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Page 1
Tyrosine hydroxylase deficiency with severe clinical course.
Zafeiriou DI, Willemsen MA, Verbeek MM, Vargiami E, Ververi A, Wevers R. Zafeiriou DI, et al. Among authors: ververi a. Mol Genet Metab. 2009 May;97(1):18-20. doi: 10.1016/j.ymgme.2009.02.001. Epub 2009 Feb 10. Mol Genet Metab. 2009. PMID: 19282209
L-2-Hydroxyglutaric aciduria presenting with severe autistic features.
Zafeiriou DI, Ververi A, Salomons GS, Vargiami E, Haas D, Papadopoulou V, Kontopoulos E, Jakobs C. Zafeiriou DI, et al. Among authors: ververi a. Brain Dev. 2008 Apr;30(4):305-7. doi: 10.1016/j.braindev.2007.09.005. Epub 2007 Nov 5. Brain Dev. 2008. PMID: 17981416
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 DI, Rodenburg RJ, Scheffer H, van den Heuvel LP, Pouwels PJ, Ververi A, Athanasiadou-Piperopoulou F, van der Knaap MS. Zafeiriou DI, et al. Among authors: ververi a. Neuropediatrics. 2008 Jun;39(3):172-5. doi: 10.1055/s-0028-1093336. Epub 2008 Nov 7. Neuropediatrics. 2008. PMID: 18991197
Childhood autism and auditory system abnormalities.
Hitoglou M, Ververi A, Antoniadis A, Zafeiriou DI. Hitoglou M, et al. Among authors: ververi a. Pediatr Neurol. 2010 May;42(5):309-14. doi: 10.1016/j.pediatrneurol.2009.10.009. Pediatr Neurol. 2010. PMID: 20399382 Review.
40 results