6 items found

Groups: Metadata-only Access Tags: Genetics Neuroscience

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    The impairment of small nerve fibers in severe sepsis and septic shock

    Abstract Background A decrease of small nerve fibers in skin biopsies during the course of critical illness has been demonstrated recently. However, the diagnostic use of skin...
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    Homozygous TBC1 domain-containing kinase (TBCK) mutation causes a novel lysos...

    Abstract Homozygous mutation of TBC1 domain-containing kinase (TBCK) is the cause of a very recently defined severe childhood disorder, which is characterized by severe...
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    Optic-nerve-transmitted eyeshine, a new type of light emission from fish eyes

    Abstract Background Most animal eyes feature an opaque pigmented eyecup to assure that light can enter from one direction only. We challenge this dogma by describing a...
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    Increased cortical activation upon painful stimulation in fibromyalgia syndrome

    Abstract Background Fibromyalgia syndrome (FMS) is a chronic condition characterized by widespread pain and associated symptoms. We investigated cerebral activation in FMS...
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    Nosological delineation of congenital ocular motor apraxia type Cogan: an obs...

    Abstract Background The nosological assignment of congenital ocular motor apraxia type Cogan (COMA) is still controversial. While regarded as a distinct entity by some...
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    SRF modulates seizure occurrence, activity induced gene transcription and hip...

    Abstract A hallmark of temporal lobe epilepsy (TLE) is hippocampal neuronal demise and aberrant mossy fiber sprouting. In addition, unrestrained neuronal activity in TLE...