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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: vargiami e. 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
Russell's diencephalic syndrome.
Zafeiriou DI, Koliouskas D, Vargiami E, Gombakis N. Zafeiriou DI, et al. Among authors: vargiami e. Neurology. 2001 Sep 11;57(5):932. doi: 10.1212/wnl.57.5.932. Neurology. 2001. PMID: 11552038 No abstract available.
Cerebellar agenesis and diabetes insipidus.
Zafeiriou DI, Vargiami E, Boltshauser E. Zafeiriou DI, et al. Among authors: vargiami e. Neuropediatrics. 2004 Dec;35(6):364-7. doi: 10.1055/s-2004-830369. Neuropediatrics. 2004. PMID: 15627945 Review.
Ethylmalonic encephalopathy: clinical and biochemical observations.
Zafeiriou DI, Augoustides-Savvopoulou P, Haas D, Smet J, Triantafyllou P, Vargiami E, Tamiolaki M, Gombakis N, van Coster R, Sewell AC, Vianey-Saban C, Gregersen N. Zafeiriou DI, et al. Among authors: vargiami e. Neuropediatrics. 2007 Apr;38(2):78-82. doi: 10.1055/s-2007-984447. Neuropediatrics. 2007. PMID: 17712735
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: vargiami e. 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
65 results