Synofzik, M. : rechercher sur Z-Library

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1

Beyond the comparator model: A multifactorial two-step account of agency

Matthis Synofzik, Gottfried Vosgerau, Albert Newen

Journal:

Consciousness and Cognition

Année:

2008

Langue:

english

Fichier:

PDF, 410 KB

english, 2008

2

Electrodes in the brain—Ethical criteria for research and treatment with deep brain stimulation for neuropsychiatric disorders

Matthis Synofzik, Thomas E. Schlaepfer

Journal:

Brain Stimulation

Année:

2011

Langue:

english

Fichier:

PDF, 410 KB

english, 2011

3

A COGNITIVE THEORY OF THOUGHTS

Gottfried Vosgerau and Matthis Synofzik

Journal:

American Philosophical Quarterly

Année:

2010

Langue:

english

Fichier:

PDF, 2.01 MB

english, 2010

4

Gangveränderungen als Frühindikator einer Demenz

M. Jamour, C. Becker, M. Synofzik, W. Maetzler

Journal:

Zeitschrift für Gerontologie und Geriatrie

Année:

2012

Langue:

german

Fichier:

PDF, 292 KB

german, 2012

5

Boudewijn Chabot, Christian Walther (2010) Ausweg am Lebensende. Selbstbestimmtes Sterben durch freiwilligen Verzicht auf Essen und Trinken

Matthis Synofzik

Journal:

Ethik in der Medizin

Année:

2011

Langue:

german

Fichier:

PDF, 590 KB

german, 2011

6

How Happy Is Too Happy? Euphoria, Neuroethics, and Deep Brain Stimulation of the Nucleus Accumbens

Synofzik, Matthis, Schlaepfer, Thomas E., Fins, Joseph J.

Journal:

AJOB Neuroscience

Année:

2012

Langue:

english

Fichier:

PDF, 188 KB

english, 2012

7

The genetic nomenclature of recessive cerebellar ataxias

Rossi, Malco, Anheim, Mathieu, Durr, Alexandra, Klein, Christine, Koenig, Michel, Synofzik, Matthis, Marras, Connie, van de Warrenburg, Bart P.

Journal:

Movement Disorders

Année:

2018

Langue:

english

Fichier:

PDF, 506 KB

english, 2018

8

I move, therefore I am: A new theoretical framework to investigate agency and ownership

Matthis Synofzik, Gottfried Vosgerau, Albert Newen

Journal:

Consciousness and Cognition

Année:

2008

Langue:

english

Fichier:

PDF, 244 KB

english, 2008

9

Wie sollen wir Patienten mit Demenz behandeln? Die ethisch problematische Funktion der Antidementiva

Matthis Synofzik, Walter Maetzler

Journal:

Ethik in der Medizin

Année:

2007

Langue:

german

Fichier:

PDF, 281 KB

german, 2007

10

Intensive coordinative training improves motor performance in degenerative cerebellar disease

Ilg, W., Synofzik, M., Brotz, D., Burkard, S., Giese, M. A., Schols, L.

Journal:

Année:

2009

Langue:

english

Fichier:

PDF, 565 KB

english, 2009

11

A neuromodulation experience registry for deep brain stimulation studies in psychiatric research: Rationale and recommendations for implementation

Matthis Synofzik, Joseph J. Fins, Thomas E. Schlaepfer

Journal:

Brain Stimulation

Année:

2012

Langue:

english

Fichier:

PDF, 67 KB

english, 2012

12

Autosomal recessive spastic ataxia of Charlevoix Saguenay (ARSACS): expanding the genetic, clinical and imaging spectrum

Matthis Synofzik, Anne S Soehn, Janina Gburek-Augustat…

Journal:

Orphanet Journal of Rare Diseases

Année:

2013

Langue:

english

Fichier:

PDF, 442 KB

english, 2013

13

X-linked Charcot-Marie-Tooth disease, Arts syndrome, and prelingual non-syndromic deafness form a disease continuum: evidence from a family with a novelPRPS1mutation

Synofzik, Matthis, Müller vom Hagen, Jennifer, Haack, Tobias B, Wilhelm, Christian, Lindig, Tobias, Beck-Wödl, Stefanie, Nabuurs, Sander B, van Kuilenburg, André BP, de Brouwer, Arjan PM, Schöls, Ludg

Journal:

Orphanet Journal of Rare Diseases

Année:

2014

Langue:

english

Fichier:

PDF, 447 KB

english, 2014

14

Videogame-based coordinative training can improve advanced, multisystemic early-onset ataxia

