Katrin Burk: search on Z-Library

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1

Friedreich Ataxia: current status and future prospects

Journal:

Cerebellum & Ataxias

Year:

2017

Language:

english

File:

PDF, 409 KB

english, 2017

2

Low impact surface hardness testing (Equotip) on porous surfaces - advances in methodology with implications for rock weathering and stone deterioration research

Wilhelm, Katrin, Viles, Heather, Burke, Órlaith

Journal:

Earth Surface Processes and Landforms

Year:

2016

Language:

english

File:

PDF, 1.17 MB

english, 2016

3

Catastrophic Limestone Decay at the Central Sanctuary of Iupiter Dolichenus at Dülük Baba Tepesi in Southern Turkey: Causes and Implications for Future Conservation

Wilhelm, Katrin, Viles, Heather, Winter, Engelbert, Burke, Órlaith, Engelstaedter, Sebastian, Coyte, Katharine Z.

Journal:

Conservation and Management of Archaeological Sites

Year:

2017

Language:

english

File:

PDF, 3.64 MB

english, 2017

4

Spectrin mutations cause spinocerebellar ataxia type 5

Ikeda, Yoshio, Dick, Katherine A, Weatherspoon, Marcy R, Gincel, Dan, Armbrust, Karen R, Dalton, Joline C, Stevanin, Giovanni, Dürr, Alexandra, Zühlke, Christine, Bürk, Katrin

Journal:

Nature Genetics

Year:

2006

Language:

english

File:

PDF, 389 KB

english, 2006

5

Primäre und sekundäre Sturzprävention in der Rehabilitation: Hinweise zur Sturzprophylaxe

Bujan, Bartosz, Döring, Christian, Sturzenegger, Christian, Bürk, Katrin

Journal:

Die Rehabilitation

Year:

2018

Language:

german

File:

PDF, 371 KB

german, 2018

6

Effectiveness of intravenous immunoglobin therapy in cerebellar ataxia associated with gluten sensitivity

Katrin Bürk, Arthur Melms, Jörg B. Schulz, Johannes Dichgans

Journal:

Annals of Neurology

Year:

2001

Language:

english

File:

PDF, 1.86 MB

english, 2001

7

Spinocerebellar ataxia type 1 (SCA1): Phenotype-genotype correlation studies in intermediate alleles

Zühlke, Christine, Dalski, Andreas, Hellenbroich, Yorck, Bubel, Stefanie, Schwinger, Eberhard, Bürk, Katrin

Journal:

European Journal of Human Genetics

Year:

2002

Language:

english

File:

PDF, 141 KB

english, 2002

8

Clinical and Magnetic Resonance Imaging Characteristics of Sporadic Cerebellar Ataxia

Bürk, Katrin, Bühring, Udo, Schulz, Jörg Bernhard, Zühlke, Christine, Hellenbroich, Yorck, Dichgans, Johannes

Journal:

Archives of Neurology

Year:

2005

Language:

english

File:

PDF, 104 KB

english, 2005

9

Cognitive function in multiple system atrophy of the cerebellar type

Katrin Bürk, Irene Daum, Udo Rüb

Journal:

Movement Disorders

Year:

2006

Language:

english

File:

PDF, 61 KB

english, 2006

10

Spinocerebellar ataxia type 1, 2, and 3 and restless legs syndrome: Striatal dopamine D2 receptor status investigated by [11C]raclopride positron emission tomography

Matthias Reimold, Christoph Globas, Marc Gleichmann, Michael Schulze, Christian Gerloff, Roland Bares, H.-J. Machulla, Katrin Bürk

Journal:

Movement Disorders

Year:

2006

Language:

english

File:

PDF, 113 KB

english, 2006

11

A novel missense mutation in CACNA1A evaluated by in silico protein modeling is associated with non-episodic spinocerebellar ataxia with slow progression

Bürk, Katrin, Kaiser, Frank J., Tennstedt, Stephanie, Schöls, Ludger, Kreuz, Friedmar R., Wieland, Thomas, Strom, Tim M., Büttner, Thomas, Hollstein, Ronja, Braunholz, Diana, Plaschke, Jens, Gillessen

Journal:

European Journal of Medical Genetics

Year:

2014

Language:

english

File:

PDF, 552 KB

english, 2014

12

Monitoring progression in Friedreich ataxia (FRDA): the use of clinical scales

Bürk, Katrin, Schulz, Stefanie R., Schulz, Jörg B.

