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F Zimprich

Showing results (21-30 of 32) with videos related to

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Neurology|September 29, 2004
Association of an ABCB1 gene haplotype with pharmacoresistance in temporal lobe epilepsyF Zimprich, R Sunder-Plassmann, E Stogmann, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|October 31, 2009
Analysis of four prevalent filaggrin mutations (R501X, 2282del4, R2447X and S3247X) in Austrian and German patients with atopic dermatitisEk Greisenegger, N Novak, L Maintz, et al.
Neurology|October 26, 2005
Inclusion body myopathy and Paget disease is linked to a novel mutation in the VCP geneD Haubenberger, R E Bittner, S Rauch-Shorny, et al.
Neurology|September 13, 2006
Andreas Rett and benign familial neonatal convulsions revisitedF Zimprich, G M Ronen, W Stögmann, et al.
European Journal of Neurology|March 24, 2017
Hereditary spastic paraplegia caused by compound heterozygous mutations outside the motor domain of the KIF1A geneM Krenn, G Zulehner, C Hotzy, et al.
European Journal of Neurology|December 4, 2008
Report of the Task Force on pre-graduate education in Europe of the education committee of the European Federation of Neurological Societies Composition of the task force of the education committee on pre-graduate educationJ M Lopes Lima, A Mesec, I M S Wilkinson, et al.
Brain : a Journal of Neurology|May 17, 2001
Distribution of a calcium channel subunit in dystrophic axons in multiple sclerosis and experimental autoimmune encephalomyelitisB Kornek, M K Storch, J Bauer, et al.
Neurology|December 13, 2006
Idiopathic generalized epilepsy phenotypes associated with different EFHC1 mutationsE Stogmann, P Lichtner, C Baumgartner, et al.
European Journal of Neurology|August 14, 2019
Genotype-guided diagnostic reassessment after exome sequencing in neuromuscular disorders: experiences with a two-step approachM Krenn, M Tomschik, J Rath, et al.
Neurogenetics|October 14, 2008
A novel mutation in the MFSD8 gene in late infantile neuronal ceroid lipofuscinosisE Stogmann, S El Tawil, J Wagenstaller, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
Neurology|September 29, 2004
Association of an ABCB1 gene haplotype with pharmacoresistance in temporal lobe epilepsyF Zimprich, R Sunder-Plassmann, E Stogmann, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|October 31, 2009
Analysis of four prevalent filaggrin mutations (R501X, 2282del4, R2447X and S3247X) in Austrian and German patients with atopic dermatitisEk Greisenegger, N Novak, L Maintz, et al.
Neurology|October 26, 2005
Inclusion body myopathy and Paget disease is linked to a novel mutation in the VCP geneD Haubenberger, R E Bittner, S Rauch-Shorny, et al.
Neurology|September 13, 2006
Andreas Rett and benign familial neonatal convulsions revisitedF Zimprich, G M Ronen, W Stögmann, et al.
European Journal of Neurology|March 24, 2017
Hereditary spastic paraplegia caused by compound heterozygous mutations outside the motor domain of the KIF1A geneM Krenn, G Zulehner, C Hotzy, et al.
European Journal of Neurology|December 4, 2008
Report of the Task Force on pre-graduate education in Europe of the education committee of the European Federation of Neurological Societies Composition of the task force of the education committee on pre-graduate educationJ M Lopes Lima, A Mesec, I M S Wilkinson, et al.
Brain : a Journal of Neurology|May 17, 2001
Distribution of a calcium channel subunit in dystrophic axons in multiple sclerosis and experimental autoimmune encephalomyelitisB Kornek, M K Storch, J Bauer, et al.
Neurology|December 13, 2006
Idiopathic generalized epilepsy phenotypes associated with different EFHC1 mutationsE Stogmann, P Lichtner, C Baumgartner, et al.
European Journal of Neurology|August 14, 2019
Genotype-guided diagnostic reassessment after exome sequencing in neuromuscular disorders: experiences with a two-step approachM Krenn, M Tomschik, J Rath, et al.
Neurogenetics|October 14, 2008
A novel mutation in the MFSD8 gene in late infantile neuronal ceroid lipofuscinosisE Stogmann, S El Tawil, J Wagenstaller, et al.
Pageof 4