Synofzik, Matthis, Schatton, Cornelia, Giese, Martin, Wolf, Julia, Schöls, Ludger, Ilg, Winfried

Journal:

Journal of Neurology

Année:

2013

Langue:

english

Fichier:

PDF, 270 KB

english, 2013

15

Phenotype and frequency of STUB1 mutations: next-generation screenings in Caucasian ataxia and spastic paraplegia cohorts

Synofzik, Matthis, Schüle, Rebecca, Schulze, Martin, Gburek-Augustat, Janina, Schweizer, Roland, Schirmacher, Anja, Krägeloh-Mann, Ingeborg, Gonzalez, Michael, Young, Peter, Züchner, Stephan, Schöls,

Journal:

Orphanet Journal of Rare Diseases

Année:

2014

Langue:

english

Fichier:

PDF, 649 KB

english, 2014

16

Misattributions of agency in schizophrenia are based on imprecise predictions about the sensory consequences of one's actions

Synofzik, M., Thier, P., Leube, D. T., Schlotterbeck, P., Lindner, A.

Journal:

Année:

2010

Langue:

english

Fichier:

PDF, 639 KB

english, 2010

17

ATAXIA WITH OPHTHALMOPLEGIA OR SENSORY NEUROPATHY IS FREQUENTLY CAUSED BY POLG MUTATIONS

Schulte, C., Synofzik, M., Gasser, T., Schols, L.

Journal:

Année:

2009

Langue:

english

Fichier:

PDF, 161 KB

english, 2009

18

Lack of enzyme activity in GBA2 mutants associated with hereditary spastic paraplegia/cerebellar ataxia (SPG46)

Sultana, Saki, Reichbauer, Jennifer, Schüle, Rebecca, Mochel, Fanny, Synofzik, Matthis, van der Spoel, Aarnoud C.

Journal:

Biochemical and Biophysical Research Communications

Année:

2015

Langue:

english

Fichier:

PDF, 823 KB

english, 2015

19

Video game-based coordinative training improves ataxia in children with degenerative ataxia

Ilg, W., Schatton, C., Schicks, J., Giese, M. A., Schols, L., Synofzik, M.

Journal:

Année:

2012

Langue:

english

Fichier:

PDF, 430 KB

english, 2012

20

Towards a common framework of grounded action cognition: Relating motor control, perception and cognition

Gentsch, Antje, Weber, Arne, Synofzik, Matthis, Vosgerau, Gottfried, Schütz-Bosbach, Simone

Journal:

Année:

2016

Langue:

english

Fichier:

PDF, 542 KB

english, 2016

21

Antisense Oligonucleotide Mediated Splice Correction of a Deep Intronic Mutation in OPA1

Bonifert, Tobias, Gonzalez Menendez, Irene, Battke, Florian, Theurer, Yvonne, Synofzik, Matthis, Schöls, Ludger, Wissinger, Bernd

Journal:

Molecular Therapy — Nucleic Acids

Année:

2016

Langue:

english

Fichier:

PDF, 979 KB

english, 2016

22

STUB1/CHIP mutations cause Gordon Holmes syndrome as part of a widespread multisystemic neurodegeneration: evidence from four novel mutations

Hayer, Stefanie Nicole, Deconinck, Tine, Bender, Benjamin, Smets, Katrien, Züchner, Stephan, Reich, Selina, Schöls, Ludger, Schüle, Rebecca, De Jonghe, Peter, Baets, Jonathan, Synofzik, Matthis

Journal:

Orphanet Journal of Rare Diseases

Année:

2017

Langue:

english

Fichier:

PDF, 1.45 MB

english, 2017

23

Individualized exergame training improves postural control in advanced degenerative spinocerebellar ataxia: A rater-blinded, intra-individually controlled trial

Schatton, Cornelia, Synofzik, Matthis, Fleszar, Zofia, Giese, Martin A., Schöls, Ludger, Ilg, Winfried

Journal:

Parkinsonism & Related Disorders

Année:

2017

Langue:

english

Fichier:

PDF, 1.07 MB

english, 2017

24

Validity and reliability of outcome measures assessing dexterity, coordination, and upper limb strength in Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay

Gagnon, Cynthia, Lessard, Isabelle, Brais, Bernard, Côté, Isabelle, Lavoie, Caroline, Synofzik, Matthis, Mathieu, Jean

Journal:

Archives of Physical Medicine and Rehabilitation

Année:

2018

Langue:

english

Fichier:

