jose,García-Díaz Juan de Dios,Rodríguez-Puyol Diego,Martínez-Miguel Patricia

Publisher

Elsevier BV

Subject

Nephrology

Reference31 articles.

1. Demonstration einer eigenartigen familiaren para amyloidose;Ostertag;Zentralbl Aug Pathol,1932

2. Amyloidogenicity and clinical phenotype associated with five novel mutations in apolipoproteinA-I;Rowczenio;Am J Pathol.,2011

3. Human lysozyme gene mutations cause hereditary systemic amyloidosis;Pepys;Nature.,1993

4. Variant apolipoproteinAI as a major constituent of a human hereditary amyloid;Nichols;Biochem Biophys Res Commun.,1988

5. Liver biopsy discloses a new apolipoproteinA-I hereditary amyloidosis in several unrelated Italian families;Obici;Gastroenterology.,2004

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. N-terminal mutants of human apolipoprotein A-I: structural perturbations associated to protein misfolding;2019-01-14

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