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Human Molecular Genetics
|
October 10, 2014
CACNA1B mutation is linked to unique myoclonus-dystonia syndrome
Justus L Groen, Arturo Andrade, Katja Ritz, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
February 5, 2015
RELN rare variants in myoclonus-dystonia
Justus L Groen, Katja Ritz, Hamid Jalalzadeh, et al.
Molecular Brain
|
January 22, 2021
Rare functional missense variants in CACNA1H: What can we learn from Writer's cramp?
Miaozhen Huang, Esther A R Nibbeling, Tjerk J Lagrand, et al.
Journal of the American Medical Directors Association
|
August 16, 2018
One Week of Hospitalization Following Elective Hip Surgery Induces Substantial Muscle Atrophy in Older Patients
Imre W K Kouw, Bart B L Groen, Joey S J Smeets, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
July 10, 2012
Phenotypes and genetic architecture of focal primary torsion dystonia
Justus L Groen, Marlot C Kallen, Bart P C van de Warrenburg, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
August 6, 2010
DYT6 dystonia: mutation screening, phenotype, and response to deep brain stimulation
Justus L Groen, Katja Ritz, Maria Fiorella Contarino, et al.
BMJ Open
|
November 17, 2025
Prevention of postamputation pain with targeted muscle reinnervation (PreventPAP trial): protocol for a national, multicentre, randomised, sham-controlled trial
Guus A H Tendijck, Jan van Schaik, Robert R Dijkman, et al.
Archives of Neurology
|
December 15, 2004
Analysis of the PINK1 gene in a large cohort of cases with Parkinson disease
Ekaterina Rogaeva, Janel Johnson, Anthony E Lang, et al.
The Journal of Nutrition
|
February 19, 2020
Protein Type, Protein Dose, and Age Modulate Dietary Protein Digestion and Phenylalanine Absorption Kinetics and Plasma Phenylalanine Availability in Humans
Stefan H M Gorissen, Jorn Trommelen, Imre W K Kouw, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
December 31, 2013
Genome-wide association study in musician's dystonia: a risk variant at the arylsulfatase G locus?
Katja Lohmann, Alexander Schmidt, Arne Schillert, et al.
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of 10
Search research articles
Search
Showing results (91-100 of 100) with videos related to
Sort By:
Page
of 10
You have reached the last page of results.
This site can display upto 100 results.
Human Molecular Genetics
|
October 10, 2014
CACNA1B mutation is linked to unique myoclonus-dystonia syndrome
Justus L Groen, Arturo Andrade, Katja Ritz, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
February 5, 2015
RELN rare variants in myoclonus-dystonia
Justus L Groen, Katja Ritz, Hamid Jalalzadeh, et al.
Molecular Brain
|
January 22, 2021
Rare functional missense variants in CACNA1H: What can we learn from Writer's cramp?
Miaozhen Huang, Esther A R Nibbeling, Tjerk J Lagrand, et al.
Journal of the American Medical Directors Association
|
August 16, 2018
One Week of Hospitalization Following Elective Hip Surgery Induces Substantial Muscle Atrophy in Older Patients
Imre W K Kouw, Bart B L Groen, Joey S J Smeets, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
July 10, 2012
Phenotypes and genetic architecture of focal primary torsion dystonia
Justus L Groen, Marlot C Kallen, Bart P C van de Warrenburg, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
August 6, 2010
DYT6 dystonia: mutation screening, phenotype, and response to deep brain stimulation
Justus L Groen, Katja Ritz, Maria Fiorella Contarino, et al.
BMJ Open
|
November 17, 2025
Prevention of postamputation pain with targeted muscle reinnervation (PreventPAP trial): protocol for a national, multicentre, randomised, sham-controlled trial
Guus A H Tendijck, Jan van Schaik, Robert R Dijkman, et al.
Archives of Neurology
|
December 15, 2004
Analysis of the PINK1 gene in a large cohort of cases with Parkinson disease
Ekaterina Rogaeva, Janel Johnson, Anthony E Lang, et al.
The Journal of Nutrition
|
February 19, 2020
Protein Type, Protein Dose, and Age Modulate Dietary Protein Digestion and Phenylalanine Absorption Kinetics and Plasma Phenylalanine Availability in Humans
Stefan H M Gorissen, Jorn Trommelen, Imre W K Kouw, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
December 31, 2013
Genome-wide association study in musician's dystonia: a risk variant at the arylsulfatase G locus?
Katja Lohmann, Alexander Schmidt, Arne Schillert, et al.
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of 10