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Cognitive phenotype in ataxia-telangiectasia.
Hoche F, Frankenberg E, Rambow J, Theis M, Harding JA, Qirshi M, Seidel K, Barbosa-Sicard E, Porto L, Schmahmann JD, Kieslich M. Hoche F, et al. Among authors: seidel k. Pediatr Neurol. 2014 Sep;51(3):297-310. doi: 10.1016/j.pediatrneurol.2014.04.027. Epub 2014 May 5. Pediatr Neurol. 2014. PMID: 25037873
Novel N-terminal truncating CLCN1 mutation in severe Becker disease.
Hoche F, Seidel K, Barbosa-Sicard E, Heidegger T, Kang JS, Koenig R, Kieslich M. Hoche F, et al. Among authors: seidel k. Muscle Nerve. 2014 Nov;50(5):866-7. doi: 10.1002/mus.24312. Epub 2014 Sep 24. Muscle Nerve. 2014. PMID: 24920213 No abstract available.
Involvement of the auditory brainstem system in spinocerebellar ataxia type 2 (SCA2), type 3 (SCA3) and type 7 (SCA7).
Hoche F, Seidel K, Brunt ER, Auburger G, Schöls L, Bürk K, de Vos RA, den Dunnen W, Bechmann I, Egensperger R, Van Broeckhoven C, Gierga K, Deller T, Rüb U. Hoche F, et al. Among authors: seidel k. Neuropathol Appl Neurobiol. 2008 Oct;34(5):479-91. doi: 10.1111/j.1365-2990.2007.00933.x. Epub 2008 Jan 24. Neuropathol Appl Neurobiol. 2008. PMID: 18221259
Degeneration of the cerebellum in Huntington's disease (HD): possible relevance for the clinical picture and potential gateway to pathological mechanisms of the disease process.
Rüb U, Hoche F, Brunt ER, Heinsen H, Seidel K, Del Turco D, Paulson HL, Bohl J, von Gall C, Vonsattel JP, Korf HW, den Dunnen WF. Rüb U, et al. Among authors: seidel k. Brain Pathol. 2013 Mar;23(2):165-77. doi: 10.1111/j.1750-3639.2012.00629.x. Epub 2012 Sep 21. Brain Pathol. 2013. PMID: 22925167 Free PMC article.
Spinocerebellar ataxia type 1 (SCA1): new pathoanatomical and clinico-pathological insights.
Rüb U, Bürk K, Timmann D, den Dunnen W, Seidel K, Farrag K, Brunt E, Heinsen H, Egensperger R, Bornemann A, Schwarzacher S, Korf HW, Schöls L, Bohl J, Deller T. Rüb U, et al. Among authors: seidel k. Neuropathol Appl Neurobiol. 2012 Dec;38(7):665-80. doi: 10.1111/j.1365-2990.2012.01259.x. Neuropathol Appl Neurobiol. 2012. PMID: 22309224
Spinocerebellar ataxia type 3 (SCA3): thalamic neurodegeneration occurs independently from thalamic ataxin-3 immunopositive neuronal intranuclear inclusions.
Rüb U, de Vos RA, Brunt ER, Sebestény T, Schöls L, Auburger G, Bohl J, Ghebremedhin E, Gierga K, Seidel K, den Dunnen W, Heinsen H, Paulson H, Deller T. Rüb U, et al. Among authors: seidel k. Brain Pathol. 2006 Jul;16(3):218-27. doi: 10.1111/j.1750-3639.2006.00022.x. Brain Pathol. 2006. PMID: 16911479 Free PMC article.
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 ER, Gierga K, Seidel K, Schultz C, Schöls L, Auburger G, Heinsen H, Ippel PF, Glimmerveen WF, Wittebol-Post D, Arai K, Deller T, de Vos RA. Rüb U, et al. Among authors: seidel k. Brain Pathol. 2005 Oct;15(4):287-95. doi: 10.1111/j.1750-3639.2005.tb00113.x. Brain Pathol. 2005. PMID: 16389941 Free PMC article.
595 results