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Best matches for Münchau A[au]:

Treatable inherited rare movement disorders. Jinnah HA et al. Mov Disord. (2018)

Phenotypic insights into ADCY5-associated disease. Chang FC et al. Mov Disord. (2016)

Novel GNB1 mutations disrupt assembly and function of G protein heterotrimers and cause global developmental delay in humans. Lohmann K et al. Hum Mol Genet. (2017)

Search results

Items: 1 to 50 of 263

1.

Single-pulse subthalamic deep brain stimulation reduces premotor-motor facilitation in Parkinson's disease.

Weissbach A, Udupa K, Ni Z, Gunraj C, Rinchon C, Baarbe J, Fasano A, Munhoz RP, Lang A, Tadic V, Brüggemann N, Münchau A, Bäumer T, Chen R.

Parkinsonism Relat Disord. 2019 Aug 7. pii: S1353-8020(19)30359-1. doi: 10.1016/j.parkreldis.2019.08.003. [Epub ahead of print]

PMID:
31427071
2.

Safety and efficacy of epigallocatechin gallate in multiple system atrophy (PROMESA): a randomised, double-blind, placebo-controlled trial.

Levin J, Maaß S, Schuberth M, Giese A, Oertel WH, Poewe W, Trenkwalder C, Wenning GK, Mansmann U, Südmeyer M, Eggert K, Mollenhauer B, Lipp A, Löhle M, Classen J, Münchau A, Kassubek J, Gandor F, Berg D, Egert-Schwender S, Eberhardt C, Paul F, Bötzel K, Ertl-Wagner B, Huppertz HJ, Ricard I, Höglinger GU; PROMESA Study Group.

Lancet Neurol. 2019 Aug;18(8):724-735. doi: 10.1016/S1474-4422(19)30141-3. Epub 2019 Jul 2.

PMID:
31278067
3.

[Model for personalized diagnostics and treatment in neurology-German Academy for Rare Neurological Diseases].

Münchau A, Schöls L, Klein C, Graessner H.

Nervenarzt. 2019 Aug;90(8):796-803. doi: 10.1007/s00115-019-0750-2. Review. German.

PMID:
31243508
4.

A peek into premonitory urges in Tourette syndrome: Temporal evolution of neurophysiological oscillatory signatures.

Niccolai V, Korczok S, Finis J, Jonas M, Thomalla G, Siebner HR, Müller-Vahl K, Münchau A, Schnitzler A, Biermann-Ruben K.

Parkinsonism Relat Disord. 2019 May 31. pii: S1353-8020(19)30260-3. doi: 10.1016/j.parkreldis.2019.05.039. [Epub ahead of print]

PMID:
31182372
5.

FAHN/SPG35: a narrow phenotypic spectrum across disease classifications.

Rattay TW, Lindig T, Baets J, Smets K, Deconinck T, Söhn AS, Hörtnagel K, Eckstein KN, Wiethoff S, Reichbauer J, Döbler-Neumann M, Krägeloh-Mann I, Auer-Grumbach M, Plecko B, Münchau A, Wilken B, Janauschek M, Giese AK, De Bleecker JL, Ortibus E, Debyser M, Lopez de Munain A, Pujol A, Bassi MT, D'Angelo MG, De Jonghe P, Züchner S, Bauer P, Schöls L, Schüle R.

Brain. 2019 Jun 1;142(6):1561-1572. doi: 10.1093/brain/awz102.

PMID:
31135052
6.

Spinocerebellar Ataxia Type 28-Phenotypic and Molecular Characterization of a Family with Heterozygous and Compound-Heterozygous Mutations in AFG3L2.

Tunc S, Dulovic-Mahlow M, Baumann H, Baaske MK, Jahn M, Junker J, Münchau A, Brüggemann N, Lohmann K.

Cerebellum. 2019 Aug;18(4):817-822. doi: 10.1007/s12311-019-01036-2.

PMID:
31111429
7.

Somatosensory-motor cortex interactions measured using dual-site transcranial magnetic stimulation.

Brown MJN, Weissbach A, Pauly MG, Vesia M, Gunraj C, Baarbé J, Münchau A, Bäumer T, Chen R.

Brain Stimul. 2019 Sep - Oct;12(5):1229-1243. doi: 10.1016/j.brs.2019.04.009. Epub 2019 Apr 23.

PMID:
31043330
8.

A hexanucleotide repeat modifies expressivity of X-linked dystonia parkinsonism.

