Abstracts of the 36th Annual Meeting of the Society of Neuropediatrics

Abstracts (HTML) List of Authors

Valsangiacomo, E

Cerebral MRI findings in adolescents with congenital heart disease

van der Knaap, M

Infantile Alexander Disease mimicking multilocular astrocytoma

Vianey-Saban Saban, C

Neonatal hypotonia with burst suppression pattern reveals non ketotic hyperglycinemia associated with P-protein deficiency

Vlaho, S

Promising treatment in a boy with creatine transporter deficiency
Calpainopathy as differential diagnosis of idiopathic hyperCKemia
Autosomal dominant CMT-Type IB (Charcot-Marie-Tooth Neuropathy) as a differential diagnosis of clinically diagnosed autosomal recessive demyelinating CMT-Type 4E
De novo deletion 17p13.1 and duplication 17p11.2 in a seven months-old male infant with the clinical features of Potocki-Lupski syndrome
Dysembryoplastic neuroepithelial tumor (DNET) in a patient with Noonan syndrome
Hypothalamic and pituitary affection after traumatic brain injury in childhood
DWI and Proton weighted MRI seems to be a highly sensitive marker of pathological activity in pediatric multiple sclerosis

Voigt, B

Validation of a parent questionnaire on cognitive development in preterm born infants at the (corrected) age of two years
Correlations between early stress experiences and later behavior regulation in premature born toddlers with low and very low birth weight at the age of two years

Vollmer, B

Microstructural alterations of motor pathways in adolescents born preterm

Vorgerd, M

Muscular hypotonia, joint contractures and elevated creatin kinase level as main symptoms for Congenital muscular dystrophy 1A (MDC 1A/congenital muscular dystrophy with laminin α 2 (merosin) deficiency)

Vry, J

6q13–6q14.1 deletion syndrome characterized by congenital myopathy, mental retardation and minor dysmorphisms – a case report