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The Application of Clinical Genetics
|
June 19, 2013
Genetic basis of Parkinson's disease: inheritance, penetrance, and expression
Claudia Schulte, Thomas Gasser
Scientific Reports
|
April 15, 2026
Investigating non-linear volume-outcome relationships in total knee arthroplasty based on a sample of more than 60,000 hospital cases from Germany, 2020-2023
Martin Roessler, Christoph Bobeth, Claudia Schulte, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
August 31, 2010
POLG, but not PEO1, is a frequent cause of cerebellar ataxia in Central Europe
Julia Schicks, Matthis Synofzik, Claudia Schulte, et al.
NPJ Parkinson'S Disease
|
December 2, 2025
TMEM175, SCARB2 and CTSB associations with Parkinson's disease risk across populations
Wenhua Sun, Claudia Schulte, Thomas Gasser, et al.
NPJ Parkinson'S Disease
|
April 13, 2026
Author Correction: TMEM175, SCARB2 and CTSB associations with Parkinson's disease risk across populations
Wenhua Sun, Claudia Schulte, Thomas Gasser, et al.
Neurology
|
September 16, 2009
Ataxia with ophthalmoplegia or sensory neuropathy is frequently caused by POLG mutations
Claudia Schulte, Matthis Synofzik, Thomas Gasser, et al.
Medizinische Klinik, Intensivmedizin Und Notfallmedizin
|
April 23, 2024
Hospital admissions following emergency medical services in Germany: analysis of 2 million hospital cases in 2022
Martin Roessler, Claudia Schulte, Christoph Bobeth, et al.
Medical Care
|
November 14, 2023
Multilevel Quality Indicators: Methodology and Monte Carlo Evidence
Martin Roessler, Claudia Schulte, Uwe Repschläger, et al.
The European Journal of Health Economics : HEPAC : Health Economics in Prevention and Care
|
November 20, 2021
Optimising the impact of COVID-19 vaccination on mortality and hospitalisations using an individual additive risk measuring approach based on a risk adjustment scheme
Danny Wende, Dagmar Hertle, Claudia Schulte, et al.
Parkinsonism & Related Disorders
|
July 25, 2016
Broad clinical phenotype in Parkinsonism associated with a base pair deletion in RAB39B and additional POLG variant
Max Güldner, Claudia Schulte, Ann-Kathrin Hauser, et al.
Page
of 17
Search research articles
Search
Showing results (1-10 of 164) with videos related to
Sort By:
Page
of 17
The Application of Clinical Genetics
|
June 19, 2013
Genetic basis of Parkinson's disease: inheritance, penetrance, and expression
Claudia Schulte, Thomas Gasser
Scientific Reports
|
April 15, 2026
Investigating non-linear volume-outcome relationships in total knee arthroplasty based on a sample of more than 60,000 hospital cases from Germany, 2020-2023
Martin Roessler, Christoph Bobeth, Claudia Schulte, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
August 31, 2010
POLG, but not PEO1, is a frequent cause of cerebellar ataxia in Central Europe
Julia Schicks, Matthis Synofzik, Claudia Schulte, et al.
NPJ Parkinson'S Disease
|
December 2, 2025
TMEM175, SCARB2 and CTSB associations with Parkinson's disease risk across populations
Wenhua Sun, Claudia Schulte, Thomas Gasser, et al.
NPJ Parkinson'S Disease
|
April 13, 2026
Author Correction: TMEM175, SCARB2 and CTSB associations with Parkinson's disease risk across populations
Wenhua Sun, Claudia Schulte, Thomas Gasser, et al.
Neurology
|
September 16, 2009
Ataxia with ophthalmoplegia or sensory neuropathy is frequently caused by POLG mutations
Claudia Schulte, Matthis Synofzik, Thomas Gasser, et al.
Medizinische Klinik, Intensivmedizin Und Notfallmedizin
|
April 23, 2024
Hospital admissions following emergency medical services in Germany: analysis of 2 million hospital cases in 2022
Martin Roessler, Claudia Schulte, Christoph Bobeth, et al.
Medical Care
|
November 14, 2023
Multilevel Quality Indicators: Methodology and Monte Carlo Evidence
Martin Roessler, Claudia Schulte, Uwe Repschläger, et al.
The European Journal of Health Economics : HEPAC : Health Economics in Prevention and Care
|
November 20, 2021
Optimising the impact of COVID-19 vaccination on mortality and hospitalisations using an individual additive risk measuring approach based on a risk adjustment scheme
Danny Wende, Dagmar Hertle, Claudia Schulte, et al.
Parkinsonism & Related Disorders
|
July 25, 2016
Broad clinical phenotype in Parkinsonism associated with a base pair deletion in RAB39B and additional POLG variant
Max Güldner, Claudia Schulte, Ann-Kathrin Hauser, et al.
Page
of 17