المؤلفون: McCormack, James P.^Aff4

المساهمون: Crommelin, Daan J. A., editor^Aff1, Sindelar, Robert D., editor^Aff2, Meibohm, Bernd, editor^Aff3

المصدر: Pharmaceutical Biotechnology : Fundamentals and Applications. :283-288

المؤلفون: Isao Ohsawa, Akiko Onuki, Fumie Oka, Yoshiyuki Matsuoka, Yuko Makita, Takashi Kobayashi, Yasuhiko Kanaguchi, Yuya Nakamura, Yusuke Suzuki, Yoshikazu Goto, Hiromichi Gotoh

المصدر: BMC Nephrology, Vol 25, Iss 1, Pp 1-7 (2024)

مصطلحات موضوعية: Fabry disease, Enzyme replacement therapy, Agalsidase alfa, Hemodialysis, Cognitive impairment, Hasegawa dementia rating scale, Diseases of the genitourinary system. Urology, RC870-923

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1471-2369

URL الوصول: https://doaj.org/article/102309544f4b4f30a488cb531556efbb

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

URL الوصول: https://doaj.org/article/145e1028133243a0aaf53d5d956f33d9

المؤلفون: Feriozzi S, Chimenti C, Reisin RC

المصدر: Drug Design, Development and Therapy, Vol Volume 18, Pp 1083-1101 (2024)

مصطلحات موضوعية: fabry disease, agalsidase alfa, enzyme replacement therapy, clinical outcome in fabry treated patients, Therapeutics. Pharmacology, RM1-950

وصف الملف: electronic resource

Relation: https://www.dovepress.com/updated-evaluation-of-agalsidase-alfa-enzyme-replacement-therapy-for-p-peer-reviewed-fulltext-article-DDDT; https://doaj.org/toc/1177-8881

URL الوصول: https://doaj.org/article/546054683cb249edac6efb3820c719b2

المؤلفون: Zewei Chen, Bo Yin, Juan Jiao, Tianyang Ye

المصدر: BMC Nephrology, Vol 25, Iss 1, Pp 1-5 (2024)

مصطلحات موضوعية: Fabry disease, Enzyme replacement therapy, Agalsidase α, Fabry nephropathy, Genetic testing, Diseases of the genitourinary system. Urology, RC870-923

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1471-2369

URL الوصول: https://doaj.org/article/b4ce314ee6b34ecda6a0d731e27455b6

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

URL الوصول: https://doaj.org/article/c127f7d8ac8b440fad79006e7c98871d

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المؤلفون: Makoto Arakawa, Yoshinori Ikeda, Hiromichi Otaka, Sanghun Iwashiro

المصدر: Molecular Genetics and Metabolism Reports, Vol 40, Iss , Pp 101122- (2024)

مصطلحات موضوعية: Agalsidase alfa, Enzyme replacement therapy, Fabry disease, Japan, Post-marketing surveillance, Real-world data, Medicine (General), R5-920, Biology (General), QH301-705.5

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2214426924000752; https://doaj.org/toc/2214-4269

URL الوصول: https://doaj.org/article/46005a26b2374345a6cd8785dc655334

المؤلفون: Lee, Chae Sung^{Aff1, IDs13023023028035_cor1}, Tsurumi, Mina, Eto, Yoshikatsu

المصدر: Orphanet Journal of Rare Diseases. 18(1)

المؤلفون: Dominique P. Germain, Ales Linhart

المصدر: Frontiers in Genetics, Vol 15 (2024)

مصطلحات موضوعية: Fabry disease, PEGylation, agalsidase, non-inferiority trial, renal function, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fgene.2024.1395287/full; https://doaj.org/toc/1664-8021

URL الوصول: https://doaj.org/article/1c858e76d54a4a80b66b9f63a998cfb0