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E Stogmann

Showing results (1-10 of 7) 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.
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.
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.
Neurogenetics|August 26, 2006
Mutations in the CLCN2 gene are a rare cause of idiopathic generalized epilepsy syndromesE Stogmann, P Lichtner, C Baumgartner, et al.
Neurology|March 18, 2009
A splice site variant in the sodium channel gene SCN1A confers risk of febrile seizuresK Schlachter, U Gruber-Sedlmayr, E Stogmann, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Neurology|September 29, 2004
Association of an ABCB1 gene haplotype with pharmacoresistance in temporal lobe epilepsyF Zimprich, R Sunder-Plassmann, E Stogmann, 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.
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.
Neurogenetics|August 26, 2006
Mutations in the CLCN2 gene are a rare cause of idiopathic generalized epilepsy syndromesE Stogmann, P Lichtner, C Baumgartner, et al.
Neurology|March 18, 2009
A splice site variant in the sodium channel gene SCN1A confers risk of febrile seizuresK Schlachter, U Gruber-Sedlmayr, E Stogmann, et al.
Pageof 1