- Polymicrogyria with dysmorphic basal ganglia? Think tubulin!
- Array comparative genomic hybridization in male infertility
- Inborn oxidative phosphorylation defect as risk factor for propofol infusion syndrome
- TUBA1A mutations: from isolated lissencephaly to familial polymicrogyria
- Immunohistochemical analysis of the oxidative phosphorylation complexes in skeletal muscle from patients with mitochondrial DNA encoded tRNA gene defects
- MITOCHONDRIAL ABNORMALITIES IN A NEWBORN WITH LACTIC ACIDOSIS AND ADRENAL CALCIFICATIONS
Role of BN-page in the diagnosis of mitochondrial DNA depletion
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Immunostaining technniques in patients with mtDNA depletion
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- Do we need to search for gr/gr deletions in infertile men in a clinical setting?
- The presence of complex V subcomplexes in patients with defective intramitochondrial protein translation.