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Neuropediatrics|May 1, 1999
Apnoea of prematurity and changes in cerebral oxygenation and cerebral blood volumeB Urlesberger, A Kaspirek, G Pichler, et al.Neuropediatrics|May 1, 1999
Respiratory chain deficiency presenting as recurrent myoglobinuria in childhoodP de Lonlay-Debeney, P Edery, V Cormier-Daire, et al.Neuropediatrics|August 30, 2000
MR patterns of hypoxic-ischemic brain damage after prenatal, perinatal or postnatal asphyxiaL T Sie, M S van der Knaap, J Oosting, et al.Neuropediatrics|August 30, 2000
Painless fractures and thermoregulation disturbances in sensory-autonomic neuropathy: electrophysiological abnormalities and sural nerve biopsyA Polo, R Aldegheri, L G Bongiovanni, et al.Neuropediatrics|August 30, 2000
Familial systemic lupus erythematosus and congenital infection-like syndromeR C Dale, S P Tang, J Z Heckmatt, et al.Neuropediatrics|April 25, 2000
A KCNQ2 splice site mutation causing benign neonatal convulsions in a Scottish familyW L Lee, C Biervert, K Hallmann, et al.Neuropediatrics|April 25, 2000
Lymphocyte inclusions in Finnish-variant late infantile neuronal ceroid lipofuscinosis (CLN5)J Rapola, B D LakeNeuropediatrics|December 19, 2001
Progressive multifocal leukoencephalopathy in a child with hyperimmunoglobulin E recurrent infection syndrome and review of the literatureL Angelini, M C Pietrogrande, M R Delle Piane, et al.Neuropediatrics|December 19, 2001
Congenital nemaline myopathy due to ACTA1-gene mutation and carnitine insufficiency: a case reportH Buxmann, R Schlösser, W Schlote, et al.Neuropediatrics|December 19, 2001
Neurological outcome in comatose children with bilateral loss of cortical somatosensory evoked potentialsG Wohlrab, E Boltshauser, B SchmittPageof 255