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

Abstracts (HTML) List of Authors

Mader, S

Acute blindness – a case report of Neuromyelitis Optica (Devic Syndrome) in adolescence

Maher, E

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

Maier, EM

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

Mainberger, F

Low-Frequency rTMS selectively modulates inhibitory intracortical networks
Impaired long term potentiation (LTP)-like plasticity in patients with high functiong autism and Asperger syndrome (HFA/AS)
Impaired motor cortex plasticity in patients with Noonan syndrome

Mall, V

Psychiatric symptoms and CK-Elevation as initial manifestations of late-onset Tay-Sachs disease
Low-Frequency rTMS selectively modulates inhibitory intracortical networks
Impaired long term potentiation (LTP)-like plasticity in patients with high functiong autism and Asperger syndrome (HFA/AS)
Impaired motor cortex plasticity in patients with Noonan syndrome
Influence of current direction in transcranial magnetic stimulation (TMS) on MEP amplitude and latency – opportunity of I wave specific evaluation and stimulation

Maroske, J

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

Marquard, K

Helmets or physiotherapy? Natural history and treatment options for non-synostotic skull deformity in children – results of a literature search

Mattes, D

Acute blindness – a case report of Neuromyelitis Optica (Devic Syndrome) in adolescence

Mattle, HP

Differences in risk-factors, aetiology and outcome between children and young adults with acute ischaemic stroke

Mauer, UM

Current practice in the management of newborns with spina bifida in Germany

Mautner, VF

Growth hormone treatment of patients with neurofibromatosis type 1

Mayatepek, E

Dopamine transporter defect: Infantile parkinsonism-dystonia with elevated dopamine metabolites in cerebrospinal fluid is genetically resolved
Optic pathway gliomas in children with neurofibromatosis type 1: a long term study in 38 patients

Mayr, J

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

Merkel, HJ

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

Meyer, D

Developmental and sex differences of somatosensory perception

Meyer, S

Neonatal hypotonia with burst suppression pattern reveals non ketotic hyperglycinemia associated with P-protein deficiency
The role of EEG in monitoring cerebral dysfunction before and after cardiac surgery in children congenital heart disease

Mildenberger, E

Temporary neonatal respiratory disorder – Early-onset-variation of Ondine's curse
Proposal on an evaluation form for the standardized indication of physiotherapy and occupational therapy and scientific application in neonatology

Moeller, F

Dynamic analysis of absence seizures in humans: all the same but all different

Moers, A von

From pediatric to adult-orientated care: the „Berliner Transitionsprogramm“
Dopamine transporter defect: Infantile parkinsonism-dystonia with elevated dopamine metabolites in cerebrospinal fluid is genetically resolved

Mohr, A

Polymicrogyria in Fetal Alcohol Syndrome

Möhring, J

EEG-fMRI: Including sleep-induced potentials in the general linear model improves spatial accordance with epileptic focus

Mole, SE

Identification of potential biomarkers and modifiers of CLN3-disease progression

Möller, F

EEG-fMRI: Including sleep-induced potentials in the general linear model improves spatial accordance with epileptic focus

Möller-Hartmann, C

ARX-mutation – phenotype and clinical course in two brothers with West Syndrome and developmental delay

Moll-Khosrawi, P

High phenotype variability in CLN3 patients with identical genotype

Morava, E

Towards the genetic defect in MEGDEL syndrome: Four novel patients

Mordekar, S

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

Muhle, H

Dynamic analysis of absence seizures in humans: all the same but all different

Mühlhausen, C

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

Müller, B

From pediatric to adult-orientated care: the „Berliner Transitionsprogramm“

Müller, HL

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

Müller, K

Diffusion tensor imaging demonstrates effectiveness of immunotherapy for Rasmussen's encephalitis
„Fixed dystonia“ syndrome after peripheral trauma in two adolescent girls
The concept of modular motor therapy in paediatric neurology

Müller-Schlüter, K

From pediatric to adult-orientated care: the „Berliner Transitionsprogramm“

Müller-Wielsch, K

Developmental retardation due to dietary vitamin B12 deficiency during infancy

Münchau, A

Impaired long term potentiation (LTP)-like plasticity in patients with high functiong autism and Asperger syndrome (HFA/AS)

Munteanu, M

ARX-mutation – phenotype and clinical course in two brothers with West Syndrome and developmental delay

Mürle, B

Macrocephaly with dilated Virchow-Robin spaces: a new clinical entity?

Müther, S

From pediatric to adult-orientated care: the „Berliner Transitionsprogramm“

Muyimbwa, J

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