Publikationen Gesamt

Publikationsliste

2017

Meles SK, Vadasz D, Renken RJ, Sitting-Wiegand E, Mayer G, Depboylu C, Reetz K, Overeem S, Pijpers A, Reesink FE, van Laar T, Heinen L, Teune LK, Höffken H, Luster M, Kesper K, Adriaanse SM, Booij J, Leenders KL, Oertel WH. FDG PRT, dopamine transporter SPECT, and olifaction: Combining biomarkers in REM sleepbehavior disorder. Mov Disord. 2017 Jul 22; doi: 10.1002/mds.27094. [Epub ahead of print]
>> PubMed

Caspers J, Mathys C, Hoffstaedter F, Südmeyer M, Cieslik EC, Rubbert C, Hartmann CJ, Eickhoff CR, Reetz K, Grefkes C, Michely J, Turowski B, Schnitzler A, Eickhoff SB. Differential functional connectivity alterations of two subdivisions within the right dlPFC in Parkinson’s disease. Frontiers in Human Neuroscience. 2017;11:288. eCollection 2017.
>> PMC

Moss DJH, Pardinas AF, Langbehn D, Lo K, Leavitt BR, Roos R, Durr A, Mead S, Track-Hd investigators, Registry investigators, Holmans P, Jones L, Tabrizi SJ. Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study. The Lancet Neurology. 2017. pii:S1474-4422(17)30161-8.
>> PubMed

Lueken U, Evens R, Balzer-Geldsetzer M, Baudrexel S, Dodel R, Gräber-Sultan S, Hilker-Roggendorf R, Kalbe E, Kaut O, Mollenhauer B, Reetz K, Schäffer E, Schmidt N, Schulz JB, Spottke A, Witt K, Linse K, Storch A, Riedel O. Psychometric properties of the apathy evaluation scale in patients with Parkinson's disease. Int J Methods Psychiatr Res. 2017 Apr 18. doi: 10.1002/mpr.1564. [Epub ahead of print]
>>  PubMed 

Lahut S, Gispert S, Ömür Ö, Depboylu C, Seidel K, Domínguez-Bautista JA, et al. Blood RNA biomarkers in prodromal PARK4 and REM sleep behavior disorder show role of complexin-1 loss for risk of Parkinson's disease. Dis Model Mech. 2017;10(5):619-631. Epub 2017.
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2016

Reetz K, Dogan I, Hilgers RD, Giunti P, Mariotti C, Durr A, Boesch S, Klopstock T, de Rivera FJ, Schöls L, Klockgether T, Bürk K, Pandolfo M, Schulz JB; Progression characteristics of the European Fridreich's Ataxia Consortium for Translational Studies (EFACTS): a 2 year cohort study. The Lancet Neurology, 2016;15(13):1346-1354. 
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Troche MS, Schumann B, Brandimore AE, Okun MS, Hegland KW. Reflex Cough and Disease Duration as Predictors of Swallowing Dysfunction in Parkinson's Disease. Dysphagia. 2016;31(6):757-764.
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Cubo E, Ramos-Arroyo MA, Martinez-Horta S, Martínez-Descalls A, Calvo S, Gil-Polo C; European HD Network. Clinical manifestation of intermediate allele carriers in Huntington disease. Neurology. 2016 Jul 8. pii:10.1212/WNL.2944.
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Heller J, Brcina N, Dogan I, Holtbernd F, Romanzetti S, Schulz JB, Schiefer J, Reetz K. Brain imaging findings in idiopathic REM sleep behavior disorder (RBD) - a systematic review on potential biomarkers for neurodegeneration. Sleep Medicine Reviews. 2017;34:23-33. Epub 2016.
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Dogan I, Tinnemann E, Romanzetti S, Mirzazade S, Costa AS, Werner CJ, Heim S, Fedosov K, Schulz S, Timmann D, Giordano IA, Klockgether T, Schulz JB and Reetz K. Cognition in Friedreich’s ataxia: a behavioral and multimodal imaging study. Annals of Clinical and Translational Neurology. 2016;3(8):572-87.
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Schrempf W, Katona I, Dogan I, Felbert VV, Wienecke M, Heller J, Maier A, Hermann A, Linse K, Brandt MD, Reichmann H, Schulz JB, Schiefer J, Oertel WH, Storch A, Weis J, Reetz K. Reduced intraepidermal nerve fiber density in patients with REM sleep behavior disorder. Parkinsonism Relat Disord. 2016;29:10-6. 
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Mengel D, Dams, J, Ziemek J, Becker J, Balzer-Geldsetzer M, Hilker R, Baudrexel S, Kalbe E, Schmidt N, Witt K, Liepelt-Scarfone I, Gräber S, Petrelli A, Neuser P, Schulte C, Wittchen HU, Riedel O, Mollenhauer B, Ebentheuer J, Trenkwalder C, Klockgether T, Spottke A, Wüllner U, Schulz JB, Reetz K, Heber IA, Ramirez A, Dodel R. Apolipoprotein E epsilon4 does not affect cognitive performance in patients with Parkinson's diseaseParkinsonism and Related Disorders 2016;8:1-18. 
>> PubMed 

