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Batlle, Alcira María del Carmen
180
2000
10
"Two new mutations (H106P and L178V) in the protoporphyrinogen oxidase gene in Argentinean patients with variegate porphyria." (2000) De Siervi, A.; Parera, V.E.; del C Batlle, A.M.; Rossetti, M.V. Human mutation. 16(6):532
"The influence of the vehicle on the synthesis of porphyrins after topical application of 5-aminolaevulinic acid. Implications in cutaneous photodynamic sensitization" (2000) Casas, A.; Fukuda, H.; Di Venosa, G.; Del C.Batlle, A.M. British Journal of Dermatology. 143(3):564-572
"Relevance of cytochrome P450 levels in the actions of enflurane and isoflurane in mice: Studies on the haem pathway" (2000) Buzaleh, A.M.; Del Carmen Martinez, M.; Del Carmen Batlle, A.M. Clinical and Experimental Pharmacology and Physiology. 27(10):796-800
"Preventive aspirin treatment of streptozotocin induced diabetes: Blockage of oxidative status and revertion of heme enzymes inhibition" (2000) Caballero, F.; Gerez, E.; Batlle, A.; Vazquez, E. Chemico-Biological Interactions. 126(3):215-225
"Porphyrin biosynthesis intermediates are not regulating δ-aminolevulinic acid transport in Saccharomyces cerevisiae" (2000) Moretti, M.B.; Garcia, S.C.; Batlle, A. Biochemical and Biophysical Research Communications. 272(3):946-950
"Mutations in familial porphyria cutanea tarda: Two novel and two previously described for hepatoerythropoietic porphyria" (2000) Mendez, M.;Rossetti, M.V.;De Siervi, A. (...)Parera, V. Human mutation. 16(3):269-270
"Effect of acetaminophen on heme metabolism in rat liver" (2000) Noriega, G.O.; Ossola, J.O.; Tomaro, M.L.; Batlle, A.M.delC. International Journal of Biochemistry and Cell Biology. 32(9):983-991
"Constitutive expression of the UGA4 gene in Saccharomyces cerevisiae depends on two positive-acting proteins, Uga3p and Uga35p" (2000) Garcia, S.C.; Moretti, M.B.; Batlle, A. FEMS Microbiology Letters. 184(2):219-224
"A novel mutation (1320InsT) identified in two Argentine families with variegate porphyria." (2000) Siervi, A.D.;Parera, V.E.;Varela, L.S. (...)Rossetti, M.V. Human mutation. 16(1):96