A triple-blinded crossover study to evaluate the short-term safety of sweet manioc starch for the treatment of glycogen storage disease type Ia von Monteiro, Vaneisse C. L., de Oliveira, Bibiana M., dos Santos, Bruna B., Sperb-Ludwig, Fernanda, Refosco, Lilia F., Nalin, Tatiele, Derks, Terry G. J., Moura de Souza, Carolina F., Schwartz, Ida V. D.

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Potential use of other starch sources in the treatment of glycogen storage disease type Ia - an in vitro study von Monteiro, Vaneisse, Colonetti, Karina, Pagno, Carlos Henrique, Schmidt, Helena Os, Sperb-Ludwig, Fernanda, Oliveira, Bibiana Mello de, Poloni, Soraia, Rios, Alessandro O, de Souza, Carolina F Moura, Schwartz, Ida Vanessa Doederlein

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Oxidative stress assessment by glutathione peroxidase activity and glutathione levels in response to selenium supplementation in patients with Mucopolysaccharidosis I, II and VI von Oliveira-Silva, José Araújo de, Yamamoto, Joyce Umbelino Pinto, Oliveira, Renata Bernardes de, Monteiro, Vaneisse Cristina Lima, Frangipani, Beatriz Jurkiewcz, Kyosen, Sandra Obikawa, Martins, Ana Maria, D'Almeida, Vânia

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Brazilian Food Reference Guide for Phenylalanine Content: A Study Based on the Perception of PKU Patients and Health Providers von Santos, Bruna Bento dos, Oliveira, Bibiana Mello de, Monteiro, Vaneisse C. Lima, Poloni, Soraia, Tonon, Tassia, Schwartz, Ida V. D.

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NDUFV1 mutations in complex I deficiency: Case reports and review of symptoms von Zanette, Vanessa, do Valle, Daniel, Telles, Bruno Augusto, Robinson, Alan J., Monteiro, Vaneisse, Santos, Mara Lucia S. F., Souza, Ricardo Lehtonen R., Beninca, Cristiane

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Evaluation of food intake in patients with mucopolysaccharidosis von Monteiro, Vaneisse Cristina Lima, Araújo de Oliveira Silva, José, Oliveira, Renata Bernardes, Frangipani, Beatriz Jurkiewicz, Dearo, Patrícia Rossetti, Previdelli, Ágatha Nogueira, Martins, Ana Maria, de Cássia Aquino, Rita, D’Almeida, Vânia

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Phenylalanine and Tyrosine Metabolism Analysis in Heterozygotes for Phenylketonuria and in Healthy Individuals von Andrade, Roseani, Monteiro, Vaneisse, Cruz, Cléber, Silva, Carla, Bastos, Adriana, Silva, Luiz

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Neurodevelopmental regression, severe generalized dystonia, and metabolic acidosis caused by POLR3A mutations von Zanette, Vanessa, Reyes, Aurelio, Johnson, Mark, do Valle, Daniel, Robinson, Alan J., Monteiro, Vaneisse, Telles, Bruno Augusto, L.R. Souza, Ricardo, S.F. Santos, Mara L, Benincá, Cristiane, Zeviani, Massimo

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NDUFV1 mutations in complex I deficiency: Case reports and review of symptoms von Zanette, Vanessa, Valle, Daniel do, Telles, Bruno Augusto, Robinson, Alan J, Monteiro, Vaneisse, Santos, Mara Lucia SF, Souza, Ricardo Lehtonen R, Benincá, Cristiane

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Neurodevelopmental regression, severe generalized dystonia, and metabolic acidosis caused by POLR3A mutations von Zanette, Vanessa, Reyes, Aurelio, Johnson, Mark, do Valle, Daniel, Robinson, Alan J, Monteiro, Vaneisse, Telles, Bruno Augusto, L R Souza, Ricardo, S F Santos, Mara L, Benincá, Cristiane, Zeviani, Massimo

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NDUFV1 mutations in complex I deficiency: Case reports and review of symptoms von Zanette, Vanessa, Valle, Daniel do, Telles, Bruno Augusto, Robinson, Alan J., Monteiro, Vaneisse, Santos, Mara Lucia S. F., Souza, Ricardo Lehtonen R., Benincá, Cristiane

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Oxidative stress assessment by glutathione peroxidase activity and glutathione levels in response to selenium supplementation in patients with Mucopolysaccharidosis I, II and VI von Oliveira-Silva, José Araújo De, Yamamoto, Joyce Umbelino Pinto, Oliveira, Renata Bernardes De, Vaneisse Cristina Lima Monteiro, Frangipani, Beatriz Jurkiewcz, Kyosen, Sandra Obikawa, Martins, Ana Maria, Vânia D’Almeida

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Oxidative stress assessment by glutathione peroxidase activity and glutathione levels in response to selenium supplementation in patients with Mucopolysaccharidosis I, II and VI von Oliveira-Silva, José Araújo De, Yamamoto, Joyce Umbelino Pinto, Oliveira, Renata Bernardes De, Vaneisse Cristina Lima Monteiro, Frangipani, Beatriz Jurkiewcz, Kyosen, Sandra Obikawa, Martins, Ana Maria, Vânia D’Almeida

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