Westenberger A, Reyes CJ, Saranza G, Dobricic V, Hanssen H, Domingo A, Laabs BH, Schaake S, Pozojevic J, Rakovic A, Grütz K, Begemann K, Walter U, Dressler D, Bauer P, Rolfs A, Münchau A, Kaiser FJ, Ozelius LJ, Jamora RD, Rosales RL, Diesta CCE, Lohmann K, König IR, Brüggemann N, Klein C.

Ann Neurol. 2019 Jun;85(6):812-822. doi: 10.1002/ana.25488. Epub 2019 May 3.

PMID:
30973967
9.

A special issue on childhood-onset movement disorders.

Ebrahimi-Fakhari D, Münchau A, Stamelou M.

Mov Disord. 2019 May;34(5):595-597. doi: 10.1002/mds.27663. Epub 2019 Apr 2. No abstract available.

PMID:
30938852
10.

De-novo KMT2B mutation in a consanguineous family: 15-Year follow-up of an Afghan dystonia patient.

Klein C, Baumann H, Olschewski L, Hanssen H, Münchau A, Ferbert A, Brüggemann N, Lohmann K.

Parkinsonism Relat Disord. 2019 Mar 25. pii: S1353-8020(19)30111-7. doi: 10.1016/j.parkreldis.2019.03.018. [Epub ahead of print] No abstract available.

PMID:
30935829
11.

Methylphenidate Can Improve Chorea in NKX2.1 and ADCY5 Mutation-positive Patients-A Report of Two Children.

Tübing J, Bohnenpoll J, Spiegler J, Gillessen-Kaesbach G, Bäumer T, Max C, Sperner J, Klein C, Münchau A.

Mov Disord Clin Pract. 2018 Apr 6;5(3):343-345. doi: 10.1002/mdc3.12608. eCollection 2018 May-Jun. No abstract available.

12.

Movement Disorders in Treatable Inborn Errors of Metabolism.

Ebrahimi-Fakhari D, Van Karnebeek C, Münchau A.

Mov Disord. 2019 May;34(5):598-613. doi: 10.1002/mds.27568. Epub 2018 Dec 17. Review.

PMID:
30557456
13.

Association of Pallidal Neurostimulation and Outcome Predictors With X-linked Dystonia Parkinsonism.

Brüggemann N, Domingo A, Rasche D, Moll CKE, Rosales RL, Jamora RDG, Hanssen H, Münchau A, Graf J, Weissbach A, Tadic V, Diesta CC, Volkmann J, Kühn A, Münte TF, Tronnier V, Klein C.

JAMA Neurol. 2019 Feb 1;76(2):211-216. doi: 10.1001/jamaneurol.2018.3777.

PMID:
30508028
14.

A recurrent de-novo ANO3 mutation causes early-onset generalized dystonia.

Tunc S, Denecke J, Olschewski L, Bäumer T, Münchau A, Lessel D, Lohmann K.

J Neurol Sci. 2019 Jan 15;396:199-201. doi: 10.1016/j.jns.2018.11.024. Epub 2018 Nov 22. No abstract available.

PMID:
30502610
15.

Sez6l2-antibody-associated progressive cerebellar ataxia: a differential diagnosis of atypical parkinsonism.

Borsche M, Hahn S, Hanssen H, Münchau A, Wandinger KP, Brüggemann N.

J Neurol. 2019 Feb;266(2):522-524. doi: 10.1007/s00415-018-9115-1. Epub 2018 Nov 20. No abstract available.

PMID:
30460451
16.

Iron overload is accompanied by mitochondrial and lysosomal dysfunction in WDR45 mutant cells.

Seibler P, Burbulla LF, Dulovic M, Zittel S, Heine J, Schmidt T, Rudolph F, Westenberger A, Rakovic A, Münchau A, Krainc D, Klein C.

Brain. 2018 Oct 1;141(10):3052-3064. doi: 10.1093/brain/awy230.

PMID:
30169597
17.

[Neuronal plasticity and neuromodulation in pediatric neurology].

Jung NH, Münchau A, Mall V.

Nervenarzt. 2018 Oct;89(10):1131-1139. doi: 10.1007/s00115-018-0586-1. Review. German.

PMID:
30141068
18.

Associative plasticity in supplementary motor area - motor cortex pathways in Tourette syndrome.

Tübing J, Gigla B, Brandt VC, Verrel J, Weissbach A, Beste C, Münchau A, Bäumer T.

Sci Rep. 2018 Aug 10;8(1):11984. doi: 10.1038/s41598-018-30504-8.

19.

Striatal Microstructure and Its Relevance for Cognitive Control.

Beste C, Moll CKE, Pötter-Nerger M, Münchau A.

Trends Cogn Sci. 2018 Sep;22(9):747-751. doi: 10.1016/j.tics.2018.06.007. Epub 2018 Jul 14. Review.

