about
Brown-Vialetto-Van Laere syndrome, a ponto-bulbar palsy with deafness, is caused by mutations in c20orf54Status dystonicus: a practice guideDifferences in globus pallidus neuronal firing rates and patterns relate to different disease biology in children with dystonia.Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signatureThe maturation of motor dexterity: or why Johnny can't go any faster.Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2The tympanic membrane displacement analyser for monitoring intracranial pressure in children.Paediatric autoimmune encephalopathies: clinical features, laboratory investigations and outcomes in patients with or without antibodies to known central nervous system autoantigens.Accuracy of stimulating electrode placement in paediatric pallidal deep brain stimulation for primary and secondary dystonia.Deep brain stimulation for childhood dystonia: Is 'where' as important as in 'whom'?Cutaneous signs are important in the diagnosis of the rare neoplasia syndrome Carney complexSGCE mutations cause psychiatric disorders: clinical and genetic characterizationNMDA receptor antibodies associated with distinct white matter syndromes.N-methyl-D-aspartate receptor antibodies in post-herpes simplex virus encephalitis neurological relapse.Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study.Central Motor Conduction Time and diffusion tensor imaging metrics in children with complex motor disorders.Visual failure without headache in idiopathic intracranial hypertensionObservation and modeling of deep brain stimulation electrode depth in the pallidal target of the developing brain.SGCE and myoclonus dystonia: motor characteristics, diagnostic criteria and clinical predictors of genotype.Pediatric Herpes Simplex Virus Encephalitis Complicated by N-Methyl-D-aspartate Receptor Antibody EncephalitisMedication use in childhood dystonia.Progression to musculoskeletal deformity in childhood dystonia.Tensor and non-tensor tractography for the assessment of the corticospinal tract of children with motor disorders: a comparative study.Classification of dystonia in childhood.Fractional anisotropy in children with dystonia or spasticity correlates with the selection for DBS or ITB movement disorder surgery.β-Propeller protein-associated neurodegeneration: a new X-linked dominant disorder with brain iron accumulation.Perceptions of symptoms and expectations of advanced therapy for Parkinson's disease: preliminary report of a Patient-Reported Outcome tool for Advanced Parkinson's disease (PRO-APD).Battery life following pallidal deep brain stimulation (DBS) in children and young people with severe primary and secondary dystonia.Interventional studies in childhood dystonia do not address the concerns of children and their carers.A field guide to current advances in paediatric movement disorders.Intrathecal baclofen trials: complications and positive yield in a pediatric cohort.Genetic, Phenotypic, and Interferon Biomarker Status in ADAR1-Related Neurological Disease.Recognizing the Common Origins of Dystonia and the Development of Human Movement: A Manifesto of Unmet Needs in Isolated Childhood Dystonias.The International Classification of Functioning (ICF) to evaluate deep brain stimulation neuromodulation in childhood dystonia-hyperkinesia informs future clinical & research priorities in a multidisciplinary model of care.l-Dopa in dystonia: A modern perspective.Clonidine use in the outpatient management of severe secondary dystonia.Efficacy of pallidal stimulation in isolated dystonia: a systematic review and meta-analysis.Burke-Fahn-Marsden dystonia severity, Gross Motor, Manual Ability, and Communication Function Classification scales in childhood hyperkinetic movement disorders including cerebral palsy: a 'Rosetta Stone' study.Clinical presentation and management of dyskinetic cerebral palsy.Bilateral globus pallidus internus deep brain stimulation for dyskinetic cerebral palsy supports success of cochlear implantation in a 5-year old ex-24 week preterm twin with absent cerebellar hemispheres.
P50
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P50
description
hulumtues
@sq
onderzoeker
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researcher
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հետազոտող
@hy
name
Jean-Pierre Lin
@ast
Jean-Pierre Lin
@en
Jean-Pierre Lin
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Jean-Pierre Lin
@nl
Jean-Pierre Lin
@sl
type
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Jean-Pierre Lin
@ast
Jean-Pierre Lin
@en
Jean-Pierre Lin
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Jean-Pierre Lin
@nl
Jean-Pierre Lin
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prefLabel
Jean-Pierre Lin
@ast
Jean-Pierre Lin
@en
Jean-Pierre Lin
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Jean-Pierre Lin
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Jean-Pierre Lin
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P1153
P106
P1153
50461740800
56828267300
56843823100
P21
P2798
P31
P496
0000-0001-9314-2259
P569
2000-01-01T00:00:00Z