Journal:

Journal of Neurochemistry

Year:

2013

Language:

english

File:

PDF, 117 KB

english, 2013

13

UCHL-1 gene in multiple system atrophy: A haplotype tagging approach

Daniel G. Healy, Patrick M. Abou-Sleiman, Niall Quinn, Kourosh R. Ahmadi, Tetsutaro Ozawa, Christoph Kamm, Ullrich Wullner, Wolfgang H. Oertel, Katrin Burk, Erik Dupont, Maria T. Pellecchia, Eduardo T

Journal:

Movement Disorders

Year:

2005

Language:

english

File:

PDF, 109 KB

english, 2005

14

Mutations in TITF1 are not relevant to sporadic and familial chorea of unknown cause

Peter Bauer, Friedmar R. Kreuz, Katrin Bürk, Carsten Saft, Jürgen Andrich, Hubert Heilemann, Olaf Riess, Ludger Schöls

Journal:

Movement Disorders

Year:

2006

Language:

english

File:

PDF, 62 KB

english, 2006

15

Exon deletions and intragenic insertions are not rare in ataxia with oculomotor apraxia 2

Veronica Bernard, Martina Minnerop, Katrin Bürk, Friedmar Kreuz, Gabriele Gillessen-Kaesbach, Christine Zühlke

Journal:

BMC Medical Genetics

Year:

2009

Language:

english

File:

PDF, 871 KB

english, 2009

16

CD8+/perforin+/granzyme B+ effector cells infiltrating cerebellum and inferior olives in gluten ataxia

Michel Mittelbronn, Jens Schittenhelm, Gellert Bakos, Rob A. De Vos, Manfred Wehrmann, Richard Meyermann, Katrin Bürk

Journal:

Year:

2010

Language:

english

File:

PDF, 458 KB

english, 2010

17

[Handbook of Clinical Neurology] The Cerebellum: From Embryology to Diagnostic Investigations Volume 154 || Scales for the clinical evaluation of cerebellar disorders

Year:

2018

Language:

english

File:

PDF, 139 KB

english, 2018

18

Aberrant functional connectivity of resting state networks related to misperceptions and intra-individual variability in Parkinson‘s disease

Miloserdov, Kristina, Schmidt-Samoa, Carsten, Williams, Kathleen, Weinrich, Christiane Anne, Kagan, Igor, Bürk, Katrin, Trenkwalder, Claudia, Bähr, Mathias, Wilke, Melanie

Journal:

NeuroImage: Clinical

Year:

2020

File:

PDF, 2.50 MB

2020

19

Antineuronal autoantibodies in neurological disorders

Journal:

BioMolecular Concepts

Year:

2011

Language:

english

File:

PDF, 89 KB

english, 2011

20

Im Grenzgebiet zwischen Bewegungsstörungen und Epilepsien

Strzelczyk, Adam, Reif, Philipp S., Bürk, Katrin, Oertel, Wolfgang H., Klein, Karl Martin

Journal:

DNP - Der Neurologe und Psychiater

Year:

2013

Language:

german

File:

PDF, 459 KB

german, 2013

21

Cognition in hereditary ataxia

Journal:

Year:

2007

Language:

english

File:

PDF, 147 KB

english, 2007

22

Comparison of three clinical rating scales in Friedreich ataxia (FRDA)

Katrin Bürk, Ulrike Mälzig, Stefanie Wolf, Suzette Heck, Konstantinos Dimitriadis, Tanja Schmitz-Hübsch, Sascha Hering, Tobias M. Lindig, Verena Haug, Dagmar Timmann, Ingrid Degen, Bernd Kruse, Jan-Ma

Journal:

Movement Disorders

Year:

