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Results: 2

Authors: De Kremer, RD Paschini-Capra, A Bacman, S Argarana, C Civallero, G Kelley, RI Guelbert, N Latini, A de Halac, IN Giner-Ayala, A Johnston, J Proujansky, R Gonzalez, I Depetris-Boldini, C Oller-Ramirez, A Angaroni, C Theaux, RA Hliba, E Juaneda, E
Citation: Rd. De Kremer et al., Barth's syndrome-like disorder: A new phenotype with a maternally inherited A3243G substitution of mitochondrial DNA (MELAS mutation), AM J MED G, 99(2), 2001, pp. 83-93

Authors: Depetris-Boldini, C Galetto, R Videla, MP Dodelson, RD
Citation: C. Depetris-boldini et al., Increased excretion of coproporphyrin I in a patient with hereditary tyrosinaemia type I: Relevant changes with NTBC treatment, J INH MET D, 22(3), 1999, pp. 227-230
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