Publikationen
2013
Julius
Verrel,
Steven
Pologe,
Wayne
Manselle,
Ulman
Lindenberger, and
Marjorie
Woollacott,
Coordination of degrees of freedom and stabilization of task variables in a complex motor skill: expertise-related differences in cello bowing, Exp Brain Res , vol. 224, no. 3, pp. 323–334, 2013.
Coordination of degrees of freedom and stabilization of task variables in a complex motor skill: expertise-related differences in cello bowing, Exp Brain Res , vol. 224, no. 3, pp. 323–334, 2013.
| DOI: | 10.1007/s00221-012-3314-2 |
N. D.
Forkert,
A.
Schmidt-Richberg,
A.
Treszl,
C.
Hilgetag,
J.
Fiehler,
Alexander
Münchau,
H.
Handels, and
K.
Boelmans,
Automated volumes-of-interest identification for classical and atypical Parkinsonian syndrome differentiation using T2’ MR imaging, Methods Inf Med , vol. 52, no. 2, pp. 128–136, 2013.
Automated volumes-of-interest identification for classical and atypical Parkinsonian syndrome differentiation using T2’ MR imaging, Methods Inf Med , vol. 52, no. 2, pp. 128–136, 2013.
| DOI: | 10.3414/ME12-01-0044 |
Joyce P. M.
van der Vegt,
Oliver J.
Hulme,
Simone
Zittel,
Kristoffer H.
Madsen,
Michael M.
Weiss,
Carsten
Buhmann,
Bastiaan R.
Bloem,
Alexander
Münchau, and
Hartwig R.
Siebner,
Attenuated neural response to gamble outcomes in drug-naive patients with Parkinson’s disease, Brain , vol. 136, no. Pt 4, pp. 1192–1203, 2013.
Attenuated neural response to gamble outcomes in drug-naive patients with Parkinson’s disease, Brain , vol. 136, no. Pt 4, pp. 1192–1203, 2013.
| DOI: | 10.1093/brain/awt027 |
P.
Bäumer,
V. F.
Mautner,
Tobias
Bäumer,
M. U.
Schuhmann,
M.
Tatagiba,
S.
Heiland,
T.
Kaestel,
M.
Bendszus, and
M.
Pham,
Accumulation of non-compressive fascicular lesions underlies NF2 polyneuropathy, J Neurol , vol. 260, no. 1, pp. 38–46, 2013.
Accumulation of non-compressive fascicular lesions underlies NF2 polyneuropathy, J Neurol , vol. 260, no. 1, pp. 38–46, 2013.
| DOI: | 10.1007/s00415-012-6581-8 |
Network HORIZON Investigators of the Huntington Study Group and European Huntington’s Disease,
A randomized, double-blind, placebo-controlled study of latrepirdine in patients with mild to moderate Huntington disease, JAMA Neurol , vol. 70, no. 1, pp. 25–33, 2013.
A randomized, double-blind, placebo-controlled study of latrepirdine in patients with mild to moderate Huntington disease, JAMA Neurol , vol. 70, no. 1, pp. 25–33, 2013.
| DOI: | 10.1001/2013.jamaneurol.382 |
2012
Denis
Ertelt,
Karsten
Witt,
Kathrin
Reetz,
Wolfgang
Frank,
Klaus
Junghanns,
Jutta
Backhaus,
Vera
Tadic,
Antonello
Pellicano,
Jan
Born, and
Ferdinand
Binkofski,
Skill memory escaping from distraction by sleep--evidence from dual-task performance, PLoS ONE , vol. 7, no. 12, pp. e50983, 2012.
Skill memory escaping from distraction by sleep--evidence from dual-task performance, PLoS ONE , vol. 7, no. 12, pp. e50983, 2012.
| DOI: | 10.1371/journal.pone.0050983 |
Stephanie
Franzkowiak,
Bettina
Pollok,
Katja
Biermann-Ruben,
Martin
Südmeyer,
Jennifer
Paszek,
Götz
Thomalla,
Melanie
Jonas,
Michael
Orth,
Alexander
Münchau, and
Alfons
Schnitzler,
Motor-cortical interaction in Gilles de la Tourette syndrome, PLoS ONE , vol. 7, no. 1, pp. e27850, 2012.
