Publikationen
2013
Christos
Ganos,
Veit
Roessner, and
Alexander
Münchau,
The functional anatomy of Gilles de la Tourette syndrome, Neurosci Biobehav Rev , vol. 37, no. 6, pp. 1050–1062, 2013.
The functional anatomy of Gilles de la Tourette syndrome, Neurosci Biobehav Rev , vol. 37, no. 6, pp. 1050–1062, 2013.
DOI: | 10.1016/j.neubiorev.2012.11.004 |
Silke
Metzger,
Carolin
Walter,
Olaf
Riess,
Raymund A. C.
Roos,
Jørgen E.
Nielsen,
David
Craufurd,
[GROUP]
REGISTRY Investigators of the European Huntington’s Disease Network, and
Huu Phuc
Nguyen,
The V471A polymorphism in autophagy-related gene ATG7 modifies age at onset specifically in Italian Huntington disease patients, PLoS ONE , vol. 8, no. 7, pp. e68951, 2013.
The V471A polymorphism in autophagy-related gene ATG7 modifies age at onset specifically in Italian Huntington disease patients, PLoS ONE , vol. 8, no. 7, pp. e68951, 2013.
DOI: | 10.1371/journal.pone.0068951 |
Andrea
Ludolph,
Veit
Roessner,
Alexander
Münchau, and
Kirsten
Müller-Vahl,
Tourette Syndrome and Other Tic Disorders in Childhood, Adolescence and Adulthood, Dtsch Arztebl Int , vol. 110, no. 16, pp. 285, 2013.
Tourette Syndrome and Other Tic Disorders in Childhood, Adolescence and Adulthood, Dtsch Arztebl Int , vol. 110, no. 16, pp. 285, 2013.
DOI: | 10.3238/arztebl.2013.0285b |
Michael
Orth, and
Alexander
Münchau,
Transcranial magnetic stimulation studies of sensorimotor networks in Tourette syndrome, Behav Neurol , vol. 27, no. 1, pp. 57–64, 2013.
Transcranial magnetic stimulation studies of sensorimotor networks in Tourette syndrome, Behav Neurol , vol. 27, no. 1, pp. 57–64, 2013.
DOI: | 10.3233/BEN-120289 |
Katja
Lohmann,
Robert A.
Wilcox,
Susen
Winkler,
Alfredo
Ramirez,
Aleksandar
Raković,
Jin-Sung
Park,
Björn
Arns,
Thora
Lohnau,
Justus
Groen,
Meike
Kasten,
Norbert
Brüggemann,
Johann
Hagenah,
Alexander
Schmidt,
Frank J.
Kaiser,
Kishore R.
Kumar,
Katja
Zschiedrich,
Daniel
Alvarez-Fischer,
Eckart
Altenmüller,
Andreas
Ferbert,
Anthony E.
Lang,
Alexander
Münchau,
Vladimir
Kostic,
Kristina
Simonyan,
Marc
Agzarian,
Laurie J.
Ozelius,
Antonius P. M.
Langeveld,
Carolyn M.
Sue,
Marina A. J.
Tijssen, and
Christine
Klein,
Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene, Ann Neurol , vol. 73, no. 4, pp. 537–545, 2013.
Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene, Ann Neurol , vol. 73, no. 4, pp. 537–545, 2013.
DOI: | 10.1002/ana.23829 |
2012
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
2011
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 |
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 |
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 |
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,
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