2009

Language:

english

File:

PDF, 111 KB

english, 2009

23

No parkinsonism in SCA2 and SCA3 despite severe neurodegeneration of the dopaminergic substantia nigra

Schöls, Ludger, Reimold, Matthias, Seidel, Kay, Globas, Christoph, Brockmann, Kathrin, Karsten Hauser, Till, Auburger, Georg, Bürk, Katrin, den Dunnen, Wilfred, Reischl, Gerald, Korf, Horst-Werner, Br

Journal:

Year:

2015

Language:

english

File:

PDF, 1.00 MB

english, 2015

24

Spinocerebellar ataxia type 17 is caused by mutations in the TATA-box binding protein

Christine Zühlke, Katrin Bürk

Journal:

Year:

2007

Language:

english

File:

PDF, 168 KB

english, 2007

25

Aberrant functional connectivity of resting state networks related to misperceptions and intra-individual variability in Parkinson‘s disease

Miloserdov, Kristina, Schmidt-Samoa, Carsten, Williams, Kathleen, Weinrich, Christiane Anne, Kagan, Igor, Bürk, Katrin, Trenkwalder, Claudia, Bähr, Mathias, Wilke, Melanie

Journal:

NeuroImage: Clinical

Year:

2020

Language:

english

File:

PDF, 2.50 MB

english, 2020

26

Phenotypical variability of expanded alleles in the TATA-binding protein gene

Christine Zühlke, Ulrike Gehlken, Yorck Hellenbroich, Eberhard Schwinger, Katrin Bürk

Journal:

Journal of Neurology

Year:

2003

Language:

english

File:

PDF, 223 KB

english, 2003

27

Induction of the cytokine TWEAK and its receptor Fn14 in ischemic stroke

Ioana Inta, Katrin Frauenknecht, Henrike Dörr, Patricia Kohlhof, Tanja Rabsilber, Gerd U. Auffarth, Linda Burkly, Michel Mittelbronn, Kyungmin Hahm, Clemens Sommer, Markus Schwaninger

Journal:

Journal of the Neurological Sciences

Year:

2008

Language:

english

File:

PDF, 706 KB

english, 2008

28

Restless legs syndrome in spinocerebellar ataxia types 1, 2, and 3

Michael Abele, Katrin Bürk, Franco Laccone, Johannes Dichgans, Thomas Klockgether

Journal:

Journal of Neurology

Year:

2001

Language:

english

File:

PDF, 187 KB

english, 2001

29

Dopamine Transporter Positron Emission Tomography in Spinocerebellar Ataxias Type 1, 2, 3, and 6

Wüllner, Ullrich, Reimold, Michael, Abele, Michael, Bürk, Katrin, Minnerop, Martina, Dohmen, Bernd-Michael, Machulla, Hans-Juergen, Bares, Roland, Klockgether, Thomas

Journal:

Archives of Neurology

Year:

2005

Language:

english

File:

PDF, 349 KB

english, 2005

30

Aprataxin mutations are a rare cause of early onset ataxia in Germany

Matthias Habeck, Christine Zühlke, KarlH.P. Bentele, Stephan Unkelbach, Wolfram Kreß, Katrin Bürk, Eberhard Schwinger, Yorck Hellenbroich

Journal:

Journal of Neurology

Year:

2004

Language:

english

File:

PDF, 183 KB

english, 2004

31

Do CTG expansions at the SCA8 locus cause ataxia?

Ludger Schöls, Ingrid Bauer, Christine Zühlke, Thorsten Schulte, Christina Kölmel, Katrin Bürk, Helge Topka, Peter Bauer, Horst Przuntek, Olaf Riess

Journal:

Annals of Neurology

Year:

2003

Language:

english

File:

PDF, 84 KB

english, 2003

32

Diagnosis and treatment of Friedreich ataxia: a European perspective

Schulz, Jörg B., Boesch, Sylvia, Bürk, Katrin, Dürr, Alexandra, Giunti, Paola, Mariotti, Caterina, Pousset, Francoise, Schöls, Ludger, Vankan, Pierre, Pandolfo, Massimo

