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1

Genomic organization and mutation analysis of three candidate genes for hereditary neuralgic amyotrophy

Gert Hünermund, Anja Schirmacher, Bernd Ringelstein, Peter Young, Giles D. Watts, Jan Meuleman, Eva Nelis, Phillip F. Chance, Vincent Timmerman, Florian Stögbauer, Gregor Kuhlenbäumer

Journal:

Year:

2004

Language:

english

File:

PDF, 75 KB

english, 2004

2

Hereditary amyloidosis of the Finnish type in a German family: Clinical and electrophysiological presentation

Rainer J. Lüttmann, Inga Teismann, Ingo W. Husstedt, E. Bernd Ringelstein, Gregor Kuhlenbäumer

Journal:

Year:

2010

Language:

english

File:

PDF, 213 KB

english, 2010

3

Febrile infection-related epilepsy syndrome (FIRES) is not caused by SCN1A, POLG, PCDH19 mutations or rare copy number variations

APPENZELLER, SILKE, HELBIG, INGO, STEPHANI, ULRICH, HÄUSLER, MARTIN, KLUGER, GERHARD, BUNGEROTH, MAY, MÜLLER, STEFANIE, KUHLENBÄUMER, GREGOR, VAN BAALEN, ANDREAS

Journal:

Developmental Medicine & Child Neurology

Year:

2012

Language:

english

File:

PDF, 195 KB

english, 2012

4

Gut microbiota in Parkinson disease in a northern German cohort

Hopfner, Franziska, Künstner, Axel, Müller, Stefanie H., Künzel, Sven, Zeuner, Kirsten E., Margraf, Nils G., Deuschl, Günther, Baines, John F., Kuhlenbäumer, Gregor

Journal:

Year:

2017

Language:

english

File:

PDF, 988 KB

english, 2017

5

Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke

Solveig Gretarsdottir, Gudmar Thorleifsson, Andrei Manolescu, Unnur Styrkarsdottir, Anna Helgadottir, Andreas Gschwendtner, Konstantinos Kostulas, Gregor Kuhlenbäumer, Steve Bevan, Thorbjorg Jonsdotti

Journal:

Annals of Neurology

Year:

2008

Language:

english

File:

PDF, 91 KB

english, 2008

6

Novel genomic techniques open new avenues in the analysis of monogenic disorders

Gregor Kuhlenbäumer, Julia Hullmann, Silke Appenzeller

Journal:

Year:

2011

Language:

english

File:

PDF, 175 KB

english, 2011

7

Painless legs and moving toes in a mother and her daughter

Rainer Dziewas, Gregor Kuhlenbäumer, Angelika Okegwo, Peter Lüdemann

Journal:

Movement Disorders

Year:

2003

Language:

english

File:

PDF, 439 KB

english, 2003

8

LINGO1 polymorphisms are associated with essential tremor in Europeans

Sandra Thier, Delia Lorenz, Michael Nothnagel, Giovanni Stevanin, Alexandra Dürr, Almut Nebel, Stefan Schreiber, Gregor Kuhlenbäumer, Günther Deuschl, Stephan Klebe

Journal:

Movement Disorders

Year:

2010

Language:

english

File:

PDF, 150 KB

english, 2010

9

No evidence for differential methylation of α-synuclein in leukocyte DNA of Parkinson's disease patients

Julia Richter, Silke Appenzeller, Ole Ammerpohl, G. Deuschl, Steffen Paschen, Norbert Brüggemann, Christine Klein, Gregor Kuhlenbäumer

Journal:

Movement Disorders

Year:

2012

Language:

english

File:

PDF, 199 KB

english, 2012

10

Zerebrale Mikroangiopathien

E.Bernd Ringelstein, Gregor Kuhlenbäumer

Journal:

Clinical Neuroradiology

Year:

2004

Language:

german

File:

PDF, 466 KB

german, 2004

11

Clinical features and molecular genetics of hereditary peripheral neuropathies

Gregor Kuhlenbäumer, Peter Young, Gert Hünermund, Bernd Ringelstein, Florian Stögbauer

Journal:

Journal of Neurology

Year:

2002

Language:

english

File:

PDF, 437 KB

english, 2002

12

Cervical artery dissection—clinical features, risk factors, therapy and outcome in 126 patients

Rainer Dziewas, Carsten Konrad, Bianca Dräger, Stefan Evers, Michael Besselmann, Peter Lüdemann, Gregor Kuhlenbäumer, Florian Stögbauer, E.Bernd Ringelstein

Journal:

Journal of Neurology

Year:

2003

Language:

english

File:

PDF, 169 KB

english, 2003

13

Neither collagen 8A1 nor 8A2 mutations play a major role in cervical artery dissection

