about
Phenotype and frequency of STUB1 mutations: next-generation screenings in Caucasian ataxia and spastic paraplegia cohortsMitochondrial aspartyl-tRNA synthetase deficiency causes leukoencephalopathy with brain stem and spinal cord involvement and lactate elevationAssessing White Matter Microstructure in Brain Regions with Different Myelin Architecture Using MRICNTNAP1 mutations cause CNS hypomyelination and neuropathy with or without arthrogryposis.Language and cognition in children with metachromatic leukodystrophy: onset and natural course in a nationwide cohort.Imaging of early brain injury and cortical plasticity.MRI classification system (MRICS) for children with cerebral palsy: development, reliability, and recommendations.The role of magnetic resonance imaging in elucidating the pathogenesis of cerebral palsy: a systematic review.Leukodystrophies and other genetic metabolic leukoencephalopathies in children and adults.Natural course of pontocerebellar hypoplasia type 2A.Demyelination load as predictor for disease progression in juvenile metachromatic leukodystrophy.Cerebral gray and white matter changes and clinical course in metachromatic leukodystrophy.Reorganization in congenital hemiparesis acquired at different gestational ages.Somatosensory system in two types of motor reorganization in congenital hemiparesis: topography and function.tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia.Gender affects body language reading.Emotion through locomotion: gender impact.Plasticity during Early Brain Development Is Determined by Ontogenetic Potential.Global and local development of gray and white matter volume in normal children and adolescents.European consensus table 2006 on botulinum toxin for children with cerebral palsy.Brain morphometry in Pontocerebellar Hypoplasia type 2.Cerebral palsy update.Limitations on the developing preterm brain: impact of periventricular white matter lesions on brain connectivity and cognition.What constitutes cerebral palsy in the twenty-first century?Growth, head growth, and neurocognitive outcome in children born very preterm: methodological aspects and selected results.Combined functional and causal connectivity analyses of language networks in children: a feasibility study.Increases in language lateralization in normal children as observed using magnetoencephalography.Language lateralization in magnetoencephalography: two tasks to investigate hemispheric dominance.An fMRI task battery for assessing hemispheric language dominance in children.Lesion characteristics driving right-hemispheric language reorganization in congenital left-hemispheric brain damage.Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation: clinical and genetic characterization and target for therapy.Decreasing prevalence in cerebral palsy: a multi-site European population-based study, 1980 to 2003.Long-term Outcome of Allogeneic Hematopoietic Stem Cell Transplantation in Patients With Juvenile Metachromatic Leukodystrophy Compared With Nontransplanted Control Patients.Postnatal human cytomegalovirus infection in preterm infants has long-term neuropsychological sequelae.Pontocerebellar hypoplasia type 2: variability in clinical and imaging findings.Clinical, neuroradiological and genetic findings in pontocerebellar hypoplasia.Microcephaly with simplified gyral pattern: MRI classification.Preserved crossed corticospinal tract and hand function despite extensive brain maldevelopment.Misleading functional magnetic resonance imaging mapping of the cortical hand representation in a 4-year-old boy with an arteriovenous malformation of the central region.Two types of ipsilateral reorganization in congenital hemiparesis: a TMS and fMRI study.
P50
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P50
description
hulumtuese
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հետազոտող
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Ingeborg Krägeloh-Mann
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Ingeborg Krägeloh-Mann
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Ingeborg Krägeloh-Mann
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Ingeborg Krägeloh-Mann
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Ingeborg Krägeloh-Mann
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Ingeborg Krägeloh-Mann
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Ingeborg Krägeloh-Mann
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Ingeborg Krägeloh-Mann
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Ingeborg Krägeloh-Mann
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Ingeborg Krägeloh-Mann
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Ingeborg Krägeloh-Mann
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Ingeborg Krägeloh-Mann
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Ingeborg Krägeloh-Mann
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viaf-305782629