Fengler S, Roeske S, Heber I, Reetz K, Schulz JB, Riedel O, Wittchen HU, Baudrexel S, Hilker-Roggendorf R, Mollenhauer B, Witt K, Schmidt N, Balzer-Geldsetzer M, Dams J, Dodel R, Gräber S, Pilotto A, Petrelli A, Fünkele S, Kassubek J, Kalbe E. Verbal memory declines more in female patients with Parkinson's disease: the importance of gender-corrected normative data. Psychological Medicine. 2016;46(11):2275-86. 
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Mathys C, Caspers J, Langner R, Südmeyer M, Grefkes C, Reetz K, Moldovan AS, Michely J, Heller J, Rickhoff CR, Turowski B, Schnitzler A, Hoffstaedter F, Eickhoff SB. Functional connectivity differences of the subthalamic nucleus related to Parkinson’s disease. Human Brain Mapping. 2016;37(3):1235-1253. 
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Heber IA, Costa AS, Werner CJ, Schöne U, Reich A, Schulz JB, Reetz K; Posterior Cortical Atrophy: A Case Report of a 6-Year Natural Progression.; Alzheimer disease and associated disorders. 2016;30(3):276-80.
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2015

Dogan I, Eickhoff CR, Fox PT, Laird AR, Schulz JB, Eickhoff SB, Reetz K. Functional connectivity modeling of consistent cortico-striatal degeneration in Huntington's disease. NeuroImage Clinical. 2015;7:640-52.
>> PMC

Schiefer J, Werner C, Reetz K. Clinical diagnosis and management in early Huntingtons disease: a review. Degenerative Neurological and Neuromuscular Disease. 2015;5:37-50.
>> Dovepress 

Reetz K, Abbas Z, Costa AS, Gras V, Tiffin-Richards F, Mirzazade S, Holschbach B, Frank RD, Vassiliadou A, Krüger T, Eitner F, Gross T, Schulz JB, Shah NJ. Increased cerebral water content in hemodialysis patients. PloS one. 2015;10(3):e0122188.
>> PMC

New AB, Robin DA, Parkinson AL, Eickhoff CR, Reetz K, Hoffstaedter F, Mathys C, Sudmeyer M, Grefkes C, Larson CR, Ramig LO, Fox PT, Eickhoff SB. The intrinsic resting state voice network in Parkinson's disease. Human brain mapping. 2015;36(5):1951-1962.
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Jauch-Chara K, Binkofski F, Loebig M, Reetz K, Jahn G, Melchert UH, Schweiger U, Oltmanns K. Blunted brain energy consumption relates to insula atrophy and impaired glucose tolerance in obesity. Diabetes. 2015;64(6):2082-2091.
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Reetz K, Dogan I, Costa AS, Dafotakis M, Fedosov K, Giunti P, Parkinson MH, Sweeney MG, Mariotti C, Panzeri M, Nanetti L, Arpa J, Sanz-Gallego I, Durr A, Charles P, Boesch S, Nachbauer W, Klopstock T, Karin I, Depondt C, Vom Hagen JM, Schols L, Giordano IA, Klockgether T, Burk K, Pandolfo M and Schulz JB. Biological and clinical characteristics of the European Friedreich’s Ataxia Consortium for Translational Studies (EFACTS) cohort: a cross-sectional analysis of baseline data. The Lancet Neurology. 2015;14(2):174-182.
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2014

Baldarçara L, Currie S, Hadjivassiliou M, Hoggard N, Jack A, Jackowski AP, Masclachi M, Parazzini C, Reetz K, Righini A, Schulz JB, Vella A, Webb SJ, Habas C. Consensus Paper: Radiological Biomarkers of Cerebellar Diseases. Cerebellum. Springer US. 2015;14(2):175-96.
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Tiffin-Richards FE, Costa AS, Holschbach B, Frank RD, Vassiliadou A, Krüger T, Kuckuck Karl, Gross T, Eitner F, Flöge J, Schulz JB, Reetz K. The Montreal Cognitive Assessment (MoCA) - A Sensitive Screening Instrument for Detecting Cognitive Impairment in Chronic Hemodialysis Patients. PLoS ONE. 2014;9(10):e106700.
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Ketteler S, Ketteler D, Vohn R, Kastrau F, Schulz JB, Reetz K, Huber W. The processing of lexical ambiguity in healthy ageing and Parkinson's disease: Role of cortico-subcortical networks. Brain Res, 2014;1581:51-63.
>> PubMed

Ana S. Costa, Frances E. Tiffin-Richards, Bernhard Holschbach, Rolf D. Frank, Athina Vassiliadou, Thilo Krüger, Frank Eitner, Theresa Gross, Nadim J. Shah, Jörg B. Schulz, Jürgen Floege and Kathrin Reetz. Clinical Predictors of Individual Cognitive Fluctuations in Patients Undergoing Hemodialysis. YAJKD. 2014;64(3):434-442.
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Nellessen N, Rottschy C, Eickhoff SB, Ketteler ST, Kuhn H, Shah NJ, et al. Specific and disease stage-dependent episodic memory-related brain activation patterns in Alzheimer's disease: a coordinate-based meta-analysis. Brain Struct Funct. 2014;220(3):1555-1571.
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Heller J, Dogan I, Schulz JB, Reetz K. Evidence for gender differences in cognition, emotion and quality of life in Parkinson’s disease? Aging and Disease. 2014;5(1):63-75. 
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Clemens B, Voß B, Pawliczek C, Mingoia G, Weyer D, Repple J, Eggermann T, Zerres K, Reetz K, Habel U. Effect of MAOA Genotype on Resting-State Networks in Healthy Participants. Cereb Cortex. 2014;(25/7):1771-1781.
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Werner C, Dogan I, Sass C, Mirzazade S, Schiefer J, Shah NJ, Schulz JB, Reetz K. Altered resting-state connectivity in Huntington's Disease. Hum Brain Mapp. 2014;35(6):2582-2593.
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Dogan I, Sass C, Mirzazade S, Kleiman A, Werner C, Pohl A, Schiefer J, Binkofski F, Schulz JB, Shah NJ, Reetz K. Neural correlates of impaired emotion processing in manifest Huntington's disease. Soc Cogn Affect Neurosci. 2014;9(5):671-680.
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2013

Freiherr J, Lundström JN, Habel U, Reetz K. Multisensory integration during aging. Frontiers in Human Neuroscience. 2013;7:863. eCollection.
>> PubMed

