Miriam Ostrozovicova

London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 23 publications

Shared Pathogenic Pathways Between REM Sleep Behavior Disorder and Neurodegenerative and Psychiatric Disorders.

Shared Pathogenic Pathways Between REM Sleep Behavior Disorder and Neurodegenerative and Psychiatric Disorders.

Journal: medRxiv : the preprint server for health sciences

Published: February 12, 2026

Shared Pathogenic Pathways Between REM Sleep Behavior Disorder and Neurodegenerative and Psychiatric Disorders.

Shared Pathogenic Pathways Between REM Sleep Behavior Disorder and Neurodegenerative and Psychiatric Disorders.

Journal: medRxiv : the preprint server for health sciences

Published: February 12, 2026

Long-Term Benefit of GPi-DBS in Two Siblings with BCL11B-Related Dystonia: An Uncommon but Potentially Treatable Condition.

Long-Term Benefit of GPi-DBS in Two Siblings with BCL11B-Related Dystonia: An Uncommon but Potentially Treatable Condition.

Journal: Movement disorders clinical practice

Published: December 18, 2025

Collaborative Genomics for Dystonia in Central and Eastern Europe: Successes Achieved, New Frontiers Ahead.

Collaborative Genomics for Dystonia in Central and Eastern Europe: Successes Achieved, New Frontiers Ahead.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: December 03, 2025

CNV-Finder: streamlining copy number variation discovery.

CNV-Finder: streamlining copy number variation discovery.

Journal: Bioinformatics advances

Published: November 13, 2025

Update on Genetic Chorea.

Update on Genetic Chorea.

Journal: Current neurology and neuroscience reports

Published: August 17, 2025

Genome-wide association study of REM sleep behavior disorder in Parkinson's disease.

Genome-wide association study of REM sleep behavior disorder in Parkinson's disease.

Journal: NPJ Parkinson's disease

Published: June 30, 2025

Genome-wide assessment identifies novel runs of homozygosity linked to Parkinson's disease etiology across diverse ancestral populations.

Genome-wide assessment identifies novel runs of homozygosity linked to Parkinson's disease etiology across diverse ancestral populations.

Journal: medRxiv : the preprint server for health sciences

Published: June 06, 2025

Genome-Wide Assessment Reveals Ancestral Differences in Homozygosity Patterns Potentially Linked to Parkinson's Disease Etiology.

Genome-Wide Assessment Reveals Ancestral Differences in Homozygosity Patterns Potentially Linked to Parkinson's Disease Etiology.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: March 27, 2025

CNV-Finder: Streamlining Copy Number Variation Discovery.

CNV-Finder: Streamlining Copy Number Variation Discovery.

Journal: bioRxiv : the preprint server for biology

Published: November 28, 2024

Combined genomics and proteomics unveils elusive variants and vast aetiologic heterogeneity in dystonia.

Combined genomics and proteomics unveils elusive variants and vast aetiologic heterogeneity in dystonia.

Journal: Brain : a journal of neurology

Published: October 04, 2024

Prevalence and Clinical Characteristics of the LRRK2 p.L1795F Variant in Central Europeans with Early-Onset and Familial Parkinson's Disease.

Prevalence and Clinical Characteristics of the LRRK2 p.L1795F Variant in Central Europeans with Early-Onset and Familial Parkinson's Disease.

Journal: Movement disorders clinical practice

Published: July 31, 2024

Showing 1-12 of 23

Last Updated: 09/26/2026