Long-term neurological outcome of a cohort of 80 patients with classical organic acidurias

Renal transplantation in 4 patients with methylmalonic aciduria: A cell therapy for metabolic disease

(2013) A. Brassier et al.   MOLECULAR GENETICS AND METABOLISM

Propionic acidemia: clinical course and outcome in 55 pediatric and adolescent patients

(2013) Sarah C Grünert et al.   Orphanet Journal of Rare Diseases

Clinical variability of isovaleric acidemia in a genetically homogeneous population

(2012) M. Dercksen et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Clinical and molecular findings in Thai patients with isolated methylmalonic acidemia

(2012) Nithiwat Vatanavicharn et al.   MOLECULAR GENETICS AND METABOLISM

Clinical and neurocognitive outcome in symptomatic isovaleric acidemia

(2012) Sarah C Grünert et al.   Orphanet Journal of Rare Diseases

Disruption of mitochondrial homeostasis in organic acidurias: insights from human and animal studies

(2011) Moacir Wajner et al.   JOURNAL OF BIOENERGETICS AND BIOMEMBRANES

Neurologic considerations in propionic acidemia

(2011) John Schreiber et al.   MOLECULAR GENETICS AND METABOLISM

Prediction of outcome in isolated methylmalonic acidurias: combined use of clinical and biochemical parameters

(2009) F. Hörster et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Long-term outcome in methylmalonic aciduria: A series of 30 French patients

(2009) M.A. Cosson et al.   MOLECULAR GENETICS AND METABOLISM

Multiple OXPHOS Deficiency in the Liver, Kidney, Heart, and Skeletal Muscle of Patients With Methylmalonic Aciduria and Propionic Aciduria

(2009) Yves de Keyzer et al.   PEDIATRIC RESEARCH

Liver hepatoblastoma and multiple OXPHOS deficiency in the follow-up of a patient with methylmalonic aciduria

(2008) M.A. Cosson et al.   MOLECULAR GENETICS AND METABOLISM