Gregor Kuhlenbäumer*, UtaS. Müller*, Michael Besselmann, Jürgen Rauterberg, Horst Robenek, Gert Hünermund, Tobias Brandt, E.Bernd Ringelstein, Florian Stögbauer

Journal:

Journal of Neurology

Year:

2004

Language:

english

File:

PDF, 195 KB

english, 2004

14

Plasma homocysteine, MTHFR C677T, CBS 844ins68bp, and MTHFD1 G1958A polymorphisms in spontaneous cervical artery dissections

Carsten Konrad, Georg A. Müller, Claus Langer, Gregor Kuhlenbäumer, Klaus Berger, Darius G. Nabavi, Rainer Dziewas, Florian Stögbauer, Erich B. Ringelstein, Ralf Junker

Journal:

Journal of Neurology

Year:

2004

Language:

english

File:

PDF, 228 KB

english, 2004

15

Arterial elongation (“redundancy”) is not a feature of spontaneous cervical artery dissection

Ralf Dittrich, Isabelle Nassenstein, Siri Harms, David Maintz, Walter Heindel, Gregor Kuhlenbäumer, Erich Bernd Ringelstein

Journal:

Journal of Neurology

Year:

2011

Language:

english

File:

PDF, 192 KB

english, 2011

16

Hereditary Neuralgic Amyotrophy (HNA) is genetically heterogeneous

Gregor Kuhlenbäumer, Jan Meuleman, Peter De Jonghe, Björn Falck, Peter Young, Gert Hünermund, Christine Van Broeckhoven, Vincent Timmerman, Florian Stögbauer

Journal:

Journal of Neurology

Year:

2001

Language:

english

File:

PDF, 218 KB

english, 2001

17

Chlamydia pneumoniaeinfection and Alzheimer’s disease: a connection to remember?

Kensuke Shima, Gregor Kuhlenbäumer, Jan Rupp

Journal:

Medical Microbiology and Immunology

Year:

2010

Language:

english

File:

PDF, 411 KB

english, 2010

18

Functional gene variants of the serotonin-synthesizing enzyme tryptophan hydroxylase 2 in migraine

Martin Marziniak, Claudia Kienzler, Gregor Kuhlenbäumer, Claudia Sommer, Rainald Mössner

Journal:

Journal of Neural Transmission

Year:

2009

Language:

english

File:

PDF, 209 KB

english, 2009

19

GeneticTPH2variants and the susceptibility for migraine: association of aTPH2haplotype with migraine without aura

Alexander Jung, Andreas Huge, Gregor Kuhlenbäumer, Steffi Kempt, Tanja Seehafer, Stefan Evers, Klaus Berger, Martin Marziniak

Journal:

Journal of Neural Transmission

Year:

2010

Language:

english

File:

PDF, 249 KB

english, 2010

20

MRI Features of Pontine Autosomal Dominant Microangiopathy and Leukoencephalopathy (PADMAL)

Xiao-Qi Ding, Christian Hagel, E. Bernd Ringelstein, Stefan Buchheit, Hermann Zeumer, Gregor Kuhlenbäumer, Silke Appenzeller, Jens Fiehler

Journal:

Journal of Neuroimaging

Year:

2010

Language:

english

File:

PDF, 314 KB

english, 2010

21

Mutations in SEPT9 cause hereditary neuralgic amyotrophy

Kuhlenbäumer, Gregor, Hannibal, Mark C, Nelis, Eva, Schirmacher, Anja, Verpoorten, Nathalie, Meuleman, Jan, Watts, Giles D J, Vriendt, Els De, Young, Peter, Stögbauer, Florian

Journal:

Nature Genetics

Year:

2005

Language:

english

File:

PDF, 287 KB

english, 2005

22

Genetic refinement of the hereditary neuralgic amyotrophy (HNA) locus at chromosome 17q25

Meuleman, Jan, Kuhlenbäumer, Gregor, Schirmacher, Anja, Wehnert, Manfred, De Jonghe, Peter, De Vriendt, Els, Young, Peter, Airaksinen, Eila, Pou-Serradell, Adolfo, Prats, José-Maria

Journal:

European Journal of Human Genetics

Year:

1999

Language:

english

File:

PDF, 287 KB

english, 1999

23

No association between NOD2 variants and Parkinson's disease

Silke Appenzeller, Sandra Thier, Frank Papengut, Christine Klein, Johann Hagenah, Meike Kasten, Daniela Berg, Karin Srulijes, Thomas Gasser, Stefan Schreiber, Günther Deuschl, Gregor Kuhlenbäumer

Journal:

Movement Disorders

Year:

2012

Language:

english

File:

PDF, 711 KB

english, 2012

24

A Sequence-Ready BAC/PAC Contig and Partial Transcript Map of Approximately 1.5 Mb in Human Chromosome 17q25 Comprising Multiple Disease Genes

