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Showing 201 - 210 results of 210 for search 'hospital de ((ninos de) OR (anos de)) la santisima trinidad.', query time: 0.66s Refine Results
  1. 201
    Metabolismo de las purinas y pirimidinas : errores hereditarios primarios y alteraciones secundarias en otros defectos genéticos /

    Metabolismo de las purinas y pirimidinas : errores hereditarios primarios y alteraciones secundarias en otros defectos genéticos / by Laróvere, Laura Elena

    Published 2002
    Thesis Book
  2. 202
    Lipofuscinosis Ceroidea Neuronal (LCNs): caracterización molecular y bioinformática del gen CLN8 en pacientes de América Latina

    Lipofuscinosis Ceroidea Neuronal (LCNs): caracterización molecular y bioinformática del gen CLN8 en pacientes de América Latina by Pesaola, Favio Nicolás

    Published 2013
    Thesis Book
  3. 203
    Evaluación en el Síndrome Metabólico del estrés oxidativo y alteraciones mitocondriales

    Evaluación en el Síndrome Metabólico del estrés oxidativo y alteraciones mitocondriales by Tarán, Mariana, Baez, María del Carmen, Scribano Parada, María de la Paz, Balceda, Ariel, Becerra, Walter, Moya, Mónica

    Published 2021
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  4. 204
    Estudio integral de las lipofuscinosis ceroideas neuronales genotipos CLN3, CNL5, CNL6, CNL7, y CNL8 en familias de Latinoamérica /

    Estudio integral de las lipofuscinosis ceroideas neuronales genotipos CLN3, CNL5, CNL6, CNL7, y CNL8 en familias de Latinoamérica / by Cismondi, Inés Adriana

    Published 2012
    Texto Completo
    Thesis Book
  5. 205
    Nonsense mediated mRNA decay affects nonsense transcripts levelsand in vitro response to gentamicin and ataluren in X-ALD

    Nonsense mediated mRNA decay affects nonsense transcripts levelsand in vitro response to gentamicin and ataluren in X-ALD by Amorosi, CA, Kemp, Stephan, Dodelson de Kremer, Raquel, Argaraña, Carlos, Ramírez Oller, Ana María

    Published 2023
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  6. 206
    Ornithine transcarbamylase deficiency: identification of mutations, computational validation, and phenotypic correlation in argentinian patients

    Ornithine transcarbamylase deficiency: identification of mutations, computational validation, and phenotypic correlation in argentinian patients by Silvera Ruíz, Silene Maite, Arranz Amo, Antonio, Dodelson de Kremer, Raquel, Larovere, Laura Elena

    Published 2022
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  7. 207
    Genetic defects in the liver phosphorylase system in Argentine patients nosological definition through a strategy of enzimatic and molecular analysis

    Genetic defects in the liver phosphorylase system in Argentine patients nosological definition through a strategy of enzimatic and molecular analysis by Agaroni, Celia Juana, Giner Ayala, Alicia, Castillo, Angéles, Paschini Capra, Agustín, Dodelson de Kremer, Raquel, Lanza, Victoria

    Published 2021
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  8. 208
    Efficacy of citrulline supplementation to decrease the risk of pulmonary hypertension after congenital heart disease surgery. A local experience

    Efficacy of citrulline supplementation to decrease the risk of pulmonary hypertension after congenital heart disease surgery. A local experience by Silvera Ruiz, Silene, Grosso, Carola L., Tablada, Elena Margot, Cabrera, Marcelo, Dodelson de Kremer, Raquel, Juaneda, Ernesto, Laróvere, Laura E.

    Published 2022
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  9. 209
    Bone Diseases as the only clinical manifestation of gaucher disease type

    Bone Diseases as the only clinical manifestation of gaucher disease type by Guelbert, Norberto, Robledo, Hugo, Becerra, Walter, Angaroni, Celia, Giner Ayala, Alicia, Ramírez Oller, Ana María, Dodelson Kremmer, Raquel

    Published 2021
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  10. 210
    Daño cronico irreversible en lupus erimatoso sistemico /

    Daño cronico irreversible en lupus erimatoso sistemico / by Drenkard, Cristina Marta

    Published 2002
    Thesis Book

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