Publikationen
2012
Katja
Lohmann,
Nils
Uflacker,
Alev
Erogullari,
Thora
Lohnau,
Susen
Winkler,
Andreas
Dendorfer,
Susanne A.
Schneider,
Alma
Osmanovic,
Marina
Svetel,
Andreas
Ferbert,
Simone
Zittel,
Andrea A.
Kühn,
Alexander
Schmidt,
Eckart
Altenmüller,
Alexander
Münchau,
Christoph
Kamm,
Matthias
Wittstock,
Andreas
Kupsch,
Elena
Moro,
Jens
Volkmann,
Vladimir
Kostic,
Frank J.
Kaiser,
Christine
Klein, and
Norbert
Brüggemann,
Identification and functional analysis of novel THAP1 mutations, Eur J Hum Genet , vol. 20, no. 2, pp. 171–175, 2012.
Identification and functional analysis of novel THAP1 mutations, Eur J Hum Genet , vol. 20, no. 2, pp. 171–175, 2012.
| DOI: | 10.1038/ejhg.2011.159 |
N.
Brüggemann,
W.
Külper,
J.
Hagenah,
P.
Bauer,
C.
Pattaro,
Vera
Tadic,
T.
Lohnau,
S.
Winkler,
H.
Tönnies,
A.
Sprenger,
P.
Pramstaller,
A.
Rolfs,
R.
Siebert,
O.
Riess,
P.
Vieregge,
K.
Lohmann, and
C.
Klein,
Autosomal dominant Parkinson’s disease in a large German pedigree, Acta Neurol Scand , vol. 126, no. 2, pp. 129–137, 2012.
Autosomal dominant Parkinson’s disease in a large German pedigree, Acta Neurol Scand , vol. 126, no. 2, pp. 129–137, 2012.
| DOI: | 10.1111/j.1600-0404.2011.01621.x |
S.
Zittel,
M.
Nickel,
N. I.
Wolf,
G.
Uyanik,
D.
Gläser,
C.
Ganos,
C.
Gerloff,
Alexander
Münchau, and
A.
Kohlschütter,
“Pelizaeus-Merzbacher-like disease” presenting as complicated hereditary spastic paraplegia, J Neurol , vol. 259, no. 11, pp. 2498–2500, 2012.
“Pelizaeus-Merzbacher-like disease” presenting as complicated hereditary spastic paraplegia, J Neurol , vol. 259, no. 11, pp. 2498–2500, 2012.
| DOI: | 10.1007/s00415-012-6617-0 |
Sergiu
Groppa,
Nicole
Werner-Petroll,
Alexander
Münchau,
Günther
Deuschl,
Matthew F. S.
Ruschworth, and
Hartwig R.
Siebner,
A novel dual-site transcranial magnetic stimulation paradigm to probe fast facilitatory inputs from ipsilateral dorsal premotor cortex to primary motor cortex, Neuroimage , vol. 62, no. 1, pp. 500–509, 2012.
A novel dual-site transcranial magnetic stimulation paradigm to probe fast facilitatory inputs from ipsilateral dorsal premotor cortex to primary motor cortex, Neuroimage , vol. 62, no. 1, pp. 500–509, 2012.
| DOI: | 10.1016/j.neuroimage.2012.05.023 |
Kishore R.
Kumar,
Anne
Weissbach,
Marcus
Heldmann,
Meike
Kasten,
Sinem
Tunc,
Carolyn M.
Sue,
Marina
Svetel,
Vladimir S.
Kostić,
Juan
Segura-Aguilar,
Alfredo
Ramirez,
David K.
Simon,
Peter
Vieregge,
Thomas F.
Münte,
Johann
Hagenah,
Christine
Klein, and
Katja
Lohmann,
Frequency of the D620N mutation in VPS35 in Parkinson disease, Arch Neurol , vol. 69, no. 10, pp. 1360–1364, 2012.
Frequency of the D620N mutation in VPS35 in Parkinson disease, Arch Neurol , vol. 69, no. 10, pp. 1360–1364, 2012.
| DOI: | 10.1001/archneurol.2011.3367 |
Christos
Ganos,
Christian
Bernreuther,
Jakob
Matschke,
Christian
Gerloff,
Alexander
Münchau, and
Frank
Leypoldt,
Ataxia and HIV: clinicopathologic correlations in a case of HIV-associated cerebellar leukoencephalopathy, Cerebellum , vol. 11, no. 3, pp. 816–819, 2012.
