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Items: 1 to 50 of 143

1.

Correspondence regarding the systematic review entitled 'Evidence-based treatment of multicystic dysplastic kidney: a systematic review'.

Printza N, Vargiami E, Kondou A, Dotis J, Stabouli S, Tsikopoulos G, Zafeiriou D.

J Pediatr Urol. 2019 May;15(3):291-292. doi: 10.1016/j.jpurol.2019.02.023. Epub 2019 Mar 19. No abstract available.

PMID:
30962010
2.

Neurological complications in childhood nephrotic syndrome: A systematic review.

Stabouli S, Chrysaidou K, Kupferman JC, Zafeiriou DI.

Eur J Paediatr Neurol. 2019 May;23(3):384-391. doi: 10.1016/j.ejpn.2019.02.007. Epub 2019 Feb 22. Review.

PMID:
30837193
3.

Test of Everyday Attention for Children (TEA-Ch): Greek Normative Data and Discriminative Validity for Children with Combined Type of Attention Deficit-Hyperactivity Disorder.

Malegiannaki AC, Aretouli E, Metallidou P, Messinis L, Zafeiriou D, Kosmidis MH.

Dev Neuropsychol. 2019 Mar-Apr;44(2):189-202. doi: 10.1080/87565641.2019.1578781. Epub 2019 Feb 20.

PMID:
30786760
4.

Sleep disorders and executive function in children and adolescents with chronic kidney disease.

Stabouli S, Gidaris D, Printza N, Dotis J, Papadimitriou E, Chrysaidou K, Papachristou F, Zafeiriou D.

Sleep Med. 2019 Mar;55:33-39. doi: 10.1016/j.sleep.2018.11.020. Epub 2018 Dec 14.

PMID:
30743208
5.

Response to "Leigh-like syndrome with mild mtDNA depletion due to the SUCLG1 variant c.626C>A".

Chinopoulos C, Wevers RA, Waterham HR, Zafeiriou D.

Mol Genet Metab Rep. 2018 Dec 13;18:10. doi: 10.1016/j.ymgmr.2018.12.002. eCollection 2019 Mar. No abstract available.

6.

Fetal ventriculomegaly: What we have and what is still missing.

D'Antonio F, Zafeiriou DI.

Eur J Paediatr Neurol. 2018 Nov;22(6):898-899. doi: 10.1016/j.ejpn.2018.11.005. No abstract available.

PMID:
30573223
7.

Arterial Stiffness in a Toddler with Neurofibromatosis Type 1 and Refractory Hypertension.

Stabouli S, Vargiami E, Maliachova O, Printza N, Dotis J, Kyriazi M, Papazoglou KO, Zafeiriou D.

Case Rep Pediatr. 2018 Oct 31;2018:5957987. doi: 10.1155/2018/5957987. eCollection 2018.

8.

Mutated SUCLG1 causes mislocalization of SUCLG2 protein, morphological alterations of mitochondria and an early-onset severe neurometabolic disorder.

Chinopoulos C, Batzios S, van den Heuvel LP, Rodenburg R, Smeets R, Waterham HR, Turkenburg M, Ruiter JP, Wanders RJA, Doczi J, Horvath G, Dobolyi A, Vargiami E, Wevers RA, Zafeiriou D.

Mol Genet Metab. 2019 Jan;126(1):43-52. doi: 10.1016/j.ymgme.2018.11.009. Epub 2018 Nov 16.

PMID:
30470562
9.

Fetal stroke and cerebrovascular disease: Advances in understanding from lenticulostriate and venous imaging, alloimmune thrombocytopaenia and monochorionic twins.

Kirkham FJ, Zafeiriou D, Howe D, Czarpran P, Harris A, Gunny R, Vollmer B.

Eur J Paediatr Neurol. 2018 Nov;22(6):989-1005. doi: 10.1016/j.ejpn.2018.08.008. Epub 2018 Sep 11. Review.

PMID:
30467085
10.

Diagnosis of tuberous sclerosis complex in the fetus.

Dragoumi P, O'Callaghan F, Zafeiriou DI.

Eur J Paediatr Neurol. 2018 Nov;22(6):1027-1034. doi: 10.1016/j.ejpn.2018.08.005. Epub 2018 Sep 12. Review.

PMID:
30279084
11.

Prenatal aspects in spinal muscular atrophy: From early detection to early presymptomatic intervention.

