Deep characterization of the anti-drug antibodies developed in Fabry disease patients, a prospective analysis from the French multicenter cohort FFABRY
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Published:2018-07-31
Issue:1
Volume:13
Page:
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ISSN:1750-1172
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Container-title:Orphanet Journal of Rare Diseases
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language:en
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Short-container-title:Orphanet J Rare Dis
Author:
Mauhin WladimirORCID, Lidove Olivier, Amelin Damien, Lamari Foudil, Caillaud Catherine, Mingozzi Federico, Dzangué-Tchoupou Gaëlle, Arouche-Delaperche Louiza, Douillard Claire, Dussol Bertrand, Leguy-Seguin Vanessa, D’Halluin Pauline, Noel Esther, Zenone Thierry, Matignon Marie, Maillot François, Ly Kim-Heang, Besson Gérard, Willems Marjolaine, Labombarda Fabien, Masseau Agathe, Lavigne Christian, Froissart Roseline, Lacombe Didier, Ziza Jean Marc, Hachulla Eric, Benveniste Olivier
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),Genetics (clinical),General Medicine
Reference25 articles.
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http://www.ncbi.nlm.nih.gov/books/NBK1292/
. [cited 7 Jan 2016]. 3. Echevarria L, Benistan K, Toussaint A, Dubourg O, Hagege AA, Eladari D, et al. X-chromosome inactivation in female patients with Fabry disease. Clin Genet. 2016;89:44–54. 4. Pan X, Ouyang Y, Wang Z, Ren H, Shen P, Wang W, et al. Genotype: a crucial but not unique factor affecting the clinical phenotypes in Fabry disease. PLoS One. 2016;11:e0161330. 5. Schiffmann R, Ries M, Timmons M, Flaherty JT, Brady RO. Long-term therapy with agalsidase alfa for Fabry disease: safety and effects on renal function in a home infusion setting. Nephrol Dial Transplant. 2006;21:345–54.
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21 articles.
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