Ataxia and HIV: clinicopathologic correlations in a case of HIV-associated cerebellar leukoencephalopathy, Cerebellum , vol. 11, no. 3, pp. 816–819, 2012.
| DOI: | 10.1007/s12311-011-0345-3 |
Anne
Grünewald,
Björn
Arns,
Philip
Seibler,
Aleksandar
Raković,
Alexander
Münchau,
Alfredo
Ramirez,
Carolyn M.
Sue, and
Christine
Klein,
ATP13A2 mutations impair mitochondrial function in fibroblasts from patients with Kufor-Rakeb syndrome, Neurobiol Aging , vol. 33, no. 8, pp. 1843.e1–7, 2012.
ATP13A2 mutations impair mitochondrial function in fibroblasts from patients with Kufor-Rakeb syndrome, Neurobiol Aging , vol. 33, no. 8, pp. 1843.e1–7, 2012.
| DOI: | 10.1016/j.neurobiolaging.2011.12.035 |
Christos
Ganos,
Ursula
Kahl,
Odette
Schunke,
Simone
Kühn,
Patrick
Haggard,
Christian
Gerloff,
Veit
Roessner,
Götz
Thomalla, and
Alexander
Münchau,
Are premonitory urges a prerequisite of tic inhibition in Gilles de la Tourette syndrome?, J Neurol Neurosurg Psychiatry , vol. 83, no. 10, pp. 975–978, 2012.
Are premonitory urges a prerequisite of tic inhibition in Gilles de la Tourette syndrome?, J Neurol Neurosurg Psychiatry , vol. 83, no. 10, pp. 975–978, 2012.
| DOI: | 10.1136/jnnp-2012-303033 |
Kai
Boelmans,
Brigitte
Holst,
Marc
Hackius,
Jürgen
Finsterbusch,
Christian
Gerloff,
Jens
Fiehler, and
Alexander
Münchau,
Brain iron deposition fingerprints in Parkinson’s disease and progressive supranuclear palsy, Mov Disord , vol. 27, no. 3, pp. 421–427, 2012.
Brain iron deposition fingerprints in Parkinson’s disease and progressive supranuclear palsy, Mov Disord , vol. 27, no. 3, pp. 421–427, 2012.
| DOI: | 10.1002/mds.24926 |
J.-M.
Lee,
E. M.
Ramos,
J.-H.
Lee,
T.
Gillis,
J. S.
Mysore,
M. R.
Hayden,
S. C.
Warby,
P.
Morrison,
M.
Nance,
C. A.
Ross,
R. L.
Margolis,
F.
Squitieri,
S.
Orobello,
S.
Di Donato,
E.
Gomez-Tortosa,
C.
Ayuso,
O.
Suchowersky,
R. J. A.
Trent,
E.
McCusker,
A.
Novelletto,
M.
Frontali,
R.
Jones,
T.
Ashizawa,
S.
Frank,
M. H.
Saint-Hilaire,
S. M.
Hersch,
H. D.
Rosas,
D.
Lucente,
M. B.
Harrison,
A.
Zanko,
R. K.
Abramson,
K.
Marder,
J.
Sequeiros,
J. S.
Paulsen,
[GROUP]
PREDICT-HD study of the Huntington Study Group (HSG),
G. B.
Landwehrmeyer,
[GROUP]
REGISTRY study of the European Huntington’s Disease Network,
R. H.
Myers,
[GROUP]
HD-MAPS Study Group,
M. E.
MacDonald,
J. F.
Gusella, and
[GROUP]
COHORT study of the HSG,
CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion, Neurology , vol. 78, no. 10, pp. 690–695, 2012.
CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion, Neurology , vol. 78, no. 10, pp. 690–695, 2012.
| DOI: | 10.1212/WNL.0b013e318249f683 |
Judith
van Gaalen,
Ronald J. E.
Pennings,
Andy J.
Beynon,
Alexander
Münchau,
Bastiaan R.
Bloem, and
Bart P. C.
van de Warrenburg,
Cervical dystonia after ear surgery, Parkinsonism Relat Disord , vol. 18, no. 5, pp. 669–671, 2012.
