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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

Udo Rüb

Institute for Clinical Neuroanatomy

J. W. Goethe-University

Frankfurt/Main

Germany

[email]@em.uni-frankfurt.de

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Institute for Clinical Neuroanatomy, J. W. Goethe-University, Frankfurt/Main, Germany. 2000 - 2008

References

  1. Spinocerebellar ataxia type 7 (SCA7): widespread brain damage in an adult-onset patient with progressive visual impairments in comparison with an adult-onset patient without visual impairments. Rüb, U., Brunt, E.R., Seidel, K., Gierga, K., Mooy, C.M., Kettner, M., Van Broeckhoven, C., Bechmann, I., La Spada, A.R., Schöls, L., den Dunnen, W., de Vos, R.A., Deller, T. Neuropathol. Appl. Neurobiol. (2008) [Pubmed]
  2. Consistent affection of the central somatosensory system in spinocerebellar ataxia type 2 and type 3 and its significance for clinical symptoms and rehabilitative therapy. Rüb, U., Seidel, K., Ozerden, I., Gierga, K., Brunt, E.R., Schöls, L., de Vos, R.A., den Dunnen, W., Schultz, C., Auburger, G., Deller, T. Brain. Research. Reviews (2007) [Pubmed]
  3. Degeneration of ingestion-related brainstem nuclei in spinocerebellar ataxia type 2, 3, 6 and 7. Rüb, U., Brunt, E.R., Petrasch-Parwez, E., Schöls, L., Theegarten, D., Auburger, G., Seidel, K., Schultz, C., Gierga, K., Paulson, H., van Broeckhoven, C., Deller, T., de Vos, R.A. Neuropathol. Appl. Neurobiol. (2006) [Pubmed]
  4. Extended pathoanatomical studies point to a consistent affection of the thalamus in spinocerebellar ataxia type 2. Rüb, U., Del Turco, D., Bürk, K., Diaz, G.O., Auburger, G., Mittelbronn, M., Gierga, K., Ghebremedhin, E., Schultz, C., Schöls, L., Bohl, J., Braak, H., Deller, T. Neuropathol. Appl. Neurobiol. (2005) [Pubmed]
  5. Spinocerebellar ataxias types 2 and 3: degeneration of the pre-cerebellar nuclei isolates the three phylogenetically defined regions of the cerebellum. Rüb, U., Gierga, K., Brunt, E.R., de Vos, R.A., Bauer, M., Schöls, L., Bürk, K., Auburger, G., Bohl, J., Schultz, C., Vuksic, M., Burbach, G.J., Braak, H., Deller, T. J. Neural. Transm (2005) [Pubmed]
  6. Spinocerebellar ataxia type 7 (SCA7): first report of a systematic neuropathological study of the brain of a patient with a very short expanded CAG-repeat. Rüb, U., Brunt, E.R., Gierga, K., Seidel, K., Schultz, C., Schöls, L., Auburger, G., Heinsen, H., Ippel, P.F., Glimmerveen, W.F., Wittebol-Post, D., Arai, K., Deller, T., de Vos, R.A. Brain Pathol. (2005) [Pubmed]
  7. Degeneration of the central vestibular system in spinocerebellar ataxia type 3 (SCA3) patients and its possible clinical significance. Rüb, U., Brunt, E.R., de Vos, R.A., Del Turco, D., Del Tredici, K., Gierga, K., Schultz, C., Ghebremedhin, E., Bürk, K., Auburger, G., Braak, H. Neuropathol. Appl. Neurobiol. (2004) [Pubmed]
  8. Damage to the reticulotegmental nucleus of the pons in spinocerebellar ataxia type 1, 2, and 3. Rüb, U., Bürk, K., Schöls, L., Brunt, E.R., de Vos, R.A., Diaz, G.O., Gierga, K., Ghebremedhin, E., Schultz, C., Del Turco, D., Mittelbronn, M., Auburger, G., Deller, T., Braak, H. Neurology (2004) [Pubmed]
  9. 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 patient. Rüb, U., Brunt, E.R., Del Turco, D., de Vos, R.A., Gierga, K., Paulson, H., Braak, H. Neuropathol. Appl. Neurobiol. (2003) [Pubmed]
  10. The nucleus raphe interpositus in spinocerebellar ataxia type 3 (Machado-Joseph disease). Rüb, U., Brunt, E.R., Gierga, K., Schultz, C., Paulson, H., de Vos, R.A., Braak, H. J. Chem. Neuroanat. (2003) [Pubmed]
  11. Thalamic involvement in a spinocerebellar ataxia type 2 (SCA2) and a spinocerebellar ataxia type 3 (SCA3) patient, and its clinical relevance. Rüb, U., Del Turco, D., Del Tredici, K., de Vos, R.A., Brunt, E.R., Reifenberger, G., Seifried, C., Schultz, C., Auburger, G., Braak, H. Brain (2003) [Pubmed]
  12. Parkinson's disease: the thalamic components of the limbic loop are severely impaired by alpha-synuclein immunopositive inclusion body pathology. Rüb, U., Del Tredici, K., Schultz, C., Ghebremedhin, E., de Vos, R.A., Jansen Steur, E., Braak, H. Neurobiol. Aging (2002) [Pubmed]
  13. Progressive supranuclear palsy: neuronal and glial cytoskeletal pathology in the higher order processing autonomic nuclei of the lower brainstem. Rüb, U., Del Tredici, K., Schultz, C., de Vos, R.A., Jansen Steur, E.N., Arai, K., Braak, H. Neuropathol. Appl. Neurobiol. (2002) [Pubmed]
  14. Spinocerebellar ataxia type 3 (Machado-Joseph disease): severe destruction of the lateral reticular nucleus. Rüb, U., de Vos, R.A., Schultz, C., Brunt, E.R., Paulson, H., Braak, H. Brain (2002) [Pubmed]
  15. Degeneration of the external cuneate nucleus in spinocerebellar ataxia type 3 (Machado-Joseph disease). Rüb, U., de Vos, R.A., Brunt, E.R., Schultz, C., Paulson, H., Del Tredici, K., Braak, H. Brain Res. (2002) [Pubmed]
  16. The premotor region essential for rapid vertical eye movements shows early involvement in Alzheimer's disease-related cytoskeletal pathology. Rüb, U., Del Tredici, K., Schultz, C., Büttner-Ennever, J.A., Braak, H. Vision Res. (2001) [Pubmed]
  17. Early involvement of the tegmentopontine reticular nucleus during the evolution of Alzheimer's disease-related cytoskeletal pathology. Rüb, U., Schultz, C., Del Tredici, K., Braak, H. Brain Res. (2001) [Pubmed]
  18. The autonomic higher order processing nuclei of the lower brain stem are among the early targets of the Alzheimer's disease-related cytoskeletal pathology. Rüb, U., Del Tredici, K., Schultz, C., Thal, D.R., Braak, E., Braak, H. Acta Neuropathol. (2001) [Pubmed]
  19. The evolution of Alzheimer's disease-related cytoskeletal pathology in the human raphe nuclei. Rüb, U., Del Tredici, K., Schultz, C., Thal, D.R., Braak, E., Braak, H. Neuropathol. Appl. Neurobiol. (2000) [Pubmed]
 
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