Preparation of electrospun shape memory polyurethane fibers in optimized electrospinning conditions via response surface methodology von Banikazemi, Simin, Rezaei, Mostafa, Rezaei, Pezhman, Babaie, Amin, Eyvazzadeh‐Kalajahi, Alireza

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Global reach of over 20 years of experience in the patient-centered Fabry Registry: Advancement of Fabry disease expertise and dissemination of real-world evidence to the Fabry com... von Wanner, Christoph, Ortiz, Alberto, Wilcox, William R., Hopkin, Robert J., Johnson, Jack, Ponce, Elvira, Ebels, Johan T., Batista, Julie L., Maski, Manish, Politei, Juan M., Martins, Ana Maria, Banikazemi, Maryam, Linhart, Aleš, Mauer, Michael, Oliveira, João P., Weidemann, Frank, Germain, Dominique P.

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Fabry disease caused by the GLA p.Phe113Leu (p.F113L) variant: Natural history in males von Oliveira, João P., Nowak, Albina, Barbey, Frédéric, Torres, Márcia, Nunes, José P., Teixeira-e-Costa, Fernando, Carvalho, Fernanda, Sampaio, Susana, Tavares, Isabel, Pereira, Odete, Soares, Ana L., Carmona, Cátia, Cardoso, Maria-Teresa, Jurca-Simina, Iulia E., Spada, Marco, Ferreira, Susana, Germain, Dominique P.

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Phenotypic characteristics of the p.Asn215Ser (p.N215S) GLA mutation in male and female patients with Fabry disease: A multicenter Fabry Registry study von Germain, Dominique P., Brand, Eva, Burlina, Alessandro, Cecchi, Franco, Garman, Scott C., Kempf, Judy, Laney, Dawn A., Linhart, Aleš, Maródi, László, Nicholls, Kathy, Ortiz, Alberto, Pieruzzi, Federico, Shankar, Suma P., Waldek, Stephen, Wanner, Christoph, Jovanovic, Ana

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A systematic review on screening for Fabry disease: prevalence of individuals with genetic variants of unknown significance von van der Tol, L, Smid, B E, Poorthuis, B J H M, Biegstraaten, M, Deprez, R H Lekanne, Linthorst, G E, Hollak, C E M

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Cardiovascular magnetic resonance demonstration of the spectrum of morphological phenotypes and patterns of myocardial scarring in Anderson-Fabry disease von Deva, Djeven Parameshvara, Hanneman, Kate, Li, Qin, Ng, Ming Yen, Wasim, Syed, Morel, Chantal, Iwanochko, Robert M, Thavendiranathan, Paaladinesh, Crean, Andrew Michael

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The effect of enzyme replacement therapy on clinical outcomes in female patients with Fabry disease – A systematic literature review by a European panel of experts von Germain, Dominique P., Arad, Michael, Burlina, Alessandro, Elliott, Perry M., Falissard, Bruno, Feldt-Rasmussen, Ulla, Hilz, Max J., Hughes, Derralynn A., Ortiz, Alberto, Wanner, Christoph, Weidemann, Frank, Spada, Marco

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Late-onset fabry disease due to the p.Phe113Leu variant: the first italian cluster of five families von Cianci, Vittoria, Pascarella, Angelo, Manzo, Lucia, Gasparini, Sara, Marsico, Oreste, Mammì, Anna, Rao, Carmelo Massimiliano, Franzutti, Claudio, Aguglia, Umberto, Ferlazzo, Edoardo

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A Proteomics-Based Analysis Reveals Predictive Biological Patterns in Fabry Disease von Tebani, Abdellah, Mauhin, Wladimir, Abily-Donval, Lenaig, Lesueur, Céline, Berger, Marc G, Nadjar, Yann, Berger, Juliette, Benveniste, Oliver, Lamari, Foudil, Laforêt, Pascal, Noel, Esther, Marret, Stéphane, Lidove, Olivier, Bekri, Soumeya

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Phenotypic characteristics of the p.Asn215Ser (p.N215S) G LA mutation in male and female patients with Fabry disease: A multicenter Fabry Registry study von Germain, Dominique P., Brand, Eva, Burlina, Alessandro, Cecchi, Franco, Garman, Scott C., Kempf, Judy, Laney, Dawn A., Linhart, Aleš, Maródi, László, Nicholls, Kathy, Ortiz, Alberto, Pieruzzi, Federico, Shankar, Suma P., Waldek, Stephen, Wanner, Christoph, Jovanovic, Ana

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