Cervical dystonia after ear surgery, Parkinsonism Relat Disord , vol. 18, no. 5, pp. 669–671, 2012.
| DOI: | 10.1016/j.parkreldis.2011.10.004 |
Meike
Kasten,
Lena
Kertelge,
Vera
Tadic,
Norbert
Brüggemann,
Alexander
Schmidt,
Joyce
van der Vegt,
Hartwig
Siebner,
Carsten
Buhmann,
Rebekka
Lencer,
Kishore R.
Kumar,
Katja
Lohmann,
Johann
Hagenah, and
Christine
Klein,
Depression and quality of life in monogenic compared to idiopathic, early-onset Parkinson’s disease, Mov Disord , vol. 27, no. 6, pp. 754–759, 2012.
Depression and quality of life in monogenic compared to idiopathic, early-onset Parkinson’s disease, Mov Disord , vol. 27, no. 6, pp. 754–759, 2012.
| DOI: | 10.1002/mds.24999 |
Oliver W.
Quarrell,
Olivia
Handley,
Kirsty
O’Donovan,
Christine
Dumoulin,
Maria
Ramos-Arroyo,
Ida
Biunno,
Peter
Bauer,
Margaret
Kline,
G. Bernhard
Landwehrmeyer, and
[GROUP]
European Huntington’s Disease Network,
Discrepancies in reporting the CAG repeat lengths for Huntington’s disease, Eur J Hum Genet , vol. 20, no. 1, pp. 20–26, 2012.
Discrepancies in reporting the CAG repeat lengths for Huntington’s disease, Eur J Hum Genet , vol. 20, no. 1, pp. 20–26, 2012.
| DOI: | 10.1038/ejhg.2011.136 |
Jennifer
Finis,
Agnes
Moczydlowski,
Bettina
Pollok,
Katja
Biermann-Ruben,
Götz
Thomalla,
Martin
Heil,
Holger
Krause,
Melanie
Jonas,
Alfons
Schnitzler, and
Alexander
Münchau,
Echoes from childhood--imitation in Gilles de la Tourette Syndrome, Mov Disord , vol. 27, no. 4, pp. 562–565, 2012.
Echoes from childhood--imitation in Gilles de la Tourette Syndrome, Mov Disord , vol. 27, no. 4, pp. 562–565, 2012.
| DOI: | 10.1002/mds.24913 |
2011
Alma
Osmanovic,
Andreas
Dendorfer,
Alev
Erogullari,
Nils
Uflacker,
Diana
Braunholz,
Aleksandar
Raković,
Gudrun
Vierke,
Conchi
Gil-Rodríguez,
Alexander
Münchau,
Melanie
Albrecht,
Norbert
Brüggemann,
Gabriele
Gillessen-Kaesbach,
Christine
Klein,
Katja
Lohmann, and
Frank J.
Kaiser,
Truncating mutations in THAP1 define the nuclear localization signal, Mov Disord , vol. 26, no. 8, pp. 1565–1567, 2011.
Truncating mutations in THAP1 define the nuclear localization signal, Mov Disord , vol. 26, no. 8, pp. 1565–1567, 2011.
| DOI: | 10.1002/mds.23611 |
Christos
Ganos,
Alexander
Münchau,
Tobias
Bäumer,
Christian
Gerloff, and
Tim
Magnus,
Seventy years of episodic stiffness: an unusual case of neuromyotonia, Mov Disord , vol. 26, no. 7, pp. 1360–1361, 2011.
Seventy years of episodic stiffness: an unusual case of neuromyotonia, Mov Disord , vol. 26, no. 7, pp. 1360–1361, 2011.
| DOI: | 10.1002/mds.23505 |
Alexander
Schmidt,
Hans-Christian
Jabusch,
Eckart
Altenmüller,
Leonie
Enders,
Rachel
Saunders-Pullman,
Susan B.
Bressman,
Alexander
Münchau,
Christine
Klein, and
Johann
Hagenah,
Phenotypic spectrum of musician’s dystonia: a task-specific disorder?, Mov Disord , vol. 26, no. 3, pp. 546–549, 2011.
Phenotypic spectrum of musician’s dystonia: a task-specific disorder?, Mov Disord , vol. 26, no. 3, pp. 546–549, 2011.
| DOI: | 10.1002/mds.23526 |
Simone
Zittel,
Tobias
Bäumer,
Norbert
Brüggemann,
Christian
Gerloff,
Christine
Klein, and
Alexander
Münchau,
Paroxysmal cervical myoclonus, Mov Disord , vol. 26, no. 13, pp. 2445–2446, 2011.
