Works by Kuhlenbäumer, Gregor

Results: 52

Real-time classification of movement patterns of tremor patients.

Published in:

Biomedical Engineering / Biomedizinische Technik, 2022, v. 67, n. 2, p. 119, doi. 10.1515/bmt-2021-0140

By:

Piepjohn, Patricia;
Bald, Christin;
Kuhlenbäumer, Gregor;
Becktepe, Jos Steffen;
Deuschl, Günther;
Schmidt, Gerhard

Publication type:

Article

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

Published in:

2016

By:

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

Publication type:

journal article

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

Published in:

2016

By:

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

Publication type:

journal article

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

Published in:

Movement Disorders, 2015, v. 30, n. 8, p. 1149, doi. 10.1002/mds.26252

By:

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

Publication type:

Article

The impact of rare variants in FUS in essential tremor.

Published in:

Movement Disorders, 2015, v. 30, n. 5, p. 721, doi. 10.1002/mds.26145

By:

Hopfner, Franziska;
Stevanin, Giovanni;
Müller, Stefanie H.;
Mundwiller, Emeline;
Bungeroth, May;
Durr, Alexandra;
Pendziwiat, Manuela;
Anheim, Mathieu;
Schneider, Susanne A.;
Tittmann, Lukas;
Klebe, Stephan;
Lorenz, Delia;
Deuschl, Günther;
Brice, Alexis;
Kuhlenbäumer, Gregor

Publication type:

Article

No association between polymorphisms in the glutamate transporter SLC1A2 and Parkinson's disease.

Published in:

Movement Disorders, 2013, v. 28, n. 9, p. 1305, doi. 10.1002/mds.25330

By:

Appenzeller, Silke;
Schulte, Claudia;
Thier, Sandra;
Hopfner, Franziska;
Pendziwiat, Manuela;
Papengut, Frank;
Klein, Christine;
Hagenah, Johann;
Kasten, Meike;
Srulijes, Karin;
Berg, Daniela;
Gasser, Thomas;
Singleton, Andrew;
Deuschl, Günther;
Kuhlenbäumer, Gregor

Publication type:

Article

The role of SCARB2 as susceptibility factor in Parkinson's disease.

Published in:

Movement Disorders, 2013, v. 28, n. 4, p. 538, doi. 10.1002/mds.25349

By:

Hopfner, Franziska;
Schulte, Eva C.;
Mollenhauer, Brit;
Bereznai, Benjamin;
Knauf, Franziska;
Lichtner, Peter;
Zimprich, Alexander;
Haubenberger, Dietrich;
Pirker, Walter;
Brücke, Thomas;
Peters, Annette;
Gieger, Christian;
Kuhlenbäumer, Gregor;
Trenkwalder, Claudia;
Winkelmann, Juliane

Publication type:

Article

No association between NOD2 variants and Parkinson's disease.

Published in:

Movement Disorders, 2012, v. 27, n. 9, p. 1191, doi. 10.1002/mds.25059

By:

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

Publication type:

Article

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

Published in:

Movement Disorders, 2012, v. 27, n. 4, p. 590, doi. 10.1002/mds.24907

By:

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

Publication type:

Article

LINGO1 polymorphisms are associated with essential tremor in Europeans.

Published in:

Movement Disorders, 2010, v. 25, n. 6, p. 717, doi. 10.1002/mds.22887

By:

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

Publication type:

Article

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

Published in:

European Journal of Human Genetics, 1999, v. 7, n. 8, p. 920, doi. 10.1038/sj.ejhg.5200384

By:

Meuleman, Jan;
Kuhlenbäumer, Gregor;
Schirmacher, Anja;
Wehnert, Manfred;
De Jonghe, Peter;
De Vriendt, Els;
Young, Peter;
Airaksinen, Eila;
Pou-Serradell, Adolfo;
Prats, José-Maria;
Ringelstein, Bernd;
Stögbauer, Florian;
Van Broeckhoven, Christine;
Timmerman, Vincent

Publication type:

Article

Mutations in SEPT9 cause hereditary neuralgic amyotrophy.

