Hakutulokset - Ida Vanessa Döederlein Schwartz

Tarkenna hakua
  1. 1
    Evaluation of orofacial motricity in patients with mucopolysaccharidosis: a cross-sectional study

    Evaluation of orofacial motricity in patients with mucopolysaccharidosis: a cross-sectional study Tekijä Giovana Sasso Turra, Ida Vanessa Döederlein Schwartz

    Julkaistu 2009
    Hae kokoteksti
    Artigo
    Lisää suosikkeihin
    Tallennettuna:
  2. 2
    Consequências da judicialização das políticas de saúde: custos de medicamentos para as mucopolissacaridoses

    Consequências da judicialização das políticas de saúde: custos de medicamentos para as mucopolissacaridoses Tekijä Débora Diniz, Marcelo Medeiros, Ida Vanessa Döederlein Schwartz

    Julkaistu 2012
    Hae kokoteksti Hae kokoteksti
    Artigo
    Lisää suosikkeihin
    Tallennettuna:
  3. 3
    Stearoyl-CoA Desaturase-1: Is It the Link between Sulfur Amino Acids and Lipid Metabolism?

    Stearoyl-CoA Desaturase-1: Is It the Link between Sulfur Amino Acids and Lipid Metabolism? Tekijä Soraia Poloni, Henk J. Blom, Ida Vanessa Döederlein Schwartz

    Julkaistu 2015
    Hae kokoteksti Hae kokoteksti
    Revisão
    Lisää suosikkeihin
    Tallennettuna:
  4. 4
    Development of an inventory to assess perceived barriers related to PKU treatment

    Development of an inventory to assess perceived barriers related to PKU treatment Tekijä Katia Irie Teruya, Eduardo Remor, Ida Vanessa Döederlein Schwartz

    Julkaistu 2020
    Hae kokoteksti Hae kokoteksti
    Artigo
    Lisää suosikkeihin
    Tallennettuna:
  5. 5
    New approaches to the treatment of orphan genetic disorders: Mitigating molecular pathologies using chemicals

    New approaches to the treatment of orphan genetic disorders: Mitigating molecular pathologies using chemicals Tekijä Renata Voltolini Velho, Fernanda Sperb‐Ludwig, Ida Vanessa Döederlein Schwartz

    Julkaistu 2015
    Hae kokoteksti Hae kokoteksti
    Revisão
    Lisää suosikkeihin
    Tallennettuna:
  6. 6
    Assessment of newborn screening in the public health system of a municipality in northern Rio Grande do Sul

    Assessment of newborn screening in the public health system of a municipality in northern Rio Grande do Sul Tekijä Tássia Tonon, Elisa Sisti, Tatiéle Nalin, Ida Vanessa Döederlein Schwartz

    Julkaistu 2018
    Hae kokoteksti Hae kokoteksti
    Artigo
    Lisää suosikkeihin
    Tallennettuna:
  7. 7
    The microbiome and inborn errors of metabolism: Why we should look carefully at their interplay?

    The microbiome and inborn errors of metabolism: Why we should look carefully at their interplay? Tekijä Karina Colonetti, Luiz Fernando Würdig Roesch, Ida Vanessa Döederlein Schwartz

    Julkaistu 2018
    Hae kokoteksti Hae kokoteksti
    Artigo
    Lisää suosikkeihin
    Tallennettuna:
  8. 8
    Infant mortality in Brazil attributable to inborn errors of metabolism associated with sudden death: a time-series study (2002–2014)

    Infant mortality in Brazil attributable to inborn errors of metabolism associated with sudden death: a time-series study (2002–2014) Tekijä Fernanda Bender, Ida Vanessa Döederlein Schwartz, Fernanda Sales Luiz Vianna

    Julkaistu 2019
    Hae kokoteksti Hae kokoteksti
    Artigo
    Lisää suosikkeihin
    Tallennettuna:
  9. 9
    Epidemiological aspects of hereditary fructose intolerance: A database study

    Epidemiological aspects of hereditary fructose intolerance: A database study Tekijä Franciele Cabral Pinheiro, Fernanda Sperb‐Ludwig, Ida Vanessa Döederlein Schwartz

    Julkaistu 2021
    Hae kokoteksti
    Revisão
    Lisää suosikkeihin
    Tallennettuna:
  10. 10
    Triagem neonatal de distúrbios metabólicos

    Triagem neonatal de distúrbios metabólicos Tekijä Carolina Fischinger Moura de Souza, Ida Vanessa Döederlein Schwartz, Roberto Giugliani

    Julkaistu 2002
    Hae kokoteksti Hae kokoteksti
    Artigo
    Lisää suosikkeihin
    Tallennettuna:
  11. 11
    Tratamento de erros inatos do metabolismo

