Publications
- Neurotransmitter disorders in childhood and differential diagnosis2010 | Publication without faculty affiliation
- Girl with congenital disorder of glycosylation - case report2009 | Publication without faculty affiliation
- Development of a human mitochondrial oligonucleotide microarray (h-MitoArray) and gene expression analysis of fibroblast cell lines from 13 patients with isolated FIFo ATP synthase deficiency2008 | Publication without faculty affiliation
- Clinical Manifestations and Results of Laboratory Examinations in Four Patients with Alpha-Mannosidosis2008 | Publication without faculty affiliation
- TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy2008 | Publication without faculty affiliation
- Globoid cell leukodystrophy (Krebbe's disease). A series of Czech patients and a survey of current views of biology and differential2006 | Publication without faculty affiliation
- Mitochondiral inheritance2005 | Publication without faculty affiliation
- Newborn screening of inherited metabolic disorders by tandem mass spectrometry2005 | Publication without faculty affiliation
- Abnormalities in succinzlpurines in fumarse deficiency.2000 | Publication without faculty affiliation
- The first polymofismus causing an amino acid exchange in patients with X-ALD.2000 | Publication without faculty affiliation
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