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Journal of Chemical Neuroanatomy|March 29, 2003

The nucleus raphe interpositus in spinocerebellar ataxia type 3 (Machado-Joseph disease)U Rüb, E R Brunt, K Gierga, et al.

Neuropathology and Applied Neurobiology|February 13, 2003

Guidelines for the pathoanatomical examination of the lower brain stem in ingestive and swallowing disorders and its application to a dysphagic spinocerebellar ataxia type 3 patientU Rüb, E R Brunt, D Del Turco, et al.

Brain Research|October 18, 2002

Degeneration of the external cuneate nucleus in spinocerebellar ataxia type 3 (Machado-Joseph disease)U Rüb, R A I de Vos, E R Brunt, et al.

Nature Genetics|October 1, 1994

Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1D L Browne, S T Gancher, J G Nutt, et al.

Journal of Neurology, Neurosurgery, and Psychiatry|October 1, 1995

Hereditary myokymia and paroxysmal ataxia linked to chromosome 12 is responsive to acetazolamideW J Lubbers, E R Brunt, H Scheffer, et al.

American Journal of Human Genetics|October 1, 1994

A gene for episodic ataxia/myokymia maps to chromosome 12p13M Litt, P Kramer, D Browne, et al.

Clinical Neuropathology|December 5, 2006

Neuronal intranuclear inclusions, dysregulation of cytokine expression and cell death in spinocerebellar ataxia type 3B O Evert, J Schelhaas, H Fleischer, et al.

The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 24, 2001

Inflammatory genes are upregulated in expanded ataxin-3-expressing cell lines and spinocerebellar ataxia type 3 brainsB O Evert, I R Vogt, C Kindermann, et al.

Brain : a Journal of Neurology|July 9, 2003

Thalamic involvement in a spinocerebellar ataxia type 2 (SCA2) and a spinocerebellar ataxia type 3 (SCA3) patient, and its clinical relevanceU Rüb, D Del Turco, K Del Tredici, et al.

Neuropathology and Applied Neurobiology|June 23, 2015

Polyglutamine aggregation in Huntington's disease and spinocerebellar ataxia type 3: similar mechanisms in aggregate formationK Seidel, S Siswanto, M Fredrich, et al.

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Showing results (11-20 of 39) with videos related to

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Journal of Chemical Neuroanatomy|March 29, 2003

The nucleus raphe interpositus in spinocerebellar ataxia type 3 (Machado-Joseph disease)U Rüb, E R Brunt, K Gierga, et al.

Neuropathology and Applied Neurobiology|February 13, 2003

Guidelines for the pathoanatomical examination of the lower brain stem in ingestive and swallowing disorders and its application to a dysphagic spinocerebellar ataxia type 3 patientU Rüb, E R Brunt, D Del Turco, et al.

Brain Research|October 18, 2002

Degeneration of the external cuneate nucleus in spinocerebellar ataxia type 3 (Machado-Joseph disease)U Rüb, R A I de Vos, E R Brunt, et al.

Nature Genetics|October 1, 1994

Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1D L Browne, S T Gancher, J G Nutt, et al.

Journal of Neurology, Neurosurgery, and Psychiatry|October 1, 1995

Hereditary myokymia and paroxysmal ataxia linked to chromosome 12 is responsive to acetazolamideW J Lubbers, E R Brunt, H Scheffer, et al.

American Journal of Human Genetics|October 1, 1994

A gene for episodic ataxia/myokymia maps to chromosome 12p13M Litt, P Kramer, D Browne, et al.

Clinical Neuropathology|December 5, 2006

Neuronal intranuclear inclusions, dysregulation of cytokine expression and cell death in spinocerebellar ataxia type 3B O Evert, J Schelhaas, H Fleischer, et al.

The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 24, 2001

Inflammatory genes are upregulated in expanded ataxin-3-expressing cell lines and spinocerebellar ataxia type 3 brainsB O Evert, I R Vogt, C Kindermann, et al.

Brain : a Journal of Neurology|July 9, 2003

Thalamic involvement in a spinocerebellar ataxia type 2 (SCA2) and a spinocerebellar ataxia type 3 (SCA3) patient, and its clinical relevanceU Rüb, D Del Turco, K Del Tredici, et al.

Neuropathology and Applied Neurobiology|June 23, 2015

Polyglutamine aggregation in Huntington's disease and spinocerebellar ataxia type 3: similar mechanisms in aggregate formationK Seidel, S Siswanto, M Fredrich, et al.

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