    Tratamento de erros inatos do metabolismo Tekijä Ida Vanessa Döederlein Schwartz, Carolina Fischinger Moura de Souza, Roberto Giugliani

    Julkaistu 2008
    Hae kokoteksti Hae kokoteksti
    Artigo
    Lisää suosikkeihin
    Tallennettuna:
  12. 12
    Treatment of inborn errors of metabolism

    Treatment of inborn errors of metabolism Tekijä Ida Vanessa Döederlein Schwartz, Carolina Fischinger Moura de Souza, Roberto Giugliani

    Julkaistu 2008
    Hae kokoteksti
    Revisão
    Lisää suosikkeihin
    Tallennettuna:
  13. 13
    Development of new treatment strategies for mucolipidosis types II and III: a study focusing on premature degradation of GNPTAB and GNPTG mRNA

    Development of new treatment strategies for mucolipidosis types II and III: a study focusing on premature degradation of GNPTAB and GNPTG mRNA Tekijä Ida Vanessa Döederlein Schwartz, Renata Voltolini Velho, Fernanda Sperb Ludwig, Taciane Alegra

    Julkaistu 2014
    Hae kokoteksti
    Artigo
    Lisää suosikkeihin
    Tallennettuna:
  14. 14
    Assessment of quality of life in Gaucher disease: A methodological approach

    Assessment of quality of life in Gaucher disease: A methodological approach Tekijä Vitória Schütt Zizemer, Tatiéle Nalin, Ida Vanessa Döederlein Schwartz, Ana Paula Vanz

    Julkaistu 2020
    Hae kokoteksti Hae kokoteksti
    Carta
    Lisää suosikkeihin
    Tallennettuna:
  15. 15
    What is known about patients’ quality of life with Phenylketonuria and their caregivers? A scoping review

    What is known about patients’ quality of life with Phenylketonuria and their caregivers? A scoping review Tekijä Eduardo Remor, Kamilla Mueller Gabe, Katia Irie Teruya, Ida Vanessa Döederlein Schwartz

    Julkaistu 2024
    Hae kokoteksti
    Revisão
    Lisää suosikkeihin
    Tallennettuna:
  16. 16
    Effects of imiglucerase on the growth and metabolism of Gaucher disease type I patients: a systematic review

    Effects of imiglucerase on the growth and metabolism of Gaucher disease type I patients: a systematic review Tekijä Divair Doneda, Cristina Brinckmann Oliveira Netto, Cileide Cunha Moulin, Ida Vanessa Döederlein Schwartz

    Julkaistu 2013
    Hae kokoteksti Hae kokoteksti
    Revisão
    Lisää suosikkeihin
    Tallennettuna:
  17. 17
    Medicamentos de alto custo para doenças raras no Brasil: o exemplo das doenças lisossômicas

    Medicamentos de alto custo para doenças raras no Brasil: o exemplo das doenças lisossômicas Tekijä Mônica Vinhas de Souza, Bárbara Krug, Paulo Dornelles Picon, Ida Vanessa Döederlein Schwartz

    Julkaistu 2010
    Hae kokoteksti Hae kokoteksti
    Revisão
    Lisää suosikkeihin
    Tallennettuna:
  18. 18
    Next-generation sequencing corroborates a probable de novo GNPTG variation previously detected by Sanger sequencing

    Next-generation sequencing corroborates a probable de novo GNPTG variation previously detected by Sanger sequencing Tekijä Nataniel Floriano Ludwig, Fernanda Sperb‐Ludwig, Renata Voltolini Velho, Ida Vanessa Döederlein Schwartz

    Julkaistu 2017
    Hae kokoteksti
    Artigo
    Lisää suosikkeihin
    Tallennettuna:
  19. 19
    Commentary: "Quality of Life in Caregivers of Children and Adolescents with Osteogenesis Imperfecta"

    Commentary: "Quality of Life in Caregivers of Children and Adolescents with Osteogenesis Imperfecta" Tekijä Ana Paula Vanz, Têmis Félix, Neusa Sica da Rocha, Ida Vanessa Döederlein Schwartz

    Julkaistu 2019
    Hae kokoteksti Hae kokoteksti
    Artigo
    Lisää suosikkeihin
    Tallennettuna:
  20. 20
    Three Main Causes of Homocystinuria: CBS, cblC and MTHFR Deficiency. What do they Have in Common?

    Three Main Causes of Homocystinuria: CBS, cblC and MTHFR Deficiency. What do they Have in Common? Tekijä Giovana Regina Weber Hoss, Soraia Poloni, Henk J. Blom, Ida Vanessa Döederlein Schwartz

    Julkaistu 2019
    Hae kokoteksti Hae kokoteksti
    Artigo
    Lisää suosikkeihin
    Tallennettuna:

Työkalut: