615 results on '"Lin, Jean-Pierre"'
Search Results
2. Dystonia in Childhood: How Insights from Paediatric Research Enrich the Network Theory of Dystonia
3. Dyskinetic crisis in GNAO1-related disorders: clinical perspectives and management strategies
4. Probabilistic mapping of deep brain stimulation in childhood dystonia
5. Harnessing cognitive strategy use for functional problems and proposed underlying mechanisms in childhood-onset dystonia
6. Pharmacological and neurosurgical management of cerebral palsy and dystonia: Clinical practice guideline update.
7. Mental health and behaviour in children with dystonia: Anxiety, challenging behaviour and the relationship to pain and self-esteem
8. Rehabilitation in childhood-onset hyperkinetic movement disorders including dystonia: Treatment change in outcomes across the ICF and feasibility of outcomes for full trial evaluation
9. Deep Brain Stimulation of the Internal Pallidum in Lesch–Nyhan Syndrome: Clinical Outcomes and Connectivity Analysis
10. Abnormal patterns of corticomuscular and intermuscular coherence in childhood dystonia
11. 'Focal Seizures in Dystonic Cerebral Palsy (DCP): rare or common or both?
12. Gross motor function outcomes following deep brain stimulation for childhood-onset dystonia: A descriptive report
13. Cross-frequency cortex–muscle interactions are abnormal in young people with dystonia.
14. Somatosensory Evoked Potentials and Central Motor Conduction Times in children with dystonia and their correlation with outcomes from Deep Brain Stimulation of the Globus pallidus internus
15. Abnormal microscale neuronal connectivity triggered by a proprioceptive stimulus in dystonia
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
17. N°62 – Abnormal dynamic neuronal connectivity in children with dystonia
18. N°64 - Deep Brain Stimulation Evoked Potentials (DBSEPs) in children with dystonia
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
24. Cognitive approach to rehabilitation in children with hyperkinetic movement disorders post-DBS
25. Clinical Reasoning: A Teenage Girl With Progressive Hyperkinetic Movements, Seizures, and Encephalopathy
26. Dyskinetic Crisis in GNAO1-Related Disorder: A Comprehensive International Delphi Study
27. Clinical and radiological features of recurrent demyelination following acute disseminated encephalomyelitis (ADEM)
28. Central Motor Conduction Time and Diffusion Tensor Imaging metrics in children with complex motor disorders
29. Reply to: “GNAO1 Haploinsufficiency Associated with a Mild Delayed‐Onset Dystonia Phenotype”
30. Metabolic patterns in brain 18F-fluorodeoxyglucose PET relate to aetiology in paediatric dystonia
31. Transition Services for Children and Young Adults with Movement Disorders: A Survey by the MDS Task Force on Pediatrics
32. GNAO1-related movement disorder with life-threatening exacerbations: movement phenomenology and response to DBS
33. Advances in pharmacotherapies for movement disorders in children: current limitations and future progress
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
37. Tensor and non-tensor tractography for the assessment of the corticospinal tract of children with motor disorders: a comparative study
38. Cognitive Functioning in Children with Pantothenate-Kinase-Associated Neurodegeneration Undergoing Deep Brain Stimulation
39. Highlighting the Dystonic Phenotype Related to GNAO1
40. Editorial: Neuronal Plasticity and Neuromodulation in Development and Developmental Disorders
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
43. Goldberg–Shprintzen megacolon syndrome with associated sensory motor axonal neuropathy
44. Role of 18F-FDG PET imaging in paediatric primary dystonia and dystonia arising from neurodegeneration with brain iron accumulation
45. Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1
46. The impact and prognosis for dystonia in childhood including dystonic cerebral palsy: a clinical and demographic tertiary cohort study
47. The tympanic membrane displacement analyser for monitoring intracranial pressure in children
48. Accuracy of stimulating electrode placement in paediatric pallidal deep brain stimulation for primary and secondary dystonia
49. Sensorimotor Integration in Childhood Dystonia and Dystonic Cerebral Palsy—A Developmental Perspective
50. The importance of neurology and genetic testing in the patient with non-cleft velopharyngeal dysfunction
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