Tizzano EF, Zafeiriou D.

Eur J Paediatr Neurol. 2018 Nov;22(6):944-950. doi: 10.1016/j.ejpn.2018.08.009. Epub 2018 Sep 3. Review.

PMID:
30219357
12.

Mortality After Pediatric Arterial Ischemic Stroke.

Beslow LA, Dowling MM, Hassanein SMA, Lynch JK, Zafeiriou D, Sun LR, Kopyta I, Titomanlio L, Kolk A, Chan A, Biller J, Grabowski EF, Abdalla AA, Mackay MT, deVeber G; International Pediatric Stroke Study Investigators.

Pediatrics. 2018 May;141(5). pii: e20174146. doi: 10.1542/peds.2017-4146.

13.

Neurological outcome at 6 and 12 months corrected age in hospitalised late preterm infants -a prospective study.

Chatziioannidis I, Kyriakidou M, Exadaktylou S, Antoniou E, Zafeiriou D, Nikolaidis N.

Eur J Paediatr Neurol. 2018 Jul;22(4):602-609. doi: 10.1016/j.ejpn.2018.02.013. Epub 2018 Mar 6.

PMID:
29571948
14.

Screening for TSC1 and TSC2 mutations using NGS in Greek children with tuberous sclerosis syndrome.

Papadopoulou A, Dinopoulos A, Koutsodontis G, Pons R, Vorgia P, Koute V, Vratimos A, Zafeiriou D.

Eur J Paediatr Neurol. 2018 May;22(3):419-426. doi: 10.1016/j.ejpn.2018.01.026. Epub 2018 Feb 9.

PMID:
29500070
15.

Intracerebral gene therapy in children with mucopolysaccharidosis type IIIB syndrome: an uncontrolled phase 1/2 clinical trial.

Tardieu M, Zérah M, Gougeon ML, Ausseil J, de Bournonville S, Husson B, Zafeiriou D, Parenti G, Bourget P, Poirier B, Furlan V, Artaud C, Baugnon T, Roujeau T, Crystal RG, Meyer C, Deiva K, Heard JM.

Lancet Neurol. 2017 Sep;16(9):712-720. doi: 10.1016/S1474-4422(17)30169-2. Epub 2017 Jul 14.

PMID:
28713035
16.

Diagnosis of tuberous sclerosis complex in a patient referred for uncontrolled hypertension and renal dysfunction: a case highlighting the importance of proper diagnostic work-up of hypertensive patients.

Sarafidis PA, Bikos A, Loutradis C, Tzikas S, Vakirlis E, Avdelidou E, Zafeiriou D, Papagianni A, Vassilikos V.

J Hypertens. 2017 Oct;35(10):2109-2114. doi: 10.1097/HJH.0000000000001423.

PMID:
28594706
17.

Application of high-resolution array comparative genomic hybridization in children with unknown syndromic microcephaly.

Tsoutsou E, Tzetis M, Giannikou K, Braoudaki M, Mitrakos A, Amenta S, Selenti N, Kanavakis E, Zafeiriou D, Kitsiou-Tzeli S, Fryssira H.

Pediatr Res. 2017 Aug;82(2):253-260. doi: 10.1038/pr.2017.65. Epub 2017 May 24.

PMID:
28422950
18.
19.

Management goals for type 1 Gaucher disease: An expert consensus document from the European working group on Gaucher disease.

Biegstraaten M, Cox TM, Belmatoug N, Berger MG, Collin-Histed T, Vom Dahl S, Di Rocco M, Fraga C, Giona F, Giraldo P, Hasanhodzic M, Hughes DA, Iversen PO, Kiewiet AI, Lukina E, Machaczka M, Marinakis T, Mengel E, Pastores GM, Plöckinger U, Rosenbaum H, Serratrice C, Symeonidis A, Szer J, Timmerman J, Tylki-Szymańska A, Weisz Hubshman M, Zafeiriou DI, Zimran A, Hollak CEM.

Blood Cells Mol Dis. 2018 Feb;68:203-208. doi: 10.1016/j.bcmd.2016.10.008. Epub 2016 Oct 24.

20.

Investigation of the motor system in two siblings with Canavan's disease: a combined transcranial magnetic stimulation (TMS) - diffusion tensor imaging (DTI) study.