Published in:

Nature Genetics, 2005, v. 37, n. 10, p. 1044, doi. 10.1038/ng1649

By:

Kuhlenbäumer, Gregor;
Hannibal, Mark C.;
Nelis, Eva;
Schirmacher, Anja;
Verpoorten, Nathalie;
Meuleman, Jan;
Watts, Giles D. J.;
de Vriendt, Els;
Young, Peter;
Stögbauer, Florian;
Halfter, Hartmut;
Irobi, Joy;
Goossens, Dirk;
Del-Favero, Jurgen;
Betz, Benjamin G.;
Hyun Hor;
Kurlemann, Gert;
Bird, Thomas D.;
Airaksinen, Ella;
Mononen, Tarja

Publication type:

Article

Chlamydia pneumoniae infection and Alzheimer's disease: a connection to remember?

Published in:

Medical Microbiology & Immunology, 2010, v. 199, n. 4, p. 283, doi. 10.1007/s00430-010-0162-1

By:

Shima, Kensuke;
Kuhlenbäumer, Gregor;
Rupp, Jan

Publication type:

Article

Validity and Prognostic Value of a Polygenic Risk Score for Parkinson's Disease.

Published in:

Genes, 2021, v. 12, n. 12, p. 1859, doi. 10.3390/genes12121859

By:

Koch, Sebastian;
Laabs, Björn-Hergen;
Kasten, Meike;
Vollstedt, Eva-Juliane;
Becktepe, Jos;
Brüggemann, Norbert;
Franke, Andre;
Krämer, Ulrike M.;
Kuhlenbäumer, Gregor;
Lieb, Wolfgang;
Mollenhauer, Brit;
Neis, Miriam;
Trenkwalder, Claudia;
Schäffer, Eva;
Usnich, Tatiana;
Wittig, Michael;
Klein, Christine;
König, Inke R.;
Lohmann, Katja;
Krawczak, Michael

Publication type:

Article

Long-Lived Individuals Show a Lower Burden of Variants Predisposing to Age-Related Diseases and a Higher Polygenic Longevity Score.

Published in:

International Journal of Molecular Sciences, 2022, v. 23, n. 18, p. N.PAG, doi. 10.3390/ijms231810949

By:

Torres, Guillermo G.;
Dose, Janina;
Hasenbein, Tim P.;
Nygaard, Marianne;
Krause-Kyora, Ben;
Mengel-From, Jonas;
Christensen, Kaare;
Andersen-Ranberg, Karen;
Kolbe, Daniel;
Lieb, Wolfgang;
Laudes, Matthias;
Görg, Siegfried;
Schreiber, Stefan;
Franke, Andre;
Caliebe, Amke;
Kuhlenbäumer, Gregor;
Nebel, Almut

Publication type:

Article

Pontine autosomal dominant microangiopathy with leukoencephalopathy: Col4A1 gene variants in the original family and sporadic stroke.

Published in:

Journal of Neurology, 2023, v. 270, n. 5, p. 2631, doi. 10.1007/s00415-023-11590-9

By:

Roos, Jessica;
Müller, Stefanie;
Giese, Anne;
Appenzeller, Silke;
Ringelstein, Erich Bernd;
Fiehler, Jens;
Berger, Klaus;
Rolfs, Arndt;
Hagel, Christian;
Kuhlenbäumer, Gregor

Publication type:

Article

Clinical and radiological differences between patients with probable cerebral amyloid angiopathy and mixed cerebral microbleeds.

Published in:

Journal of Neurology, 2020, v. 267, n. 12, p. 3602, doi. 10.1007/s00415-020-10038-8

By:

Jensen-Kondering, Ulf R.;
Weiler, Caroline;
Langguth, Patrick;
Larsen, Naomi;
Flüh, Charlotte;
Kuhlenbäumer, Gregor;
Jansen, Olav;
Margraf, Nils G.

