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Browsing by Author Zafeiriou, D.I.
Showing results 1 to 4 of 4
| Full Text | Issue Date | Title | Author(s) | | 2010 | Tyrosine hydroxylase deficiency: a treatable disorder of brain catecholamine biosynthesis. | Willemsen, M.A.A.P.; Verbeek, M.M.; Kamsteeg, E.J.; Rijk-van Andel, J.F. de; Aeby, A., et al |
| 2009 | Tyrosine hydroxylase deficiency with severe clinical course. | Zafeiriou, D.I.; Willemsen, M.A.A.P.; Verbeek, M.M.; Vargiami, E.; Ververi, A., et al |
| 2008 | MR spectroscopy and serial magnetic resonance imaging in a patient with mitochondrial cystic leukoencephalopathy due to complex I deficiency and NDUFV1 mutations and mild clinical course. | Zafeiriou, D.I.; Rodenburg, R.J.; Scheffer, H.; Heuvel, L.P.v.d.; Pouwels, P.J., et al |
| 2008 | Two Greek siblings with sepiapterin reductase deficiency. | Verbeek, M.M.; Willemsen, M.A.A.P.; Wevers, R.A.; Lagerwerf, A.J.; Abeling, N.G., et al |
Showing results 1 to 4 of 4
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