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1دورية أكاديمية
المؤلفون: Ana Jovanovic, Eve Miller-Hodges, Felicia Castriota, Shweta Takyar, Heena Howitt, Olulade Ayodele
المصدر: Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-37 (2024)
مصطلحات موضوعية: Fabry disease, Agalsidase alfa, Agalsidase beta, Migalastat, Health-related quality of life, SF-36, Medicine
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1750-1172
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2دورية أكاديمية
المؤلفون: Renzo Mignani, Claudio Americo, Filippo Aucella, Yuri Battaglia, Vittoria Cianci, Annamaria Sapuppo, Chiara Lanzillo, Fabio Pennacchiotti, Luciano Tartaglia, Giacomo Marchi, Federico Pieruzzi
المصدر: Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-9 (2024)
مصطلحات موضوعية: Anti-drug antibodies, Fabry disease, Enzyme replacement therapy, Agalsidase beta, Infusion time, Infusion-associated reactions, Medicine
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1750-1172
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3دورية أكاديمية
المؤلفون: Lee, Chae SungAff1, IDs13023023028035_cor1, Tsurumi, Mina, Eto, Yoshikatsu
المصدر: Orphanet Journal of Rare Diseases. 18(1)
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4دورية أكاديمية
المؤلفون: Chae Sung Lee, Mina Tsurumi, Yoshikatsu Eto
المصدر: Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-9 (2023)
مصطلحات موضوعية: Fabry disease, Enzyme replacement therapy, Agalsidase beta, Infusion time, Infusion-associated reaction, Medicine
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1750-1172
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5دورية أكاديمية
المؤلفون: Dutra-Clarke, Marina, Tapia, Daisy, Curtin, Emily, Rünger, Dennis, Lee, Grace K, Lakatos, Anita, Alandy-Dy, Zyza, Freedkin, Linda, Hall, Kathy, Ercelen, Nesrin, Alandy-Dy, Jousef, Knight, Margaret, Pahl, Madeleine, Lombardo, Dawn, Kimonis, Virginia
مصطلحات موضوعية: Biomedical and Clinical Sciences, Clinical Sciences, Orphan Drug, Pediatric, Neurodegenerative, Kidney Disease, Rare Diseases, Peripheral Neuropathy, Neurosciences, Chronic Pain, Biotechnology, Pain Research, Fabry disease, Enzyme replacement therapy, Agalsidase beta, Globotriaosylceramide, GL-3, GLA gene, Biochemistry and Cell Biology, Genetics, Clinical sciences
وصف الملف: application/pdf
URL الوصول: https://escholarship.org/uc/item/3hr6979k
https://escholarship.org/content/qt3hr6979k/qt3hr6979k.pdf -
6دورية أكاديمية
المؤلفون: Jovanovic, Ana, Miller-Hodges, Eve, Castriota, Felicia, Takyar, Shweta, Howitt, Heena, Ayodele, OluladeAff3, IDs1302302403131y_cor6
المصدر: Orphanet Journal of Rare Diseases. 19(1)
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7دورية أكاديمية
المؤلفون: Mignani, RenzoAff1, IDs13023024030495_cor1, Americo, Claudio, Aucella, Filippo, Battaglia, Yuri, Cianci, Vittoria, Sapuppo, Annamaria, Lanzillo, Chiara, Pennacchiotti, Fabio, Tartaglia, Luciano, Marchi, Giacomo, Pieruzzi, FedericoAff11, Aff12
المصدر: Orphanet Journal of Rare Diseases. 19(1)
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8دورية أكاديمية
المؤلفون: Eleonora Riccio, Carlo Garofalo, Ivana Capuano, Pasquale Buonanno, Guido Iaccarino, Teodolinda Di Risi, Massimo Imbriaco, Federica Riccio Cuomo, Antonio Pisani
المصدر: Genetics in Medicine Open, Vol 1, Iss 1, Pp 100805- (2023)
مصطلحات موضوعية: Agalsidase alfa, Agalsidase beta, Enzymatic replacement therapy, Fabry disease, Switch, Genetics, QH426-470, Medicine
وصف الملف: electronic resource
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9دورية أكاديمية
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10دورية أكاديمية
المؤلفون: Christoph Wanner, Ulla Feldt‐Rasmussen, Ana Jovanovic, Aleš Linhart, Meng Yang, Elvira Ponce, Eva Brand, Dominique P. Germain, Derralynn A. Hughes, John L. Jefferies, Ana Maria Martins, Albina Nowak, Bojan Vujkovac, Frank Weidemann, Michael L. West, Alberto Ortiz
المصدر: ESC Heart Failure, Vol 7, Iss 3, Pp 825-834 (2020)
مصطلحات موضوعية: Agalsidase beta, Enzyme replacement therapy, Fabry disease, Cardiomyopathy, Kidney function, Female patients, Diseases of the circulatory (Cardiovascular) system, RC666-701
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2055-5822