PDF, 2.29 MB

english, 2018

25

Hemodialysis in MNGIE transiently reduces serum and urine levels of thymidine and deoxyuridine, but not CSF levels and neurological function

Röeben, Benjamin, Marquetand, Justus, Bender, Benjamin, Billing, Heiko, Haack, Tobias B., Sanchez-Albisua, Iciar, Schöls, Ludger, Blom, Henk J., Synofzik, Matthis

Journal:

Orphanet Journal of Rare Diseases

Année:

2017

Langue:

english

Fichier:

PDF, 674 KB

english, 2017

26

Biallelic Parkin (PARK2) mutations can cause a bvFTD phenotype without clinically relevant parkinsonism

Zimmermann, Milan, Wilke, Carlo, Schulte, Claudia, Hoffmann, Jessica, Klopfer, Jasmin, Reimold, Matthias, Brockmann, Kathrin, Synofzik, Matthis

Journal:

Parkinsonism & Related Disorders

Année:

2018

Langue:

english

Fichier:

PDF, 385 KB

english, 2018

27

The experience of agency: an interplay between prediction and postdiction

Synofzik, Matthis, Vosgerau, Gottfried, Voss, Martin

Journal:

Frontiers in Psychology

Année:

2013

Langue:

english

Fichier:

PDF, 1.16 MB

english, 2013

28

Nerve ultrasound characterizes AMN polyneuropathy as inhomogeneous and focal hypertrophic

Rattay, Tim W., Just, Jennifer, Röben, Benjamin, Hengel, Holger, Schüle, Rebecca, Synofzik, Matthis, Söhn, Anne S., Winter, Natalie, Dammeier, Nele, Schöls, Ludger, Grimm, Alexander

Journal:

Orphanet Journal of Rare Diseases

Année:

2018

Langue:

english

Fichier:

PDF, 2.03 MB

english, 2018

29

Recommendations for patient screening in ultra-rare inherited metabolic diseases: what have we learned from Niemann-Pick disease type C?

Sobrido, María-Jesús, Bauer, Peter, de Koning, Tom, Klopstock, Thomas, Nadjar, Yann, Patterson, Marc C, Synofzik, Matthis, Hendriksz, Chris J

Journal:

Orphanet Journal of Rare Diseases

Année:

2019

Fichier:

PDF, 680 KB

2019

30

Documenting the psychometric properties of the scale for the assessment and rating of ataxia to advance trial readiness of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay

Bourcier, Dax, BÃ©langer, Mathieu, CÃ´tÃ©, Isabelle, Brais, Bernard, Synofzik, Matthis, Brisson, Jean-Denis, Rodrigue, Xavier, Gagnon, Maude-Marie, Mathieu, Jean, Gagnon, Cynthia

Journal:

Journal of the Neurological Sciences

Année:

2020

Fichier:

PDF, 2.71 MB

2020

31

Sustained dopaminergic response of parkinsonism and depression in POLG-associated parkinsonism

Matthis Synofzik, Friedrich Asmus, Matthias Reimold, Ludger Schöls, Daniela Berg

Journal:

Movement Disorders

Année:

2010

Langue:

english

Fichier:

PDF, 287 KB

english, 2010

32

Long-term effects of coordinative training in degenerative cerebellar disease

Winfried Ilg, Doris Brötz, Susanne Burkard, Martin A. Giese, Ludger Schöls, Matthis Synofzik

Journal:

Movement Disorders

Année:

2010

Langue:

english

Fichier:

PDF, 459 KB

english, 2010

33

POLG, but not PEO1, is a frequent cause of cerebellar ataxia in Central Europe

Julia Schicks, Matthis Synofzik, Claudia Schulte, Ludger Schöls

Journal:

Movement Disorders

Année:

2010

Langue:

english

Fichier:

PDF, 645 KB

english, 2010

34

Complex hyperkinetic movement disorders associated with POLG mutations

Matthis Synofzik, Rebecca SchüLe, Claudia Schulte, Rejko KrüGer, Tobias Lindig, Ludger SchöLs, Friedrich Asmus

Journal:

Movement Disorders

Année:

2010

Langue:

english

Fichier:

PDF, 558 KB

english, 2010

35

Atypical juvenile parkinsonism in a consanguineous SPG15 family

Julia Schicks, Matthis Synofzik, Hjörvar Pétursson, Johanna Huttenlocher, Matthias Reimold, Ludger Schöls, Peter Bauer

Journal:

Movement Disorders

Année:

2011

Langue:

english

Fichier:

