Abstracts of the 39th Annual Meeting of the Society of Neuropediatrics

Abstracts (HTML) Autorenliste

Abel, L

Mutation analysis of KCNAB1 in rolandic epilepsy

Abela, L

Fatal outcome of rhino-orbital-cerebral mucormycosis due to bilateral internal carotid occlusion in a child after hematopoietic stem cell transplantation

Abicht, A

A new heterozygote sequence variant of the CDKL5 Gene as the underlying cause of intractable early infantile epilepsy

Adler, C

Activities of daily living in children with hemiparesis: Influence of cognitive functions and motor competence on quality of performance
Outcome measurement in clinical pediatric neurorehabilitation: assessment of motor and process skills evaluates the effect of therapy in the area of activity of daily living

Ahlbory, K

Nicolaides-Baraitser Syndrome

Ahlenstiel, T

Neurological outcome in pediatric patients with hemolytic uremic syndrome caused by Escherichia coli O104:H4

Ahting, U

Mitochondriopathy due to mutations in MTFMT: a predominant neurologic phenotype
Molecular diagnosis in mitochondrial respiratory chain deficiency using exome sequencing
The German network for mitochondrial disorders (mitoNET)

Aiello, C

Ataxia, cognitive impairment, and ocular motor apraxia with cerebellar cysts and dysplasia: A new form of dystroglycanopathy?

Alber, M

Early childhood onset progressive myoclonic epilepsy phenotype caused by KCTD7 mutations

Albers, J

Retrospective evaluation of antiepileptic drugs in patients with CDKL5 mutations

Albers, K

Jacobsen syndrome: a rare differential diagnosis of multifocal white matter lesions

Albrecht, B

Genotype-phenotype correlation in congenital muscular dystrophies with defective O-glycosylation of #CHR:alpha_LOWER#-dystroglycan
Tetrasomy X and neuropathy: double trouble or extended phenotype?

Albrecht, U

Visual disorders in children with cerebral palsy
Epilepsy in children with cerebral palsy

Arnold, C

Visual disorders in children with cerebral palsy

Asmussen, M

Jacobsen syndrome: a rare differential diagnosis of multifocal white matter lesions

Assmann, B

Atypical Infantile neuroaxonal dystrophy: a case report
Choreatic movement disorder due to tyrosine hydroxylase deficiency caused by a novel mutation in the TH gene
Case report: cerebral atrophy-induced hygroma in a 3-month-old floppy infant: Unusual and severe manifestation of 5-methylentetrahydrofolate reductase (MTHFR) deficiency
Behçet disease – a rare differential diagnosis of inflammatory CNS disease in children

Au, K von

Ocular myasthenia with both AChR and MuSK antibodies

Auffermann, H

Which covariates influence effectiveness of intensified robotic-assisted treadmill therapy in children with cerebral palsy

Auvin, S

Retrospective evaluation of antiepileptic drugs in patients with CDKL5 mutations