Is Hereditary Transthyretin Amyloidosis the Third Leading Cause of Monogenic Chronic Kidney Disease, Only Behind ADPKD and Alport Disease?

Keywords: Transthyretin, Amyloidosis, Cardiorenal syndrome, Exome sequencing, TTR gene

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:American journal of nephrology 2022-12, Vol.53 (8-9), p.624-627
Hauptverfasser: Allinovi, Marco, Bergesio, Franco, Cappelli, Francesco, Chiappini, Maria Grazia, Santostefano, Marisa, Argirò, Alessia, Catalucci, Tullio, Parise, Alberto, Zampieri, Mattia, Perfetto, Federico
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 627
container_issue 8-9
container_start_page 624
container_title American journal of nephrology
container_volume 53
creator Allinovi, Marco
Bergesio, Franco
Cappelli, Francesco
Chiappini, Maria Grazia
Santostefano, Marisa
Argirò, Alessia
Catalucci, Tullio
Parise, Alberto
Zampieri, Mattia
Perfetto, Federico
description Keywords: Transthyretin, Amyloidosis, Cardiorenal syndrome, Exome sequencing, TTR gene
doi_str_mv 10.1159/000526955
format Article
fullrecord <record><control><sourceid>gale_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1159_000526955</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A729281514</galeid><sourcerecordid>A729281514</sourcerecordid><originalsourceid>FETCH-LOGICAL-c427t-e0e3cfbc3858d43ad189a5e5b1e77ad254e1d512b7070b9d32dd276951d73b1a3</originalsourceid><addsrcrecordid>eNpt0c9v0zAUB3ALgVgZHLgjZGkSAokM_4jr5IRCC2ysMA7lHDnxS2OW2MV2DvkX-KtJla1i0uTDs-zPe5L9ReglJeeUivwDIUSwZS7EI7SgKaNJvpTkMVoQJkiSkVycoGch_CaEsozIp-iEL3mayyVZoL-XAV-AB22i8iPeemVDbEcP0Vhc9GPnjHbBBBxbwNvWeI03oLSxO7xSQwDsGvzdWbcDa2q8ar071CujLYx4bQKoAO_xte1G_AlaYzUu1j-v1lgddt3e-XinPj5HTxrVBXhxW0_Rry-ft6uLZHP99XJVbJI6ZTImQIDXTVXzTGQ65UrTLFcCREVBSqWZSIFqQVkliSRVrjnTmsnpd6iWvKKKn6K389y9d38GCLHsTaih65QFN4SSSZ4uKc8zNtGzme5UB6WxjYte1QdeFpLlLKOCppM6f0BNS0NvamehMdP5vYY3_zW0oLrYBtcN0Tgb7sN3M6y9C8FDU-696aegSkrKQ_TlMfrJvr591lD1oI_yLusJvJrBjfI78Edw7D978Lr49mMW5V43_B-lTbtQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2734613982</pqid></control><display><type>article</type><title>Is Hereditary Transthyretin Amyloidosis the Third Leading Cause of Monogenic Chronic Kidney Disease, Only Behind ADPKD and Alport Disease?</title><source>MEDLINE</source><source>Karger Journals</source><creator>Allinovi, Marco ; Bergesio, Franco ; Cappelli, Francesco ; Chiappini, Maria Grazia ; Santostefano, Marisa ; Argirò, Alessia ; Catalucci, Tullio ; Parise, Alberto ; Zampieri, Mattia ; Perfetto, Federico</creator><creatorcontrib>Allinovi, Marco ; Bergesio, Franco ; Cappelli, Francesco ; Chiappini, Maria Grazia ; Santostefano, Marisa ; Argirò, Alessia ; Catalucci, Tullio ; Parise, Alberto ; Zampieri, Mattia ; Perfetto, Federico</creatorcontrib><description>Keywords: Transthyretin, Amyloidosis, Cardiorenal syndrome, Exome sequencing, TTR gene</description><identifier>ISSN: 0250-8095</identifier><identifier>EISSN: 1421-9670</identifier><identifier>DOI: 10.1159/000526955</identifier><identifier>PMID: 36349760</identifier><language>eng</language><publisher>Basel, Switzerland: S. Karger AG</publisher><subject>Amyloid Neuropathies, Familial - complications ; Amyloid Neuropathies, Familial - genetics ; Amyloidosis ; Chronic kidney failure ; Complications and side effects ; Humans ; Mutation ; Perspective ; Polycystic Kidney, Autosomal Dominant - complications ; Polycystic Kidney, Autosomal Dominant - genetics ; Renal Insufficiency, Chronic - complications ; Renal Insufficiency, Chronic - genetics ; Risk factors</subject><ispartof>American journal of nephrology, 2022-12, Vol.53 (8-9), p.624-627</ispartof><rights>2022 