• <em>PLEKHG5</em>-related autosomal recessive lower motor neuron disease with dysmyelination in peripheral nerves
• A class-specific effect of dysmyelination on the excitability of hippocampal interneurons
• A hypomyelinating leukodystrophy in German Shepherd dogs
• A Mouse Model System to Study Peroxisomal Roles in Neurodegeneration of Peroxisome Biogenesis Disorders
• A novel case of concurrent occurrence of demyelinating-polyneuropathy-causing PMP22 duplication and SOX10 gene mutation producing severe hypertrophic neuropathy
• A novel mouse model of CMT1B identifies hyperglycosylation as a new pathogenetic mechanism
• A Novel Vitronectin Peptide Facilitates Differentiation of Oligodendrocytes from Human Pluripotent Stem Cells (Synthetic ECM for Oligodendrocyte Differentiation)
• A role of oligodendrocytes in information processing
• Abnormalities of Cerebral White Matter Microstructure in Children With New-Onset, Untreated Idiopathic-Generalized Epilepsy
• Age-Dependent Increase in Schmidt-Lanterman Incisures and a Cadm4-Associated Membrane Skeletal Complex in Fatty Acid 2-hydroxylase Deficient Mice: a Mouse Model of Spastic Paraplegia SPG35
• Alpha-Asaronol Alleviates Dysmyelination by Enhancing Glutamate Transport Through the Activation of PPARgamma-GLT-1 Signaling in Hypoxia-Ischemia Neonatal Rats
• Alpha-Asaronol Alleviates Dysmyelination by Enhancing Glutamate Transport Through the Activation of PPARγ-GLT-1 Signaling in Hypoxia-Ischemia Neonatal Rats
• Alpha-asaronol promoted oligodendrocyte precursor cell differentiation and improved myelination as an activator PPARγ
• Alterations of Oligodendrocyte and Myelin Energy Metabolism in Multiple Sclerosis
• Alzheimer's disease alters oligodendrocytic glycolytic and ketolytic gene expression
• Assembly and Function of the Juxtaparanodal Kv1 Complex in Health and Disease
• Assessing regional intracortical myelination in schizophrenia spectrum and bipolar disorders using the optimized T1w/T2w-ratio
• Assessment of myelination in infants and young children by T1 relaxation time measurements using the magnetization-prepared 2 rapid acquisition gradient echoes sequence
• Association between Diffusion Tensor Imaging, inflammation and immunological alterations in unipolar and bipolar depression: A review
• Associations of alcohol use, HIV infection, and age with brain white matter microstructure
• Baroreflex sensitivity is associated with markers of hippocampal gliosis and dysmyelination in patients with psychosis
• Canine models of Charcot-Marie-Tooth: MTMR2, MPZ, and SH3TC2 variants in golden retrievers with congenital hypomyelinating polyneuropathy
• Case of acute onset ataxia caused by <em>Klebsiella pneumoniae</em> sepsis with the appearance of anti-GD1b antibody
• CIDP, CMT1B, or CMT1B plus CIDP?
