Treffer 1 - 3 von 3 für Suche 'Boldini, Catalina D.', Suchdauer: 0,54s Treffer weiter einschränken
  1. 1
    Mucopolysaccharidosis type VII (β-glucuronidase deficiency): A chronic variant with an oligosymptomatic severe skeletal dysplasia

    Mucopolysaccharidosis type VII (β-glucuronidase deficiency): A chronic variant with an oligosymptomatic severe skeletal dysplasia von de Kremer, Raquel D., Givogri, Irene, Argaraña, Carlos E., Hliba, Ernesto, Conci, Rene, Boldini, Catalina D., Capra, Ana P.


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  2. 2
    Leukodystrophy and CSF purine abnormalities associated with isolated 3-methylcrotonyl-CoA carboxylase deficiency

    Leukodystrophy and CSF purine abnormalities associated with isolated 3-methylcrotonyl-CoA carboxylase deficiency von DODELSON DE KREMER, Raquel, LATINI, Alexandra, SUORMALA, Terttu, BAUMGARTNER, E. Regula, LAROVERE, Laura, CIVALLERO, Gabriel, GUELBERT, Norberto, PASCHINI-CAPRA, Ana, DEPETRIS-BOLDINI, Catalina, QUIROGA MAYOR, Carlos

    Veröffentlicht in Metabolic brain disease

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  3. 3
    Barth's syndrome-like disorder: A new phenotype with a maternally inherited A3243G substitution of mitochondrial DNA (MELAS mutation)

    Barth's syndrome-like disorder: A new phenotype with a maternally inherited A3243G substitution of mitochondrial DNA (MELAS mutation) von De Kremer, Raquel Dodelson, Paschini-Capra, Ana, Bacman, Sandra, Argaraña, Carlos, Civallero, Gabriel, Kelley, Richard I., Guelbert, Norberto, Latini, Alexandra, de Halac, Inés Noher, Giner-Ayala, Alicia, Johnston, Jennifer, Proujansky, Roy, Gonzalez, Iris, Depetris-Boldini, Catalina, Oller-Ramírez, Ana, Angaroni, Celia, Theaux, Ricardo A., Hliba, Ernesto, Juaneda, Ernesto


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