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Annals of Neurology
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December 26, 2021
Variants in Mitochondrial ATP Synthase Cause Variable Neurologic Phenotypes
Michael Zech, Robert Kopajtich, Katja Steinbrücker, et al.
Ebiomedicine
|
June 29, 2026
Trio analysis in dystonia identifies de novo KLC1 variants in a kinesinopathy with distinct motor and neurodevelopmental features
Elisa Peirano, Laura O'Regan, Philip Harrer, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 5, 2021
Scoring Algorithm-Based Genomic Testing in Dystonia: A Prospective Validation Study
Michael Zech, Robert Jech, Sylvia Boesch, et al.
Annals of Neurology
|
February 2, 2026
Fibroblast Transcriptomics in Molecular Diagnostics of a Comprehensive Dystonia Cohort
Alice Saparov, Ivana Dzinovic, Theresa Brunet, et al.
Annals of Neurology
|
June 20, 2025
Deep Brain Stimulation for VPS16-Related Dystonia: A Multicenter Study
Tatiana Svorenova, Luigi M Romito, Ahmet Kaymak, et al.
American Journal of Human Genetics
|
April 19, 2023
POLR1A variants underlie phenotypic heterogeneity in craniofacial, neural, and cardiac anomalies
Kelly Smallwood, Kristin E N Watt, Satoru Ide, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 10, 2023
Rare variants in <i>PPFIA3</i> cause delayed development, intellectual disability, autism, and epilepsy
Maimuna S Paul, Sydney L Michener, Hongling Pan, et al.
Brain : a Journal of Neurology
|
June 11, 2025
Deciphering DST-associated disorders: biallelic variants affecting DST-b cause a congenital myopathy
Maureen Jacob, Heike Kölbel, Philip Harrer, et al.
Annals of Neurology
|
August 19, 2020
Loss-of-Function Variants in HOPS Complex Genes VPS16 and VPS41 Cause Early Onset Dystonia Associated with Lysosomal Abnormalities
Dora Steel, Michael Zech, Chen Zhao, et al.
Human Mutation
|
April 13, 2021
Clinical, neuroimaging, and molecular spectrum of TECPR2-associated hereditary sensory and autonomic neuropathy with intellectual disability
Sonja Neuser, Barbara Brechmann, Gali Heimer, et al.
Page
of 20
Search research articles
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Showing results (171-180 of 196) with videos related to
Sort By:
Page
of 20
Annals of Neurology
|
December 26, 2021
Variants in Mitochondrial ATP Synthase Cause Variable Neurologic Phenotypes
Michael Zech, Robert Kopajtich, Katja Steinbrücker, et al.
Ebiomedicine
|
June 29, 2026
Trio analysis in dystonia identifies de novo KLC1 variants in a kinesinopathy with distinct motor and neurodevelopmental features
Elisa Peirano, Laura O'Regan, Philip Harrer, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 5, 2021
Scoring Algorithm-Based Genomic Testing in Dystonia: A Prospective Validation Study
Michael Zech, Robert Jech, Sylvia Boesch, et al.
Annals of Neurology
|
February 2, 2026
Fibroblast Transcriptomics in Molecular Diagnostics of a Comprehensive Dystonia Cohort
Alice Saparov, Ivana Dzinovic, Theresa Brunet, et al.
Annals of Neurology
|
June 20, 2025
Deep Brain Stimulation for VPS16-Related Dystonia: A Multicenter Study
Tatiana Svorenova, Luigi M Romito, Ahmet Kaymak, et al.
American Journal of Human Genetics
|
April 19, 2023
POLR1A variants underlie phenotypic heterogeneity in craniofacial, neural, and cardiac anomalies
Kelly Smallwood, Kristin E N Watt, Satoru Ide, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 10, 2023
Rare variants in <i>PPFIA3</i> cause delayed development, intellectual disability, autism, and epilepsy
Maimuna S Paul, Sydney L Michener, Hongling Pan, et al.
Brain : a Journal of Neurology
|
June 11, 2025
Deciphering DST-associated disorders: biallelic variants affecting DST-b cause a congenital myopathy
Maureen Jacob, Heike Kölbel, Philip Harrer, et al.
Annals of Neurology
|
August 19, 2020
Loss-of-Function Variants in HOPS Complex Genes VPS16 and VPS41 Cause Early Onset Dystonia Associated with Lysosomal Abnormalities
Dora Steel, Michael Zech, Chen Zhao, et al.
Human Mutation
|
April 13, 2021
Clinical, neuroimaging, and molecular spectrum of TECPR2-associated hereditary sensory and autonomic neuropathy with intellectual disability
Sonja Neuser, Barbara Brechmann, Gali Heimer, et al.
Page
of 20