Rozwój funkcji poznawczych u dzieci z mukopolisacharydozą typu I (choroba Hurler) leczonych enzymatycznie laronidazą by Marta Biernacka, Anna Jakubowska-Winecka, Anna Tylki-Szymańska

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Aplicación móvil para guiar el tratamiento en pacientes con Mucopolisacáridosis Tipo I by Maria Fernanda Jimbo Patiño, Carlos Julio Guillén Berrezueta, Rosa Angélica Ordóñez Zhunio

Subjects: “…aplicación móvil, mucopolisacáridosis tipo i; síndrome de hurler; paciente pediátrico; guía.…”
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Ultrasound imaging for assessing aortic phenotypes: A preclinical tool for measuring cardiac disease model progression and therapeutic effect by James Cao, Alex Jayyosi, Jennifer Nietupski, Giulio Tomassy, Ingeborg M. Langohr, Michelle Potter, Srinivas Rao, Dinesh S. Bangari, Xiaoyou Ying

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α-mannosidosis diagnosis in Brazilian patients with MPS-like symptoms by Maryana Marins, Marco Antonio Curiati, Caio Perez Gomes, Renan Paulo Martin, Priscila Nicolicht-Amorim, Joyce Umbelino da Silva Yamamoto, Vânia D’Almeida, Ana Maria Martins, João Bosco Pesquero

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Advancements in the Treatment of Mucopolysaccharidoses: From Established Therapies to Gene Therapy by Joanna Wanat, Wojciech Homa, Aleksandra Warunek, Gabriela Gronowicz, Izabela Dzikowska, Agata Siejka, Daria Stefaniak, Weronika Zielińska, Michał Chról

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