Paroxysmal cervical myoclonus, Mov Disord , vol. 26, no. 13, pp. 2445–2446, 2011.
| DOI: | 10.1002/mds.23913 |
Alexander Münchau,
Luxie loxie-hannah hannah-anna…blume, Mov Disord , vol. 26, no. 5, pp. 931–932, 2011.
Luxie loxie-hannah hannah-anna…blume, Mov Disord , vol. 26, no. 5, pp. 931–932, 2011.
| DOI: | 10.1002/mds.23491 |
Christoph
Kamm,
Nils
Uflacker,
Friedrich
Asmus,
Christoph
Schrader,
Alexander
Wolters,
Matthias
Wittstock,
Jens
Pahnke,
Thomas
Gasser,
Jens
Volkmann,
Alexander
Münchau,
Johann
Hagenah,
Reiner
Benecke,
Christine
Klein, and
Katja
Lohmann,
No evidence for THAP1/DYT6 variants as disease modifiers in DYT1 dystonia, Mov Disord , vol. 26, no. 11, pp. 2136–2137, 2011.
No evidence for THAP1/DYT6 variants as disease modifiers in DYT1 dystonia, Mov Disord , vol. 26, no. 11, pp. 2136–2137, 2011.
| DOI: | 10.1002/mds.23777 |
Carsten
Saft,
Jörg T.
Epplen,
Stefan
Wieczorek,
G. Bernhard
Landwehrmeyer,
Raymund A. C.
Roos,
Justo Garcia
de Yebenes,
Matthias
Dose,
Sarah J.
Tabrizi,
David
Craufurd,
[GROUP]
REGISTRY Investigators of the European Huntington’s Disease Network, and
Larissa
Arning,
NMDA receptor gene variations as modifiers in Huntington disease: a replication study, PLoS Curr , vol. 3, pp. RRN1247, 2011.
NMDA receptor gene variations as modifiers in Huntington disease: a replication study, PLoS Curr , vol. 3, pp. RRN1247, 2011.
| DOI: | 10.1371/currents.RRN1247 |
Frank
Leypoldt,
Manuel A.
Friese,
Josef
Böhm, and
Tobias
Bäumer,
Multiple enlarged nerves on neurosonography: an unusual paraneoplastic case, Muscle Nerve , vol. 43, no. 5, pp. 756–758, 2011.
Multiple enlarged nerves on neurosonography: an unusual paraneoplastic case, Muscle Nerve , vol. 43, no. 5, pp. 756–758, 2011.
| DOI: | 10.1002/mus.22010 |
Michael
Orth,
[GROUP]
European Huntington’s Disease Network,
O. J.
Handley,
C.
Schwenke,
S.
Dunnett,
E. J.
Wild,
S. J.
Tabrizi, and
G. B.
Landwehrmeyer,
Observing Huntington’s disease: the European Huntington’s Disease Network’s REGISTRY, J Neurol Neurosurg Psychiatry , vol. 82, no. 12, pp. 1409–1412, 2011.
Observing Huntington’s disease: the European Huntington’s Disease Network’s REGISTRY, J Neurol Neurosurg Psychiatry , vol. 82, no. 12, pp. 1409–1412, 2011.
| DOI: | 10.1136/jnnp.2010.209668 |
Julius
Verrel,
Rémy
Cuisinier,
Ulman
Lindenberger, and
Nicolas
Vuillerme,
Local and global effects of neck muscle vibration during stabilization of upright standing, Exp Brain Res , vol. 210, no. 2, pp. 313–324, 2011.
Local and global effects of neck muscle vibration during stabilization of upright standing, Exp Brain Res , vol. 210, no. 2, pp. 313–324, 2011.
| DOI: | 10.1007/s00221-011-2636-9 |
Sarah
Schiebler,
Alexander
Schmidt,
Simone
Zittel,
Tobias
Bäumer,
Christian
Gerloff,
Christine
Klein, and
Alexander
Münchau,
Arm tremor in cervical dystonia--is it a manifestation of dystonia or essential tremor?, Mov Disord , vol. 26, no. 10, pp. 1789–1792, 2011.
