Search Results - "Visbeck, A"

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  1. 1
    Mutation analysis of the spastin gene (SPG4) in patients in Germany with autosomal dominant hereditary spastic paraplegia

    Mutation analysis of the spastin gene (SPG4) in patients in Germany with autosomal dominant hereditary spastic paraplegia by Sauter, S., Miterski, B., Klimpe, S., Bönsch, D., Schöls, L., Visbeck, A., Papke, T., Hopf, H.C., Engel, W., Deufel, T., Epplen, J.T., Neesen, J.

    Published in Human mutation (01-08-2002)
    “…Hereditary spastic paraplegias (HSP) comprise a genetically and clinically heterogeneous group of neurodegenerative disorders characterized by progressive…”
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  2. 2
    Adaptive frequency decomposition of EEG with subsequent expert system analysis

    Adaptive frequency decomposition of EEG with subsequent expert system analysis by Herrmann, C.S, Arnold, T, Visbeck, A, Hundemer, H.-P, Hopf, H.C

    Published in Computers in biology and medicine (01-11-2001)
    “…We present a hybrid system for automatic analysis of clinical routine EEG, comprising a spectral analysis and an expert system. EEG raw data are transformed…”
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  3. 3
    Dysarthria-clumsy hand syndrome due to infarction of the cerebral peduncle

    Dysarthria-clumsy hand syndrome due to infarction of the cerebral peduncle by Urban, P P, Hopf, H C, Visbeck, A, Fleischer, S, Andreas, J

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  4. 4
    The risk of abducens palsy after diagnostic lumbar puncture

    The risk of abducens palsy after diagnostic lumbar puncture by THÖMKE, F, MIKA-GRÜTTNER, A, VISBECK, A, BRÜHL, K

    Published in Neurology (08-02-2000)
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  5. 5
    Mutation analysis of the spastin gene ( SPG4 ) in patients in Germany with autosomal dominant hereditary spastic paraplegia: SPG4 MUTATIONS IN HSP

    Mutation analysis of the spastin gene ( SPG4 ) in patients in Germany with autosomal dominant hereditary spastic paraplegia: SPG4 MUTATIONS IN HSP by Sauter, S., Miterski, B., Klimpe, S., Bönsch, D., Schöls, L., Visbeck, A., Papke, T., Hopf, H.C., Engel, W., Deufel, T., Epplen, J.T., Neesen, J.

    Published in Human mutation (01-08-2002)
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  6. 6
    Vasculitic Wallenberg syndrome with detection of anti‐proteinase 3 antibodies in the cerebrospinal fluid of a patient with severe Wegener's granulomatosis and only mild kidney involvement

    Vasculitic Wallenberg syndrome with detection of anti‐proteinase 3 antibodies in the cerebrospinal fluid of a patient with severe Wegener's granulomatosis and only mild kidney involvement by Faust, Justus, Visbeck, Anke, Fitzek, Sabine, Fitzek, Clemens, Orth, Thomas, Wandel, Eveline, Mayet, Werner J.

    Published in Nephrology, dialysis, transplantation (01-06-2000)
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  7. 7
    Color‐Coded Duplex Ultrasonography of the Origin of the Vertebral Artery: Normal Values of Flow Velocities

    Color‐Coded Duplex Ultrasonography of the Origin of the Vertebral Artery: Normal Values of Flow Velocities by Kuhl, Valerio, Tettenborn, Barbara, Eicke, B. Martin, Visbeck, Anke, Meckes, Stefanie

    Published in Journal of neuroimaging (01-01-2000)
    “…The introduction of color‐coded duplex ultrasonography has improved the ease of performing ultrasound investigations of the vertebral arteries. So far, normal…”
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  8. 8
    Dysarthria-clumsy hand syndrome due to infarction of the cerebral peduncle

    Dysarthria-clumsy hand syndrome due to infarction of the cerebral peduncle by Urban, P P, Hopf, H C, Visbeck, A, Fleischer, S, Andreas, J

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