Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Eleni A. Vagiakou"'
Publikováno v:
Brain and Development. 24:732-735
A 12-month-old boy with progressive cranial nerve palsies followed by ventilatory failure demanding artificial ventilation, generalized muscle weakness, and rapid progression to death at the age of 21 months is described. The patient had normal early
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61e7a3f2ca5d8c9e84c1a97fc7790f7a
https://doi.org/10.1016/s0387-7604(02)00085-2
https://doi.org/10.1016/s0387-7604(02)00085-2
Autor:
Eleni A. Vagiakou, Basilios Tsagris, Stamatia Dimou, Maria Moustaki, Petros M. Zeis, Angeliki Skardoutsou, Konstantinos A. Voudris
Publikováno v:
Seizure. 11(6):377-380
This study aimed to investigate whether carbamazepine, sodium valproate or phenobarbital as monotherapy in ambulatory epileptic children with adequate sun exposure have some effect on their bone metabolism based on the determination of total serum al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fee67092e69d04c3c2cdfa32f2510ad4
Autor:
Eleni A. Vagiakou, Petros M. Zeis, Ioanna Haronitis, Konstantinos A. Voudris, Angeliki Skaardoutsou
Publikováno v:
European Journal of Paediatric Neurology. 5:199-202
Acute necrotizing encephalopathy following influenza A is frequently reported from Japan and Taiwan but is very rarely seen in Western countries. We describe a 10-year-old boy with acute necrotizing encephalopathy, who developed symmetrical thalamic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed4170479b140c2452bc51d283b6872c
https://doi.org/10.1053/ejpn.2000.0511
https://doi.org/10.1053/ejpn.2000.0511
Autor:
Eleni A. Vagiakou, Angeliki Skardoutsou, Dimitrios Gionnis, Sotiria Mastroyianni, Efstathia Katsarou, Panagiotis Mavromatis, Konstantinos A. Voudris
Publikováno v:
Journal of Child Neurology. 18:570-572
Acute necrotizing encephalopathy is a severe parainfectious disorder with a clear racial predilection for Oriental children living in the Far East. The prognosis was originally reported as grave; however, a mild form of the disease has recently been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d99ce5fdf24de0719da98d4cc812b8d8
https://doi.org/10.1177/08830738030180081301
https://doi.org/10.1177/08830738030180081301
Publikováno v:
Pediatric Dermatology. 20:371-373
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0347e86adafca2c92d2e5de39a75e1d9
https://doi.org/10.1046/j.1525-1470.2003.20326_3.x
https://doi.org/10.1046/j.1525-1470.2003.20326_3.x
Publikováno v:
Journal of Child Neurology. 17:904-906
Two infants with congenital microcephaly associated with the factor V Leiden mutation are described. In both cases, brain magnetic resonance imaging (MRI) revealed cerebral atrophy and porencephalic cystic lesions, which were probably attributable to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c2f42ac5b1e75a9f41a5b60cf7a959bd
https://doi.org/10.1177/08830738020170123001
https://doi.org/10.1177/08830738020170123001
Autor:
George Magoufis, Sotiria Mastroyianni, Angeliki Skardoutsou, Konstantinos A. Voudris, Eleni A. Vagiakou, Peter M. Koukoutsakis
Publikováno v:
Journal of child neurology. 22(4)
A 13-year-old Greek girl with pyruvate kinase deficiency and moya moya angiographic pattern is reported. She also had raised serum lipoprotein (a) concentration and was homozygous for the C677T mutation of the methylenetetrahydrofolate reductase gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f945476259f12bef349e5230590af31
https://pubmed.ncbi.nlm.nih.gov/17621533
https://pubmed.ncbi.nlm.nih.gov/17621533
Autor:
Sotiria Mastroyianni, Angeliki Skardoutsou, Eleni A. Vagiakou, Yvonne Dimitriou, Konstantinos A. Voudris
Publikováno v:
Journal of child neurology. 21(10)
Several cases with cerebral infarctions associated with the factor V Leiden mutation have been reported. However, bearing in mind the large number of asymptomatic individuals with the factor V Leiden mutation, additional risk factors for cerebral inf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97e09532717a5d990903380dd044f2a3
https://pubmed.ncbi.nlm.nih.gov/17005112
https://pubmed.ncbi.nlm.nih.gov/17005112
Autor:
Yboni Dimitriou, Eleni A. Vagiakou, Angeliki Skardoutsou, Konstantinos A. Voudris, Sotiria Mastroyianni
Publikováno v:
Journal of child neurology. 19(1)
A 3-month-old male infant with cytomegalovirus infection and intractable partial seizures was treated with ganciclovir for 6 weeks. The drug was well tolerated, and virus shedding in the cerebrospinal fluid and urine was eliminated, although infantil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fbc7ee5822de01c008d058081fc202c2
https://pubmed.ncbi.nlm.nih.gov/15032385
https://pubmed.ncbi.nlm.nih.gov/15032385
Publikováno v:
Seizure. 12(8)
A case of a 7-year-old male with epilepsy who developed non-convulsive status epilepticus (NCSE) with electroclinical features consistent with those of atypical absence seizures after adjunctive antiepileptic therapy of tiagabine (TGB) is reported. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::821f18251868ace9733c9e72d868a670
https://pubmed.ncbi.nlm.nih.gov/14630501
https://pubmed.ncbi.nlm.nih.gov/14630501