PMID:
30017252
20.

European Multicentre Tics in Children Studies (EMTICS): protocol for two cohort studies to assess risk factors for tic onset and exacerbation in children and adolescents.

Schrag A, Martino D, Apter A, Ball J, Bartolini E, Benaroya-Milshtein N, Buttiglione M, Cardona F, Creti R, Efstratiou A, Gariup M, Georgitsi M, Hedderly T, Heyman I, Margarit I, Mir P, Moll N, Morer A, Müller N, Müller-Vahl K, Münchau A, Orefici G, Plessen KJ, Porcelli C, Paschou P, Rizzo R, Roessner V, Schwarz MJ, Steinberg T, Tagwerker Gloor F, Tarnok Z, Walitza S, Dietrich A, Hoekstra PJ; EMTICS Collaborative Group.

Eur Child Adolesc Psychiatry. 2019 Jan;28(1):91-109. doi: 10.1007/s00787-018-1190-4. Epub 2018 Jul 7.

21.

Altered perception-action binding modulates inhibitory control in Gilles de la Tourette syndrome.

Petruo V, Bodmer B, Brandt VC, Baumung L, Roessner V, Münchau A, Beste C.

J Child Psychol Psychiatry. 2019 Sep;60(9):953-962. doi: 10.1111/jcpp.12938. Epub 2018 Jun 20.

PMID:
29924402
22.

Mutations in VPS13D lead to a new recessive ataxia with spasticity and mitochondrial defects.

Seong E, Insolera R, Dulovic M, Kamsteeg EJ, Trinh J, Brüggemann N, Sandford E, Li S, Ozel AB, Li JZ, Jewett T, Kievit AJA, Münchau A, Shakkottai V, Klein C, Collins CA, Lohmann K, van de Warrenburg BP, Burmeister M.

Ann Neurol. 2018 Jun;83(6):1075-1088. doi: 10.1002/ana.25220. Epub 2018 Jun 30.

23.

Prospective evaluation of Globus pallidus internus deep brain stimulation in Huntington's disease.

Zittel S, Tadic V, Moll CKE, Bäumer T, Fellbrich A, Gulberti A, Rasche D, Brüggemann N, Tronnier V, Münchau A.

Parkinsonism Relat Disord. 2018 Jun;51:96-100. doi: 10.1016/j.parkreldis.2018.02.030. Epub 2018 Feb 20.

PMID:
29486999
24.

Novel homozygous variants in ATCAY, MCOLN1, and SACS in complex neurological disorders.

Manzoor H, Brüggemann N, Hussain HMJ, Bäumer T, Hinrichs F, Wajid M, Münchau A, Naz S, Lohmann K.

Parkinsonism Relat Disord. 2018 Jun;51:91-95. doi: 10.1016/j.parkreldis.2018.02.005. Epub 2018 Feb 6.

PMID:
29449188
25.

The temporal relationship between premonitory urges and covert compulsions in patients with obsessive-compulsive disorder.

Brandt VC, Hermanns J, Beck C, Bäumer T, Zurowski B, Münchau A.

Psychiatry Res. 2018 Apr;262:6-12. doi: 10.1016/j.psychres.2018.01.041. Epub 2018 Feb 20.

PMID:
29407570
26.

Spatio-temporal dynamics of cortical drive to human subthalamic nucleus neurons in Parkinson's disease.

Sharott A, Gulberti A, Hamel W, Köppen JA, Münchau A, Buhmann C, Pötter-Nerger M, Westphal M, Gerloff C, Moll CKE, Engel AK.

Neurobiol Dis. 2018 Apr;112:49-62. doi: 10.1016/j.nbd.2018.01.001. Epub 2018 Jan 4.

27.

Tics and Tourette syndrome - surplus of actions rather than disorder?

Beste C, Münchau A.

Mov Disord. 2018 Feb;33(2):238-242. doi: 10.1002/mds.27244. Epub 2017 Dec 26. Review. No abstract available.

PMID:
29278288
28.

Boys in a famous choir: Singing and ticcing.

Tunc S, Münchau A.

Ann Neurol. 2017 Dec;82(6):1029-1031. doi: 10.1002/ana.25112.

PMID:
29265544
29.

Perceived and real tic suppression ability and its relation to impulsivity.

Brandt VC, Herrmann K, Kerner Auch Koerner J, Münchau A.

Mov Disord. 2017 Dec;32(12):1795-1796. doi: 10.1002/mds.27202. Epub 2017 Oct 27. No abstract available.

PMID:
29076594
30.