S. Karger AG, Basel</rights><rights>COPYRIGHT 2022 S. Karger AG</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0002-1664-1238</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,2427,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36349760$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Allinovi, Marco</creatorcontrib><creatorcontrib>Bergesio, Franco</creatorcontrib><creatorcontrib>Cappelli, Francesco</creatorcontrib><creatorcontrib>Chiappini, Maria Grazia</creatorcontrib><creatorcontrib>Santostefano, Marisa</creatorcontrib><creatorcontrib>Argirò, Alessia</creatorcontrib><creatorcontrib>Catalucci, Tullio</creatorcontrib><creatorcontrib>Parise, Alberto</creatorcontrib><creatorcontrib>Zampieri, Mattia</creatorcontrib><creatorcontrib>Perfetto, Federico</creatorcontrib><title>Is Hereditary Transthyretin Amyloidosis the Third Leading Cause of Monogenic Chronic Kidney Disease, Only Behind ADPKD and Alport Disease?</title><title>American journal of nephrology</title><addtitle>Am J Nephrol</addtitle><description>Keywords: Transthyretin, Amyloidosis, Cardiorenal syndrome, Exome sequencing, TTR gene</description><subject>Amyloid Neuropathies, Familial - complications</subject><subject>Amyloid Neuropathies, Familial - genetics</subject><subject>Amyloidosis</subject><subject>Chronic kidney failure</subject><subject>Complications and side effects</subject><subject>Humans</subject><subject>Mutation</subject><subject>Perspective</subject><subject>Polycystic Kidney, Autosomal Dominant - complications</subject><subject>Polycystic Kidney, Autosomal Dominant - genetics</subject><subject>Renal Insufficiency, Chronic - complications</subject><subject>Renal Insufficiency, Chronic - genetics</subject><subject>Risk factors</subject><issn>0250-8095</issn><issn>1421-9670</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpt0c9v0zAUB3ALgVgZHLgjZGkSAokM_4jr5IRCC2ysMA7lHDnxS2OW2MV2DvkX-KtJla1i0uTDs-zPe5L9ReglJeeUivwDIUSwZS7EI7SgKaNJvpTkMVoQJkiSkVycoGch_CaEsozIp-iEL3mayyVZoL-XAV-AB22i8iPeemVDbEcP0Vhc9GPnjHbBBBxbwNvWeI03oLSxO7xSQwDsGvzdWbcDa2q8ar071CujLYx4bQKoAO_xte1G_AlaYzUu1j-v1lgddt3e-XinPj5HTxrVBXhxW0_Rry-ft6uLZHP99XJVbJI6ZTImQIDXTVXzTGQ65UrTLFcCREVBSqWZSIFqQVkliSRVrjnTmsnpd6iWvKKKn6K389y9d38GCLHsTaih65QFN4SSSZ4uKc8zNtGzme5UB6WxjYte1QdeFpLlLKOCppM6f0BNS0NvamehMdP5vYY3_zW0oLrYBtcN0Tgb7sN3M6y9C8FDU-696aegSkrKQ_TlMfrJvr591lD1oI_yLusJvJrBjfI78Edw7D978Lr49mMW5V43_B-lTbtQ</recordid><startdate>20221201</startdate><enddate>20221201</enddate><creator>Allinovi, Marco</creator><creator>Bergesio, Franco</creator><creator>Cappelli, Francesco</creator><creator>Chiappini, Maria Grazia</creator><creator>Santostefano, Marisa</creator><creator>Argirò, Alessia</creator><creator>Catalucci, Tullio</creator><creator>Parise, Alberto</creator><creator>Zampieri, Mattia</creator><creator>Perfetto, Federico</creator><general>S. Karger AG</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-1664-1238</orcidid></search><sort><creationdate>20221201</creationdate><title>Is Hereditary Transthyretin Amyloidosis the Third Leading Cause of Monogenic Chronic Kidney Disease, Only Behind ADPKD and Alport Disease?