Abstracts for the 30th Annual Meeting of the Society for Neuropediatrics (Gesellschaft für Neuropädiatrie)

Abstracts (HTML) List of Authors

Nagel, S.

Alpers-Huttenlocher syndrome: mitochondrial diseases of brain and liver

Neophytou, B.

Neurological features of the CCFDN (congenital cataracts facial dysmorphism neuropathy)-syndrome

Neubauer, B.

Beta-2-glykoprotein 1 antibodies in an infant with recurrent strokes and familial predisposition for systemic lupus erythematosus
Mutations in the sodium channel gene SCN1A in myoclonic epilepsies of infancy

Neubauer, B. A.

X-linked lissencephaly with abnormal genitalia (XLAG) associated with renal phosphate wasting and exocrine pancreatic insufficiency
Fluctuating ataxia in a child with short-intestine-syndrome and D-lactate acidosis

Neuberger, J.

Asymptomatic cortical atrophy of the cerebellum after intoxication with an antiseptic agent
Posterior reversible encephalopathy associated with hypertension in an acute, streptococcal glomerulonephritis

Neuen-Jacob, E.

Congenital peripheral neuropathy with optic atrophy and symmetric white matter lesions

Neumaier Probst, E.

Alpers-Huttenlocher syndrome: mitochondrial diseases of brain and liver

Neville, B.

Novelty event related potential abnormalities in children with infantile spasms

Nowak-Göttl, U.

Recurrent arterial ischemic stroke in childhood: the role of prothrombotic disorders and underlying conditions
The factor V G1691A mutation is significantly associated with childhood porencephaly in white children – a case-control-study