Research map: Expanding the Motor Phenotype and Molecular Spectrum of NAA15 ‐Related Disorder: Two Cases of Isolated Childhood‐Onset Gait Dystonia

Back to the article

Papers in this map

  1. N omenclature of genetic movement disorders: R ecommendations of the international P arkinson and movement disorder society task force · Connie Marras · 2016 · 288 citations · Cited by this paper
  2. Childhood‐Onset Movement Disorders at the Forefront: From Genes to Precision Therapy · Kathryn Yang · 2026 · Related
  3. Nomenclature of Genetic Movement Disorders: Recommendations of the International Parkinson and Movement Disorder Society Task Force – An Update · Lara Mariah Lange · 2022 · 142 citations · Cited by this paper
  4. Physical Activity and Exercise for People with Parkinson's Disease: The Past, Present, and Future · 2026 · Related
  5. Truncating Variants in NAA15 Are Associated with Variable Levels of Intellectual Disability, Autism Spectrum Disorder, and Congenital Anomalies · Hanyin Cheng · 2018 · 91 citations · Cited by this paper
  6. Spatiotemporal Progression Patterns of Striatal Dopamine Depletion and Cerebral Hypoperfusion in Parkinson's Disease · 2026 · Related
  7. Neurodevelopmental Gene‐Related Dystonia‐Parkinsonism with Onset in Adults: A Case with NAA15 Variant · Igor Straka · 2022 · 16 citations · Cited by this paper
  8. Movement Disorders: Volume 41, Number 7, July 2026 · 2026 · Related
  9. Neurodevelopmental Gene‐Related Dystonia: A Pediatric Case with NAA15 Variant · Dèlia Yubero · 2022 · 15 citations · Cited by this paper
  10. Parabrachial Npy1r ‐Expressing Neurons Drive Pain in a Mouse Model of Parkinson's Disease · 2026 · Related
  11. Childhood‐Onset Lower Limb Focal Dystonia Due to a NAA15 Variant: A Case Report · Federica Rachele Danti · 2024 · 6 citations · Cited by this paper
  12. Alzheimer's Disease Cerebrospinal Fluid Biomarkers Predict Survival in Progressive Supranuclear Palsy · 2026 · Related
  13. Cortical Myoclonus and Complex Paroxysmal Dyskinesias in a Patient with NAA15 Variant · Elena Freri · 2024 · 6 citations · Cited by this paper
  14. Addressing the Challenges of Translating LRRK2 Biology into Disease‐Modifying Therapies: The LRRK2 Investigative Therapeutics Exchange Initiative · 2026 · Related
  15. Genomic Landscape and Phenotypic Spectrum of Autosomal Recessive Cerebellar Ataxia in China · 2026 · Related
  16. DNA Repair Pathway Variants Are Enriched in Individuals with Biallelic AAGGG CANVAS and RFC1 ‐Related Disease · 2026 · Related
  17. Epilepsy‐Dyskinesia Syndromes: The Venn Diagram of Genetic Epilepsy and Movement Disorders · 2026 · Related

Source: OpenAlex (CC0)