White Matter Microstructure of the Human Mirror Neuron System is Related to Symptom Severity in Adults with Autism.

Fründt O, Schulz R, Schöttle D, Cheng B, Thomalla G, Braaß H, Ganos C, David N, Peiker I, Engel AK, Bäumer T, Münchau A.

J Autism Dev Disord. 2018 Feb;48(2):417-429. doi: 10.1007/s10803-017-3332-9.

PMID:
29027066
31.

A novel, in-frame KMT2B deletion in a patient with apparently isolated, generalized dystonia.

Lange LM, Tunc S, Tennstedt S, Münchau A, Klein C, Assmann B, Lohmann K.

Mov Disord. 2017 Oct;32(10):1495-1497. doi: 10.1002/mds.27137. Epub 2017 Sep 18. No abstract available. Erratum in: Mov Disord. 2018 Jan;33(1):184.

PMID:
28921672
32.

Alcohol improves cerebellar learning deficit in myoclonus-dystonia: A clinical and electrophysiological investigation.

Weissbach A, Werner E, Bally JF, Tunc S, Löns S, Timmann D, Zeuner KE, Tadic V, Brüggemann N, Lang A, Klein C, Münchau A, Bäumer T.

Ann Neurol. 2017 Oct;82(4):543-553. doi: 10.1002/ana.25035. Epub 2017 Sep 25.

PMID:
28869676
33.

Treatable inherited rare movement disorders.

Jinnah HA, Albanese A, Bhatia KP, Cardoso F, Da Prat G, de Koning TJ, Espay AJ, Fung V, Garcia-Ruiz PJ, Gershanik O, Jankovic J, Kaji R, Kotschet K, Marras C, Miyasaki JM, Morgante F, Munchau A, Pal PK, Rodriguez Oroz MC, Rodríguez-Violante M, Schöls L, Stamelou M, Tijssen M, Uribe Roca C, de la Cerda A, Gatto EM; International Parkinson's Disease Movement Disorders Society Task Force on Rare Movement Disorders.

Mov Disord. 2018 Jan;33(1):21-35. doi: 10.1002/mds.27140. Epub 2017 Sep 1. Review.

34.

Involvement of obliquus capitis inferior muscle in dystonic head tremor.

Schramm A, Huber D, Möbius C, Münchau A, Kohl Z, Bäumer T.

Parkinsonism Relat Disord. 2017 Nov;44:119-123. doi: 10.1016/j.parkreldis.2017.07.034. Epub 2017 Aug 1.

PMID:
28802760
35.

Imitation inhibition in children with Tourette syndrome.

Brandt VC, Moczydlowski A, Jonas M, Boelmans K, Bäumer T, Brass M, Münchau A.

J Neuropsychol. 2019 Mar;13(1):82-95. doi: 10.1111/jnp.12132. Epub 2017 Aug 12.

PMID:
28801946
36.

Evidence for enhanced multi-component behaviour in Tourette syndrome - an EEG study.

Brandt VC, Stock AK, Münchau A, Beste C.

Sci Rep. 2017 Aug 10;7(1):7722. doi: 10.1038/s41598-017-08158-9.

37.

Author response: Munchausen syndrome by genetics: Next-generation challenges for clinicians.

Zittel S, Alvarez-Fischer D, Schweiger U, Klein C, Münchau A.

Neurology. 2017 Jul 18;89(3):307. doi: 10.1212/WNL.0000000000004133. No abstract available.

PMID:
28716878
38.

Influence of L-dopa on subtle motor signs in heterozygous Parkin- and PINK1 mutation carriers.

Weissbach A, König IR, Hückelheim K, Pramstaller PP, Werner E, Brüggemann N, Tadic V, Lohmann K, Bäumer T, Münchau A, Kasten M, Klein C.

Parkinsonism Relat Disord. 2017 Sep;42:95-99. doi: 10.1016/j.parkreldis.2017.07.003. Epub 2017 Jul 8.

PMID:
28716427
39.

Hereditary Dystonia Overview.

Klein C, Lohmann K, Marras C, Münchau A.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2019.
2003 Oct 28 [updated 2017 Jun 22].

40.

Investigation of previously implicated genetic variants in chronic tic disorders: a transmission disequilibrium test approach.

