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Till Voigtländer

Showing results (1-10 of 30) with videos related to

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Orvosi Hetilap|November 24, 2004
[Diagnosis of paraneoplastic neurological syndromes]Gábor Géza Kovács, Till Voigtländer
Acta Neuropathologica|January 13, 2005
Pathogenesis of prion diseasesUrsula Unterberger, Till Voigtländer, Herbert Budka
Journal of the Neurological Sciences|October 2, 2007
Refsum disease due to the splice-site mutation c.135-2A>G before exon 3 of the PHYH gene, diagnosed eight years after detection of retinitis pigmentosaJosef Finsterer, Günther Regelsberger, Till Voigtländer
Journal of the Neurological Sciences|July 19, 2011
Deterioration of anti-Yo-associated paraneoplastic cerebellar degenerationJosef Finsterer, Till Voigtländer, Wolfgang Grisold
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 10, 2008
Non-manifesting Refsum heterozygotes carrying the c.135-2A>G PAHX gene transitionJosef Finsterer, Günther Regelsberger, Till Voigtländer
Gene|November 17, 2012
Epilepsy in adult X-linked adrenoleucodystrophy due to the deletion c.1415-1416delAG in exon 5 of the ABCD1-geneEva Brownstone, Till Voigtländer, Ulf Baumhackl, et al.
The Journal of Infection|August 6, 2005
Anti-GQ1b-negative Miller-Fisher syndrome with lower cranial nerve involvement from parasinusoidal aspergillomaJosef Finsterer, Anton Niedermayr, Peter G Weigl, et al.
The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry|June 5, 2004
Rationale for diagnosing human prion diseaseGábor G Kovács, Till Voigtländer, Ellen Gelpi, et al.
Acta Neuropathologica|August 13, 2002
Distribution of intraneuronal immunoreactivity for the prion protein in human prion diseasesGabor G Kovacs, Till Voigtländer, Johannes A Hainfellner, et al.
Clinical Biochemistry|May 26, 2007
Diagnosis of X-linked adrenoleukodystrophy in blood leukocytesUrsula Unterberger, Günther Regelsberger, Regina Sundt, et al.
Pageof 3

Showing results (1-10 of 30) with videos related to

Sort By:
Pageof 3
Orvosi Hetilap|November 24, 2004
[Diagnosis of paraneoplastic neurological syndromes]Gábor Géza Kovács, Till Voigtländer
Acta Neuropathologica|January 13, 2005
Pathogenesis of prion diseasesUrsula Unterberger, Till Voigtländer, Herbert Budka
Journal of the Neurological Sciences|October 2, 2007
Refsum disease due to the splice-site mutation c.135-2A>G before exon 3 of the PHYH gene, diagnosed eight years after detection of retinitis pigmentosaJosef Finsterer, Günther Regelsberger, Till Voigtländer
Journal of the Neurological Sciences|July 19, 2011
Deterioration of anti-Yo-associated paraneoplastic cerebellar degenerationJosef Finsterer, Till Voigtländer, Wolfgang Grisold
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 10, 2008
Non-manifesting Refsum heterozygotes carrying the c.135-2A>G PAHX gene transitionJosef Finsterer, Günther Regelsberger, Till Voigtländer
Gene|November 17, 2012
Epilepsy in adult X-linked adrenoleucodystrophy due to the deletion c.1415-1416delAG in exon 5 of the ABCD1-geneEva Brownstone, Till Voigtländer, Ulf Baumhackl, et al.
The Journal of Infection|August 6, 2005
Anti-GQ1b-negative Miller-Fisher syndrome with lower cranial nerve involvement from parasinusoidal aspergillomaJosef Finsterer, Anton Niedermayr, Peter G Weigl, et al.
The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry|June 5, 2004
Rationale for diagnosing human prion diseaseGábor G Kovács, Till Voigtländer, Ellen Gelpi, et al.
Acta Neuropathologica|August 13, 2002
Distribution of intraneuronal immunoreactivity for the prion protein in human prion diseasesGabor G Kovacs, Till Voigtländer, Johannes A Hainfellner, et al.
Clinical Biochemistry|May 26, 2007
Diagnosis of X-linked adrenoleukodystrophy in blood leukocytesUrsula Unterberger, Günther Regelsberger, Regina Sundt, et al.
Pageof 3