Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Angeliki Skardoutsou"'
Autor:
Panagiotis Primikiris, Antonios Marmarinos, Dimitrios Gourgiotis, Charalampos Tsentidis, Angeliki Skardoutsou
Publikováno v:
Minerva Pediatrics.
BACKROUND In the present study we investigated the levels of proapoptotic Caspase-9 and antiapoptotic Bcl-2 proteins in the sera of children and adolescents with idiopathic epilepsy and tried to relate the findings to the patients clinical parameters
Publikováno v:
Clinical Genetics. 37:30-34
We report our findings in four cases of metachromatic leukodystrophy diagnosed in Greece during the last 4 years. The age of onset and the clinical symptoms were those described for the late infantile form of the disease. However, one patient retaine
Autor:
Konstantinos A. Voudris, Masashi Mizuguchi, Angeliki Skardoutsou, Dimitrios Gionnis, Sotiria Mastroyianni
Publikováno v:
Journal of Child Neurology. 21:872-879
Acute necrotizing encephalopathy of childhood is a novel type of parainfectious encephalopathy with a racial and geographic predilection, rarely reported from other than East Asian areas. The objective was to describe the clinical, imaging, and other
Autor:
Anastasia Garoufi, Konstantinos A. Voudris, Achilleas Attilakos, Eustathia Katsarou, Sotiria Mastroyianni, Stamatia Dimou, Angeliki Skardoutsou
Publikováno v:
Journal of Child Neurology. 20:513-516
The purpose of this study was to investigate, by a prospective, self-controlled method, whether early treatment with carbamazepine monotherapy can alter bone metabolism in ambulatory epileptic children with adequate sun exposure, based on the determi
Autor:
Achilleas Attilakos, Sotiria Mastroyianni, Konstantinos A. Voudris, Angeliki Skardoutsou, Eustathia Katsarou, Stamatia Dimou, Anastasia Garoufi
Publikováno v:
Clinica Chimica Acta. 350:175-180
Background Serum total amylase and lipase activities have been determined in epileptic patients treated with polytherapy using enzyme-inducing anticonvulsant drugs; however, to our knowledge, serum total amylase, pancreatic amylase and lipase activit
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
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
Autor:
Rebecca Gooding, Constantinos J. Stefanidis, Efstathia Katsarou, Angeliki Skardoutsou, Luba Kalaydjieva, Anastasia Garoufi, Sotiria Mastroyianni, Konstantinos A. Voudris
Publikováno v:
European Journal of Pediatrics. 166:747-749
Congenital cataracts-facial dysmorphism-neuropathy syndrome (CCFDN, MIM: 604168), is a recently delineated neurogenetic disease causing recurrent episodes of rhabdomyolysis; prevention and early diagnosis of rhabdomyolysis should be part of the clini
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
Publikováno v:
Pediatric Dermatology. 20:371-373