Arm tremor in cervical dystonia--is it a manifestation of dystonia or essential tremor?, Mov Disord , vol. 26, no. 10, pp. 1789–1792, 2011.
| DOI: | 10.1002/mds.23837 |
Nils Daniel
Forkert,
Alexander
Schmidt-Richberg,
Brigitte
Holst,
Alexander
Münchau,
Heinz
Handels, and
Kai
Boelmans,
Image-based classification of parkinsonian syndromes using T2’-atlases, Stud Health Technol Inform , vol. 169, pp. 465–469, 2011.
Image-based classification of parkinsonian syndromes using T2’-atlases, Stud Health Technol Inform , vol. 169, pp. 465–469, 2011.
Julius Verrel,
A formal and data-based comparison of measures of motor-equivalent covariation, J Neurosci Methods , vol. 200, no. 2, pp. 199–206, 2011.
A formal and data-based comparison of measures of motor-equivalent covariation, J Neurosci Methods , vol. 200, no. 2, pp. 199–206, 2011.
| DOI: | 10.1016/j.jneumeth.2011.04.006 |
Alexander
Münchau,
Götz
Thomalla, and
Veit
Roessner,
[Somatosensory phenomena and the role of sensorimotor circuits in Gilles de la Tourette syndrome], Z Kinder Jugendpsychiatr Psychother , vol. 39, no. 3, pp. 161–169, 2011.
[Somatosensory phenomena and the role of sensorimotor circuits in Gilles de la Tourette syndrome], Z Kinder Jugendpsychiatr Psychother , vol. 39, no. 3, pp. 161–169, 2011.
| DOI: | 10.1024/1422-4917/a000091 |
Danielle C.
Cath,
Tammy
Hedderly,
Andrea G.
Ludolph,
Jeremy S.
Stern,
Tara
Murphy,
Andreas
Hartmann,
Virginie
Czernecki,
Mary May
Robertson,
Davide
Martino,
Alexander
Münchau,
R.
Rizzo, and
[GROUP]
ESSTS Guidelines Group,
European clinical guidelines for Tourette syndrome and other tic disorders. Part I: assessment, Eur Child Adolesc Psychiatry , vol. 20, no. 4, pp. 155–171, 2011.
European clinical guidelines for Tourette syndrome and other tic disorders. Part I: assessment, Eur Child Adolesc Psychiatry , vol. 20, no. 4, pp. 155–171, 2011.
| DOI: | 10.1007/s00787-011-0164-6 |
Veit
Roessner,
Kerstin J.
Plessen,
Aribert
Rothenberger,
Andrea G.
Ludolph,
Renata
Rizzo,
Liselotte
Skov,
Gerd
Strand,
Jeremy S.
Stern,
Cristiano
Termine,
Pieter J.
Hoekstra, and
[GROUP]
ESSTS Guidelines Group,
European clinical guidelines for Tourette syndrome and other tic disorders. Part II: pharmacological treatment, Eur Child Adolesc Psychiatry , vol. 20, no. 4, pp. 173–196, 2011.
European clinical guidelines for Tourette syndrome and other tic disorders. Part II: pharmacological treatment, Eur Child Adolesc Psychiatry , vol. 20, no. 4, pp. 173–196, 2011.
| DOI: | 10.1007/s00787-011-0163-7 |
Cara
Verdellen,
Jolande
van de Griendt,
Andreas
Hartmann,
Tara
Murphy, and
[GROUP]
ESSTS Guidelines Group,
European clinical guidelines for Tourette syndrome and other tic disorders. Part III: behavioural and psychosocial interventions, Eur Child Adolesc Psychiatry , vol. 20, no. 4, pp. 197–207, 2011.
European clinical guidelines for Tourette syndrome and other tic disorders. Part III: behavioural and psychosocial interventions, Eur Child Adolesc Psychiatry , vol. 20, no. 4, pp. 197–207, 2011.
| DOI: | 10.1007/s00787-011-0167-3 |
Kirsten R.
Müller-Vahl,
Danielle C.
Cath,
Andrea E.
Cavanna,
Sandra
Dehning,
Mauro
Porta,
Mary M.
Robertson,
Veerle
Visser-Vandewalle, and
[GROUP]
ESSTS Guidelines Group,
European clinical guidelines for Tourette syndrome and other tic disorders. Part IV: deep brain stimulation, Eur Child Adolesc Psychiatry , vol. 20, no. 4, pp. 209–217, 2011.