• Clinical and genetic spectrum of hereditary spastic paraplegia in Chinese children
• Cognitive Dysfunction After Analgesia and Sedation: Out of the Operating Room and Into the Pediatric Intensive Care Unit
• Comparative role of SOX10 gene in the gliogenesis of central, peripheral, and enteric nervous systems
• Conduction slowing, conduction block and temporal dispersion in demyelinating, dysmyelinating and axonal neuropathies: Electrophysiology meets pathology
• COVID-19 Proned Ventilation and Its Possible Association With Foot Drop: A Case Series
• Curcumin-cyclodextrin/cellulose nanocrystals improve the phenotype of Charcot-Marie-Tooth-1A transgenic rats through the reduction of oxidative stress
• Deficiency of galactosy-lceramidase in adult oligodendrocytes worsens disease severity during chronic experimental allergic encephalomyelitis
• Deficiency of galactosyl-ceramidase in adult oligodendrocytes worsens disease severity during chronic experimental allergic encephalomyelitis
• Deficiency of galactosylceramidase in adult oligodendrocytes worsens the neurological deficits and shortens the survival during chronic experimental allergic encephalomyelitis
• Deletion of the Thrombin Proteolytic Site in Neurofascin 155 Causes Disruption of Nodal and Paranodal Organization
• Distinct Changes in Calpain and Calpastatin during PNS Myelination and Demyelination in Rodent Models
• Docking protein 6 (DOK6) selectively docks the neurotrophic signaling transduction to restrain peripheral neuropathy
• Downregulation of PMP22 ameliorates myelin defects in iPSC-derived human organoid cultures of CMT1A
• Dysmyelination and glycolipid interference caused by phenylalanine in phenylketonuria
• Dysmyelination by Oligodendrocyte-Specific Ablation of Ninj2 Contributes to Depressive-Like Behaviors
• Early Changes in Skeletal Muscle of Young C22 Mice, A Model of Charcot-Marie-Tooth 1A
• Epidural Anesthesia and Continuous Epidural Analgesia in a Pediatric Patient With Pelizaeus-Merzbacher Disease: A Case Report
• Ermin deficiency leads to compromised myelin, inflammatory milieu, and susceptibility to demyelinating insult
• Exosomal Lipid Biomarkers of Oligodendrocyte Pathology to Predict Scoliosis in Children with Cerebral Palsy
• Fibulin 5, a human Wharton's jelly-derived mesenchymal stem cells-secreted paracrine factor, attenuates peripheral nervous system myelination defects through the Integrin-RAC1 signaling axis
• Four mutations in MITF, SOX10 and PAX3 genes were identified as genetic causes of waardenburg syndrome in four unrelated Iranian patients: case report
• Further delineation of HIDEA syndrome
• Glial progenitor cell-based repair of the dysmyelinated brain: Progression to the clinic
• Gut and oral microbiome modulate molecular and clinical markers of schizophrenia-related symptoms: A transdiagnostic, multilevel pilot study
• HDAC3 Inhibition Stimulates Myelination in a CMT1A Mouse Model
• Histopathology of the trigeminal ganglion and nerve: A historical review
• Human stem cell-derived oligodendrocytes: From humanized animal models to cell therapy in myelin diseases
• Hypomyelinating leukodystrophies in adults: Clinical and genetic features
• Impaired Autophagy in Krabbe Disease: The Role of BCL2 and Beclin-1 Phosphorylation
• In Silico Structural Analysis Predicting the Pathogenicity of PLP1 Mutations in Multiple Sclerosis
• Inhomogeneous magnetization transfer MRI of white matter structures in the hypomyelinated shiverer mouse brain
• Interference of commissural connections through the genu of the corpus callosum specifically impairs sensorimotor gating
• Intermittent lipid nanoparticle mRNA administration prevents cortical dysmyelination associated with arginase deficiency
• Intracarotid Transplantation of Skin-Derived Precursor Schwann Cells Promotes Functional Recovery After Acute Ischemic Stroke in Rats
• Jitter patterns in conventional concentric needle electromyography recordings of regenerating motor units
• Loss of oligodendrocyte ErbB receptor signaling leads to hypomyelination, reduced density of parvalbumin-expressing interneurons, and inhibitory function in the auditory cortex
• Magnetic Resonance Imaging and Spectroscopy Analysis in a Pelizaeus-Merzbacher Disease Rat Model
• Magnetic resonance imaging of disorders with white matter changes in children and adolescents: a pictorial essay
• Maternal Blood Lipid Biomarkers of Oligodendrocyte Pathology to Predict Fetal Alcohol Spectrum Disorders
• Mechanisms and treatment strategies of demyelinating and dysmyelinating Charcot-Marie-Tooth disease
• Mek/ERK1/2-MAPK and PI3K/Akt/mTOR signaling plays both independent and cooperative roles in Schwann cell differentiation, myelination and dysmyelination
• Melatonin pretreatment alleviates the long-term synaptic toxicity and dysmyelination induced by neonatal Sevoflurane exposure via MT1 receptor-mediated Wnt signaling modulation
• Metformin treatment reduces inflammation, dysmyelination and disease severity in a mouse model of multiple sclerosis, experimental autoimmune encephalomyelitis
• Microglia-Mediated Neurodegeneration in Perinatal Brain Injuries
• Movement disorders in hereditary spastic paraplegias
• Myelin Defects in Niemann-Pick Type C Disease: Mechanisms and Possible Therapeutic Perspectives
• Myelin in Alzheimer's disease: culprit or bystander?