Publication type:

Article

Autosomal dominant epilepsy with auditory features: a new LGI1 family including a phenocopy with cortical dysplasia.

Published in:

Journal of Neurology, 2016, v. 263, n. 1, p. 11, doi. 10.1007/s00415-015-7921-2

By:

Klein, Karl;
Pendziwiat, Manuela;
Cohen, Rony;
Appenzeller, Silke;
Kovel, Carolien;
Rosenow, Felix;
Koeleman, Bobby;
Kuhlenbäumer, Gregor;
Sheintuch, Liron;
Veksler, Ronel;
Friedman, Alon;
Afawi, Zaid;
Helbig, Ingo

Publication type:

Article

Arterial elongation ('redundancy') is not a feature of spontaneous cervical artery dissection.

Published in:

Journal of Neurology, 2011, v. 258, n. 2, p. 250, doi. 10.1007/s00415-010-5737-7

By:

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

Publication type:

Article

Aberrations of dermal connective tissue in patients with cervical artery dissection (sCAD).

Published in:

Journal of Neurology, 2008, v. 255, n. 3, p. 340, doi. 10.1007/s00415-008-0585-4

By:

Uhlig, Phillip;
Bruckner, Peter;
Dittrich, Ralf;
Ringelstein, E. Bernd;
Kuhlenbäumer, Gregor;
Hansen, Uwe

Publication type:

Article

Family and literature analysis demonstrates phenotypic effect of two variants in the calpain-3 gene.

Published in:

Neurogenetics, 2023, v. 24, n. 4, p. 273, doi. 10.1007/s10048-023-00728-6

By:

Tomforde, Maike;
Steinbach, Meike;
Haack, Tobias B.;
Kuhlenbäumer, Gregor

Publication type:

Article

Evidence for pathogenicity of variant ATM Val1729Leu in a family with ataxia telangiectasia.

Published in:

Neurogenetics, 2021, v. 22, n. 2, p. 143, doi. 10.1007/s10048-021-00639-4

By:

Shalash, Ali S.;
Rösler, Thomas W.;
Salama, Mohamed;
Pendziwiat, Manuela;
Müller, Stefanie H.;
Hopfner, Franziska;
Höglinger, Günter U.;
Kuhlenbäumer, Gregor

Publication type:

Article

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

Published in:

Journal of Neuroimaging, 2010, v. 20, n. 2, p. 134, doi. 10.1111/j.1552-6569.2008.00336.x

By:

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

Publication type:

Article

Painless legs and moving toes in a mother and her daughter.

Published in:

Movement Disorders, 2003, v. 18, n. 6, p. 718, doi. 10.1002/mds.10435

By:

Dziewas, Rainer;
Kuhlenbäumer, Gregor;
Okegwo, Angelika;
Lüdemann, Peter

Publication type:

Article

Novel septin 9 repeat motifs altered in neuralgic amyotrophy bind and bundle microtubules.

Published in:

Journal of Cell Biology, 2013, v. 203, n. 6, p. 895, doi. 10.1083/jcb.201308068

By:

Bai, Xiaobo;
Bowen, Jonathan R.;
Knox, Tara K.;
Zhou, Kaifeng;
Pendziwiat, Manuela;
Kuhlenbäumer, Gregor;
Sindelar, Charles V.;
Spiliotis, Elias T.

Publication type:

Article

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

Published in:

International Journal of Neuropsychopharmacology, 2004, v. 7, n. 2, p. 183, doi. 10.1017/s146114570400416x

By:

Katharina Domschke;
Christine M. Freitag;
Gregor Kuhlenbäumer;
Anja Schirmacher;
Philipp Sand;
Peter Nyhuis;
Christian Jacob;
Jürgen Fritze;
Petra Franke;
Marcella Rietschel;
Henk S. Garritsen;
Rolf Fimmers;
Markus M. Nöthen;
Klaus-Peter Lesch;
Florian Stögbauer

Publication type:

Article

K-variant BCHE and pesticide exposure: Gene-environment interactions in a case–control study of Parkinson’s disease in Egypt.