European clinical guidelines for Tourette syndrome and other tic disorders. Part IV: deep brain stimulation, Eur Child Adolesc Psychiatry , vol. 20, no. 4, pp. 209–217, 2011.
| DOI: | 10.1007/s00787-011-0166-4 |
2010
Lena
Kertelge,
Norbert
Brüggemann,
Alexander
Schmidt,
Vera
Tadic,
Claudia
Wisse,
Sylwia
Dankert,
Laura
Drude,
Joyce
van der Vegt,
Hartwig
Siebner,
Heike
Pawlack,
Peter P.
Pramstaller,
Maria Isabel
Behrens,
Alfredo
Ramirez,
Dirk
Reichel,
Carsten
Buhmann,
Johann
Hagenah,
Christine
Klein,
Katja
Lohmann, and
Meike
Kasten,
Impaired sense of smell and color discrimination in monogenic and idiopathic Parkinson’s disease, Mov Disord , vol. 25, no. 15, pp. 2665–2669, 2010.
Impaired sense of smell and color discrimination in monogenic and idiopathic Parkinson’s disease, Mov Disord , vol. 25, no. 15, pp. 2665–2669, 2010.
| DOI: | 10.1002/mds.23272 |
Norbert
Brüggemann,
Johann
Hagenah,
Kathrin
Reetz,
Alexander
Schmidt,
Meike
Kasten,
Inga
Buchmann,
Susanne
Eckerle,
Manfred
Bähre,
Alexander
Münchau,
Ana
Djarmati,
Joyce
van der Vegt,
Hartwig
Siebner,
Ferdinand
Binkofski,
Alfredo
Ramirez,
Maria I.
Behrens, and
Christine
Klein,
Recessively inherited parkinsonism: effect of ATP13A2 mutations on the clinical and neuroimaging phenotype, Arch Neurol , vol. 67, no. 11, pp. 1357–1363, 2010.
Recessively inherited parkinsonism: effect of ATP13A2 mutations on the clinical and neuroimaging phenotype, Arch Neurol , vol. 67, no. 11, pp. 1357–1363, 2010.
| DOI: | 10.1001/archneurol.2010.281 |
C.
Eggers,
A.
Schmidt,
J.
Hagenah,
N.
Brüggemann,
J. C.
Klein,
Vera
Tadic,
L.
Kertelge,
M.
Kasten,
F.
Binkofski,
H.
Siebner,
B.
Neumaier,
G. R.
Fink,
R.
Hilker, and
C.
Klein,
Progression of subtle motor signs in PINK1 mutation carriers with mild dopaminergic deficit, Neurology , vol. 74, no. 22, pp. 1798–1805, 2010.
Progression of subtle motor signs in PINK1 mutation carriers with mild dopaminergic deficit, Neurology , vol. 74, no. 22, pp. 1798–1805, 2010.
| DOI: | 10.1212/WNL.0b013e3181e0f79c |
Alkomiet
Hasan,
Aribert
Rothenberger,
Alexander
Münchau,
Thomas
Wobrock,
Peter
Falkai, and
Veit
Roessner,
Oral delta 9-tetrahydrocannabinol improved refractory Gilles de la Tourette syndrome in an adolescent by increasing intracortical inhibition: a case report, J Clin Psychopharmacol , vol. 30, no. 2, pp. 190–192, 2010.
Oral delta 9-tetrahydrocannabinol improved refractory Gilles de la Tourette syndrome in an adolescent by increasing intracortical inhibition: a case report, J Clin Psychopharmacol , vol. 30, no. 2, pp. 190–192, 2010.
| DOI: | 10.1097/JCP.0b013e3181d236ec |
Meike
Kasten,
Lena
Kertelge,
Norbert
Brüggemann,
Joyce
van der Vegt,
Alexander
Schmidt,
Vera
Tadic,
Carsten
Buhmann,
Susanne
Steinlechner,
Maria Isabel
Behrens,
Alfredo
Ramirez,
Ferdinand
Binkofski,
Hartwig
Siebner,
Heiner
Raspe,
Johann
Hagenah,
Rebekka
Lencer, and
Christine
Klein,
Nonmotor symptoms in genetic Parkinson disease, Arch Neurol , vol. 67, no. 6, pp. 670–676, 2010.
