Search research articles
Contact Us
Filters
Showing results (1-10 of 267) with videos related to
Page
of 27
Sort By:
Movement Disorders : Official Journal of the Movement Disorder Society
|
August 24, 2019
Rediscovery of repeat expansions: Solving the unsolved cases
Katja Lohmann, Norbert Brüggemann
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics
|
July 24, 2014
Next generation sequencing and the future of genetic diagnosis
Katja Lohmann, Christine Klein
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 19, 2012
Familial idiopathic basal ganglia calcification: unraveling the first genetic cause
Katja Lohmann, Christine Klein
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 24, 2021
Importance of Methylation Pattern: Episignatures as a Novel Instrument in Diagnostics
Mirja Thomsen, Katja Lohmann
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 20, 2018
Disease-causing or benign? challenges in genetic variant interpretation and limitations of ClinVar
Sonja Petkovic, Katja Lohmann
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 30, 2013
Genetics of dystonia: what's known? What's new? What's next?
Katja Lohmann, Christine Klein
Current Neurology and Neuroscience Reports
|
March 12, 2017
Update on the Genetics of Dystonia
Katja Lohmann, Christine Klein
Neurogenetics
|
March 22, 2014
The many faces of TUBB4A mutations
Katja Lohmann, Christine Klein
Movement Disorders Clinical Practice
|
July 18, 2022
<i>PRKRAP1</i> and Other Pseudogenes in Movement Disorders: The Troublemakers in Genetic Analyses Are More Than Genomic Fossils
Francesca Magrinelli, Katja Lohmann
Neurology
|
November 7, 2008
Parkinson disease(s): is "Parkin disease" a distinct clinical entity?
Christine Klein, Katja Lohmann
Page
of 27
Search research articles
Search
Showing results (1-10 of 267) with videos related to
Sort By:
Page
of 27
Movement Disorders : Official Journal of the Movement Disorder Society
|
August 24, 2019
Rediscovery of repeat expansions: Solving the unsolved cases
Katja Lohmann, Norbert Brüggemann
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics
|
July 24, 2014
Next generation sequencing and the future of genetic diagnosis
Katja Lohmann, Christine Klein
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 19, 2012
Familial idiopathic basal ganglia calcification: unraveling the first genetic cause
Katja Lohmann, Christine Klein
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 24, 2021
Importance of Methylation Pattern: Episignatures as a Novel Instrument in Diagnostics
Mirja Thomsen, Katja Lohmann
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 20, 2018
Disease-causing or benign? challenges in genetic variant interpretation and limitations of ClinVar
Sonja Petkovic, Katja Lohmann
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 30, 2013
Genetics of dystonia: what's known? What's new? What's next?
Katja Lohmann, Christine Klein
Current Neurology and Neuroscience Reports
|
March 12, 2017
Update on the Genetics of Dystonia
Katja Lohmann, Christine Klein
Neurogenetics
|
March 22, 2014
The many faces of TUBB4A mutations
Katja Lohmann, Christine Klein
Movement Disorders Clinical Practice
|
July 18, 2022
<i>PRKRAP1</i> and Other Pseudogenes in Movement Disorders: The Troublemakers in Genetic Analyses Are More Than Genomic Fossils
Francesca Magrinelli, Katja Lohmann
Neurology
|
November 7, 2008
Parkinson disease(s): is "Parkin disease" a distinct clinical entity?
Christine Klein, Katja Lohmann
Page
of 27