Journal:

Nature Reviews Neurology (formerly Nature Clinical Practice Neurology)

Year:

2009

Language:

english

File:

PDF, 879 KB

english, 2009

33

KCNC3: phenotype, mutations, channel biophysics—a study of 260 familial ataxia patients

Karla P. Figueroa, Natali A. Minassian, Giovanni Stevanin, Michael Waters, Vartan Garibyan, Sylvie Forlani, Adam Strzelczyk, Katrin Bürk, Alexis Brice, Alexandra Dürr, Diane M. Papazian, Stefan M. Pul

Journal:

Year:

2010

Language:

english

File:

PDF, 180 KB

english, 2010

34

Mutation of the highly conserved cysteine residue 131 of the SCA14 associated PRKCG gene in a family with slow progressive cerebellar ataxia

Andreas Dalski, Beate Mitulla, Katrin Bürk, Christoph Schattenfroh, Eberhard Schwinger, Christine Zühlke

Journal:

Journal of Neurology

Year:

2006

Language:

english

File:

PDF, 49 KB

english, 2006

35

Friedreich and dominant ataxias: quantitative differences in cerebellar dysfunction measurements

Tanguy Melac, Audrey, Mariotti, Caterina, Filipovic Pierucci, Antoine, Giunti, Paola, Arpa, Javier, Boesch, Sylvia, Klopstock, Thomas, Müller vom Hagen, Jennifer, Klockgether, Thomas, Bürk, Katrin, Sc

Journal:

Journal of Neurology Neurosurgery & Psychiatry

Year:

2017

Language:

english

File:

PDF, 443 KB

english, 2017

36

A functional polymorphism regulating dopamine β-hydroxylase influences against Parkinson's disease

Daniel G. Healy, Patrick M. Abou-Sleiman, Tetsutaro Ozawa, Andrew J. Lees, Kailash Bhatia, Kourosh R. Ahmadi, Ullrich Wullner, Jose Berciano, J. Carsten Moller, Christoph Kamm, Katrin Burk, Paolo Barr

Journal:

Annals of Neurology

Year:

2004

Language:

english

File:

PDF, 125 KB

english, 2004

37

High prevalence of CSF-containing cysts in superficial hemosiderosis of the central nervous system

Katrin Bürk, Martin Skalej, Johannes Dichgans

Journal:

Journal of Neurology

Year:

2001

Language:

english

File:

PDF, 138 KB

english, 2001

38

Spinocerebellar ataxia 28: a novel AFG3L2 mutation in a German family with young onset, slow progression and saccadic slowing

Zühlke, Christine, Mikat, Barbara, Timmann, Dagmar, Wieczorek, Dagmar, Gillessen-Kaesbach, Gabriele, Bürk, Katrin

Journal:

Cerebellum & Ataxias

Year:

2015

Language:

english

File:

PDF, 412 KB

english, 2015

39

Neurological symptoms in patients with biopsy proven celiac disease

Katrin Bürk, Marie-Louise Farecki, Georg Lamprecht, Guenter Roth, Patrice Decker, Michael Weller, Hans-Georg Rammensee, Wolfang Oertel

Journal:

Movement Disorders

Year:

2009

Language:

english

File:

PDF, 62 KB

english, 2009

40

Treatment of paroxysmal dyskinesias

Strzelczyk, Adam, Bürk, Katrin, Oertel, Wolfgang H

Journal:

Expert Opinion on Pharmacotherapy

Year:

2011

Language:

english

File:

PDF, 256 KB

english, 2011

41

Mesial temporal lobe epilepsy in a patient with spinocerebellar ataxia type 13 (SCA13)

Bürk, Katrin, Strzelczyk, Adam, Reif, Philipp S., Figueroa, Karla P., Pulst, Stefan M., Zühlke, Christine, Oertel, Wolfgang H., Hamer, Hajo M., Rosenow, Felix

Journal:

International Journal of Neuroscience

Year:

2013

Language:

english

File:

PDF, 433 KB

english, 2013

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