María Victoria Rossetti

Familial Porphyria Cutanea Tarda: Characterization of Seven Novel Uroporphyrinogen Decarboxylase Mutations and Frequency of Common Hemochromatosis Alleles

Manuel Méndez, Lonnie Sorkin, María Victoria Rossetti et al. · The American Journal of Human Genetics · 1998 · 57 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

The role of inherited and acquired factors in the development of porphyria cutanea tarda in the Argentinean population

Manuel Méndez, María Victoria Rossetti, Alcira Batlle et al. · Journal of the American Academy of Dermatology · 2005 · 46 citations · Full text

Life Sciences, Biology, Genetics +5

Identification and characterization of hydroxymethylbilane synthase mutations causing acute intermittent porphyria: Evidence for an ancestral founder of the common G111R mutation

Adriana De Siervi, María Victoria Rossetti, Victoria Estela Parera et al. · American Journal of Medical Genetics · 1999 · 42 citations

Life Sciences, Genetics, Molecular Genetics +17

Acute intermittent porphyria: Biochemical and clinical analysis in the Argentinean population

Adriana De Siervi, María Victoria Rossetti, Victoria Estela Parera et al. · Clinica Chimica Acta · 1999 · 28 citations

Life Sciences, Biochemistry, Clinical Sciences +9

Enzymic polymerization of porphobilinogen into uroporphyrinogens

Alcira Batlle, María Victoria Rossetti · International Journal of Biochemistry · 1977 · 26 citations

Life Sciences, Biochemistry, Molecular Biology +10