E R Brunt - JoVE Visualize

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Human Genetics|December 1, 1995

Refinement by linkage analysis in two large families of the candidate region of the third locus (SCA3) for autosomal dominant cerebellar ataxia type IC C Verschuuren-Bemelmans, E R Brunt, M Burton, et al.

Neuropathology and Applied Neurobiology|August 13, 2004

Degeneration of the central vestibular system in spinocerebellar ataxia type 3 (SCA3) patients and its possible clinical significanceU Rüb, E R Brunt, R A I de Vos, et al.

Human Genetics|May 26, 1998

Three novel KCNA1 mutations in episodic ataxia type I familiesH Scheffer, E R Brunt, G J Mol, et al.

Early Human Development|September 25, 2009

Neurophysiological evaluation in children with Friedreich's ataxiaD A Sival, G J du Marchie Sarvaas, O F Brouwer, et al.

Neuropathology and Applied Neurobiology|February 1, 2013

Involvement of the cholinergic basal forebrain nuclei in spinocerebellar ataxia type 2 (SCA2)U Rüb, K Farrag, K Seidel, et al.

Neuropathology and Applied Neurobiology|June 24, 2011

The HSPB8-BAG3 chaperone complex is upregulated in astrocytes in the human brain affected by protein aggregation diseasesK Seidel, J Vinet, W F A den Dunnen, et al.

Neurology|April 1, 1996

Botulinum toxin versus trihexyphenidyl in cervical dystonia: a prospective, randomized, double-blind controlled trialJ W Brans, R Lindeboom, J W Snoek, et al.

Neuropathology and Applied Neurobiology|November 7, 2006

Degeneration of ingestion-related brainstem nuclei in spinocerebellar ataxia type 2, 3, 6 and 7U Rüb, E R Brunt, E Petrasch-Parwez, et al.

Journal of Neural Transmission (Vienna, Austria : 1996)|March 24, 2005

Spinocerebellar ataxias types 2 and 3: degeneration of the pre-cerebellar nuclei isolates the three phylogenetically defined regions of the cerebellumU Rüb, K Gierga, E R Brunt, et al.

Neuropathology and Applied Neurobiology|January 29, 2008

Involvement of the auditory brainstem system in spinocerebellar ataxia type 2 (SCA2), type 3 (SCA3) and type 7 (SCA7)F Hoche, K Seidel, E R Brunt, et al.

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Showing results (21-30 of 39) with videos related to

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Human Genetics|December 1, 1995

Refinement by linkage analysis in two large families of the candidate region of the third locus (SCA3) for autosomal dominant cerebellar ataxia type IC C Verschuuren-Bemelmans, E R Brunt, M Burton, et al.

Neuropathology and Applied Neurobiology|August 13, 2004

Degeneration of the central vestibular system in spinocerebellar ataxia type 3 (SCA3) patients and its possible clinical significanceU Rüb, E R Brunt, R A I de Vos, et al.

Human Genetics|May 26, 1998

Three novel KCNA1 mutations in episodic ataxia type I familiesH Scheffer, E R Brunt, G J Mol, et al.

Early Human Development|September 25, 2009

Neurophysiological evaluation in children with Friedreich's ataxiaD A Sival, G J du Marchie Sarvaas, O F Brouwer, et al.

Neuropathology and Applied Neurobiology|February 1, 2013

Involvement of the cholinergic basal forebrain nuclei in spinocerebellar ataxia type 2 (SCA2)U Rüb, K Farrag, K Seidel, et al.

Neuropathology and Applied Neurobiology|June 24, 2011

The HSPB8-BAG3 chaperone complex is upregulated in astrocytes in the human brain affected by protein aggregation diseasesK Seidel, J Vinet, W F A den Dunnen, et al.

Neurology|April 1, 1996

Botulinum toxin versus trihexyphenidyl in cervical dystonia: a prospective, randomized, double-blind controlled trialJ W Brans, R Lindeboom, J W Snoek, et al.

Neuropathology and Applied Neurobiology|November 7, 2006

Degeneration of ingestion-related brainstem nuclei in spinocerebellar ataxia type 2, 3, 6 and 7U Rüb, E R Brunt, E Petrasch-Parwez, et al.

Journal of Neural Transmission (Vienna, Austria : 1996)|March 24, 2005

Spinocerebellar ataxias types 2 and 3: degeneration of the pre-cerebellar nuclei isolates the three phylogenetically defined regions of the cerebellumU Rüb, K Gierga, E R Brunt, et al.

Neuropathology and Applied Neurobiology|January 29, 2008

Involvement of the auditory brainstem system in spinocerebellar ataxia type 2 (SCA2), type 3 (SCA3) and type 7 (SCA7)F Hoche, K Seidel, E R Brunt, et al.

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