</title><author>Allinovi, Marco ; Bergesio, Franco ; Cappelli, Francesco ; Chiappini, Maria Grazia ; Santostefano, Marisa ; Argirò, Alessia ; Catalucci, Tullio ; Parise, Alberto ; Zampieri, Mattia ; Perfetto, Federico</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c427t-e0e3cfbc3858d43ad189a5e5b1e77ad254e1d512b7070b9d32dd276951d73b1a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Amyloid Neuropathies, Familial - complications</topic><topic>Amyloid Neuropathies, Familial - genetics</topic><topic>Amyloidosis</topic><topic>Chronic kidney failure</topic><topic>Complications and side effects</topic><topic>Humans</topic><topic>Mutation</topic><topic>Perspective</topic><topic>Polycystic Kidney, Autosomal Dominant - complications</topic><topic>Polycystic Kidney, Autosomal Dominant - genetics</topic><topic>Renal Insufficiency, Chronic - complications</topic><topic>Renal Insufficiency, Chronic - genetics</topic><topic>Risk factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Allinovi, Marco</creatorcontrib><creatorcontrib>Bergesio, Franco</creatorcontrib><creatorcontrib>Cappelli, Francesco</creatorcontrib><creatorcontrib>Chiappini, Maria Grazia</creatorcontrib><creatorcontrib>Santostefano, Marisa</creatorcontrib><creatorcontrib>Argirò, Alessia</creatorcontrib><creatorcontrib>Catalucci, Tullio</creatorcontrib><creatorcontrib>Parise, Alberto</creatorcontrib><creatorcontrib>Zampieri, Mattia</creatorcontrib><creatorcontrib>Perfetto, Federico</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of nephrology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Allinovi, Marco</au><au>Bergesio, Franco</au><au>Cappelli, Francesco</au><au>Chiappini, Maria Grazia</au><au>Santostefano, Marisa</au><au>Argirò, Alessia</au><au>Catalucci, Tullio</au><au>Parise, Alberto</au><au>Zampieri, Mattia</au><au>Perfetto, Federico</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Is Hereditary Transthyretin Amyloidosis the Third Leading Cause of Monogenic Chronic Kidney Disease, Only Behind ADPKD and Alport Disease?</atitle><jtitle>American journal of nephrology</jtitle><addtitle>Am J Nephrol</addtitle><date>2022-12-01</date><risdate>2022</risdate><volume>53</volume><issue>8-9</issue><spage>624</spage><epage>627</epage><pages>624-627</pages><issn>0250-8095</issn><eissn>1421-9670</eissn><abstract>Keywords: Transthyretin, Amyloidosis, Cardiorenal syndrome, Exome sequencing, TTR gene</abstract><cop>Basel, Switzerland</cop><pub>S. Karger AG</pub><pmid>36349760</pmid><doi>10.1159/000526955</doi><tpages>4</tpages><orcidid>https://orcid.org/0000-0002-1664-1238</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0250-8095
ispartof American journal of nephrology, 2022-12, Vol.53 (8-9), p.624-627
issn 0250-8095
1421-9670
language eng
recordid cdi_crossref_primary_10_1159_000526955
source MEDLINE; Karger Journals
subjects Amyloid Neuropathies, Familial - complications
Amyloid Neuropathies, Familial - genetics
Amyloidosis
Chronic kidney failure
Complications and side effects
Humans
Mutation
Perspective
Polycystic Kidney, Autosomal Dominant - complications
Polycystic Kidney, Autosomal Dominant - genetics
Renal Insufficiency, Chronic - complications
Renal Insufficiency, Chronic - genetics
Risk factors
title Is Hereditary Transthyretin Amyloidosis the Third Leading Cause of Monogenic Chronic Kidney Disease, Only Behind ADPKD and Alport Disease?
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-11T06%3A57%3A04IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Is%20Hereditary%20Transthyretin%20Amyloidosis%20the%20Third%20Leading%20Cause%20of%20Monogenic%20Chronic%20Kidney%20Disease,%20Only%20Behind%20ADPKD%20and%20Alport%20Disease?&rft.jtitle=American%20journal%20of%20nephrology&rft.au=Allinovi,%20Marco&rft.date=2022-12-01&rft.volume=53&rft.issue=8-9&rft.spage=624&rft.epage=627&rft.pages=624-627&rft.issn=0250-8095&rft.eissn=1421-9670&rft_id=info:doi/10.1159/000526955&rft_dat=%3Cgale_cross%3EA729281514%3C/gale_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2734613982&rft_id=info:pmid/36349760&rft_galeid=A729281514&rfr_iscdi=true