Maria V. Rossetti
B, Argentina
Last Updated: 09/26/2026
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Found 10 publications
Acute Intermittent Porphyria in a Man with Dual Enzyme Deficiencies.
Journal: Case reports in genetics
Published: August 19, 2020
Role of ABCB1 and glutathione S-transferase gene variants in the association of porphyria cutanea tarda and human immunodeficiency virus infection.
Journal: Biomedical reports
Published: June 24, 2020
Clinical, biochemical, and genetic characterization of acute hepatic porphyrias in a cohort of Argentine patients.
Journal: Molecular genetics & genomic medicine
Published: October 19, 2018
Haplotype Study in Argentinean Variegate Porphyria Patients.
Journal: Human heredity
Published: July 28, 2015
Acute intermittent porphyria in Argentina: an update.
Journal: BioMed research international
Published: October 09, 2014
Characterization of variegate porphyria mutations using a minigene approach.
Journal: JIMD reports
Published: July 08, 2014
Photodynamic inactivation of Gram-positive bacteria employing natural resources.
Journal: Journal of photochemistry and photobiology. B, Biology
Published: November 08, 2013
An odd case of heteroallelic acute intermittent porphyria in the Argentinean population.
Journal: Cellular and molecular biology (Noisy-le-Grand, France)
Published: February 20, 2013
Functional associations of genetic variants involved in the clinical manifestation of erythropoietic protoporphyria in the Argentinean population.
Journal: Journal of the European Academy of Dermatology and Venereology : JEADV
Published: May 18, 2012
Molecular analysis of the UROD gene in 17 Argentinean patients with familial porphyria cutanea tarda: characterization of four novel mutations.
Journal: Molecular genetics and metabolism
Published: December 07, 2011
Showing 1-10 of 10
Last Updated: 09/26/2026