Search research articles
Contact Us
Filters
Showing results (11-20 of 32) with videos related to
Page
of 4
Sort By:
Muscle & Nerve
|
December 5, 2000
An autosomal dominant early adult-onset distal muscular dystrophy
F 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 pruritus
E K Greisenegger, A Zimprich, F Zimprich, et al.
Neurology
|
February 12, 2004
Vestibular processing in human paramedian precuneus as shown by electrical cortical stimulation
G Wiest, F Zimprich, D Prayer, et al.
European Journal of Neurology
|
May 14, 2013
Postictal psychosis in temporal lobe epilepsy: a case-control study
E 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 complement
S 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 cells
H 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 disorder
M 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 gravis
H 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 sclerosis
A 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 mRNA
H Cetin, A Wöhrer, I Rittelmeyer, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 32) with videos related to
Sort By:
Page
of 4
Muscle & Nerve
|
December 5, 2000
An autosomal dominant early adult-onset distal muscular dystrophy
F 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 pruritus
E K Greisenegger, A Zimprich, F Zimprich, et al.
Neurology
|
February 12, 2004
Vestibular processing in human paramedian precuneus as shown by electrical cortical stimulation
G Wiest, F Zimprich, D Prayer, et al.
European Journal of Neurology
|
May 14, 2013
Postictal psychosis in temporal lobe epilepsy: a case-control study
E 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 complement
S 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 cells
H 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 disorder
M 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 gravis
H 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 sclerosis
A 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 mRNA
H Cetin, A Wöhrer, I Rittelmeyer, et al.
Page
of 4