PDF, 273 KB

english, 2011

36

Retinal nerve fiber layer loss in multiple system atrophy

M.Dominik Fischer, Matthis Synofzik, Robert Heidlauf, Julia Schicks, Karin Srulijes, Christoph Kernstock, Daniela Berg, Ludger Schöls, Ulrich Schiefer

Journal:

Movement Disorders

Année:

2011

Langue:

english

Fichier:

PDF, 880 KB

english, 2011

37

Cerebrospinal fluid fatty acids in glucocerebrosidase-associated Parkinson's disease

Stefan P. Schmid, Erwin D. Schleicher, Alexander Cegan, Christian Deuschle, Stephanie Baur, Ann-Kathrin Hauser, Matthis Synofzik, Karin Srulijes, Kathrin Brockmann, Daniela Berg, Walter Maetzler

Journal:

Movement Disorders

Année:

2012

Langue:

english

Fichier:

PDF, 1.12 MB

english, 2012

38

Reply to Carruthers

Matthis Synofzik, Gottfried Vosgerau, Albert Newen

Journal:

Consciousness and Cognition

Année:

2009

Langue:

english

Fichier:

PDF, 109 KB

english, 2009

39

Me or not me – An optimal integration of agency cues?

Matthis Synofzik, Gottfried Vosgerau, Axel Lindner

Journal:

Consciousness and Cognition

Année:

2009

Langue:

english

Fichier:

PDF, 121 KB

english, 2009

40

Philosophieren über die Rätsel des Gehirns

M. Synofzik, L. Huber, U. Wiesing

Journal:

Année:

2004

Langue:

german

Fichier:

PDF, 522 KB

german, 2004

41

PEG-Ernährung bei fortgeschrittener Demenz

Journal:

Année:

2007

Langue:

german

Fichier:

PDF, 818 KB

german, 2007

42

Wirksam, indiziert - und dennoch ohne Nutzen?

Matthis Synofzik

Journal:

Zeitschrift für Gerontologie und Geriatrie

Année:

2006

Langue:

german

Fichier:

PDF, 283 KB

german, 2006

43

Severe orthostatic dysregulation associated with Wolfram syndrome

Matthis Synofzik, Daniel Weiss, Jite Erharhaghen, Rejko Krüger, Ludger Schöls

Journal:

Journal of Neurology

Année:

2010

Langue:

english

Fichier:

PDF, 230 KB

english, 2010

44

Die neuen Möglichkeiten der Neurowissenschaften und ihre ethischen Implikationen

Matthis Synofzik

Journal:

Ethik in der Medizin

Année:

2005

Langue:

german

Fichier:

PDF, 815 KB

german, 2005

45

Kognition

Matthis Synofzik

Journal:

Ethik in der Medizin

Année:

2006

Langue:

german

Fichier:

PDF, 289 KB

german, 2006

46

Wolfram Höfling (Hrsg.) (2005) Das sog. Wachkoma. Rechtliche, medizinische und ethische Aspekte. (Reihe Recht-Ethik-Gesundheit, Band 1)

Matthis Synofzik

Journal:

Ethik in der Medizin

Année:

2006

Langue:

german

Fichier:

PDF, 141 KB

german, 2006

47

Ethically Justified, Clinically Applicable Criteria for Physician Decision-Making in Psychopharmacological Enhancement

Matthis Synofzik

Journal:

Année:

2009

Langue:

english

Fichier:

PDF, 320 KB

english, 2009

48

Restless Legs and Substantia Nigra Hypoechogenicity are Common Features in Friedreich’s Ataxia

Matthis Synofzik, Jana Godau, Tobias Lindig, Ludger Schöls, Daniela Berg

Journal:

Année:

2011

Langue:

english

Fichier:

PDF, 138 KB

english, 2011

49

Mutations in the PDYN gene (SCA23) are not a frequent cause of dominant ataxia in Central Europe

J Schicks, M Synofzik, C Beetz, F Schiele, L Schöls

Journal:

Clinical Genetics

Année:

2011

Langue:

english

Fichier:

PDF, 473 KB

english, 2011

50

Amplicon-based high-throughput pooled sequencing identifies mutations in CYP7B1 and SPG7 in sporadic spastic paraplegia patients

NA Schlipf, R Schüle, S Klimpe, KN Karle, M Synofzik, J Schicks, O Riess, L Schöls, P Bauer

Journal:

Clinical Genetics

Année:

2011

Langue:

english

Fichier:

PDF, 1000 KB

english, 2011