Hubers AA, van Duijn E, Roos RA, Craufurd D, Rickards H, Landwehrmeyer GB, van der Mast RC, Giltay EJ, REGISTRY investigators of the European Huntington’s Disease Network. Suicidal ideation in a European Huntington’s disease population. Journal of Affective Disorders. 2013;151(1):248-258.
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Costa AS, Reich A, Fimm B, Ketteler ST, Schulz JB, Reetz K. Evidence on the sensitivity of the MoCA alternate-forms in monitoring cognitive change in early Alzheimer’s disease. Dement Geriatr Cogn Disord. 2013;37(1-2):95-103.
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Jacobi H, Reetz K, Tezenas du Montcel S, Bauer P, Mariotti C, Nanetti L, Rakawicz M, Sulek A, Durr A, Chrales P, Filla A, Antenora A, Schöls L, Schicks J, Infante J, Kang J-S, Timmann D, Di Fabo R, Masciullo M, Baliko L, Bela M, Boesch S, Bürk K, Peltz A, Schultz, JB, Dufaure-Gare I, Klockgether T. Biological and clinical characteristics of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 in the longitudinal RISCA study: analysis of baseline data. Lancet Neurol. 2013;12(7):650-658. *Shared first authorship.
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Reetz K, Costa AS, Mirzazade S, Lehmann A, Juzek A, Rakowicz M, Boguslawska R, Schöls L, Linnemann C, Mariotti C, Gristoli M, Dürr A, van de Warrenburg BP, Timmann D, Pandolfo M, Bauer P, Jacobi H, Hauser TK, Klockgether T, Schulz JB; axia Study Group Investigators. Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6. Brain. 2013;136(Pt 3):905-917.
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Heber IA, Coenen VA, Reetz K, Schulz JB, Hoellig A, Fimm B, Kronenbuerger M. Cognitive effects of deep brain stimulation for essential tremor: evaluation at 1 and 6 years. J Neural Transm. 2013;120(11):1569-1577.
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Rottschy C, Kleiman A, Dogan I, Langner R, Mirzazade S, Kronenbuerger M, Werner C, Shah NJ, Schulz JB, Eickhoff SB, Reetz K. Diminished activation of motor working-memory networks in Parkinson’s Disease. PLoS One. 2013;8(4):e61786.
>> PubMed

Dogan I, Sass C, Mirzazade S, Kleiman A, Werner C, Pohl A, Schiefer J, Binkofski F, Schulz JB, Shah NJ, Reetz K. Neural correlates of impaired emotion processing in manifest Huntington's disease. Soc Cogn Affect Neurosci. 2014;9(5):671-80. Epub 2013.
>> PubMed

Rottschy C, Caspers S, Roski C, Reetz K, Dogan I, Schulz JB, Zilles K, Laird AR, Fox PT, Eickhoff SB. Differentiated parietal connectivity of frontal regions for "what" and "where" memory. Brain Struct Funct. 2013;218(6):1551-1567.
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Dogan I, Eickhoff SB, Schulz JB, Shah NJ, Laird AR, Fox PT, Reetz K. Consistent neurodegeneration and its association with clinical progression in Huntington's disease: A coordinate-based meta-analysis. Neurodegenerative Disorders. 2013;12(1):23-35.
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2012

Ertelt D, Witt K, Reetz K, Frank W, Junghanns K, Backhaus J, Tadic V, Pellicano A, Born J, Binkofski F. Skill memory escaping from distraction by sleep-evidence from dual-task performance. PLoS One. 2012;7(12):e50983.
>> PubMed

Reetz K, Romanzetti S, Dogan I, Sass C, Werner CJ, Schiefer J, Schulz JB, Shah NJ. Increased brain tissue sodium concentration in Huntington's Disease - A sodium imaging study at 4T. Neuroimage. 2012;63(1):517-524.
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Reetz K, Dogan I, Rolfs A, Binkofski F, Schulz JB, Laird AR, Fox PT, Eickhoff SB. Investigating function and connectivity of morphometric findings - Exemplified on cerebellar atrophy in spinocerebellar ataxia 17 (SCA17). Neuroimage. 2012;62(3):1354-1366.
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Costa AS, Fimm B, Friesen P, Soundjock H, Rottschy C, Gross T, Eitner F, Reich A, Schulz JB, Nasreddine ZS, Reetz K. Alternate-form reliability of the montreal cognitive assessment screening test in a clinical setting. Dement Geriatr Cogn Disord. 2012;33(6):379-384.
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Rottschy C, Langner R, Dogan I, Reetz K, Laird AR, Schulz JB, Fox PT, Eickhoff SB. Modelling neural correlates of working memory – A coordinate based Meta-Analysis. Neuroimage. 2012;60(1):830-846.
>> PubMed

Nickl-Jockschat T, Kleiman A, Schulz JB, Schneider F, Laird AR, Fox PT, Eickhoff SB, Reetz K. Neuroanatomic changes and their association with cognitive decline in mild cognitive impairment: a meta-analysis. Brain Struct Funct. 2012;217(1):115-125.
>> PubMed

2011

Reetz K, Kleiman A, Klein C, Lencer R, Zühlke C, Brockmann K, Rolfs A, Binkofski F. CAG repeats determine brain atrophy in Spinocerebellar Ataxia 17: A VBM Study. PloS One. 2011;6(1):e15125.
>> PubMed

2010

Brüggemann N, Hagenah J, Reetz K, Schmidt A, Kasten M, Buchmann I, Eckerle S, Bähre M, Münchau A, Djarmati A, von der Vegt J, Siebner HR, Binkofski F, Ramirez A, Behrens M, Klein C. Recessively inherited parkinsonism: Effect of ATP13A2 mutations on the clinical and neuroimaging phenotype. Archives of Neurology. 2010;67(11):1357-1363.
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Reetz K, Tadic V, Kasten M, Brüggemann N, Schmidt A, Hagenah J, Pramstaller PP, Ramirez A, Behrens MI, Siebner HR, Klein C, Binkofski F. Structural imaging in the presymptomatic stage of genetically determined parkinsonism. Neurobiol Dis. 2010;39(3):402-408.
>> PubMed 

Stanley K, Hagenah J, Brüggemann N, Reetz K, Severt L, Klein C, Yu Q, derby C, Pullman, S, Saunders-Pullman, R. Digitized spiral analysis is a promising early motor marker for Parkinson Disease. Parkinsonism Relat Disord. 2010;16(3):233-234.
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Reetz K, Lencer R, Hagenah J, Gaser C, Tadic V, Walter U, Wolters A, Steinlechner S, Zühlke C, Brockmann K, Klein C, Rolfs A, Binkofski F. Structural changes associated with progression of motor deficits in spinocerebellar ataxia 17. Cerebellum. 2010;9(2):210-217.
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Carbon M, Reetz K, Ghilardi MF, Dhawan V, Eidelberg D. Early Parkinson's Disease: Longitudinal Changes in Brain Activity during Sequence Learning. Neurobiol Dis. 2010;37(2):455-460. *Shared first authorship.
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2009

Djarmati A, Hagenah J, Reetz K, Winkler S, Behrens MI, Pawlack H, Lohmann K, Ramirez A, Tadic V, Brüggemann N, Berg D, Siebner HR, Lang AE, Pramstaller PP, Binkofski F, Kostic VS, Gasser T, Klein C. ATP13A2 variants in early-onset Parkinson's disease patients and controls. Mov Disord. 2009;24(14):2104-2111.
>> PubMed

