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F Zimprich

Showing results (11-20 of 32) with videos related to

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Muscle & Nerve|December 5, 2000
An autosomal dominant early adult-onset distal muscular dystrophyF Zimprich, A Djamshidian, J A Hainfellner, et al.
Clinical and Experimental Dermatology|June 3, 2009
Analysis of the prodynorphin promoter polymorphism in atopic dermatitis and disease-related pruritusE K Greisenegger, A Zimprich, F Zimprich, et al.
Neurology|February 12, 2004
Vestibular processing in human paramedian precuneus as shown by electrical cortical stimulationG Wiest, F Zimprich, D Prayer, et al.
European Journal of Neurology|May 14, 2013
Postictal psychosis in temporal lobe epilepsy: a case-control studyE Hilger, F Zimprich, R Jung, et al.
The American Journal of Pathology|August 1, 1993
The demyelinating potential of antibodies to myelin oligodendrocyte glycoprotein is related to their ability to fix complementS J Piddlesden, H Lassmann, F Zimprich, et al.
Journal of Immunology (Baltimore, Md. : 1950)|October 1, 1991
Nucleocapsid or spike protein-specific CD4+ T lymphocytes protect against coronavirus-induced encephalomyelitis in the absence of CD8+ T cellsH Körner, A Schliephake, J Winter, et al.
International Review of Psychiatry (Abingdon, England)|April 28, 2007
The stigma of mental illness: anticipation and attitudes among patients with epileptic, dissociative or somatoform pain disorderM Freidl, S Piralic Spitzl, W Prause, et al.
European Journal of Neurology|January 3, 2013
The effect of early prednisolone treatment on the generalization rate in ocular myasthenia gravisH Zach, H Cetin, E Hilger, et al.
Neuroscience|April 17, 2002
Altered expression of voltage-dependent calcium channel alpha(1) subunits in temporal lobe epilepsy with Ammon's horn sclerosisA Djamshidian, R Grassl, M Seltenhammer, et al.
Clinical Genetics|January 11, 2016
The c.65-2A>G splice site mutation is associated with a mild phenotype in Danon disease due to the transcription of normal LAMP2 mRNAH Cetin, A Wöhrer, I Rittelmeyer, et al.
Pageof 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
Muscle & Nerve|December 5, 2000
An autosomal dominant early adult-onset distal muscular dystrophyF Zimprich, A Djamshidian, J A Hainfellner, et al.
Clinical and Experimental Dermatology|June 3, 2009
Analysis of the prodynorphin promoter polymorphism in atopic dermatitis and disease-related pruritusE K Greisenegger, A Zimprich, F Zimprich, et al.
Neurology|February 12, 2004
Vestibular processing in human paramedian precuneus as shown by electrical cortical stimulationG Wiest, F Zimprich, D Prayer, et al.
European Journal of Neurology|May 14, 2013
Postictal psychosis in temporal lobe epilepsy: a case-control studyE Hilger, F Zimprich, R Jung, et al.
The American Journal of Pathology|August 1, 1993
The demyelinating potential of antibodies to myelin oligodendrocyte glycoprotein is related to their ability to fix complementS J Piddlesden, H Lassmann, F Zimprich, et al.
Journal of Immunology (Baltimore, Md. : 1950)|October 1, 1991
Nucleocapsid or spike protein-specific CD4+ T lymphocytes protect against coronavirus-induced encephalomyelitis in the absence of CD8+ T cellsH Körner, A Schliephake, J Winter, et al.
International Review of Psychiatry (Abingdon, England)|April 28, 2007
The stigma of mental illness: anticipation and attitudes among patients with epileptic, dissociative or somatoform pain disorderM Freidl, S Piralic Spitzl, W Prause, et al.
European Journal of Neurology|January 3, 2013
The effect of early prednisolone treatment on the generalization rate in ocular myasthenia gravisH Zach, H Cetin, E Hilger, et al.
Neuroscience|April 17, 2002
Altered expression of voltage-dependent calcium channel alpha(1) subunits in temporal lobe epilepsy with Ammon's horn sclerosisA Djamshidian, R Grassl, M Seltenhammer, et al.
Clinical Genetics|January 11, 2016
The c.65-2A>G splice site mutation is associated with a mild phenotype in Danon disease due to the transcription of normal LAMP2 mRNAH Cetin, A Wöhrer, I Rittelmeyer, et al.
Pageof 4