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Parkinsonism & Related Disorders
|
February 25, 2023
TAOK1-related neurodevelopmental disorder: A new differential diagnosis for childhood-onset tremor?
Astrid Blaschek, Alexandra Sitzberger, Melanie Brugger, et al.
Rapid Communications in Mass Spectrometry : RCM
|
December 15, 2015
A novel methylation derivatization method for δ(18)O analysis of individual carbohydrates by gas chromatography/pyrolysis-isotope ratio mass spectrometry
Marco M Lehmann, Maria Fischer, Jan Blees, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 21, 2024
Genome Aggregation Database Version 4-Allele Frequency Changes and Impact on Variant Interpretation in Dystonia
Elisabetta Indelicato, Anna Eberl, Sylvia Boesch, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 15, 2023
Dystonia in ATP Synthase Defects: Reconnecting Mitochondria and Dopamine
Elisabetta Indelicato, Sylvia Boesch, Niccolo' E Mencacci, et al.
Annals of Clinical and Translational Neurology
|
May 27, 2026
Prominent Movement Disorders in RNU2-2-Related Spliceosomopathy
Magdalena Krygier, Ugo Sorrentino, Matias Wagner, et al.
Reproductive Biology
|
December 28, 2017
Elective frozen-thawed embryo transfer (FET) in women at risk for ovarian hyperstimulation syndrome
Josef Zech, Ana Brandao, Michael Zech, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)
|
September 30, 2024
Tremor-Dominant Movement Disorder in <i>ANKRD11-</i> Associated KBG Syndrome
Antonia M Stehr, Thomas Koeglsperger, Maureen Jacob, et al.
Neurogenetics
|
December 3, 2021
Correction to: Myoclonic dystonia phenotype related to a novel calmodulin-binding transcription activator 1 sequence variant
Ivana Dzinovic, Tereza Serranová, Clement Prouteau, et al.
Case Reports in Neurological Medicine
|
March 9, 2026
Mixed Movement Disorder Caused by <i>ADCY5</i> Pathogenic Variant Successfully Treated With Caffeine: A Case From Ukraine
Eugenia Tsoma, Taras Studeniak, Robert Jech, et al.
Neurogenetics
|
March 7, 2021
Myoclonic dystonia phenotype related to a novel calmodulin-binding transcription activator 1 sequence variant
Ivana Dzinovic, Tereza Serranová, Clement Prouteau, et al.
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of 20
Search research articles
Search
Showing results (61-70 of 195) with videos related to
Sort By:
Page
of 20
Parkinsonism & Related Disorders
|
February 25, 2023
TAOK1-related neurodevelopmental disorder: A new differential diagnosis for childhood-onset tremor?
Astrid Blaschek, Alexandra Sitzberger, Melanie Brugger, et al.
Rapid Communications in Mass Spectrometry : RCM
|
December 15, 2015
A novel methylation derivatization method for δ(18)O analysis of individual carbohydrates by gas chromatography/pyrolysis-isotope ratio mass spectrometry
Marco M Lehmann, Maria Fischer, Jan Blees, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 21, 2024
Genome Aggregation Database Version 4-Allele Frequency Changes and Impact on Variant Interpretation in Dystonia
Elisabetta Indelicato, Anna Eberl, Sylvia Boesch, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 15, 2023
Dystonia in ATP Synthase Defects: Reconnecting Mitochondria and Dopamine
Elisabetta Indelicato, Sylvia Boesch, Niccolo' E Mencacci, et al.
Annals of Clinical and Translational Neurology
|
May 27, 2026
Prominent Movement Disorders in RNU2-2-Related Spliceosomopathy
Magdalena Krygier, Ugo Sorrentino, Matias Wagner, et al.
Reproductive Biology
|
December 28, 2017
Elective frozen-thawed embryo transfer (FET) in women at risk for ovarian hyperstimulation syndrome
Josef Zech, Ana Brandao, Michael Zech, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)
|
September 30, 2024
Tremor-Dominant Movement Disorder in <i>ANKRD11-</i> Associated KBG Syndrome
Antonia M Stehr, Thomas Koeglsperger, Maureen Jacob, et al.
Neurogenetics
|
December 3, 2021
Correction to: Myoclonic dystonia phenotype related to a novel calmodulin-binding transcription activator 1 sequence variant
Ivana Dzinovic, Tereza Serranová, Clement Prouteau, et al.
Case Reports in Neurological Medicine
|
March 9, 2026
Mixed Movement Disorder Caused by <i>ADCY5</i> Pathogenic Variant Successfully Treated With Caffeine: A Case From Ukraine
Eugenia Tsoma, Taras Studeniak, Robert Jech, et al.
Neurogenetics
|
March 7, 2021
Myoclonic dystonia phenotype related to a novel calmodulin-binding transcription activator 1 sequence variant
Ivana Dzinovic, Tereza Serranová, Clement Prouteau, et al.
Page
of 20