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Anti-NMDA-receptor encephalitis in a 3 year old patient with chromosome 6p21.32 microdeletion including the HLA cluster
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Palatal insufficiency as isolated sign of GQ1b antibody syndrome
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Hashimoto encephalopathy and antibodies against dimethylargininase-1: a rare cause of cognitive decline in a pediatric Down's syndrome patient
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Perisylvian polymicrogyria, infantile spasms and arthrogryposis : the severe end of the spectrum of congenital bilateral perisylvian polymicrogyria
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Subcomplexes of mitochondrial complex V reveal mutations in mitochondrial DNA
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Childhood narcolepsy with partial facial cataplexy: a diagnostic dilemma
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MECHANISM OF LACTIC ACIDOSIS IN PATIENTS WITH THE PROPOFOL INFUSION SYNDROME (PRIS)
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Hippocampal atrophy and developmental regression as first sign of linear scleroderma "en coup de sabre"
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Limbic encephalitis as presentation of a SAP deficiency
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Vagus nerve stimulation for refractory status epilepticus