Work

Renal amyloidosis caused by apolipoprotein A-II without a genetic mutation in the coding sequence

Year: 2011

Type: article

Study design: Case Report

Source: Clinical and Experimental Nephrology

DOI: 10.1007/s10157-011-0483-4

Authors: Ryuji Morizane, Toshiaki Monkawa, Konosuke Konishi, Akinori Hashiguchi, Mitsuharu Ueda, Yukio Ando, Hirobumi Tokuyama, Koichi Hayashi, Matsuhiko Hayashi, Hiroshi Itoh

Institutions: Keio University, Keio University Hospital, Kumamoto University

Language: English

Topic: Amyloidosis: Diagnosis, Treatment, Outcomes

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funder: Japan Society for the Promotion of Science

Awards: Analysis of autoantibodies for targeting pathogenesis and therapyof misfolding diseases, Hepatocyte replacement therapy for familial amybidotic polyneuropathy combining iPS cells and gene-repair therapy

OpenAlex ID: W2031280077

FWCI: 0.259

Cites: 14

Cited by: 15

Related to: 10