Van Nuenen BFL, Weiss MM, Bloem BR, Reetz K, van Eimeren T, Lohmann K, Hagenah J, Pramstaller PP, Binkofski F, Klein C and Siebner HR. Heterozygous carriers of a Parkin or PINK1 mutation share a common functional endophenotype. Neurology. 2009;72(12):1041-1047.
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Reetz K, Gaser C, Klein C, Hagenah J, Buchel C, Gottschalk S, Pramstaller PP, Siebner HR, Binkofski F. Structural findings in the basal ganglia in genetically determined and idiopathic Parkinson’s disease. Movement Disorders. 2009;24(1): 99-103.
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Rief W, Nestoriuc Y, von Lilienfeld-Toal A, Dogan I, Schreiber F, Hofmann SG, Barsky AJ, Avorn J. Differences in adverse effect reporting in placebo groups in SSRI and tricyclic antidepressant trials: a systematic review and meta-analysis. Drug Saf. 2009;32(11):1041-56.
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2008

Reetz K, Lencer R, Steinlechner S, Gaser C, Hagenah J, Buchel C, Petersen D, Kock N, Djarmati A, Siebner HR, Klein C, Binkofski F. Limbic and frontal cortical degeneration is associated with psychiatric symptoms in PINK1 mutation carriers. Biol Psychiatry. 2008;64(3):241-247.
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Reetz K, Siebner HR, Gaser C, Hagenah J, Buchel C, Kasten M, Petersen D, Pramstaller PP, Klein C, Binkofski F. Premotor gray matter volume is associated with clinical findings in idiopathic and genetically determined Parkinson’s disease. The Open Neuroimaging Journal. 2008;2:102-105.
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2007

Binkofski F, Reetz K, Gaser C, Hilker R, Hagenah J, Hedrich K, van Eimeren T, Thiel A, Buchel C, Pramstaller PP, Siebner HR, Klein C. Morphometric fingerprint of asymptomatic Parkin and PINK1 mutation carriers in the basal ganglia. Neurology. 2007;69(9):842-850. *Shared first authorship.
>> PubMed

Binkofski F, Reetz K, Blangero A. Tactile agnosia and tactile apraxia: crosstalk between the action and perception streams in AIP. Behavioural and Brain Sciences. 2007;30(2):201-202.
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Schrickel JW, Brixius K, Herr C, Clemen CS, Sasse P, Reetz K, Grohe C, Meyer R, Tiemann, K, Schroder R, Bloch W, Nickenig G, Fleischmann BK, Noegel AA, Schwinger RH, Lewalter T. Enhanced heterogeneity of myocardial conduction and severe cardiac electrical instability in annexin A7-deficient mice. Cardiovasc Res. 2007;76(2):257-268.
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Hagenah J, Reetz K, Zuhlke C, Rolfs A, Binkofski F, Klein C. Predominant dystonia with marked cerebellar atrophy: a rare phenotype in familia dystonia. Neurology. 2007;68:2157-2158.
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Hiller A, Hagenah JM, Djarmati A, Hedrich K, Reetz K, Schneider-Gold C, Kress W, Munchau A, Klein C. Phenotypic spectrum of PINK1-associated parkinsonism in 15 mutation carriers from 1 family. Mov Disord. 2007;22:145-147.
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2006

Hedrich K, Hagenah J, Djarmati A, Hiller A, Lohnau T, Lasek K, Grunewald A, Hilker R, Steinlechner S, Boston H, Kock N, Schneider-Gold C, Kress W, Siebner H, Binkofski F, Lencer R, Munchau A, Klein C. Clinical spectrum of homozygous and heterozygous PINK1 mutations in a large German family with Parkinson disease: role of a single hit? Arch Neurol. 2006;63(6):833-838.
>> PubMed