Motor-cortical interaction in Gilles de la Tourette syndrome, PLoS ONE , vol. 7, no. 1, pp. e27850, 2012.
| DOI: | 10.1371/journal.pone.0027850 |
Julius
Verrel,
Martin
Lövdén, and
Ulman
Lindenberger,
Normal aging reduces motor synergies in manual pointing, Neurobiol Aging , vol. 33, no. 1, pp. 200.e1–10, 2012.
Normal aging reduces motor synergies in manual pointing, Neurobiol Aging , vol. 33, no. 1, pp. 200.e1–10, 2012.
| DOI: | 10.1016/j.neurobiolaging.2010.07.006 |
Julius
Verrel,
Martin
Lövdén, and
Ulman
Lindenberger,
Older adults show preserved equilibrium but impaired step length control in motor-equivalent stabilization of gait, PLoS ONE , vol. 7, no. 12, pp. e52024, 2012.
Older adults show preserved equilibrium but impaired step length control in motor-equivalent stabilization of gait, PLoS ONE , vol. 7, no. 12, pp. e52024, 2012.
| DOI: | 10.1371/journal.pone.0052024 |
Julius
Verrel,
Didier
Pradon, and
Nicolas
Vuillerme,
Persistence of motor-equivalent postural fluctuations during bipedal quiet standing, PLoS ONE , vol. 7, no. 10, pp. e48312, 2012.
Persistence of motor-equivalent postural fluctuations during bipedal quiet standing, PLoS ONE , vol. 7, no. 10, pp. e48312, 2012.
| DOI: | 10.1371/journal.pone.0048312 |
Alexander
Schmidt,
Kishore R.
Kumar,
Katharina
Redyk,
Anne
Grünewald,
Matthias
Leben,
Alexander
Münchau,
Carolyn M.
Sue,
Johann
Hagenah,
Hans
Hartmann,
Katja
Lohmann,
Hans-Jürgen
Christen, and
Christine
Klein,
Two faces of the same coin: benign familial infantile seizures and paroxysmal kinesigenic dyskinesia caused by PRRT2 mutations, Arch Neurol , vol. 69, no. 5, pp. 668–670, 2012.
Two faces of the same coin: benign familial infantile seizures and paroxysmal kinesigenic dyskinesia caused by PRRT2 mutations, Arch Neurol , vol. 69, no. 5, pp. 668–670, 2012.
| DOI: | 10.1001/archneurol.2012.187 |
Simone
Zittel,
Maxim
Bester,
Christian
Gerloff,
Alexander
Münchau, and
Frank
Leypoldt,
Symptomatic paroxysmal kinesigenic choreoathetosis as primary manifestation of multiple sclerosis, J Neurol , vol. 259, no. 3, pp. 557–558, 2012.
Symptomatic paroxysmal kinesigenic choreoathetosis as primary manifestation of multiple sclerosis, J Neurol , vol. 259, no. 3, pp. 557–558, 2012.
| DOI: | 10.1007/s00415-011-6188-5 |
Christos
Ganos,
Alexander
Münchau,
Brigitte
Holst,
Gregor
Schlüter,
Christian
Gerloff, and
Gökhan
Uyanik,
Teaching neuroimages: oculodentodigital dysplasia: hypomyelination and syndactyly, Neurology , vol. 79, no. 16, pp. e140, 2012.
Teaching neuroimages: oculodentodigital dysplasia: hypomyelination and syndactyly, Neurology , vol. 79, no. 16, pp. e140, 2012.
| DOI: | 10.1212/WNL.0b013e31826e9b51 |
Christos
Ganos,
Simone
Zittel,
Christian
Gerloff,
Alexander
Münchau, and
Tobias
Bäumer,
The complex movement disorder of Kasabach-Merritt syndrome associated with a basal ganglia lesion, Mov Disord , vol. 27, no. 4, pp. 591–593, 2012.