• Myelin-Independent Therapeutic Potential of Canine Glial-Restricted Progenitors Transplanted in Mouse Model of Dysmyelinating Disease
• Myelination synchronizes cortical oscillations by consolidating parvalbumin-mediated phasic inhibition
• Nanoscale volumetric fluorescence imaging via photochemical sectioning
• Nanostructure-specific X-ray tomography reveals myelin levels, integrity and axon orientations in mouse and human nervous tissue
• Neurological Manifestations of Congenital Cytomegalovirus Infection at a Tertiary Care Centre from Southern India
• Neurological Waardenburg-Shah syndrome: a diagnostic challenge in a child with skin hypopigmentation and neurological manifestation
• Novel <em>SOX10</em> Mutations in Waardenburg Syndrome: Functional Characterization and Genotype-Phenotype Analysis
• Novel Homozygous FA2H Variant Causing the Full Spectrum of Fatty Acid Hydroxylase-Associated Neurodegeneration (SPG35)
• Novel syndromic neurodevelopmental disorder caused by <em>de novo</em> deletion of <em>CHASERR</em>, a long noncoding RNA
• Novel syndromic neurodevelopmental disorder caused by de novo deletion of <em>CHASERR</em> , a long noncoding RNA
• Oligodendrocyte pathology in fetal alcohol spectrum disorders
• Oligodendrocyte pathology in Huntington's disease: from mechanisms to therapeutics
• Oligodendrocyte Precursor Cells Transplantation Improves Stroke Recovery <em>via</em> Oligodendrogenesis, Neurite Growth and Synaptogenesis
• Pelizaeus-Merzbacher Disease with <em>PLP1</em> Exon 1 Duplication, Previously Misdiagnosed as Cerebral Palsy: a Case Report
• PLEKHG5-related autosomal recessive lower motor neuron disease with dysmyelination in peripheral nerves
• Promyelinating drugs promote functional recovery in an autism spectrum disorder mouse model of Pitt-Hopkins syndrome
• Rac1 and Rac3 have opposite functions in Schwann cells during developmental myelination
• Renewal of oligodendrocyte lineage reverses dysmyelination and CNS neurodegeneration through corrected N-acetylaspartate metabolism
• Role of SNAREs and Rabs in Myelin Regulation
• SARM1 knockout does not rescue neuromuscular phenotypes in a Charcot-Marie-Tooth disease Type 1A mouse model
• Secondary Degeneration Impairs Myelin Ultrastructural Development in Adulthood following Adolescent Neurotrauma in the Rat Optic Nerve
• Severe DNM1 encephalopathy with dysmyelination due to recurrent splice site pathogenic variant
• Soluble dimeric prion protein ligand activates Adgrg6 receptor but does not rescue early signs of demyelination in PrP-deficient mice
• SOX10: 20 years of phenotypic plurality and current understanding of its developmental function
• Sulfatide in health and disease. The evaluation of sulfatide in cerebrospinal fluid as a possible biomarker for neurodegeneration
• Temporal pole blurring in temporal lobe epilepsy revealed by 3D Edge-Enhancing Gradient Echo MRI
• The pathogenesis of, and pharmacological treatment for, Canavan disease
• Transplantation of Human Glial Progenitors to Immunodeficient Neonatal Mice with Amyotrophic Lateral Sclerosis (SOD1/rag2)
• Utilizing hiPSC-derived oligodendrocytes to study myelin pathophysiology in neuropsychiatric and neurodegenerative disorders