<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-29T04:08:40Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/23639" metadataPrefix="mets">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/23639</identifier><datestamp>2024-11-28T21:55:50Z</datestamp><setSpec>com_20.500.12105_15322</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>col_20.500.12105_16967</setSpec></header><metadata><mets xmlns="http://www.loc.gov/METS/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" ID="&#xa;&#x9;&#x9;&#x9;&#x9;DSpace_ITEM_20.500.12105-23639" TYPE="DSpace ITEM" PROFILE="DSpace METS SIP Profile 1.0" xsi:schemaLocation="http://www.loc.gov/METS/ http://www.loc.gov/standards/mets/mets.xsd" OBJID="&#xa;&#x9;&#x9;&#x9;&#x9;hdl:20.500.12105/23639">
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                  <mods:namePart>Cisneros-Barroso, Eugenia</mods:namePart>
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                  <mods:namePart>Gorram, F</mods:namePart>
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                  <mods:namePart>Ribot-Sansó, Maria Antonia</mods:namePart>
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                  <mods:namePart>Alarcon, F</mods:namePart>
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                  <mods:namePart>Nuel, G</mods:namePart>
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                  <mods:namePart>González-Moreno, Juan</mods:namePart>
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                  <mods:namePart>Rodríguez, A</mods:namePart>
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                  <mods:namePart>Hernandez-Rodriguez, Jessica</mods:namePart>
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                  <mods:namePart>Amengual-Cladera, Emilia</mods:namePart>
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                  <mods:namePart>Ripoll-Vera, Tomás</mods:namePart>
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                  <mods:namePart>Losada-López, Inés</mods:namePart>
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                  <mods:namePart>Heine-Suñer, Damián</mods:namePart>
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                  <mods:namePart>Plante-Bordeneuve, V</mods:namePart>
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                  <mods:dateAccessioned encoding="iso8601">2024-10-09T06:33:59Z</mods:dateAccessioned>
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                  <mods:dateIssued encoding="iso8601">2023-08-31</mods:dateIssued>
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               <mods:identifier type="citation">Cisneros-Barroso E, Gorram F, Ribot-Sansó MA, Alarcon F, Nuel G, González-Moreno J, et al. Disease risk estimates in V30M variant transthyretin amyloidosis (A-ATTRv) from Mallorca. Orphanet J Rare Dis. 2023 Aug 31;18(1):255.</mods:identifier>
               <mods:identifier type="other">https://hdl.handle.net/20.500.13003/19389</mods:identifier>
               <mods:identifier type="uri">https://hdl.handle.net/20.500.12105/23639</mods:identifier>
               <mods:identifier type="pubmedID">37653545</mods:identifier>
               <mods:identifier type="doi">10.1186/s13023-023-02865-5</mods:identifier>
               <mods:identifier type="e-issn">1750-1172</mods:identifier>
               <mods:identifier type="journal">Orphanet journal of rare diseases</mods:identifier>
               <mods:identifier type="scopus">2-s2.0-85169400056</mods:identifier>
               <mods:identifier type="wos">1059595600003</mods:identifier>
               <mods:identifier type="pui">L2025198040</mods:identifier>
               <mods:abstract>Background: Variant transthyretin amyloidosis (A-ATTRv) is an autosomal dominant disease caused by a range of TTR gene variants which entail great phenotypical heterogeneity and penetrance. In Majorca, the A-ATTRv caused by the V30M gene variant (A-ATTRV30M) is the most common. Since asymptomatic carriers are at risk of developing the disease, estimating age of onset is vital for proper management and follow-up. Thus, the aim of this study was to estimate age-related penetrance in ATTRV30M variant carriers from Majorca. Methods: The disease risk among carriers from ATTRV30M families from Majorca was estimated by Non-parametric survival estimation. Factors potentially involved in the disease expression, namely gender and parent of origin were also analysed. Results: A total of 48 heterozygous ATTRV30M families (147 affected patients and 123 were asymptomatic carriers) were included in the analysis. Penetrance progressively increased from 6% at 30 years to 75% at 90 years of age. In contrast to other European populations, we observe a similar risk for both males and females, and no difference of risk according to the parent of origin. Conclusions: In this first study assessing the age-related penetrance of ATTRV30M variant in Majorcan families, no effect of gender or parent of origin was observed. These findings will be helpful for improving management and follow-up of TTR variant carrier individuals.</mods:abstract>
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                  <mods:title>Disease risk estimates in V30M variant transthyretin amyloidosis (A-ATTRv) from Mallorca</mods:title>
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               <mods:genre>research article</mods:genre>
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