A. Skardoutsou

发表

Early Alteration in Bone Metabolism in Epileptic Children Receiving Carbamazepine Monotherapy Owing to the Induction of Hepatic Drug-Metabolizing Enzymes

A. Attilakos, A. Garoufi, E. Katsarou, 2005 .

Brain Hamartoma in an Infant with Bannayan-Riley-Ruvalcaba Syndrome: Patient Report and Review of the Literature

T. Karpathios, V. Tsagris, K. Voudris, 2000 .

Acute Necrotizing Encephalopathy of Childhood in Non-Asian Patients: Report of Three Cases and Literature Review

M. Mizuguchi, K. Voudris, A. Skardoutsou, 2006, Journal of child neurology.

Different Additional Risk Factors for Cerebral Infarctions Associated With the Factor V Leiden Mutation in a Family

K. Voudris, A. Skardoutsou, S. Mastroyianni, 2006, Journal of child neurology.

Early Alteration in Bone Metabolism in Epileptic Children Receiving Carbamazepine Monotherapy Owing to the Induction of Hepatic Drug—Metabolizing Enzymes

A. Attilakos, A. Garoufi, E. Katsarou, 2005, Journal of child neurology.

Moya Moya Syndrome in a Child With Pyruvate Kinase Deficiency and Combined Prothrombotic Factors

G. Magoufis, P. Koukoutsakis, K. Voudris, 2007, Journal of child neurology.

Immunoglobulin A and M levels in premature infants with gastroenteritis

G. Papaevangelou, E. Kourea, P. Panayotou, 1971, Archives of disease in childhood.

Infection-triggered familial or recurrent cases of acute necrotizing encephalopathy caused by mutations in a component of the nuclear pore, RANBP2.

M. Adams, A. Fasano, A. Bassuk, 2009, American journal of human genetics.

Pre-eruptive neurologic manifestations associated with multiple cerebral infarcts in varicella.

P. Spyridis, G. Tsolas, C. Karayanni, 1995, Pediatric neurology.

Infantile progressive bulbar palsy with deafness

K. Voudris, A. Skardoutsou, E. Vagiakou, 2002, Brain and Development.

Early-onset severe neurological involvement and D409H homozygosity in Gaucher disease: outcome of enzyme replacement therapy.

H. Michelakakis, E. Dimitriou, M. Moraitou, 2002, Blood cells, molecules & diseases.

Non-convulsive status epilepticus associated with tiagabine therapy in children

K. Voudris, A. Skardoutsou, E. Vagiakou, 2003, Seizure.

Alkaline phosphatase and its isoenzyme activity for the evaluation of bone metabolism in children receiving anticonvulsant monotherapy

M. Moustaki, P. Zeis, K. Voudris, 2002, Seizure.

Serum total amylase, pancreatic amylase and lipase activities in epileptic children treated with sodium valproate monotherapy

A. Attilakos, A. Garoufi, E. Katsarou, 2006, Brain and Development.

Serum amylase, pancreatic amylase and lipase concentrations in epileptic children treated with carbamazepine monotherapy.

A. Attilakos, A. Garoufi, E. Katsarou, 2004, Clinica chimica acta; international journal of clinical chemistry.

Acute Necrotizing Encephalopathy Associated With Parainfluenza Virus in a Caucasian Child

E. Katsarou, K. Voudris, A. Skardoutsou, 2003, Journal of child neurology.

Long-Term Findings on Brain Magnetic Resonance Imaging in Acute Encephalopathy With Bilateral Striatal Necrosis Associated With Measles

K. Voudris, A. Skardoutsou, E. Vagiakou, 2002, Journal of child neurology.

Acute striatal necrosis following measles in children

K. Voudris, A. Skardoutsou, E. Vagiakou, 2001, Brain and Development.

Congenital Microcephaly in Two Infants With the Factor V Leiden Mutation

K. Voudris, A. Skardoutsou, E. Vagiakou, 2002, Journal of child neurology.

Congenital cataracts facial dysmorphism neuropathy (CCFDN) syndrome: a rare cause of parainfectious rhabdomyolysis

L. Kalaydjieva, C. Stefanidis, E. Katsarou, 2007, European Journal of Pediatrics.

Lobar holoprosencephaly.

M. Servitzoglou, P. Pavone, E. Parano, 2002, Journal of child neurology.

Infantile Spasms in an Infant With Cytomegalovirus Infection Treated With Ganciclovir

K. Voudris, A. Skardoutsou, S. Mastroyianni, 2004, Journal of child neurology.

Early and persistent increase in serum lipoprotein (a) concentrations in epileptic children treated with carbamazepine and sodium valproate monotherapy

A. Attilakos, A. Garoufi, E. Katsarou, 2006, Epilepsy Research.

Canavan disease: findings in four new cases

M. Rolland, P. Divry, H. Michelakakis, 1991, Journal of Inherited Metabolic Disease.

Congenital asymmetric crying facies and agenesis of corpus callosum

K. Voudris, A. Skardoutsou, E. Vagiakou, 2003, Brain and Development.

Tuberous sclerosis and congenital lymphedema

K. Voudris, A. Skardoutsou, E. Vagiakou, 2003, Pediatric dermatology.

Acute disseminated encephalomyelitis associated with parainfluenza virus infection of childhood

K. Voudris, A. Skardoutsou, E. Vagiakou, 2002, Brain and Development.

Bcl-2 and caspase-9 serum levels in children and adolescents with idiopathic epilepsy and active seizures

C. Tsentidis, D. Gourgiotis, A. Marmarinos, 2022, Minerva Pediatrics.