Nonmotor symptoms in genetic Parkinson disease, Arch Neurol , vol. 67, no. 6, pp. 670–676, 2010.
| DOI: | 10.1001/archneurol.67.6.670 |
Julius
Verrel,
Martin
Lövdén, and
Ulman
Lindenberger,
Motor-equivalent covariation stabilizes step parameters and center of mass position during treadmill walking, Exp Brain Res , vol. 207, no. 1–2, pp. 13–26, 2010.
Motor-equivalent covariation stabilizes step parameters and center of mass position during treadmill walking, Exp Brain Res , vol. 207, no. 1–2, pp. 13–26, 2010.
| DOI: | 10.1007/s00221-010-2424-y |
Jennifer
Paszek,
Bettina
Pollok,
Katja
Biermann-Ruben,
Kirsten
Müller-Vahl,
Veit
Roessner,
Götz
Thomalla,
Mary M.
Robertson,
Michael
Orth,
Alfons
Schnitzler, and
Alexander
Münchau,
Is it a tic?--Twenty seconds to make a diagnosis, Mov Disord , vol. 25, no. 8, pp. 1106–1108, 2010.
Is it a tic?--Twenty seconds to make a diagnosis, Mov Disord , vol. 25, no. 8, pp. 1106–1108, 2010.
| DOI: | 10.1002/mds.23053 |
Tobias
Bäumer,
Götz
Thomalla,
Johan
Kroeger,
Melanie
Jonas,
Christian
Gerloff,
Friedhelm Christoph
Hummel,
Kirsten
Müller-Vahl,
Alfons
Schnitzler,
Hartwig Roman
Siebner,
Michael
Orth, and
Alexander
Münchau,
Interhemispheric motor networks are abnormal in patients with Gilles de la Tourette syndrome, Mov Disord , vol. 25, no. 16, pp. 2828–2837, 2010.
Interhemispheric motor networks are abnormal in patients with Gilles de la Tourette syndrome, Mov Disord , vol. 25, no. 16, pp. 2828–2837, 2010.
| DOI: | 10.1002/mds.23418 |
Melanie
Jonas,
Götz
Thomalla,
Katja
Biermann-Ruben,
Hartwig Roman
Siebner,
Kirsten
Müller-Vahl,
Tobias
Bäumer,
Christian
Gerloff,
Alfons
Schnitzler,
Michael
Orth, and
Alexander
Münchau,
Imitation in patients with Gilles de la Tourette syndrome--a behavioral study, Mov Disord , vol. 25, no. 8, pp. 991–999, 2010.
Imitation in patients with Gilles de la Tourette syndrome--a behavioral study, Mov Disord , vol. 25, no. 8, pp. 991–999, 2010.
| DOI: | 10.1002/mds.22994 |
Kirsten
Müller-Vahl,
Ines
Dodel,
Norbert
Müller,
Alexander
Münchau,
Jens Peter
Reese,
Monika
Balzer-Geldsetzer,
Richard
Dodel, and
Wolfgang H.
Oertel,
Health-related quality of life in patients with Gilles de la Tourette’s syndrome, Mov Disord , vol. 25, no. 3, pp. 309–314, 2010.
Health-related quality of life in patients with Gilles de la Tourette’s syndrome, Mov Disord , vol. 25, no. 3, pp. 309–314, 2010.
| DOI: | 10.1002/mds.22900 |
Julius Verrel,
Distributional properties and variance-stabilizing transformations for measures of uncontrolled manifold effects, J Neurosci Methods , vol. 191, no. 2, pp. 166–170, 2010.
Distributional properties and variance-stabilizing transformations for measures of uncontrolled manifold effects, J Neurosci Methods , vol. 191, no. 2, pp. 166–170, 2010.
| DOI: | 10.1016/j.jneumeth.2010.06.016 |
Ines
Dodel,
Jens Peter
Reese,
Norbert
Müller,
Alexander
Münchau,
Monika
Balzer-Geldsetzer,
Jürgen
Wasem,
Wolfgang H.
Oertel,
Richard
Dodel, and
Kirsten
Müller-Vahl,
Cost of illness in patients with Gilles de la Tourette’s syndrome, J Neurol , vol. 257, no. 7, pp. 1055–1061, 2010.
Cost of illness in patients with Gilles de la Tourette’s syndrome, J Neurol , vol. 257, no. 7, pp. 1055–1061, 2010.
| DOI: | 10.1007/s00415-010-5458-y |
Simone
Zittel,
Christian K. E.
