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

Abstracts (HTML) List of Authors

Haas, D

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

Haas-Lude, K

Growth hormone treatment of patients with neurofibromatosis type 1

Hadders-Algra, M

Evaluation of general movements in infants with an electromagnetic tracking system – first steps towards the discrimination of variability of spontaneous movements

Haefeli, WE

Patient safety on a paediatric neurology ward – prevention of drug administration errors by cooperation with clinical pharmacists

Haege, G

Use of guidelines improves the neurological outcome in glutaric aciduria type I

Haffner, D

Pontine tegmental cap dysplasia: case report of a „new“ disorder with associated cortical malformation

Hahn, A

Clinical neurophysiology for differentiation between Pelizaeus-Merzbacher Disease and Pelizaeus-Merzbacher-like Disease
Singultus as main seizure type in a patient with primary generalized epilepsy

Hahn, G

Case report of a 1-year old girl with β-ureidopropionase deficiency and development of cystic encephalomalacia

Hanisch, E

Experiences with Laparoscopic Adjustable Gastric banding (LAGB) and Sleeve Gastrectomy (SG) in the treatment of patients with childhood craniopharyngioma and morbid obesity

Hanke, G

Patient safety on a paediatric neurology ward – prevention of drug administration errors by cooperation with clinical pharmacists

Hannak, D

Steadiness/stability of antiepileptic drugs in serum, plasma and whole-blood samples under various storage methods

Harting, I

Use of guidelines improves the neurological outcome in glutaric aciduria type I

Hartmann, H

L-2-hydroxyglutaric aciduria: Infantile versus adult late-onset manifestation
Neurological complications following renal transplantation in infants and children: A retrospective single centre study

Hartmann, K

Dronabinol for the treatment of unspecific pain, restlessness and spasticity in neuropaediatrics

Haschemi, M

The concept of modular motor therapy in paediatric neurology

Hasselmann, O

Leigh Syndrome: typical phenotype but atypical mitochondrial mutation – a case report

Haud, N

RNASET2-deficient cystic leukoencephalopathy: a new lysosomal disorder

Häusler, M

Lupus erythematosus and Aicardi-Goutières Syndrome: a continuum of immune mediated diseases

Heales, S

Dopamine transporter defect: Infantile parkinsonism-dystonia with elevated dopamine metabolites in cerebrospinal fluid is genetically resolved

Hechler, T

Quantitative Sensory Testing in children and adolescents with cerebral palsy
Developmental and sex differences of somatosensory perception

Heinen, F

Impaired motor cortex plasticity in patients with Noonan syndrome

Henneke, M

Clinical neurophysiology for differentiation between Pelizaeus-Merzbacher Disease and Pelizaeus-Merzbacher-like Disease
RNASET2-deficient cystic leukoencephalopathy: a new lysosomal disorder

Henschen, M

Is the assessment of general movements helpful for the prediction of the neurodevelopmental outcome in a child with symptomatic congenital CMV infection?

Hentschel, R

Long-term follow up of preterms below 33 weeks of gestation at school age

Henze, G

Impairment of executive functions in pediatric posterior fossa tumor survivors

Heringer, J

Use of guidelines improves the neurological outcome in glutaric aciduria type I

Hermann, E

Neurodevelopmental long-term outcome in VLBW preterm infants born in 2000–2004

Hernáiz Driever, P

Impairment of executive functions in pediatric posterior fossa tumor survivors

Hertzberg, C

Lupus erythematosus and Aicardi-Goutières Syndrome: a continuum of immune mediated diseases

Hessenauer, M

Remi-Pro: a standardized method to document the course of remission and finding of therapeutic goals in children and adolescents after severe acquired brain-lesions

Heyer, C

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)

Hiener, U

Intracranial hypertension in a boy with infantile hypophosphatasia requiring shunt installation

Hilbig, K

Ketogenic diet in children with difficult to treat epilepsies – 6 years of clinical experience

Hoche, F

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
Dysembryoplastic neuroepithelial tumor (DNET) in a patient with Noonan syndrome
DWI and Proton weighted MRI seems to be a highly sensitive marker of pathological activity in pediatric multiple sclerosis

Hoffmann, GF

Dopamine transporter defect: Infantile parkinsonism-dystonia with elevated dopamine metabolites in cerebrospinal fluid is genetically resolved
Use of guidelines improves the neurological outcome in glutaric aciduria type I

Hofmann-Peters, A

MRI abnormalities associated with Vigabatrin treatment – a longitudinal case study and an atypical case
Autosomal dominant nocturnal frontal lobe epilepsy in mother and daughter treated with an unusual combination of anticonvulsants
Ketogenic diet in children with difficult to treat epilepsies – 6 years of clinical experience

Höger, C

FMR2 gene deletion as a cause of non-specific mental retardation and autistic behavior in two brothers

Holinski-Feder, E

6q13–6q14.1 deletion syndrome characterized by congenital myopathy, mental retardation and minor dysmorphisms – a case report
ARX-mutation – phenotype and clinical course in two brothers with West Syndrome and developmental delay

Holthausen, H

Asymmetrical localisation of the motor cortex after perinatally acquired intracerebral hemorrhage: Volume shift versus neuroplasticity

Hoppe-Tichy, T

Patient safety on a paediatric neurology ward – prevention of drug administration errors by cooperation with clinical pharmacists

Horber, V

Eyelid myoclonia with absences (Jeavons syndrome): An unrecognized generalized epileptic syndrome?

Horváth, R

BARTH SYNDROME with a new mutation without cardial involvement
Leigh Syndrome: typical phenotype but atypical mitochondrial mutation – a case report

Hoy, L

Neurological complications following renal transplantation in infants and children: A retrospective single centre study

Huber-Zeyringer, A

Urodynamic findings by routine preoperative assessment in 46 scoliotic patients

Hübner, A

Case report of a 1-year old girl with β-ureidopropionase deficiency and development of cystic encephalomalacia

Huppke, B

European paediatric patients with neuromyelitis optica: a good prognosis for most and seronegative to NMO-IgG

Huppke, P

European paediatric patients with neuromyelitis optica: a good prognosis for most and seronegative to NMO-IgG
Developmental retardation due to dietary vitamin B12 deficiency during infancy

Hurlstone, A

RNASET2-deficient cystic leukoencephalopathy: a new lysosomal disorder

Husain, R

ADAMTS13 dysfunction and a novel frameshift mutation in the TREX1 gene in a patient with Aicardi-Goutières syndrome