Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Alejandra Gonzalez-Duarte"'
Autor:
Roy Freeman, Alejandra Gonzalez‐Duarte, Fabio Barroso, Marta Campagnolo, Sharika Rajan, Jennifer Garcia, Jee Young Kim, Ningshan Wang, Lucas Orellana, Christopher Gibbons
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 9, Iss 9, Pp 1370-1383 (2022)
Abstract Objective To determine the sensitivity and specificity of cutaneous amyloid deposition in relation to patient‐reported measures in the earliest disease stage of hereditary ATTR amyloidosis (ATTRv). Methods In a cross‐sectional study, we
Externí odkaz:
https://doaj.org/article/8b09026792cb4814b07a1bf400e47db4
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 23, p 13158 (2021)
Transthyretin (TTR) amyloidogenesis involves the formation, aggregation, and deposition of amyloid fibrils from tetrameric TTR in different organs and tissues. While the result of amyloidoses is the accumulation of amyloid fibrils resulting in end-or
Externí odkaz:
https://doaj.org/article/9b2f326323a24b0c80f1c5a9038fdbbc
Autor:
Luca Gentile, Teresa Coelho, Angela Dispenzieri, Isabel Conceição, Márcia Waddington-Cruz, Arnt Kristen, Jonas Wixner, Igor Diemberger, Juan Gonzalez-Moreno, Eve Cariou, Mathew S. Maurer, Violaine Planté-Bordeneuve, Pablo Garcia-Pavia, Ivailo Tournev, Jose Gonzalez-Costello, Alejandra Gonzalez Duarte, Martha Grogan, Anna Mazzeo, Doug Chapman, Pritam Gupta, Oliver Glass, Leslie Amass, the THAOS investigators
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-12 (2023)
Abstract Background Transthyretin amyloidosis (ATTR amyloidosis) is a progressive, multisystemic, life-threatening disease resulting from the deposition of variant or wild-type (ATTRwt amyloidosis) transthyretin amyloid fibrils in various tissues and
Externí odkaz:
https://doaj.org/article/f0832100674d4cab8c8856c8ba65b280
Autor:
Roy Freeman, Alejandra Gonzalez‐Duarte, Fabio Barroso, Marta Campagnolo, Sharika Rajan, Jennifer Garcia, Jee Young Kim, Ningshan Wang, Lucas Orellana, Christopher Gibbons
Publikováno v:
Annals of Clinical and Translational Neurology. 9:1370-1383
To determine the sensitivity and specificity of cutaneous amyloid deposition in relation to patient-reported measures in the earliest disease stage of hereditary ATTR amyloidosis (ATTRv).In a cross-sectional study, we analyzed 88 individuals with TTR
Autor:
Christopher Gibbons, Bailey Bellaire, Ningshan Wang, Roy Freeman, Charles Adler, Mitchell Miglis, Stuart Isaacson, Virgilio Gerald Evidente, Michael Soileau, Mark Gudesblatt, Guillaume Lamotte, Rajeev Kumar, Melita Petrossian, Maria Alejandra Gonzalez Duarte, Pravin Khemani, Marie-Helene Saint-Hilaire, Nikolaus McFarland, Hemant Pandey, Oleg Yerstein, Alexandru Barboi, Andrew Liu, Todd Levine
Publikováno v:
Wednesday, April 26.
Autor:
Santiago Mier y Teran-Ellis, Humberto A Estrada-Rodriguez, Javier E Anaya-Ayala, Gabriel Lopez-Pena, Emmanuel Contreras-Jimenez, Rosa X Dominguez-Vega, Alejandra Gonzalez-Duarte, Carlos A Hinojosa
Publikováno v:
Vascular.
Objective The bilateral presentation of Carotid Body Tumors (CBT) is rare; the surgical resection of these masses remains the mainstay management due to the malignant potential. We aim to describe, classify, and quantify baroreceptor failure (BRF) af
Autor:
Mathew S Maurer, Marianna Fontana, John Berk, Finn Gustafsson, Marcus Simoes, Martha Grogan, Fábio Fernandes, Robert L Gottlieb, Milos Kubanek, Steen Poulsen, Thibaud Damy, Igor Diemberger, Nobuhiro Tahara, Wen-Chung Yu, W.H. Wilson Tang, Laura Obici, Alejandra Gonzalez-Duarte, Yoshiki Sekijima, Matthew T White, Seth Arum, Patrick Y Jay, John Vest, Julian D Gillmore
Publikováno v:
Journal of Cardiac Failure. 29:550
Autor:
Parag Kale, Mathew S Maurer, Marianna Fontana, Martha Grogan, Fábio Fernandes, Tomas Palecek, Mark S Taylor, Rebecca R Hung, Alejandra Gonzalez-Duarte, Steen Poulsen, Erwan Donal, Federico Perfetto, Kenichi Tsujita, Wen-Chung Yu, Nitasha Sarswat, Matthew T White, Seth Arum, Patrick Y Jay, John Vest, Julian Gillmore
Publikováno v:
Journal of Cardiac Failure. 29:552
Autor:
