Abstracts of the 38th Annual Meeting of the Society of Neuropediatrics

Abstracts (HTML) List of Authors

Machuta, K

Integration of Armeo Spring Pediatrics in inpatient Rehabilitation of children and adolescents with Hemiparesis

Mainberger, F

Attention deficit in patients with Noonan Syndrome (NS)

Makhani, N

Hiccups, Vomiting and the Brain

Mall, V

Hypocretin-level during therapy with intravenous immunglobulines in an early stage of narcolepsy with cataplexy in childhood
Unusual presentation of juvenile Pompe disease in infancy with preceding immune thrombocytopenia
Macrocerebellum: not a clinical and neuroimaging entity
Attention deficit in patients with Noonan Syndrome (NS)
Acetazolamide as treatment for GLUT1 deficiency syndrome?

Mallmann, R

Subacute sclerosing panencephalitis

Marquardt, T

Treatment of infantile Pompe s disease with enzyme replacement therapy in Germany and Austria

Massot Taurus, A

Mutations in PCDH19 and Epilepsy: Presentation of a Spanish family with phenotypic heterogeneity

Maxonus, I

Intranasal insulin may influence motor activities and behaviour in Phelan McDermid Syndrom

May, T

Burdens of parents with epileptic children – Results of a study using a short-form of the German version of the Impact-on-Family-Scale

Mayatepek, E

Sudden bilateral sensorineural deafness in a 5 years old girl with blue sclerae, keratoconus, hypermobility of the joints and hyperelasticity of the skin with a mutation in the ZNF469 gene encoding for Brittle-Cornea-Syndrome
Brown-Vialetto-Van Laere syndrome: A riboflavin-unresponsive patient with a novel mutation in the C20orf54 gene

Mayer, T

Valproate induced nocturnal enuresis – a seldom side effect?

Mayr, J

Pyruvate dehydrogenase deficiency: Novel PDHA1 mutation in a child with progressive encephalopathy

Meier, T

DELOS Phase III Study with Idebenone (Catena®) in Duchenne Muscular Dystrophy

Meitinger, T

Mitochondrial Encephalopathies caused by defective mitochondrial translation

Mellies, U

Myasthenic symptoms: From initial presentation to diagnosis

Mengel, E

Respiration and its correlation with motoric function in non-classic Pompe disease
Treatment of infantile Pompe s disease with enzyme replacement therapy in Germany and Austria

Merfort, J

Neuroborreliosis as a chameleon – mimicking tuberculous meningitis

Merkenschlager, A

Cerebellar Infarction and Coarctation of the Aorta – causal relation or coincidence?
Shaking the head without end – bobble-head doll syndrome in no-no direction

Meyer, S

The role of Cochrane reviews in child neurology: A systematic analysis
Melatonin does not influence sleep-deprivation electroencephalogram recordings in children

Middelhoff, C

Symptomatic Treatment of Tomaculous Polyneuropathy with Methylprednisolone

Milkereit, D

KCNQ2(NMF134)-mutant mice as a model for severe neonatal epilepsy

Miny, P

Mosaic ring chromosome 3 in a child with epilepsy and developmental delay

Möllers, M

Microcephaly – Capillary Malformation Syndrome: A new syndrome with severe epilepsy – the first german patient

Moll-Khosrawi, P

Statistical properties of the jNCL scoring system according to Kohlschütter (1988)

Moog, U

Encephalocraniocutaneous lipomatosis (ECCL) – a case report

Morellini, F

KCNQ2(NMF134)-mutant mice as a model for severe neonatal epilepsy

Morris-Rosendahl, D

Microcephaly – Capillary Malformation Syndrome: A new syndrome with severe epilepsy – the first german patient

Muehlhausen, C

Pseudotumor cerebri in an 8 month old infant

Mueller, A

Visual diagnosis of Morbus Niemann Pick Typ C

Mueller, G

Validity of the clinical neurological state and nerve conduction velocity in diagnosing diabetic peripheral neuropathy

Muhle, H

Clinical characterization of myoclonic-astatic epilepsy
The role of vitamin B6 deficiency in infantile epilepsies of unknown etiology

Müller, A

Long-term Outcome after Vegetative State due to Near-Drowning and Quality of Life of the Families

Müller, I

Stem cell transplantation (SCT) in metachromatic leukodystrophy (MLD) – results from 9 patients

Müller, M

Tick-borne encephalitis: four cases in young vaccinated children
CT Perfusion and CT Angiography in children and juvenile patients during an attack of migraine with aura

Müller-Felber, W

Familial mutation in ACTA1 gene – clinical variability
Multiple sclerosis and periodic fever syndromes: Characterization of clinical symptoms

Munteanu, M

Mutation in the Fukutin-Gene (FKTN) as cause of a mild congenital muscular dystrophy
Myasthenic symptoms: From initial presentation to diagnosis
Deletion 22q13 (Phelan-McDermid-Syndrom) in two children with delayed development of speech and muscular hypotonia

Münter, S

Symptomatic Treatment of Tomaculous Polyneuropathy with Methylprednisolone

Muntoni, F

A novel variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy and hearing loss – a differential diagnosis in floppy infant syndrome

Møller, R

The role of vitamin B6 deficiency in infantile epilepsies of unknown etiology