Search Results - "DE LUCCA, Marisel"

Amiodarone and Miltefosine Act Synergistically against Leishmania mexicana and Can Induce Parasitological Cure in a Murine Model of Cutaneous Leishmaniasis by SERRANO-MARTIN, Xenón, PAYARES, Gilberto, DE LUCCA, Marisel, MARTINEZ, Juan Carlos, MENDOZA-LEON, Alexis, BENAIM, Gustavo

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The 1, 2, 3 of laboratory animal experimentation by Romero-Fernandez, Wilber, Batista-Castro, Zenia, De Lucca, Marisel, Ruano, Ana, García-Barceló, María, Rivera-Cervantes, Marta, García-Rodríguez, Julio, Sánchez-Mateos, Soledad

“…The slow scientific development in Latin America in recent decades has delayed the incorporation of laboratory animal experimentation; however, this situation…”
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MELAS a clinically and genetically heterogeneous syndrome by Casique, Liliana, De Lucca, Marisel, Mahfoud, Antonieta, Luis Ramírez, José

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Independent origin for m.3243A>G mitochondrial mutation in three Venezuelan cases of MELAS syndrome by Florez, Ingrid, Pirrone, Irune, Casique, Liliana, Domínguez, Carmen Luisa, Mahfoud, Antonieta, Rodríguez, Tania, Rodríguez, Daniel, De Lucca, Marisel, Ramírez, José Luis

“…Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) is a multisystem and progressive neurodegenerative mitochondrial…”
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Hallazgos clínicos y espectro mutacional en pacientes venezolanos con diagnóstico tardío de fenilcetonuria by Mahfoud Hawilou, Antonieta, De Lucca Osorio, Marisel, Domínguez Méndez, Carmen Luisa, Arias León, Isabel, Casique Albornoz, Liliana, Araujo Hernández, Katiuska, Rodríguez Obregón, Tania, Bottaro Omaña, Magaly, Colmenares Torrealba, Ana Rosa, López Oquendo, María Elena, Giamporcaro de Merzon, Rosa Maria

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Glucocerebrosidase mutations are also found in subjects with early-onset parkinsonism from Venezuela by Eblan, Michael J., Nguyen, Joann, Ziegler, Shira G., Lwin, Alicia, Hanson, Melissa, Gallardo, Marisol, Weiser, Roberto, De Lucca, Marisel, Singleton, Andrew, Sidransky, Ellen

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El 1, 2, 3 de la experimentación con animales de laboratorio by Romero-Fernandez, Wilber, Batista-Castro, Zenia, De Lucca, Marisel, Ruano, Ana, García-Barceló, María, Rivera-Cervantes, Marta, García-Rodríguez, Julio, Sánchez-Mateos, Soledad

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Improving phenylketonuria genotyping by screening for the IVS4 + 5g > t mutation in the PAH gene by De Lucca, Marisel, Arias, Isabel, Casique, Liliana, Araujo, Katiuska, Merzon, Rosa María

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Characterization of cystathionine β-synthase gene mutations in homocystinuric Venezuelan patients: identification of one novel mutation in exon 6 by De Lucca, Marisel, Casique, Liliana

“…This study describes for the first time the cystathionine β-synthase (CBS) gene mutations in Venezuelan patients. A total of five disease-causing mutations…”
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El 1, 2, 3 de la experimentación con animales de laboratorio by Romero-Fernandez, Wilber, Batista-Castro, Zenia, De Lucca, Marisel, Ruano, Ana, García-Barceló, María, Rivera-Cervantes, Marta, García-Rodríguez, Julio, Sánchez-Mateos, Soledad

“…El lento desarrollo científico experimentado en América Latina en las últimas décadas ha retrasado la incorporación de la experimentación con animales de…”
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El 1, 2, 3 de la experimentación con animales de laboratorio by Romero-Fernandez, Wilber, Batista-Castro, Zenia, De Lucca, Marisel, Ruano, Ana, García-Barceló, María, Rivera-Cervantes, Marta, García-Rodríguez, Julio, Sánchez-Mateos, Soledad

“…RESUMEN El lento desarrollo científico experimentado en América Latina en las últimas décadas ha retrasado la incorporación de la experimentación con animales…”
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Molecular basis of phenylketonuria in Venezuela: Presence of two novel null mutations by De Lucca, Marisel, Pérez, Belén, Desviat, Lourdes R., Ugarte, Magdalena

“…This report describes the mutational spectrum and linked haplotypes of the phenylalanine hydroxylase gene in Venezuela. In this study, we have detected…”
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Molecular characterization of phenylalanine hydroxylase deficiency in Chile by Pérez, Belén, Desviat, Lourdes R., De Lucca, Marisel, Cornejo, Veronica, Raimann, Erna, Ugarte, Magdalena

“…Both the haplotype distribution and the mutational spectrum of the phenylalanine hydroxylase (PAH) gene has been defined for the Chilean phenylketonuria (PKU)…”
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Evidence in Latin America of recurrence of V388M, a phenylketonuria mutation with high in vitro residual activity by DESVIAT, L. R, PEREZ, B, DE LUCCA, M, CORNEJO, V, SCHMIDT, B, UGARTE, M

“…Phenylketonuria mutation V388M is frequent in the Iberian Peninsula. In vitro, the V388M mutant enzyme has similar immunoreactive protein and phenylalanine…”
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Mutation analysis of phenylketonuria in South Brazil by Pérez, Belén, Desviat, Lourdes R., De Lucca, Marisel, Schmidt, Benjamin, Loghin-Grosso, Nicole, Giugliani, Roberto, Pires, Ricardo F., Ugarte, Magdalena

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