Zafeiriou D - Search Results

1

Three Individuals with PURA Syndrome in a Cohort of Patients with Neuromuscular Disease.

Mroczek M, Zafeiriou D, Gurgel-Gianetti J, Vilela Morais de Azevedo B, Roos A, Bartels E, Kohlschmidt N, Phadke R, Feng L, Duff J, Töpf A, Straub V. Mroczek M, et al. Among authors: zafeiriou d. Neuropediatrics. 2021 Oct;52(5):390-393. doi: 10.1055/s-0040-1715625. Epub 2020 Dec 22. Neuropediatrics. 2021. PMID: 33352606

2

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.

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

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

5

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

6

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

7

The Complex Interplay of Cortex, Cerebellum, and Age in a Cohort of Pediatric Patients With Tuberous Sclerosis Complex.

Sidira C, Vargiami E, Anastasiou A, Talimtzi P, Kyriazi M, Dragoumi P, Spanou M, Ntinopoulos A, Dalpa E, Evangeliou A, Zafeiriou DI. Sidira C, et al. Pediatr Neurol. 2021 Oct;123:43-49. doi: 10.1016/j.pediatrneurol.2021.06.009. Epub 2021 Jun 26. Pediatr Neurol. 2021. PMID: 34399109

8

Neuromuscular diseases and their cardiac manifestations under the spectrum of cardiovascular imaging.

Alexandridis GM, Pagourelias ED, Fragakis N, Kyriazi M, Vargiami E, Zafeiriou D, Vassilikos VP. Alexandridis GM, et al. Among authors: zafeiriou d. Heart Fail Rev. 2022 Nov;27(6):2045-2058. doi: 10.1007/s10741-022-10260-8. Epub 2022 Jul 20. Heart Fail Rev. 2022. PMID: 35857244 Review.

9

Xeroderma pigmentosum group G with severe neurological involvement and features of Cockayne syndrome in infancy.

Zafeiriou DI, Thorel F, Andreou A, Kleijer WJ, Raams A, Garritsen VH, Gombakis N, Jaspers NG, Clarkson SG. Zafeiriou DI, et al. Pediatr Res. 2001 Mar;49(3):407-12. doi: 10.1203/00006450-200103000-00016. Pediatr Res. 2001. PMID: 11228268

10

Self-mutilation and mental retardation: clues to congenital insensitivity to pain with anhidrosis.

Zafeiriou DI, Vargiami E, Economou M, Gombakis N. Zafeiriou DI, et al. J Pediatr. 2004 Feb;144(2):284. doi: 10.1016/S0022-3476(03)00385-8. J Pediatr. 2004. PMID: 14760280 No abstract available.

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