Rare GBA1 genotype in two siblings with a severe bone phenotype of type 1 Gaucher disease by Paskulin, Livia D., Starosta, Rodrigo T., Zizemer, Vitoria S., Basgalupp, Suelen, Schwartz, Ida Vanessa D.

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Taliglucerase-alpha and type 1 Gaucher disease: A five-year follow-up by Paskulin, Livia D., Zizemer, Vitória S., Vairo, Filippo, Schwartz, Ida V.D.

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Breastfeeding in Gaucher disease: is taliglicerase-alpha safe? by Paskulin, Livia D., Dornelles, Alicia Dorneles, Nalin, Tatiele, Quevedo, Amanda, Tirelli, Kristiane Michellin, Schwartz, Ida Vanessa Doederlein

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The impact of taliglucerase alfa in the bone of type I Gaucher disease by Paskulin, Livia D., Bertholdo, Débora, Vanz, Ana Paula, Vairo, Filippo, Vedolin, Leonardo, Schwartz, Ida Vanessa D.

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Taliglucerase alfa and type 1 Gaucher disease: a south Brazilian experience by Paskulin, Livia, Vairo, Filippo, Schwartz, Ida Vanessa D

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The prognostic value of the serum ferritin in a southern Brazilian cohort of patients with Gaucher disease by Koppe, Tiago, Doneda, Divair, Siebert, Marina, Paskulin, Livia, Camargo, Matheus, Tirelli, Kristiane Michelin, Vairo, Filippo, Daudt, Liane, Schwartz, Ida Vanessa D

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