Gregor Kuhlenbäumer, , Anja Schirmacher, , Jan Meuleman, Fadel Tissir, Jurgen Del-Favero, Florian Stögbauer, Peter Young, Bernd Ringelstein, Christine Van Broeckhoven, Vincent Timmerman

Journal:

Year:

1999

Language:

english

File:

PDF, 159 KB

english, 1999

25

Norepinephrine transporter (NET) promoter and 5′-UTR polymorphisms: association analysis in panic disorder

Yoo J. Lee, Christa Hohoff, Katharina Domschke, Philipp Sand, Gregor Kuhlenbäumer, Anja Schirmacher, Christine M. Freitag, Jobst Meyer, Gerald Stöber, Petra Franke, Markus M. Nöthen, Jürgen Fritze, Ro

Journal:

Neuroscience Letters

Year:

2005

Language:

english

File:

PDF, 68 KB

english, 2005

26

Absence of mutations in the prion-protein gene in a large cohort of HMSN patients

Olga Koop, Vincent Timmerman, Peter de Jonghe, Bernd Ringelstein, Peter Young, Gregor Kuhlenbäumer

Journal:

Neuromuscular Disorders

Year:

2005

Language:

english

File:

PDF, 59 KB

english, 2005

27

Genotype–phenotype analysis in patients with giant axonal neuropathy

Gregor Kuhlenbäumer

Journal:

Neuromuscular Disorders

Year:

2008

Language:

english

File:

PDF, 49 KB

english, 2008

28

Absence of mutations in peripheral myelin protein-22, myelin protein zero, and connexin 32 in autosomal recessive Dejerine-Sottas syndrome

Florian Stögbauer, Peter Young, Heiko Wiebusch, Vincent Timmerman, Gregor Kuhlenbäumer, Eva Nelis, E.Bernd Ringelstein, Gerd Kurlemann, Gerd Assmann, Christine Van Broeckhoven, Harald Funke

Journal:

Neuroscience Letters

Year:

1998

Language:

english

File:

PDF, 55 KB

english, 1998

29

Diagnostic guidelines for hereditary neuralgic amyotrophy or heredofamilial neuritis with brachial plexus predilection

Gregor Kuhlenbäumer, Florian Stögbauer, Vincent Timmerman, Peter De Jonghe

Journal:

Neuromuscular Disorders

Year:

2000

Language:

english

File:

PDF, 44 KB

english, 2000

30

Hereditary and non-hereditary microangiopathies in the young. An up-date

E. Bernd Ringelstein, Ilka Kleffner, Ralf Dittrich, Gregor Kuhlenbäumer, Martin A. Ritter

Journal:

Journal of the Neurological Sciences

Year:

2010

Language:

english

File:

PDF, 727 KB

english, 2010

31

Association of the functional V158M catechol-O-methyl-transferase polymorphism with panic disorder in women

Domschke, Katharina, Freitag, Christine M., Kuhlenbäumer, Gregor, Schirmacher, Anja, Sand, Philipp, Nyhuis, Peter, Jacob, Christian, Fritze, Jürgen, Franke, Petra, Rietschel, Marcella, Garritsen, Henk

Journal:

The International Journal of Neuropsychopharmacology

Year:

2004

Language:

english

File:

PDF, 69 KB

english, 2004

32

Differential aggregation properties of alpha-synuclein isoforms

Bungeroth, May, Appenzeller, Silke, Regulin, Annika, Völker, Wolfgang, Lorenzen, Inken, Grötzinger, Joachim, Pendziwiat, Manuela, Kuhlenbäumer, Gregor

Journal:

Neurobiology of Aging

Year:

2014

Language:

english

File:

PDF, 2.00 MB

english, 2014

33

Rare variants in ANO3 are not a susceptibility factor in essential tremor

Hopfner, Franziska, Bungeroth, May, Pendziwiat, Manuela, Tittmann, Lukas, Deuschl, Günther, Schneider, Susanne A., Kuhlenbäumer, Gregor

Journal:

Parkinsonism & Related Disorders

Year:

2014

Language:

english

File:

PDF, 164 KB

english, 2014

34

Hereditary Peripheral Neuropathies ||

Kuhlenbäumer, Gregor, Stögbauer, Florian, Ringelstein, E. Bernd, Young, Peter

Year:

2005

Language:

english

File:

PDF, 3.12 MB

english, 2005

35

Hereditary Peripheral Neuropathies || Hereditary sensory and autonomic neuropathies (HSAN)

Kuhlenbäumer, Gregor, Stögbauer, Florian, Ringelstein, E. Bernd, Young, Peter

Year:

2005

Language:

english

File:

