Zafeiriou DI - Search Results

1

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. Neuropediatrics. 2008 Jun;39(3):172-5. doi: 10.1055/s-0028-1093336. Epub 2008 Nov 7. Neuropediatrics. 2008. PMID: 18991197

2

Protracted course of N-acetylaspartic aciduria in two non-Jewish siblings: identical clinical and magnetic resonance imaging findings.

Zafeiriou DI, Kleijer WJ, Maroupoulos G, Anastasiou AL, Augoustidou-Savvopoulou P, Papadopoulou F, Kontopoulos EE, Fagan E, Payne S. Zafeiriou DI, et al. Brain Dev. 1999 Apr;21(3):205-8. Brain Dev. 1999. PMID: 10372908

3

Atypical and variable clinical presentation of glutaric aciduria type I.

Zafeiriou DI, Zschocke J, Augoustidou-Savvopoulou P, Mauromatis I, Sewell A, Kontopoulos E, Katzos G, Hoffmann GF. Zafeiriou DI, et al. Neuropediatrics. 2000 Dec;31(6):303-6. doi: 10.1055/s-2000-12943. Neuropediatrics. 2000. PMID: 11508549

4

Serial magnetic resonance imaging findings in mucopolysaccharidosis IIIB (Sanfilippo's syndrome B).

Zafeiriou DI, Savvopoulou-Augoustidou PA, Sewell A, Papadopoulou F, Badouraki M, Vargiami E, Gombakis NP, Katzos GS. Zafeiriou DI, et al. Brain Dev. 2001 Oct;23(6):385-9. doi: 10.1016/s0387-7604(01)00242-x. Brain Dev. 2001. PMID: 11578848 Clinical Trial.

5

Cerebellar agenesis and diabetes insipidus.

Zafeiriou DI, Vargiami E, Boltshauser E. Zafeiriou DI, et al. Neuropediatrics. 2004 Dec;35(6):364-7. doi: 10.1055/s-2004-830369. Neuropediatrics. 2004. PMID: 15627945 Review.

6

Possible genotype-phenotype correlations in children with mild clinical course of Canavan disease.

Tacke U, Olbrich H, Sass JO, Fekete A, Horvath J, Ziyeh S, Kleijer WJ, Rolland MO, Fisher S, Payne S, Vargiami E, Zafeiriou DI, Omran H. Tacke U, et al. Among authors: zafeiriou di. Neuropediatrics. 2005 Aug;36(4):252-5. doi: 10.1055/s-2005-865865. Neuropediatrics. 2005. PMID: 16138249

7

Childhood autism and associated comorbidities.

Zafeiriou DI, Ververi A, Vargiami E. Zafeiriou DI, et al. Brain Dev. 2007 Jun;29(5):257-72. doi: 10.1016/j.braindev.2006.09.003. Epub 2006 Nov 7. Brain Dev. 2007. PMID: 17084999 Review.

8

3-Hydroxy-3-methylglutaryl coenzyme a lyase deficiency with reversible white matter changes after treatment.

Zafeiriou DI, Vargiami E, Mayapetek E, Augoustidou-Savvopoulou P, Mitchell GA. Zafeiriou DI, et al. Pediatr Neurol. 2007 Jul;37(1):47-50. doi: 10.1016/j.pediatrneurol.2007.02.007. Pediatr Neurol. 2007. PMID: 17628222

9

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. Neuropediatrics. 2007 Apr;38(2):78-82. doi: 10.1055/s-2007-984447. Neuropediatrics. 2007. PMID: 17712735

10

Serial magnetic resonance imaging and neurophysiological studies in multiple sulphatase deficiency.

Zafeiriou DI, Vargiami E, Papadopoulou K, Dimitriou E, Mavridou I, Santamaria R, Canals I, Michelakakis H. Zafeiriou DI, et al. Eur J Paediatr Neurol. 2008 May;12(3):190-4. doi: 10.1016/j.ejpn.2007.07.015. Epub 2007 Sep 18. Eur J Paediatr Neurol. 2008. PMID: 17881260

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