Ana Paschini-Capra

Leukodystrophy and CSF Purine Abnormalities Associated with Isolated 3-Methylcrotonyl-CoA Carboxylase Deficiency

Raquel Dodelson de Kremer, Alexandra Latini, Terttu Suormala et al. · Metabolic Brain Disease · 2002 · 26 citations

Barth's syndrome-like disorder: A new phenotype with a maternally inherited A3243G substitution of mitochondrial DNA (MELAS mutation)

Raquel Dodelson de Kremer, Ana Paschini-Capra, Sandra R. Bacman et al. · American Journal of Medical Genetics · 2001 · 21 citations

Glycogen storage disease type Ia in Argentina: two novel glucose-6-phosphatase mutations affecting protein stability

Celia J. Angaroni, Raquel Dodelson de Kremer, Carlos E. Argaraña et al. · Molecular Genetics and Metabolism · 2004 · 13 citations

Protein Stability, Biochemistry, Genetics +6

Evaluation of the biotinidase activity in hepatic glycogen storage disease patients. Undescribed genetic finding associated with atypical enzymatic behavior: an outlook

Celia J. Angaroni, Alicia Giner-Ayala, Lorena P. Hill et al. · Journal of Inherited Metabolic Disease · 2010 · 10 citations