Published in:

Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-35003-4

By:

Rösler, Thomas W.;
Salama, Mohamed;
Shalash, Ali S.;
Khedr, Eman M.;
El-Tantawy, Abdelhalim;
Fawi, Gharib;
El-Motayam, Amal;
El-Seidy, Ehab;
El-Sherif, Mohamed;
El-Gamal, Mohamed;
Moharram, Mohamed;
El-Kattan, Mohammad;
Abdel-Naby, Muhammad;
Ashour, Samia;
Müller, Ulrich;
Dempfle, Astrid;
Kuhlenbäumer, Gregor;
Höglinger, Günter U.

Publication type:

Article

HLA and KIR genetic association and NK cells in anti-NMDAR encephalitis.

Published in:

Frontiers in Immunology, 2024, p. 1, doi. 10.3389/fimmu.2024.1423149

By:

Peris Sempere, Vicente;
Guo Luo;
Muñiz-Castrillo, Sergio;
Pinto, Anne-Laurie;
Picard, Géraldine;
Rogemond, Véronique;
Titulaer, Maarten J.;
Finke, Carsten;
Leypoldt, Frank;
Kuhlenbäumer, Gregor;
Jones, Hannah F.;
Dale, Russell C.;
Binks, Sophie;
Irani, Sarosh R.;
Bastiaansen, Anna E.;
de Vries, Juna M.;
de Bruijn, Marienke A. A. M.;
Roelen, Dave L.;
Tae-Joon Kim;
Kon Chu

Publication type:

Article

Cerebrospinal Fluid Biomarkers in Cerebral Amyloid Angiopathy: New Data and Quantitative Meta-Analysis.

Published in:

Frontiers in Aging Neuroscience, 2022, v. 14, p. 1, doi. 10.3389/fnagi.2022.783996

By:

Margraf, Nils G.;
Jensen-Kondering, Ulf;
Weiler, Caroline;
Leypoldt, Frank;
Maetzler, Walter;
Philippen, Sarah;
Bartsch, Thorsten;
Flüh, Charlotte;
Röcken, Christoph;
Möller, Bettina;
Royl, Georg;
Neumann, Alexander;
Brüggemann, Norbert;
Roeben, Benjamin;
Schulte, Claudia;
Bender, Benjamin;
Berg, Daniela;
Kuhlenbäumer, Gregor

Publication type:

Article

Determinants of Platelet-Leukocyte Aggregation and Platelet Activation in Stroke.

Published in:

Cerebrovascular Diseases, 2015, v. 39, n. 3/4, p. 176, doi. 10.1159/000375396

By:

Schmalbach, Barbara;
Stepanow, Olga;
Jochens, arne;
Riedel, Christian;
Deuschl, Günther;
Kuhlenbäumer, Gregor

Publication type:

Article

Archimedes Spiral Ratings: Determinants and Population‐Based Limits of Normal.

Published in:

Movement Disorders Clinical Practice, 2024, v. 11, n. 10, p. 1257, doi. 10.1002/mdc3.14201

By:

Hopfner, Franziska;
Tietz, Anja;
D'Elia, Yuri;
Pattaro, Cristian;
Becktepe, Jos S.;
Gögele, Martin;
Barin, Laura;
Pramstaller, Peter P.;
Kuhlenbäumer, Gregor;
Melotti, Roberto

Publication type:

Article

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

Published in:

Journal of Neural Transmission, 2009, v. 116, n. 7, p. 815, doi. 10.1007/s00702-009-0236-7

By:

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

Publication type:

Article

Decreased Cerebrospinal Fluid Amyloid Beta 38, 40, 42, and 43 Levels in Sporadic and Hereditary Cerebral Amyloid Angiopathy.

Published in:

Annals of Neurology, 2023, v. 94, n. 1, p. 205, doi. 10.1002/ana.26671

By:

Kuhlenbäumer, Gregor;
Jensen‐Kondering, Ulf;
Margraf, Nils G.