Kimiskidis VK, Papaliagkas V, Papagiannopoulos S, Zafeiriou D, Kazis D, Tsatsali-Foroglou E, Kouvatsou Z, Kapina V, Koutsonikolas D, Anogianakis G, Geroukis T, Bostantjopoulou S.

Metab Brain Dis. 2017 Apr;32(2):307-310. doi: 10.1007/s11011-017-9955-x. Epub 2017 Jan 28.

PMID:
28130616
21.

The Spectrum of Niemann-Pick Type C Disease in Greece.

Mavridou I, Dimitriou E, Vanier MT, Vilageliu L, Grinberg D, Latour P, Xaidara A, Lycopoulou L, Bostantjopoulou S, Zafeiriou D, Michelakakis H.

JIMD Rep. 2017;36:41-48. doi: 10.1007/8904_2016_41. Epub 2017 Jan 20.

22.

Stroke and Hypertension in Children and Adolescents.

Kupferman JC, Zafeiriou DI, Lande MB, Kirkham FJ, Pavlakis SG.

J Child Neurol. 2017 Mar;32(4):408-417. doi: 10.1177/0883073816685240. Epub 2016 Dec 26. Review.

PMID:
28019129
23.

Neuroradiological, neurophysiological and molecular findings in infantile Krabbe disease: two case reports.

Vargiami E, Papathanasiou E, Batzios S, Kyriazi M, Dimitriou E, Anastasiou A, Michelakakis H, Giese AK, Zafeiriou DI.

Balkan J Med Genet. 2016 Aug 2;19(1):85-90. eCollection 2016 Jul 1.

24.

Brittle Hair, Photosensitivity, Brain Hypomyelination and Immunodeficiency: Clues to Trichothiodystrophy.

Farmaki E, Nedelkopoulou N, Delli F, Sarafidis K, Zafeiriou DI.

Indian J Pediatr. 2017 Jan;84(1):89-90. doi: 10.1007/s12098-016-2209-9. Epub 2016 Jul 30. No abstract available.

PMID:
27473476
25.

The brainstem in late preterm birth: Born small-for-gestational-age is the "tip of the iceberg".

Zafeiriou DI.

Clin Neurophysiol. 2016 Sep;127(9):3178-3179. doi: 10.1016/j.clinph.2016.05.366. Epub 2016 Jun 11. No abstract available.

PMID:
27353720
26.

Exome Sequencing and the Management of Neurometabolic Disorders.

Tarailo-Graovac M, Shyr C, Ross CJ, Horvath GA, Salvarinova R, Ye XC, Zhang LH, Bhavsar AP, Lee JJ, Drögemöller BI, Abdelsayed M, Alfadhel M, Armstrong L, Baumgartner MR, Burda P, Connolly MB, Cameron J, Demos M, Dewan T, Dionne J, Evans AM, Friedman JM, Garber I, Lewis S, Ling J, Mandal R, Mattman A, McKinnon M, Michoulas A, Metzger D, Ogunbayo OA, Rakic B, Rozmus J, Ruben P, Sayson B, Santra S, Schultz KR, Selby K, Shekel P, Sirrs S, Skrypnyk C, Superti-Furga A, Turvey SE, Van Allen MI, Wishart D, Wu J, Wu J, Zafeiriou D, Kluijtmans L, Wevers RA, Eydoux P, Lehman AM, Vallance H, Stockler-Ipsiroglu S, Sinclair G, Wasserman WW, van Karnebeek CD.

N Engl J Med. 2016 Jun 9;374(23):2246-55. doi: 10.1056/NEJMoa1515792. Epub 2016 May 25.

27.

Multiple Coronary Artery Microfistulas in a Girl with Kleefstra Syndrome.

Vargiami E, Ververi A, Al-Mutawa H, Gioula G, Gerou S, Rouvalis F, Kambouris M, Zafeiriou DI.

Case Rep Genet. 2016;2016:3056053. doi: 10.1155/2016/3056053. Epub 2016 Apr 30.

28.

Neurological Involvement in a Thalassemic Child Receiving Deferiprone.

Economou M, Teli A, Gourtsa V, Vargiami E, Zafeiriou D.

J Pediatr Hematol Oncol. 2016 Jul;38(5):406. doi: 10.1097/MPH.0000000000000579. No abstract available.

PMID:
27164520
29.

An emerging cause of concern in Europe: Zika virus, the developing CNS and the pediatric neurologist.

