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Abstracts of the 35th Annual Meeting of the Society of Neuropediatrics
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Laccone, F.
The Preserved Speech Variant of Rett syndrome: Specificity of atypicality?
Lackner, H.
Opsoklonus-Myoklonus-Syndrom
Landgraf, M.
Toxic effects of lamotrigine ingestion in children
Therapy of headaches in children and adolescents with TENS (Transcutaneous Electrical Nerve Stimulation) – An observational study of the Children's Hospital of the University of Leipzig
Chronic fatigue and pain syndrome caused by persistent intoxication with cactus spurge in a 12-year-old girl
Lauffer, H.
Insights into the regulation of eating behavior: fMRI, peripheral physiology and multichannel EEG in children and adolescents with obesity
Le, Q.
KCNQ potassium channels are critical determinants of neuronal network activity in neonatal mouse brain
Lebrun, A. H.
Retention of lysosomal protein CLN5 in the endoplasmic reticulum causes neuronal ceroid lipofuscinosis in Asian sibship
Ledvinova, J.
GM1 gangliosidosis and Morquio B disease: Expression analysis of missense mutations affecting the catalytic site of acid β-galactosidase
Lehmann-Horn, F.
A rare Ca2+ channel mutation R528G identified in a patient with autosomal dominant hypokalemic periodic paralysis (HypoPP-1)
Lehner, K.
Fast recovery after 5 months in persistent vegetative state
Leiz, S.
Accessory nipple as key symptom in diagnosis of Mowat-Wilson syndrome
Monosomy 9pter-p22 in a boy with neonatal hypoglycemia, epilepsy, facial dysmorphism and hypotonia
Lerche, H.
Screening for 15q13.3 microdeletions in Benign Rolandic Epilepsy and related syndromes
Lettau, M.
Neurocysticercosis in a 10 year-old boy in Germany
Limperopoulos, C.
Life with only one half of the cerebellum: Outcome in children with severe unilateral cerebellar hypoplasia
Lindbichler, F.
Severe central hypomyelination in an infant with mtDNA depletion caused by RRM2B gene mutations
Lindhout, D.
VACENC – A retrospective and prospective study of clinical and genetic characteristics of vaccine encephalopathies: preliminary clinical data
Logeswaran, T.
Severe dilative Cardiomyopathy in mucopolysaccharidosis type 1 (Hurler's Syndrome)
Lombet, A.
Microglia express functional NMDA receptors: A novel finding and a promise for innovative treatment of excitotoxic and inflammatory brain disease
Lorenz, I.
Fractionated stereotactic radiosurgery of a large intracranial arteriovenous malformation (AVM) – A case report
Lorenz, N.
Severe dilative Cardiomyopathy in mucopolysaccharidosis type 1 (Hurler's Syndrome)
Loron, G.
Microglia express functional NMDA receptors: A novel finding and a promise for innovative treatment of excitotoxic and inflammatory brain disease
Lotte, J.
Provocation of seizures by vaccination with children suffering from SCN1A-mutation
Patients with Dravet's syndrome and SCN1A-mutation with a benign course of illness – A case report with 6 patients
Lotze, M.
Insights into the regulation of eating behavior: fMRI, peripheral physiology and multichannel EEG in children and adolescents with obesity
Lücke, T.
Neurodevelopmental follow-up of school-age children with congenital kidney disease and consecutive chronic renal failure
M. Scheie: Failure of enzyme replacement therapy to prevent CNS- and spinal-lesions
Ludwig, H. C.
Hydrocephalus as a rare clinical symptom in a patient with multiple sulfatase deficiency
Luef, G.
Oxcarbazepine accelerates steroid elimination in young men with epilepsy due to cytochrome P450 3A4 induction
Lütjen, S.
Hemiplegic migraine with cerebellar atrophy: A second pediatric case
Clinical long term follow-up of children presenting with a severe acute disseminated encephalomyelitis (ADEM)