Dispenzieri, Angela, Coelho, Teresa, Conceição, Isabel, Waddington-Cruz, Márcia, Wixner, Jonas, Kristen, Arnt V., Rapezzi, Claudio, Planté-Bordeneuve, Violaine, Gonzalez-Moreno, Juan, Maurer, Mathew S., Grogan, Martha, Chapman, Doug, Amass, Leslie, Pavia, Pablo Garcia, Tarnev, Ivaylo, Costello, Jose Gonzalez, Briseno, Maria Alejandra Gonzalez Duarte, Schmidt, Hartmut, Drachman, Brian, Barroso, Fabio Adrian, Yamashita, Taro, Lairez, Olivier, Sekijima, Yoshiki, Vita, Giuseppe, Jeon, Eun-Seok, Hanna, Mazen, Slosky, David, Luigetti, Marco, LoRusso, Samantha, Beamud, Francisco Munoz, Adams, David, Moelgaard, Henning, Press, Rayomand, Cirami, Calogero Lino, Nienhuis, Hans, Plana, Josep Maria Campistol, Inamo, Jocelyn, Jacoby, Daniel, Emdin, Michele, Quan, Dianna, Hummel, Scott, Witteles, Ronald, Dori, Amir, Shah, Sanjiv, Lenihan, Daniel, Azevedo, Olga, Murali, Srinivas, Zivkovic, Sasa, Low, Soon Chai, Nativi-Nicolau, Jose, Fine, Nowell, Tallaj, Jose, Tschoepe, Carsten, Torrón, Roberto Fernandéz, Polydefkis, Michael, Merlini, Giampaolo, Badelita, Sorina, Gottlieb, Stephen, Tauras, James, Correia, Edileide Barros, Ventura, Hector, Gess, Burkhard, Darstein, Felix, Oh, Jeeyoung, Marburger, Tessa, Van Cleemput, Johan, Salutto, Valeria Lujan, Parman, Yesim, Chao, Chi-Chao, Sarswat, Nitasha, Mueller, Christopher, Steidley, David, Ralph, Jeffrey, Warner, Alberta, Cotts, William, Hoffman, James, Rugiero, Marcelo, Misawa, Sonoko, Blanco, Jose Luis Munoz, Davila, Lucia Galan, Sadeh, Menachem, Luo, Jin, Kyriakides, Theodoros, Wang, Annabel, Kaufmann, Horacio
Publikováno v:
Orphanet journal of rare diseases, 17(1):236. BMC
Dispenzieri, A, Coelho, T, Conceição, I, Waddington-Cruz, M, Wixner, J, Kristen, A V, Rapezzi, C, Planté-Bordeneuve, V, Gonzalez-Moreno, J, Maurer, M S, Grogan, M, Chapman, D, Amass, L & the THAOS investigators 2022, ' Clinical and genetic profile of patients enrolled in the Transthyretin Amyloidosis Outcomes Survey (THAOS) : 14-year update ', Orphanet Journal of Rare Diseases, vol. 17, no. 1, 236 . https://doi.org/10.1186/s13023-022-02359-w
Dispenzieri, A, Coelho, T, Conceição, I, Waddington-Cruz, M, Wixner, J, Kristen, A V, Rapezzi, C, Planté-Bordeneuve, V, Gonzalez-Moreno, J, Maurer, M S, Grogan, M, Chapman, D, Amass, L & the THAOS investigators 2022, ' Clinical and genetic profile of patients enrolled in the Transthyretin Amyloidosis Outcomes Survey (THAOS) : 14-year update ', Orphanet Journal of Rare Diseases, vol. 17, no. 1, 236 . https://doi.org/10.1186/s13023-022-02359-w
Background Transthyretin amyloidosis (ATTR amyloidosis) is a rare, life-threatening disease caused by the accumulation of variant or wild-type (ATTRwt amyloidosis) transthyretin amyloid fibrils in the heart, peripheral nerves, and other tissues and o
Autor:
Jose Nativi-Nicolau, Alfonso Siu, Angela Dispenzieri, Mathew S. Maurer, Claudio Rapezzi, Arnt V. Kristen, Pablo Garcia-Pavia, Samantha LoRusso, Márcia Waddington-Cruz, Olivier Lairez, Ronald Witteles, Doug Chapman, Leslie Amass, Martha Grogan, Fabio Adrian Barroso, Johan Van Cleemput, Nowell Fine, Hartmut Schmidt, Burkhard Gess, Henning Moelgaard, Violaine Planté-Bordeneuve, David Adams, Jocelyn Inamo, Giuseppe Vita, Calogero Lino Cirami, Marco Luigetti, Michele Emdin, Yoshiki Sekijima, Taro Yamashita, Eun-Seok Jeon, Maria Alejandra Gonzalez Duarte Briseno, Hans Nienhuis, Olga Azevedo, Josep Maria Campistol Plana, Juan Gonzalez Moreno, Jose Gonzalez Costello, Jonas Wixner, Yesim Parman, Sanjiv Shah, Dianna Quan, Tessa Marburger, Michael Polydefkis, Stephen Gottlieb, Jeffrey Ralph, Nitasha Sarswat, Jin Luo, Srinivas Murali, William Cotts, Brian Drachman, David Steidley, Scott Hummel, David Slosky, Hector Ventura, Daniel Jacoby, James Hoffman, James Tauras, Sasa Zivkovic, Jose Tallaj, Daniel Lenihan, Christopher Mueller
Publikováno v:
DDFV. Repositorio Institucional de la Universidad Francisco de Vitoria
instname
JACC: CardioOncology
instname
JACC: CardioOncology
Background Transthyretin amyloid cardiomyopathy results from the accumulation of wild-type (ATTRwt) or variant (ATTRv) transthyretin amyloid fibrils in the myocardium. THAOS (Transthyretin Amyloidosis Outcomes Survey) is a global, longitudinal, obser
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5369d2058a7bfe227022ccac8c626932
http://hdl.handle.net/10641/3093
http://hdl.handle.net/10641/3093