Publication type:

Article

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

Published in:

Annals of Neurology, 2008, v. 64, n. 4, p. 402, doi. 10.1002/ana.21480

By:

Gretarsdottir, Solveig;
Thorleifsson, Gudmar;
Manolescu, Andrei;
Styrkarsdottir, Unnur;
Helgadottir, Anna;
Gschwendtner, Andreas;
Kostulas, Konstantinos;
Kuhlenbäumer, Gregor;
Bevan, Steve;
Jonsdottir, Thorbjorg;
Bjarnason, Hjordis;
Saemundsdottir, Jona;
Palsson, Stefan;
Arnar, David O.;
Holm, Hilma;
Thorgeirsson, Gudmundur;
Valdimarsson, Einar Mar;
Sveinbjörnsdottir, Sigurlaug;
Gieger, Christian;
Berger, Klaus

Publication type:

Article

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

Published in:

Developmental Medicine & Child Neurology, 2012, v. 54, n. 12, p. 1144, doi. 10.1111/j.1469-8749.2012.04435.x

By:

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

Publication type:

Article

Candidate variants in TUB are associated with familial tremor.

Published in:

PLoS Genetics, 2020, v. 16, n. 9, p. 1, doi. 10.1371/journal.pgen.1009010

By:

Sailani, M. Reza;
Jahanbani, Fereshteh;
Abbott, Charles W.;
Lee, Hayan;
Zia, Amin;
Rego, Shannon;
Winkelmann, Juliane;
Hopfner, Franziska;
Khan, Tahir N.;
Katsanis, Nicholas;
Müller, Stefanie H.;
Berg, Daniela;
Lyman, Katherine M.;
Mychajliw, Christian;
Deuschl, Günther;
Bernstein, Jonathan A.;
Kuhlenbäumer, Gregor;
Snyder, Michael P.

Publication type:

Article

Aβ38 and Aβ43 do not differentiate between Alzheimer's disease and cerebral amyloid angiopathy.

Published in:

Annals of Clinical & Translational Neurology, 2024, v. 11, n. 3, p. 806, doi. 10.1002/acn3.51987

By:

Dargvainiene, Justina;
Jensen‐Kondering, Ulf;
Bender, Benjamin;
Berg, Daniela;
Brüggemann, Norbert;
Flüh, Charlotte;
Markewitz, Robert;
Neumann, Alexander;
Röben, Benjamin;
Röcken, Christoph;
Royl, Georg;
Schulte, Claudia;
Wandinger, Klaus‐Peter;
Weiler, Caroline;
Margraf, Nils G.;
Kuhlenbäumer, Gregor

Publication type:

Article

Whole‐exome and HLA sequencing in Febrile infection‐related epilepsy syndrome.

Published in:

Annals of Clinical & Translational Neurology, 2020, v. 7, n. 8, p. 1429, doi. 10.1002/acn3.51062

By:

Helbig, Ingo;
Barcia, Giulia;
Pendziwiat, Manuela;
Ganesan, Shiva;
Mueller, Stefanie H.;
Helbig, Katherine L.;
Vaidiswaran, Priya;
Xian, Julie;
Galer, Peter D.;
Afawi, Zaid;
Specchio, Nicola;
Kluger, Gerhard;
Kuhlenbäumer, Gregor;
Appenzeller, Silke;
Wittig, Michael;
Kramer, Uri;
Baalen, Andreas;
Nabbout, Rima

Publication type:

Article

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

Published in:

Journal of Neurology, 2004, v. 251, n. 10, p. 1242, doi. 10.1007/s00415-004-0523-z

By:

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

Publication type:

Article

Neither collagen 8A1 nor 8A2 mutations play a major role in cervical artery dissection: A mutation analysis and linkage study.