Moll,
Norbert
Brüggemann,
Vera
Tadic,
Wolfgang
Hamel,
Meike
Kasten,
Katja
Lohmann,
Thora
Lohnau,
Susen
Winkler,
Christian
Gerloff,
Rainer
Schönweiler,
Johann
Hagenah,
Christine
Klein,
Alexander
Münchau, and
Susanne A.
Schneider,
Clinical neuroimaging and electrophysiological assessment of three DYT6 dystonia families, Mov Disord , vol. 25, no. 14, pp. 2405–2412, 2010.
Clinical neuroimaging and electrophysiological assessment of three DYT6 dystonia families, Mov Disord , vol. 25, no. 14, pp. 2405–2412, 2010.
| DOI: | 10.1002/mds.23279 |
Johan
Kroeger,
Tobias
Bäumer,
Melanie
Jonas,
John C.
Rothwell,
Hartwig R.
Siebner, and
Alexander
Münchau,
Charting the excitability of premotor to motor connections while withholding or initiating a selected movement, Eur J Neurosci , vol. 32, no. 10, pp. 1771–1779, 2010.
Charting the excitability of premotor to motor connections while withholding or initiating a selected movement, Eur J Neurosci , vol. 32, no. 10, pp. 1771–1779, 2010.
| DOI: | 10.1111/j.1460-9568.2010.07442.x |
Stephanie
Franzkowiak,
Bettina
Pollok,
Katja
Biermann-Ruben,
Martin
Südmeyer,
Jennifer
Paszek,
Melanie
Jonas,
Götz
Thomalla,
Tobias
Bäumer,
Michael
Orth,
Alexander
Münchau, and
Alfons
Schnitzler,
Altered pattern of motor cortical activation-inhibition during voluntary movements in Tourette syndrome, Mov Disord , vol. 25, no. 12, pp. 1960–1966, 2010.
Altered pattern of motor cortical activation-inhibition during voluntary movements in Tourette syndrome, Mov Disord , vol. 25, no. 12, pp. 1960–1966, 2010.
| DOI: | 10.1002/mds.23186 |
K.-F.
Heise,
B.
Steven,
G.
Liuzzi,
G.
Thomalla,
M.
Jonas,
K.
Müller-Vahl,
P.
Sauseng,
Alexander
Münchau,
C.
Gerloff, and
F. C.
Hummel,
Altered modulation of intracortical excitability during movement preparation in Gilles de la Tourette syndrome, Brain , vol. 133, no. Pt 2, pp. 580–590, 2010.
Altered modulation of intracortical excitability during movement preparation in Gilles de la Tourette syndrome, Brain , vol. 133, no. Pt 2, pp. 580–590, 2010.
| DOI: | 10.1093/brain/awp299 |
Michael
Schellenbach,
Martin
Lövdén,
Julius
Verrel,
Antonio
Krüger, and
Ulman
Lindenberger,
Adult age differences in familiarization to treadmill walking within virtual environments, Gait Posture , vol. 31, no. 3, pp. 295–299, 2010.
Adult age differences in familiarization to treadmill walking within virtual environments, Gait Posture , vol. 31, no. 3, pp. 295–299, 2010.
| DOI: | 10.1016/j.gaitpost.2009.11.008 |
2009
Ana
Djarmati,
Susanne A.
Schneider,
Katja
Lohmann,
Susen
Winkler,
Heike
Pawlack,
Johann
Hagenah,
Norbert
Brüggemann,
Simone
Zittel,
Tania
Fuchs,
Aleksandar
Raković,
Alexander
Schmidt,
Hans-Christian
Jabusch,
Robert
Wilcox,
Vladimir S.
Kostić,
Hartwig
Siebner,
Eckart
Altenmüller,
Alexander
Münchau,
Laurie J.
Ozelius, and
Christine
Klein,
Mutations in THAP1 (DYT6) and generalised dystonia with prominent spasmodic dysphonia: a genetic screening study, Lancet Neurol , vol. 8, no. 5, pp. 447–452, 2009.
Mutations in THAP1 (DYT6) and generalised dystonia with prominent spasmodic dysphonia: a genetic screening study, Lancet Neurol , vol. 8, no. 5, pp. 447–452, 2009.
| DOI: | 10.1016/S1474-4422(09)70083-3 |
