Gabriel Civallero

Twelve different enzyme assays on dried-blood filter paper samples for detection of patients with selected inherited lysosomal storage diseases

Gabriel Civallero, Kristiane Michelin, J. De Mari et al. · Clinica Chimica Acta · 2006 · 120 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +16

Extended use of a selective inhibitor of acid lipase for the diagnosis of Wolman disease and cholesteryl ester storage disease

Gabriel Civallero, J. De Mari, Camila Matzenbacher Bittar et al. · Gene · 2014 · 28 citations

Life Sciences, Biochemistry, Enzymology +12

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

Life Sciences, Biochemistry, Pathobiology +8

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

Life Sciences, Genetics, Molecular Genetics +17

Reliable detection of mucopolysacchariduria in dried-urine filter paper samples

Gabriel Civallero, Fernanda Bender, Ana Paula Gomes et al. · Clinica Chimica Acta · 2012 · 19 citations

Life Sciences, Biochemistry, Clinical Biochemistry +6