Abdulkadir M, Londono D, Gordon D, Fernandez TV, Brown LW, Cheon KA, Coffey BJ, Elzerman L, Fremer C, Fründt O, Garcia-Delgar B, Gilbert DL, Grice DE, Hedderly T, Heyman I, Hong HJ, Huyser C, Ibanez-Gomez L, Jakubovski E, Kim YK, Kim YS, Koh YJ, Kook S, Kuperman S, Leventhal B, Ludolph AG, Madruga-Garrido M, Maras A, Mir P, Morer A, Müller-Vahl K, Münchau A, Murphy TL, Plessen KJ, Roessner V, Shin EY, Song DH, Song J, Tübing J, van den Ban E, Visscher F, Wanderer S, Woods M, Zinner SH, King RA, Tischfield JA, Heiman GA, Hoekstra PJ, Dietrich A.

Eur Arch Psychiatry Clin Neurosci. 2018 Apr;268(3):301-316. doi: 10.1007/s00406-017-0808-8. Epub 2017 May 29.

41.

The Basal Ganglia Striosomes Affect the Modulation of Conflicts by Subliminal Information-Evidence from X-Linked Dystonia Parkinsonism.

Beste C, Mückschel M, Rosales R, Domingo A, Lee L, Ng A, Klein C, Münchau A.

Cereb Cortex. 2018 Jul 1;28(7):2243-2252. doi: 10.1093/cercor/bhx125.

PMID:
28505262
42.

Dysfunctions in striatal microstructure can enhance perceptual decision making through deficits in predictive coding.

Beste C, Mückschel M, Rosales R, Domingo A, Lee L, Ng A, Klein C, Münchau A.

Brain Struct Funct. 2017 Nov;222(8):3807-3817. doi: 10.1007/s00429-017-1435-x. Epub 2017 May 2.

PMID:
28466359
43.

Adult-onset ataxia or developmental disorder with seizures: two sides of missense changes in CACNA1A.

Balck A, Hanssen H, Hellenbroich Y, Lohmann K, Münchau A.

J Neurol. 2017 Jul;264(7):1520-1522. doi: 10.1007/s00415-017-8494-z. Epub 2017 Apr 28. No abstract available.

PMID:
28455667
44.

Facial twitches in ADCY5-associated disease - Myokymia or myoclonus? An electromyography study.

Tunc S, Brüggemann N, Baaske MK, Hartmann C, Grütz K, Westenberger A, Klein C, Münchau A, Bäumer T.

Parkinsonism Relat Disord. 2017 Jul;40:73-75. doi: 10.1016/j.parkreldis.2017.04.013. Epub 2017 Apr 20.

PMID:
28442302
45.

Associations of specific psychiatric disorders with isolated focal dystonia, and monogenic and idiopathic Parkinson's disease.

Steinlechner S, Hagenah J, Rumpf HJ, Meyer C, John U, Bäumer T, Brüggemann N, Kasten M, Münchau A, Klein C, Lencer R.

J Neurol. 2017 Jun;264(6):1076-1084. doi: 10.1007/s00415-017-8488-x. Epub 2017 Apr 11.

PMID:
28401296
46.

CAPN1 mutations are associated with a syndrome of combined spasticity and ataxia.

Tadic V, Klein C, Hinrichs F, Münchau A, Lohmann K, Brüggemann N.

J Neurol. 2017 May;264(5):1008-1010. doi: 10.1007/s00415-017-8464-5. Epub 2017 Mar 20. No abstract available.

PMID:
28321562
47.

[On the fast track to diagnosis : Recommendations for patients without a diagnosis].

Stieber C, Mücke M, Windheuser IC, Grigull L, Klawonn F, Tunc S, Münchau A, Klockgether T.

Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2017 May;60(5):517-522. doi: 10.1007/s00103-017-2535-8. German.

PMID:
28289775
48.

Striatal dysfunction in X-linked dystonia-parkinsonism is associated with disease progression.

Brüggemann N, Rosales RL, Waugh JL, Blood AJ, Domingo A, Heldmann M, Jamora RD, Münchau A, Münte TF, Lee LV, Buchmann I, Klein C.

Eur J Neurol. 2017 May;24(5):680-686. doi: 10.1111/ene.13256. Epub 2017 Feb 25.

PMID:
28236370
49.

Quantitative Sensory Testing in adults with Autism Spectrum Disorders.

Fründt O, Grashorn W, Schöttle D, Peiker I, David N, Engel AK, Forkmann K, Wrobel N, Münchau A, Bingel U.

J Autism Dev Disord. 2017 Apr;47(4):1183-1192. doi: 10.1007/s10803-017-3041-4.

PMID:
28160223
50.

Munchausen syndrome by genetics: Next-generation challenges for clinicians.

Zittel S, Lohmann K, Bauer P, Klein C, Münchau A.

Neurology. 2017 Mar 7;88(10):1000-1001. doi: 10.1212/WNL.0000000000003695. Epub 2017 Feb 3. No abstract available.

PMID:
28159884

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