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Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family
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Two novel mitochondrial DNA mutations in muscle tissue of a patient with limb-girdle myopathy
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A novel mitochondrial transfer RNA(Asn) mutation causing multiorgan failure
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A new mitochondrial point mutation in the transfer RNA(Leu) gene in a patient with a clinical phenotype resembling Kearns-Sayre syndrome.
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Association of ipsilateral motor automatisms and contralateral dystonic posturing - A clinical feature differentiating medial from neocortical temporal lobe epilepsy.