Acute Intermittent Porphyria in a Man with Dual Enzyme Deficiencies von Rossetti, M. V., Batlle, A., Tomassi, L., Varela, L. S., Assali, L. Abou, Cerbino, G. N., Parera, V. E.

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Photodynamic inactivation of Gram-positive bacteria employing natural resources von Mamone, L, Di Venosa, G, Gándara, L, Sáenz, D, Vallecorsa, P, Schickinger, S, Rossetti, M V, Batlle, A, Buzzola, F, Casas, A

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Changes in actin and E-cadherin expression induced by 5-aminolevulinic acid photodynamic therapy in normal and Ras-transfected human mammary cell lines von Di Venosa, G., Rodriguez, L., Mamone, L., Gándara, L., Rossetti, M.V., Batlle, A., Casas, A.

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Functional associations of genetic variants involved in the clinical manifestation of erythropoietic protoporphyria in the Argentinean population von Colombo, F.P., Rossetti, M.V., Méndez, M., Martínez, J.E., Enríquez de Salamanca, R., del C. Batlle, A.M., Parera, V.E.

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Familial Porphyria Cutanea Tarda: Characterization of Seven Novel Uroporphyrinogen Decarboxylase Mutations and Frequency of Common Hemochromatosis Alleles von Mendez, Manuel, Sorkin, Lonnie, Rossetti, Maria Victoria, Astrin, Kenneth H., Batlle, Alcira M. del C., Parera, Victoria E., Aizencang, Gerardo, Desnick, Robert J.

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Acute intermittent porphyria: Biochemical and clinical analysis in the Argentinean population von De Siervi, Adriana, Rossetti, Marı́a V, Parera, Victoria E, Mendez, Manuel, Varela, Laura S, del C. Batlle, Alcira M

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Two new mutations (H106P and L178V) in the protoporphyrinogen oxidase gene in Argentinean patients with variegate porphyria von De Siervi, Adriana, Parera, Victoria E., del C. Batlle, Alcira M., Rossetti, María V.

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The role of ALA‐S and ALA‐D in regulating porphyrin biosynthesis in a normal and a HEM R+ mutant strain of Saccharomyces cerevisiae von García, S. Correa, Moretti, M. Bermúdez, Cardalda, C., Rossetti, M. V., del C. Batlle, A. M.

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Haplotype Study in Argentinean Variegate Porphyria Patients von Granata, Bárbara Xoana, Parera, Victoria Estela, Batlle, Alcira, Rossetti, María Victoria

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A novel mutation (1320InsT) identified in two Argentine families with variegate porphyria von Siervi, Adriana De, Parera, Victoria E., Varela, Laura S., Batlle, Alcira M del C, Rossetti, María V.

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Identification and characterization of two novel mutations that produce acute intermittent porphyria: A 3-base deletion (841-843delGGA) and a missense mutation (T35M) von Siervi, Adriana De, Cádiz, Débora E. Weiss, Parera, Victoria E., del C. Batlle, Alcira M., Rossetti, Maria Victoria

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Acute intermittent porphyria: Characterization of two novel mutations in the porphobilinogen deaminase gene, one amino acid deletion (453-455delAGC) and one splicing aceptor site m... von De Siervi, Adriana, Mendez, Manuel, Parera, Victoria Estela, Varela, Laura, Batlle, Alcira M. del C., Rossetti, Maria Victoria

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Porphyrin biosynthesis in normal and haem mutants of Saccharomyces cerevisiae. Studies on the inheritance of the HEM R+ phenotype von De Siervi, A., Rossetti, M.V., Lezama, D., del C. Batlle, A.M.

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Porfirias poco frecuentes: Casos detectados en la población argentina von Melito, V A, Rossetti, M V, Parera, V E, Batlle

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The role of inherited and acquired factors in the development of porphyria cutanea tarda in the Argentinean population von Méndez, Manuel, Rossetti, María V., Del C. Batlle, Alcira M., Parera, Victoria E.

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ROL DE LA VARIANTE NM_004827.3:c.421C>A DEL GEN ABCG2. EN EL DESENCADENAMIENTO DE LA PORFIRIA CUTÁNEA TARDÍA EN INDIVIDUOS INFECTADOS CON VIH von Buscalia, ML, Zuccoli, J, Melito, V, Rossetti, MV, Parera, V, Buzaleh, AM

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Soluble and Particulate Porphobilinogen-Deaminase from Dark-Grown Euglena gracilis von Rossetti, M. V., Juknat, A. A., Batlle, A. M. del C.

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S-adenosyl- l-methionine and lead intoxication: Its therapeutic effect varying the route of administration von Paredes, Sergio R., Fukuda, Haydee, Kozicki, Pablo A., Rossetti, Maria V., Conti, Honorina, Batlle, Alcira M.del C.

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Zinc Aminolevulinic Acid Dehydratase Reactivation Index as a Tool for Diagnosis of Lead Exposure von Polo, C.F., Afonso, S.G., Navone, N.M., Rossetti, M.V., Batlle, A.M.D.

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Identification and characterization of hydroxymethylbilane synthase mutations causing acute intermittent porphyria: Evidence for an ancestral founder of the common G111R mutation von De Siervi, A., Rossetti, M. V., Parera, V. E., Astrin, K. H., Aizencang, G. I., Glass, I. A., del C. Batlle, A. M., Desnick, R. J.

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