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Movement Disorders : Official Journal of the Movement Disorder Society
|
December 10, 2009
Sustained dopaminergic response of parkinsonism and depression in POLG-associated parkinsonism
Matthis Synofzik, Friedrich Asmus, Matthias Reimold, et al.
Cerebellum (London, England)
|
April 25, 2012
Characterizing POLG ataxia: clinics, electrophysiology and imaging
Matthis Synofzik, Karin Srulijes, Jana Godau, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 16, 2022
Reply to: "Risk Disclosure in Prodromal Parkinson's Disease"
Eva Schaeffer, Inken Toedt, Susanne Köhler, et al.
Neurochemistry International
|
December 11, 2012
Genetics and iron in the systems biology of Parkinson's disease and some related disorders
Claudia Funke, Susanne A Schneider, Daniela Berg, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
August 5, 2021
Risk Disclosure in Prodromal Parkinson's Disease
Eva Schaeffer, Inken Toedt, Susanne Köhler, et al.
Neuro-Degenerative Diseases
|
June 11, 2011
Transcranial sonography reveals cerebellar, nigral, and forebrain abnormalities in Friedreich's ataxia
Matthis Synofzik, Jana Godau, Tobias Lindig, et al.
Cerebellum (London, England)
|
September 25, 2010
Restless legs and substantia nigra hypoechogenicity are common features in Friedreich's ataxia
Matthis Synofzik, Jana Godau, Tobias Lindig, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 16, 2004
Five-year follow-up study of hyperechogenicity of the substantia nigra in Parkinson's disease
Daniela Berg, Berthold Merz, Karlheinz Reiners, et al.
European Radiology
|
April 13, 2011
Three-dimensional magnetic resonance spectroscopic imaging in the substantia nigra of healthy controls and patients with Parkinson's disease
Adriane Gröger, Grzegorz Chadzynski, Jana Godau, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)
|
March 4, 2009
Genetic analysis of coding SNPs in blood-brain barrier transporter MDR1 in European Parkinson's disease patients
Claudia Funke, Anne S Soehn, Juergen Tomiuk, et al.
Page
of 55
Search research articles
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Showing results (71-80 of 547) with videos related to
Sort By:
Page
of 55
Movement Disorders : Official Journal of the Movement Disorder Society
|
December 10, 2009
Sustained dopaminergic response of parkinsonism and depression in POLG-associated parkinsonism
Matthis Synofzik, Friedrich Asmus, Matthias Reimold, et al.
Cerebellum (London, England)
|
April 25, 2012
Characterizing POLG ataxia: clinics, electrophysiology and imaging
Matthis Synofzik, Karin Srulijes, Jana Godau, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 16, 2022
Reply to: "Risk Disclosure in Prodromal Parkinson's Disease"
Eva Schaeffer, Inken Toedt, Susanne Köhler, et al.
Neurochemistry International
|
December 11, 2012
Genetics and iron in the systems biology of Parkinson's disease and some related disorders
Claudia Funke, Susanne A Schneider, Daniela Berg, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
August 5, 2021
Risk Disclosure in Prodromal Parkinson's Disease
Eva Schaeffer, Inken Toedt, Susanne Köhler, et al.
Neuro-Degenerative Diseases
|
June 11, 2011
Transcranial sonography reveals cerebellar, nigral, and forebrain abnormalities in Friedreich's ataxia
Matthis Synofzik, Jana Godau, Tobias Lindig, et al.
Cerebellum (London, England)
|
September 25, 2010
Restless legs and substantia nigra hypoechogenicity are common features in Friedreich's ataxia
Matthis Synofzik, Jana Godau, Tobias Lindig, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 16, 2004
Five-year follow-up study of hyperechogenicity of the substantia nigra in Parkinson's disease
Daniela Berg, Berthold Merz, Karlheinz Reiners, et al.
European Radiology
|
April 13, 2011
Three-dimensional magnetic resonance spectroscopic imaging in the substantia nigra of healthy controls and patients with Parkinson's disease
Adriane Gröger, Grzegorz Chadzynski, Jana Godau, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)
|
March 4, 2009
Genetic analysis of coding SNPs in blood-brain barrier transporter MDR1 in European Parkinson's disease patients
Claudia Funke, Anne S Soehn, Juergen Tomiuk, et al.
Page
of 55