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Experimental evidence of oxidative stress in plasma of homocystinuric patients: A possible role for homocysteine

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Segmental uniparental disomy leading to homozygosity for a pathogenic mutation in three recessive metabolic diseases

(2011) Belén Pérez et al.   MOLECULAR GENETICS AND METABOLISM

Different altered pattern expression of genes related to apoptosis in isolated methylmalonic aciduria cblB type and combined with homocystinuria cblC type

(2010) Ana Jorge-Finnigan et al.   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE

Isolated remethylation disorders: do our treatments benefit patients?

(2010) Manuel Schiff et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Genetic and cellular studies of oxidative stress in methylmalonic aciduria (MMA) cobalamin deficiency type C (cblC) with homocystinuria (MMACHC)

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Homocysteine promotes proliferation and activation of microglia

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Mitochondrial dysfunction in mut methylmalonic acidemia

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