Gioula G, Nunes ML, Zafeiriou DI.

Eur J Paediatr Neurol. 2016 Jul;20(4):497-9. doi: 10.1016/j.ejpn.2016.04.017. Epub 2016 Apr 28. No abstract available.

PMID:
27160366
30.

Nephrocalcinosis and Renal Failure in Lesch-Nyhan Syndrome: Report of Two Familial Cases and Review of the Literature.

Vargiami E, Printza N, Papadimiditriou E, Batzios S, Kyriazi M, Papachristou F, Zafeiriou DI.

Urology. 2016 Nov;97:194-196. doi: 10.1016/j.urology.2016.04.004. Epub 2016 Apr 11. Review.

PMID:
27079129
31.

Benign epilepsy with centrotemporal spikes: Relationship between type of seizures and response to medication in a Greek population.

Gkampeta A, Fidani L, Zafeiriou D, Pavlou E.

J Neurosci Rural Pract. 2015 Oct-Dec;6(4):545-8. doi: 10.4103/0976-3147.165420.

32.

Bayley-III scales at 12 months of corrected age in preterm infants: Patterns of developmental performance and correlations to environmental and biological influences.

Velikos K, Soubasi V, Michalettou I, Sarafidis K, Nakas C, Papadopoulou V, Zafeiriou D, Drossou V.

Res Dev Disabil. 2015 Oct-Nov;45-46:110-9. doi: 10.1016/j.ridd.2015.07.014. Epub 2015 Jul 28.

PMID:
26232203
33.

Brainstem Auditory Evoked Potentials in Boys with Autism: Still Searching for the Hidden Truth.

Ververi A, Vargiami E, Papadopoulou V, Tryfonas D, Zafeiriou D.

Iran J Child Neurol. 2015 Spring;9(2):21-8.

34.

Association between iron deficiency and febrile seizures.

Papageorgiou V, Vargiami E, Kontopoulos E, Kardaras P, Economou M, Athanassiou-Mataxa M, Kirkham F, Zafeiriou DI.

Eur J Paediatr Neurol. 2015 Sep;19(5):591-6. doi: 10.1016/j.ejpn.2015.05.009. Epub 2015 Jun 12.

PMID:
26112262
35.

Stüve-Wiedemann syndrome in a neonate.

Sarafidis K, Piretzi K, Agakidou E, Kohlhase J, Zafeiriou D.

Pediatr Int. 2015 Apr;57(2):302-4. doi: 10.1111/ped.12431.

PMID:
25868946
36.

Mobilization of circulating progenitor cells following brain injury in premature neonates could be indicative of an endogenous repair process. A pilot study.

Efstathiou N, Soubasi V, Koliakos G, Kyriazis G, Zafeiriou DI, Slavakis A, Kantziou K, Pozotou T, Chatzizisi O, Drosou-Agakidou V.

Hippokratia. 2015 Apr-Jun;19(2):141-7.

37.

Paroxysmal tonic upward gaze of childhood "plus": an oculomotor channelopathy?

Zafeiriou DI.

Eur J Paediatr Neurol. 2015 May;19(3):278-9. doi: 10.1016/j.ejpn.2015.03.003. Epub 2015 Mar 13. No abstract available.

PMID:
25800877
38.

Growth hormone replacement therapy in Costello syndrome.

Triantafyllou P, Christoforidis A, Vargiami E, Zafeiriou DI.

Growth Horm IGF Res. 2014 Dec;24(6):271-5. doi: 10.1016/j.ghir.2014.10.001.

PMID:
25459872
39.

Association of brain-derived neurotrophic factor (BDNF) and elongator protein complex 4 (ELP4) polymorphisms with benign epilepsy with centrotemporal spikes in a Greek population.

Gkampeta A, Fidani L, Clarimón J, Kalinderi K, Katopodi T, Zafeiriou D, Pavlou E.

Epilepsy Res. 2014 Dec;108(10):1734-9. doi: 10.1016/j.eplepsyres.2014.09.005. Epub 2014 Sep 22.

PMID:
25301525
40.

Comparative Study of Refractive Errors, Strabismus, Microsaccades, and Visual Perception Between Preterm and Full-Term Children With Infantile Cerebral Palsy.

Kozeis N, Panos GD, Zafeiriou DI, de Gottrau P, Gatzioufas Z.

