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3. Dyskinetic crisis in GNAO1-related disorders: clinical perspectives and management strategies

6. Pharmacological and neurosurgical management of cerebral palsy and dystonia: Clinical practice guideline update.

16. N°61 – Abnormal event-related modulation of sensorimotor cortex alpha/mu activity indicates impaired sensorimotor processing in young people with dystonia and dystonic cerebral palsy

19. The emerging spectrum of foetal acetylcholine receptor antibody-associated disorders (FARAD)

20. Polymicrogyria and deletion 22q11.2 syndrome: Window to the etiology of a common cortical malformation

21. Transitional Care for Young People with Movement Disorders: Consensus‐Based Recommendations from the MDS Task Force on Pediatrics

22. Motor assessments in cerebral palsy : a study of the mechanisms of equinus, the functional neuromuscular angle, clonus, alternating movements and posture

23. Neuroimaging in encephalitis: analysis of imaging findings and interobserver agreement

26. Dyskinetic Crisis in GNAO1-Related Disorder: A Comprehensive International Delphi Study

34. Clinical rating scale for pantothenate kinase‐associated neurodegeneration: A pilot study

35. Metabolic patterns in brain 18F-fluorodeoxyglucose PET relate to aetiology in paediatric dystonia.

36. Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study

38. Cognitive Functioning in Children with Pantothenate-Kinase-Associated Neurodegeneration Undergoing Deep Brain Stimulation

39. Highlighting the Dystonic Phenotype Related to GNAO1

41. SGCE and myoclonus dystonia: motor characteristics, diagnostic criteria and clinical predictors of genotype

42. Genotype–phenotype correlation in a large population of muscular dystrophy patients with LAMA2 mutations

45. Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1

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