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Katrin Bürk

Showing results (11-20 of 41) with videos related to

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European Journal of Human Genetics : EJHG|April 26, 2002
Spinocerebellar ataxia type 1 (SCA1): phenotype-genotype correlation studies in intermediate allelesChristine Zühlke, Andreas Dalski, Yorck Hellenbroich, et al.
Clinical Neuropathology|January 17, 2013
Multiple system atrophy of the cerebellar type (MSA-C) with concomitant beta-amyloid and tau pathologyBartosz Bujan, Markus J Hofer, Wolfgang H Oertel, et al.
Neurodegenerative Disease Management|March 11, 2021
Cerebral venous thrombosis, neutropenia and iron-deficiency anemia in Huntington diseaseFarinaz Tabibian, Iman Adibi, Parisa Emami Ardestani, et al.
Archives of Neurology|June 16, 2005
Clinical and magnetic resonance imaging characteristics of sporadic cerebellar ataxiaKatrin Bürk, Udo Bühring, Jörg Bernhard Schulz, et al.
BMC Medical Genetics|September 12, 2009
Exon deletions and intragenic insertions are not rare in ataxia with oculomotor apraxia 2Veronica Bernard, Martina Minnerop, Katrin Bürk, et al.
Cerebellum & Ataxias|December 18, 2015
Spinocerebellar ataxia 28: a novel AFG3L2 mutation in a German family with young onset, slow progression and saccadic slowingChristine Zühlke, Barbara Mikat, Dagmar Timmann, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|July 23, 2009
CD8(+)/perforin/granzyme B(+) effector cells infiltrating cerebellum and inferior olives in gluten ataxiaMichel Mittelbronn, Jens Schittenhelm, Gellert Bakos, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 31, 2006
Spinocerebellar ataxia type 1, 2, and 3 and restless legs syndrome: striatal dopamine D2 receptor status investigated by [11C]raclopride positron emission tomographyMatthias Reimold, Christoph Globas, Marc Gleichmann, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 11, 2006
Mutations in TITF1 are not relevant to sporadic and familial chorea of unknown causePeter Bauer, Friedmar R Kreuz, Katrin Bürk, et al.
Journal of Neurology|May 28, 2004
Aprataxin mutations are a rare cause of early onset ataxia in GermanyMatthias Habeck, Christine Zühlke, Karl H P Bentele, et al.
Pageof 5

Showing results (11-20 of 41) with videos related to

Sort By:
Pageof 5
European Journal of Human Genetics : EJHG|April 26, 2002
Spinocerebellar ataxia type 1 (SCA1): phenotype-genotype correlation studies in intermediate allelesChristine Zühlke, Andreas Dalski, Yorck Hellenbroich, et al.
Clinical Neuropathology|January 17, 2013
Multiple system atrophy of the cerebellar type (MSA-C) with concomitant beta-amyloid and tau pathologyBartosz Bujan, Markus J Hofer, Wolfgang H Oertel, et al.
Neurodegenerative Disease Management|March 11, 2021
Cerebral venous thrombosis, neutropenia and iron-deficiency anemia in Huntington diseaseFarinaz Tabibian, Iman Adibi, Parisa Emami Ardestani, et al.
Archives of Neurology|June 16, 2005
Clinical and magnetic resonance imaging characteristics of sporadic cerebellar ataxiaKatrin Bürk, Udo Bühring, Jörg Bernhard Schulz, et al.
BMC Medical Genetics|September 12, 2009
Exon deletions and intragenic insertions are not rare in ataxia with oculomotor apraxia 2Veronica Bernard, Martina Minnerop, Katrin Bürk, et al.
Cerebellum & Ataxias|December 18, 2015
Spinocerebellar ataxia 28: a novel AFG3L2 mutation in a German family with young onset, slow progression and saccadic slowingChristine Zühlke, Barbara Mikat, Dagmar Timmann, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|July 23, 2009
CD8(+)/perforin/granzyme B(+) effector cells infiltrating cerebellum and inferior olives in gluten ataxiaMichel Mittelbronn, Jens Schittenhelm, Gellert Bakos, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 31, 2006
Spinocerebellar ataxia type 1, 2, and 3 and restless legs syndrome: striatal dopamine D2 receptor status investigated by [11C]raclopride positron emission tomographyMatthias Reimold, Christoph Globas, Marc Gleichmann, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 11, 2006
Mutations in TITF1 are not relevant to sporadic and familial chorea of unknown causePeter Bauer, Friedmar R Kreuz, Katrin Bürk, et al.
Journal of Neurology|May 28, 2004
Aprataxin mutations are a rare cause of early onset ataxia in GermanyMatthias Habeck, Christine Zühlke, Karl H P Bentele, et al.
Pageof 5