Lasek K, Lencer R, Gaser C, Hagenah J, Walter U, Wolters A, Kock N, Steinlechner S, Nagel M, Zuhlke C, Nitschke MF, Brockmann K, Klein C, Rolfs A, Binkofski F. Morphological basis for the spectrum of clinical deficits in spinocerebellar ataxia 17 (SCA17). Brain. 2006;129(Pt9):2341-2352.
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Pisella L, Binkofski F, Lasek K, Toni I, Rossetti Y. No double-dissociation between optic ataxia and visual agnosia: Multiple sub-streams for multiple visuo-manual integrations. Neuropsychologia. 2006;44(13):2734-2748.
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Hesselmann V, Maarouf M, Hunsche S, Lasek K, Schaaf M, Krug B, Lackner K, Sturm V, Wedekind C. Functional MRI for immediate monitoring stereotactic thalamotomy in a patient with essential tremor. Eur Radiol. 2006;16(10):2229-2233.
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2004

Hesselmann V, Girnus R, Wedekind C, Hunsche S, Bunke J, Schulte O, Sorger B, Lasek K, Krug B, Sturm V, Lackner K. Functional MRI using multiple receiver coils: BOLD signal changes and signal-to-noise ratio for three-dimensional-PRESTO vs. single shot EPI in comparison to a standard quadrature head coil. J Magn Reson Imaging. 2004;20(2):321-326.
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Hesselmann V, Sorger B, Lasek K, Guntinas-Lichius O, Krug B, Sturm V, Goebel R, Lackner K. Discriminating the cortical representation sites of tongue and up movement by functional MRI. Brain Topogr. 2004;16(3):159-167.
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Hesselmann V, Sorger B, Girnus R, Lasek K, Maarouf M, Wedekind C, Bunke J, Schulte O, Krug B, Lackner K, Sturm V. Intraoperative functional MRI as a new approach to monitor deep brain stimulation in Parkinson's disease. Eur Radiol. 2004;14(4):686-690.
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2001

Brixius K, Hoischen S, Reuter H, Lasek K, Schwinger RH. Force/shortening-frequency relationship in multicellular muscle strips and single cardiomyocytes of human failing and nonfailing hearts. J Card Fail. 2001;7(4):335-341.
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Herr C, Smyth N, Ullrich S, Yun F, Sasse P, Hescheler J, Fleischmann B, Lasek K, Brixius K, Schwinger RHG, Fässler R, Schröder R, Noegel, AA. Loss of annexin A7 leads to alterations in frequency-induced shortening of isolated murine cardiomyocytes. Mol Cell Biol. 2001;21(13):4119-4128.
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Brixius K, Hoischen S, Zobel C, Lasek K, Schwinger RH. [The Ca(2+) sensitizers CGP 48506 and EMD 57033, but not the Na(+) channel modulator BDF 9148, prolong relaxation in isolated cardiomyocytes of the guinea pig]. Z Kardiol. 2001;90(4):286-291.
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Bücher

Reetz K and Binkofski F. Magnetic Resonance Imaging in Movement Disorders – A guide for clinicians and scientists. Ed. Tuite and Dagher, Chapter 14: Ataxia. p. 204-228. Oxford University Press 2013 in press.
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Reetz K, Binkofski F and Eggers C. Parkinson-Syndrom, Chorea Huntington (pages 549-561) in Funktionelle MRT in Psychiatrie und Neurologie, 2. Auflage. Herausgeber: Schneider, Fink. Verlag: Springer, Heidelberg. 2012. (ISBN: 978-3-540-20474-9)  
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Reetz K. „Bildgebung genetischer Aspekte des Parkinson-Syndroms“ In: Frank Schneider (Ed.) „Positionen der Psychiatrie“; (pages 153-157). Springer Verlag Heidelberg, 2012 (ISBN: 978-3-642-25475-8).
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Reetz K and Binkofski F. „Structural abnormalities in Parkinson’s disease – MRI and related methods“ In David Eidelberg (Ed.) „Imaging in Parkinson’s Disease“; (pages 32-50). Oxford University Press New York, 2011 (ISBN: 978-0-19-539348-4).
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Reetz K and Binkofski F. “Apraxia” In Stefano F Cappa et al., (Ed) “Cognitive Neurology – a clinical textbook”, (pages 67-88). Oxford University Press, 2008 (ISBN: 978-0-19-856927-5)
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