Published in:

Journal of Neurology, 2004, v. 251, n. 3, p. 357, doi. 10.1007/s00415-004-0335-1

By:

Kuhlenbäumer, Gregor;
Müller, Uta S.;
Besselmann, Michael;
Rauterberg, J&uumlrgen;
Robenek, Horst;
Hünermund, Gert;
Brandt, Tobias;
Ringelstein, E. Bernd;
Stögbauer, Florian

Publication type:

Article

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

Published in:

Journal of Neurology, 2003, v. 250, n. 10, p. 1179, doi. 10.1007/s00415-003-0174-5

By:

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

Publication type:

Article

Clinical features and molecular genetics of hereditary peripheral neuropathies.

Published in:

Journal of Neurology, 2002, v. 249, n. 12, p. 1629, doi. 10.1007/s00415-002-0946-3

By:

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

Publication type:

Article

Hereditary Neuralgic Amyotrophy (HNA) is genetically heterogeneous.

Published in:

Journal of Neurology, 2001, v. 248, n. 10, p. 861

By:

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

Publication type:

Article

Two-Stage Convolutional Neural Network for Classification of Movement Patterns in Tremor Patients.

Published in:

Information (2078-2489), 2024, v. 15, n. 4, p. 231, doi. 10.3390/info15040231

By:

Weede, Patricia;
Smietana, Piotr Dariusz;
Kuhlenbäumer, Gregor;
Deuschl, Günther;
Schmidt, Gerhard

Publication type:

Article

Validation of the QUEST for German-speaking countries.

Published in:

International Journal of Neuroscience, 2016, v. 126, n. 2, p. 127, doi. 10.3109/00207454.2015.1077241

By:

Hopfner, Franziska;
Nebel, Adelheid;
Lyons, Kelly E.;
Tröster, Alexander I.;
Kuhlenbäumer, Gregor;
Deuschl, Günther;
Martinez-Martin, Pablo

Publication type:

Article

Broad Phenotypic Heterogeneity due to a Novel SCN1A Mutation in a Family With Genetic Epilepsy With Febrile Seizures Plus.

Published in:

2014

By:

Goldberg-Stern, Hadassa;
Aharoni, Sharon;
Afawi, Zaid;
Bennett, Odeya;
Appenzeller, Silke;
Pendziwiat, Manuela;
Kuhlenbäumer, Gregor;
Basel-Vanagaite, Lina;
Shuper, Avinoam;
Korczyn, Amos D.;
Helbig, Ingo

Publication type:

Case Study

Genetic TPH2 variants and the susceptibility for migraine: association of a TPH2 haplotype with migraine without aura.

Published in:

Journal of Neural Transmission, 2010, v. 117, n. 11, p. 1253, doi. 10.1007/s00702-010-0468-6

By:

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

Publication type:

Article

Electroencephalography based delirium screening in acute supratentorial stroke.

Published in:

BMC Neurology, 2024, v. 24, n. 1, p. 1, doi. 10.1186/s12883-024-03942-3

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Hermann, Gesine;
Baumgarte, Friederike;
Welzel, Julius;
Nydahl, Peter;
Kuhlenbäumer, Gregor;
Margraf, Nils Gerd

Publication type:

Article

Large‐Scale Screening: Phenotypic and Mutational Spectrum in Isolated and Combined Dystonia Genes.

Published in:

Movement Disorders, 2024, v. 39, n. 3, p. 526, doi. 10.1002/mds.29693

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Thomsen, Mirja;
Marth, Katrin;
Loens, Sebastian;
Everding, Judith;
Junker, Johanna;
Borngräber, Friederike;
Ott, Fabian;
Jesús, Silvia;
Gelderblom, Mathias;
Odorfer, Thorsten;
Kuhlenbäumer, Gregor;
Kim, Han‐Joon;
Schaeffer, Eva;
Becktepe, Jos;
Kasten, Meike;
Brüggemann, Norbert;
Pfister, Robert;
Kollewe, Katja;
Krauss, Joachim K.;
Lohmann, Ebba

Publication type:

Article

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

Published in:

Human Mutation, 2011, v. 32, n. 2, p. 144, doi. 10.1002/humu.21400

By:

Kuhlenbäumer, Gregor;
Hullmann, Julia;
Appenzeller, Silke

Publication type:

Article