Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Alejandro Andrés-Gracia"'
Autor:
Inmaculada Moreno-Gázquez, Raquel Pérez-Palacios, Lucia Abengochea-Quílez, Carmen Lahuerta Pueyo, Ana Roteta Unceta Barrenechea, Alejandro Andrés Gracia, Miguel Angel Aibar Arregui, Sebastián Menao Guillén
Publikováno v:
BMC Research Notes, Vol 16, Iss 1, Pp 1-8 (2023)
Abstract Objective Wild-type transthyretin (ATTRwt) amyloidosis is caused by the misfolding and deposition of the transthyretin protein (TTR) in the absence of mutations in the TTR gene. Studies regarding the variant form of ATTR amyloidosis (ATTRv)
Externí odkaz:
https://doaj.org/article/5d80bc7fe1bd4ec4a469ac90eff5f42d
Autor:
Anyuli Gracia Gutiérrez, Raquel Pérez-Palacios, Ana Roteta Unceta-Barrenechea, Jorge Melero Polo, Pablo Revilla Martí, Esperanza Bueno Juana, Alejandro Andrés Gracia, Miguel Ángel Aibar Arregui, Saida Atienza Ayala
Publikováno v:
Cardiology Journal. 30:266-275
Background: Cardiac amyloidosis (CA), following a non-invasive diagnosis, constitutes an increasingly prevalent heart failure (HF) etiology. This study aims to determine which echocardiography findings help to diagnose cardiac amyloidosis in patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0155a62c67fcd7d3c00ddf3b69a70d35
https://doi.org/10.5603/cj.a2021.0085
https://doi.org/10.5603/cj.a2021.0085
Autor:
Ana, Roteta Unceta-Barrenechea, Jorge, Melero Polo, Alejandro, Andrés Gracia, Pablo, Revilla Martí, Sebastian, Menao Guillén, Carmen, Lahuerta Pueyo, Raquel, Pérez-Palacios, Inmaculada, Moreno Gázquez, Anyuli Gracia, Gutiérrez, Miguel Ángel, Aibar Arregui
Publikováno v:
Acta Cardiol Sin
BACKGROUND: Cardiac involvement is common in amyloidosis, and the vast majority of cases of amyloid cardiomyopathy are attributed to primary amyloidosis or transthyretin amyloidosis (ATTR). Although the coexistence of scintigraphy suggestive of ATTR
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::493c2b203d9b3fa30a15ceb0ca31bb91
https://pubmed.ncbi.nlm.nih.gov/35273438
https://pubmed.ncbi.nlm.nih.gov/35273438
Autor:
Sebastián Menao Guillén, Miguel Ángel Aibar Arregui, Carmen Lahuerta Pueyo, Alejandro Andrés Gracia, Ana Roteta Unceta Barrenechea, Pablo Revilla Martí, Jorge Melero Polo
Publikováno v:
Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis. 28(2)
We have read with great interest the article written by Akinboboye et al. ‘DISCOVERY: prevalence of transthyretin (TTR) mutations in a US-centric patient population suspected of having cardiac amyl...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::774d14ff2520fa71933333aa781513dd
https://pubmed.ncbi.nlm.nih.gov/32456532
https://pubmed.ncbi.nlm.nih.gov/32456532
Autor:
Carmen Lahuerta, Alejandro Andrés Gracia, Natalia Guillén, Victor Sorribas, Sebastián Menao, Esperanza Bueno-Juana, Miguel A. Aibar, Anyuli Gracia-Gutierrez
Publikováno v:
International journal of cardiology. 301
Transthyretin amyloidosis can be either the wild-type (ATTR-wt) or the hereditary form (ATTR-m) with autosomal dominant inheritance. ATTR seems to be an underdiagnosed disease, despite now being recognized as one of the most frequent causes of heart
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::808d3506872951c33d518b361a73c962
https://pubmed.ncbi.nlm.nih.gov/31740141
https://pubmed.ncbi.nlm.nih.gov/31740141
Autor:
Alejandro Andrés-Gracia, Isabel Torres-Courchoud, Raquel Martínez-Gil, Miguel Angel Torralba-Cabeza, Miguel Angel Aibar-Arregui
Publikováno v:
Revista Española de Cardiología (English Edition). 70:297-299
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6da86ed0377309c7b43d5f047eb156e4
https://doi.org/10.1016/j.rec.2016.07.001
https://doi.org/10.1016/j.rec.2016.07.001
Autor:
Alejandro Andrés-Gracia, Miguel Angel Torralba-Cabeza, Isabel Torres-Courchoud, Miguel Angel Aibar-Arregui, Raquel Martínez-Gil
Publikováno v:
Revista Española de Cardiología. 70:297-299
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0292c8f02e7e8116b22156524c563888
https://doi.org/10.1016/j.recesp.2016.06.007
https://doi.org/10.1016/j.recesp.2016.06.007
Clinical manifestations in hereditary amyloidosis with the variant Glu54Gln transthyretin: a comment
Autor:
Carmen Lahuerta Pueyo, Ana Roteta Unceta Barrenechea, Alejandro Andrés Gracia, Sebastián Menao Guillén, Miguel Ángel Aibar Arregui, Miguel Ángel Torralba Cabeza, Jorge Melero Polo
Publikováno v:
Amyloid. 27:144-144
We have read with great interest the article written by Jercan A et al. [1] ‘Clinical manifestations in hereditary amyloidosis with the variant Glu54Gln transthyretin’, where nine cases of amyloido...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51e5a1c9eda938b07ba6bb075614f6ae
https://doi.org/10.1080/13506129.2019.1710126
https://doi.org/10.1080/13506129.2019.1710126
Autor:
Javier Banzo-Marraco, Alejandro Andrés Gracia, Paula Razola-Alba, Leticia Tardín-Cardoso, Ely Francisco Rambalde-Pacheco, Enrique Prats-Rivera
Publikováno v:
Revista espanola de medicina nuclear e imagen molecular. 33(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24a9e55feed6ca0878aec5f0f6f1a718
https://pubmed.ncbi.nlm.nih.gov/24388591
https://pubmed.ncbi.nlm.nih.gov/24388591