PDF, 116 KB

english, 2005

36

Testing for alcohol sensitivity of tremor amplitude in a large cohort with essential tremor

Hopfner, Franziska, Erhart, Tatjana, Knudsen, Karina, Lorenz, Delia, Schneider, Susanne A., Zeuner, Kirsten E., Deuschl, Günther, Kuhlenbäumer, Gregor

Journal:

Parkinsonism & Related Disorders

Year:

2015

Language:

english

File:

PDF, 430 KB

english, 2015

37

Autosomal dominant epilepsy with auditory features: a newLGI1family including a phenocopy with cortical dysplasia

Klein, Karl Martin, Pendziwiat, Manuela, Cohen, Rony, Appenzeller, Silke, de Kovel, Carolien G. F., Rosenow, Felix, Koeleman, Bobby P. C., Kuhlenbäumer, Gregor, Sheintuch, Liron, Veksler, Ronel, Fried

Journal:

Journal of Neurology

Year:

2016

Language:

english

File:

PDF, 660 KB

english, 2016

38

Early-onset parkinsonism due to compound heterozygous POLG mutations

Rempe, Torge, Kuhlenbäumer, Gregor, Krüger, Stefanie, Biskup, Saskia, Matschke, Jakob, Hagel, Christian, Deuschl, Günther, van Eimeren, Thilo

Journal:

Parkinsonism & Related Disorders

Year:

2016

Language:

english

File:

PDF, 162 KB

english, 2016

39

Mutations in HTRA2 are not a common cause of familial classic ET

Hopfner, Franziska, Müller, Stefanie H., Lorenz, Delia, Appenzeller, Silke, Klebe, Stephan, Deuschl, Günther, Kuhlenbäumer, Gregor

Journal:

Movement Disorders

Year:

2015

Language:

english

File:

PDF, 171 KB

english, 2015

40

Alpha synuclein and crystallin expression in human lens in Parkinson's disease

Klettner, Alexa, Richert, Elisabeth, Kuhlenbäumer, Gregor, Nölle, Bernhard, Bhatia, Kailash P., Deuschl, Günter, Roider, Johann, Schneider, Susanne A.

Journal:

Movement Disorders

Year:

2016

Language:

english

File:

PDF, 809 KB

english, 2016

41

Early- and late-onset essential tremor patients represent clinically distinct subgroups

Hopfner, Franziska, Ahlf, Anjuli, Lorenz, Delia, Klebe, Stephan, Zeuner, Kirsten E., Kuhlenbäumer, Gregor, Deuschl, Günther

Journal:

Movement Disorders

Year:

2016

Language:

english

File:

PDF, 501 KB

english, 2016

42

Topography of essential tremor

Chen, Wei, Hopfner, Franziska, Szymczak, Silke, Granert, Oliver, Müller, Stefanie H., Kuhlenbäumer, Gregor, Deuschl, Günther

Journal:

Parkinsonism & Related Disorders

Year:

2017

Language:

english

File:

PDF, 1.11 MB

english, 2017

43

Acute physical exercise improves shifting in adolescents at school: evidence for a dopaminergic contribution

Berse, Timo, Rolfes, Kathrin, Barenberg, Jonathan, Dutke, Stephan, Kuhlenbäumer, Gregor, Völker, Klaus, Winter, Bernward, Wittig, Michael, Knecht, Stefan

Journal:

Frontiers in Behavioral Neuroscience

Year:

2015

Language:

english

File:

PDF, 610 KB

english, 2015

44

Role of ANO3 mutations in dystonia: A large-scale mutational screening study

Olschewski, Luisa, Jesús, Silvia, Kim, Han-Joon, Tunc, Sinem, Löns, Sebastian, Junker, Johanna, Zeuner, Kirsten E., Kühn, Andrea A., Kuhlenbäumer, Gregor, Schäffer, Eva, Berg, Daniela, Kasten, Meike,

Journal:

Parkinsonism & Related Disorders

Year:

2019

Language:

english

File:

PDF, 465 KB

english, 2019

45

Use of β2-adrenoreceptor agonist and antagonist drugs and risk of Parkinson disease

Hopfner, Franziska, Wod, Mette, Höglinger, Günter U., Blaabjerg, Morten, Rösler, Thomas W., Kuhlenbäumer, Gregor, Christensen, Kaare, Deuschl, Günther, Pottegård, Anton

Journal:

Year:

2019

Language:

english

File:

PDF, 187 KB

english, 2019

46

Parkinson disease genetics: too early to predict progression?

Kuhlenbäumer, Gregor, Berg, Daniela

Journal:

Nature Reviews Neurology (formerly Nature Clinical Practice Neurology)

Year:

2019

Language:

english

File:

PDF, 523 KB

english, 2019