The complex movement disorder of Kasabach-Merritt syndrome associated with a basal ganglia lesion, Mov Disord , vol. 27, no. 4, pp. 591–593, 2012.
| DOI: | 10.1002/mds.24911 |
Sergiu
Groppa,
Boris H.
Schlaak,
Alexander
Münchau,
Nicole
Werner-Petroll,
Janin
Dünnweber,
Tobias
Bäumer,
Bart F. L.
van Nuenen, and
Hartwig R.
Siebner,
The human dorsal premotor cortex facilitates the excitability of ipsilateral primary motor cortex via a short latency cortico-cortical route, Hum Brain Mapp , vol. 33, no. 2, pp. 419–430, 2012.
The human dorsal premotor cortex facilitates the excitability of ipsilateral primary motor cortex via a short latency cortico-cortical route, Hum Brain Mapp , vol. 33, no. 2, pp. 419–430, 2012.
| DOI: | 10.1002/hbm.21221 |
Christos
Ganos,
Timo
Ogrzal,
Alfons
Schnitzler, and
Alexander
Münchau,
The pathophysiology of echopraxia/echolalia: relevance to Gilles de la Tourette syndrome, Mov Disord , vol. 27, no. 10, pp. 1222–1229, 2012.
The pathophysiology of echopraxia/echolalia: relevance to Gilles de la Tourette syndrome, Mov Disord , vol. 27, no. 10, pp. 1222–1229, 2012.
| DOI: | 10.1002/mds.25103 |
Katja
Biermann-Ruben,
Anastasia
Miller,
Stephanie
Franzkowiak,
Jennifer
Finis,
Bettina
Pollok,
Claudia
Wach,
Martin
Südmeyer,
Melanie
Jonas,
Götz
Thomalla,
Kirsten
Müller-Vahl,
Alexander
Münchau, and
Alfons
Schnitzler,
Increased sensory feedback in Tourette syndrome, Neuroimage , vol. 63, no. 1, pp. 119–125, 2012.
Increased sensory feedback in Tourette syndrome, Neuroimage , vol. 63, no. 1, pp. 119–125, 2012.
| DOI: | 10.1016/j.neuroimage.2012.06.059 |
S.
Zittel,
J.
Kroeger,
J. P. M.
van der Vegt,
H. R.
Siebner,
N.
Brüggemann,
A.
Ramirez,
M. I.
Behrens,
C.
Gerloff,
Tobias
Bäumer,
C.
Klein, and
Alexander
Münchau,
Motor pathway excitability in ATP13A2 mutation carriers: a transcranial magnetic stimulation study, Parkinsonism Relat Disord , vol. 18, no. 5, pp. 590–594, 2012.
Motor pathway excitability in ATP13A2 mutation carriers: a transcranial magnetic stimulation study, Parkinsonism Relat Disord , vol. 18, no. 5, pp. 590–594, 2012.
| DOI: | 10.1016/j.parkreldis.2011.10.020 |
Kai
Boelmans,
Christian
Gerloff, and
Alexander
Münchau,
Long-lasting effect of levodopa on holmes’ tremor, Mov Disord , vol. 27, no. 9, pp. 1097–1098, 2012.
Long-lasting effect of levodopa on holmes’ tremor, Mov Disord , vol. 27, no. 9, pp. 1097–1098, 2012.
| DOI: | 10.1002/mds.24005 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
Anne
Weissbach,
Katharina
Siegesmund,
Norbert
Brüggemann,
Alexander
Schmidt,
Meike
Kasten,
Irene
Pichler,
Hiltrud
Muhle,
Ebba
Lohmann,
Thora
Lohnau,
Eberhard
Schwinger,
Johann
Hagenah,
Ulrich
Stephani,
Peter P.
Pramstaller,
Christine
Klein, and
Katja
Lohmann,
Exome sequencing in a family with restless legs syndrome, Mov Disord , vol. 27, no. 13, pp. 1686–1689, 2012.
Exome sequencing in a family with restless legs syndrome, Mov Disord , vol. 27, no. 13, pp. 1686–1689, 2012.
| DOI: | 10.1002/mds.25191 |
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 |
2011
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 |
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 |
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 |
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.
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