J Child Neurol. 2015 Jul;30(8):972-5. doi: 10.1177/0883073814549248. Epub 2014 Oct 7.

PMID:
25296927
41.

Neurophysiologic evaluation of infants with congenital hypothyroidism before and after treatment.

Triantafyllou P, Katzos G, Rousso I, Zafeiriou D.

Acta Neurol Belg. 2015 Jun;115(2):129-36. doi: 10.1007/s13760-014-0331-x. Epub 2014 Jul 23.

PMID:
25052510
42.

High-fidelity over the somatosensory cortex revisited: back to basics.

Zafeiriou DI, Vargiami E.

Clin Neurophysiol. 2015 Feb;126(2):223-4. doi: 10.1016/j.clinph.2014.06.009. Epub 2014 Jun 25. No abstract available.

PMID:
25022793
43.

Moyamoya syndrome and neurofibromatosis type 1.

Vargiami E, Sapountzi E, Samakovitis D, Batzios S, Kyriazi M, Anastasiou A, Zafeiriou DI.

Ital J Pediatr. 2014 Jun 21;40:59. doi: 10.1186/1824-7288-40-59.

44.

Early-onset diabetes mellitus and neurodevelopmental retardation: the first Greek case of Wolcott-Rallison syndrome.

Triantafyllou P, Vargiami E, Vagianou I, Badouraki M, Julier C, Zafeiriou DI.

J Pediatr Endocrinol Metab. 2014 Sep;27(9-10):967-70. doi: 10.1515/jpem-2013-0469.

PMID:
24859506
45.

Multiple endocrine disorders associated with adrenomyeloneuropathy and a novel mutation of the ABCD1 gene.

Triantafyllou P, Economou M, Vlachaki E, Aggelaki M, Athanassiou-Mataxa M, Michelakaki E, Zafeiriou DI.

Pediatr Neurol. 2014 Jun;50(6):622-4. doi: 10.1016/j.pediatrneurol.2014.01.027. Epub 2014 Jan 16.

PMID:
24685009
46.

Severe clinical presentation in monozygotic twins with 10p15.3 microdeletion syndrome.

Vargiami E, Ververi A, Kyriazi M, Papathanasiou E, Gioula G, Gerou S, Al-Mutawa H, Kambouris M, Zafeiriou DI.

Am J Med Genet A. 2014 Mar;164A(3):764-8. doi: 10.1002/ajmg.a.36329. Epub 2013 Dec 19.

PMID:
24357427
47.

Clinical course and seizure outcome of idiopathic childhood epilepsy: determinants of early and long-term prognosis.

Dragoumi P, Tzetzi O, Vargiami E, Pavlou E, Krikonis K, Kontopoulos E, Zafeiriou DI.

BMC Neurol. 2013 Dec 18;13:206. doi: 10.1186/1471-2377-13-206.

48.

Update on transcobalamin deficiency: clinical presentation, treatment and outcome.

Trakadis YJ, Alfares A, Bodamer OA, Buyukavci M, Christodoulou J, Connor P, Glamuzina E, Gonzalez-Fernandez F, Bibi H, Echenne B, Manoli I, Mitchell J, Nordwall M, Prasad C, Scaglia F, Schiff M, Schrewe B, Touati G, Tchan MC, Varet B, Venditti CP, Zafeiriou D, Rupar CA, Rosenblatt DS, Watkins D, Braverman N.

J Inherit Metab Dis. 2014 May;37(3):461-73. doi: 10.1007/s10545-013-9664-5. Epub 2013 Dec 5.

PMID:
24305960
49.

Incontinentia pigmenti: a skin, brain, and eye matter.

Zafeiriou DI, Vargiami E, Hatzidimitriou V, Kyriazi M.

J Pediatr. 2013 Nov;163(5):1520. doi: 10.1016/j.jpeds.2013.06.029. Epub 2013 Jul 26. No abstract available.

PMID:
23896188
50.

Endothelial activation and inflammation biomarkers in children and adolescents with sickle cell disease.

Hatzipantelis ES, Pana ZD, Gombakis N, Taparkou A, Tzimouli V, Kleta D, Zafeiriou DJ, Garipidou V, Kanakoudi F, Athanassiou M.

Int J Hematol. 2013 Aug;98(2):158-63. doi: 10.1007/s12185-013-1392-y. Epub 2013 Jun 27.

PMID:
23807289

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