Stearoyl-CoA Desaturase-1: Is It the Link between Sulfur Amino Acids and Lipid Metabolism?

Por Soraia Poloni, Henk J. Blom, Ida V. D. Schwartz
Publicado em 2015-06-01

New approaches to the treatment of orphan genetic disorders: Mitigating molecular pathologies using chemicals

Por Renata V. Velho, Fernanda Sperb- ludwig, Ida V.D. Schwartz
Publicado no Anais da Academia Brasileira de Ciências (2015)

Glycogen storage disease type I: clinical and laboratory profile

Por Berenice L. Santos, Carolina F.M. de Souza, Lavinia Schuler-Faccini, Lilia Refosco, Matias Epifanio, Tatiele Nalin, Sandra M.G. Vieira, Ida V.D. Schwartz
Publicado em 2014-12-01

Nutritional Status and Body Composition in Patients With Hepatic Glycogen Storage Diseases Treated With Uncooked Cornstarch—A Controlled Study

Por Bruna B. dos Santos MSc, Tatiéle Nalin PhD, Kamila C. Grokoski MSc, Ingrid D. S. Perry PhD, Lilia F. Refosco MSc, Filippo P. Vairo PhD, Carolina F. M. Souza PhD, Ida V. D. Schwartz PhD
Publicado em 2017-09-01

Correction: Biotinidase deficiency: Genotype-biochemical phenotype association in Brazilian patients.

Por Taciane Borsatto, Fernanda Sperb-Ludwig, Samyra E Lima, Maria R S Carvalho, Pablo A S Fonseca, José S Camelo, Erlane M Ribeiro, Paula F V de Medeiros, Charles M Lourenço, Carolina F M de Souza, Raquel Boy, Têmis M Félix, Camila M Bittar, Louise L C Pinto, Eurico C Neto, Henk J Blom, Ida V D Schwartz
Publicado em 2017-01-01