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Journal Article
Glia, ISSN 0894-1491, 01/2016, Volume 64, Issue 1, pp. 155 - 174
Protein zero (P0) is the major structural component of peripheral myelin. Lack of this adhesion protein from Schwann cells causes a severe dysmyelinating... 
glia‐axonal support | myelin | Schwann cell | Dejerine‐Sottas syndrome | oligodendrocyte | neurodegeneration | neuropathy | Charcot‐Marie‐tooth disease | hereditary spastic paraplegia (SPG‐2) | Dejerine-Sottas syndrome | Oligodendrocyte | Myelin | Neurodegeneration | Charcot-Marie-tooth disease | Glia-axonal support | Neuropathy | Hereditary spastic paraplegia (SPG-2) | MARIE-TOOTH-DISEASE | COLONY-STIMULATING FACTOR | glia-axonal support | MAJOR STRUCTURAL PROTEIN | NEUROSCIENCES | MICE HETEROZYGOUSLY DEFICIENT | hereditary spastic paraplegia (SPG-2) | MOUSE MODEL | PELIZAEUS-MERZBACHER-DISEASE | CENTRAL-NERVOUS-SYSTEM | SCHWANN-CELL DEVELOPMENT | BASIC-PROTEIN | INHERITED DEMYELINATING NEUROPATHIES | Motor Activity - physiology | Optic Nerve - pathology | Phrenic Nerve - pathology | Myelin-Associated Glycoprotein - metabolism | Myelin Sheath - metabolism | Brain - metabolism | Sciatic Nerve - metabolism | Myelin Proteolipid Protein - metabolism | Female | Phrenic Nerve - metabolism | Myelin Sheath - pathology | Sciatic Nerve - pathology | Mice, Inbred C57BL | Kaplan-Meier Estimate | Axons - metabolism | Neural Conduction - physiology | Mice, Knockout | Mortality, Premature | Animals | Myelin Proteolipid Protein - genetics | Axons - pathology | Brain - pathology | Myelin P0 Protein - genetics | Myelin P0 Protein - metabolism | Optic Nerve - metabolism | Analysis | Myelin proteins | Proteins | Preservation | Rodents | Index Medicus
Journal Article
Neuron, ISSN 0896-6273, 2002, Volume 36, Issue 4, pp. 585 - 596
Journal Article
Journal Article
NeuroMolecular Medicine, ISSN 1535-1084, 12/2014, Volume 16, Issue 4, pp. 821 - 844
An ongoing challenge in children presenting with motor delay/impairment early in life is to identify neurogenetic disorders with a clinical phenotype, which... 
Neurology | Cerebral palsy | Neurosciences | Biomedicine | Masqueraders | Internal Medicine | Spastic, dyskinetic, and ataxic phenotypes | Neurogenetic | RISK-FACTORS | PRETERM INFANTS | NEUROSCIENCES | COENZYME-Q10 DEFICIENCY | CEREBELLAR-ATAXIA | INTRAVENTRICULAR HEMORRHAGE | ACIDURIA TYPE-I | GLUTARIC ACIDURIA | GLOBUS-PALLIDUS INTERNUS | PELIZAEUS-MERZBACHER DISEASE | DEEP BRAIN-STIMULATION | Brain - embryology | Leukoencephalopathies - genetics | Genomics | Humans | Movement Disorders - diagnosis | Child, Preschool | Male | Nervous System Diseases - diagnosis | Stroke - congenital | Exome | Asphyxia Neonatorum - genetics | Brain Diseases, Metabolic - diagnosis | Cerebral Palsy - diagnosis | Leukoencephalopathies - diagnosis | Chromosome Disorders - diagnosis | Child | Hypoxia, Brain - diagnosis | Infant, Newborn | Brain Diseases, Metabolic - genetics | Neurotransmitter Agents - metabolism | Lysosomal Storage Diseases, Nervous System - genetics | Movement Disorders - genetics | Muscle Spasticity - genetics | Cerebral Palsy - genetics | Hypoxia, Brain - genetics | Cell Movement | Tissue Array Analysis | Stroke - diagnosis | Genetic Diseases, Inborn - genetics | Developmental Disabilities - genetics | Nervous System Diseases - genetics | Molecular Diagnostic Techniques | Diagnostic Errors | Asphyxia Neonatorum - diagnosis | Adult | Female | Birth Injuries - genetics | Developmental Disabilities - diagnosis | Genetic Diseases, Inborn - diagnosis | Globus Pallidus - pathology | Lysosomal Storage Diseases, Nervous System - diagnosis | Mitochondrial Diseases - genetics | Diagnosis, Differential | Genome-Wide Association Study | Leukoencephalopathies - metabolism | Birth Injuries - diagnosis | Muscle Spasticity - diagnosis | Chromosome Disorders - genetics | Mitochondrial Diseases - diagnosis | Medical colleges | Molecular genetics | Children's hospitals | Development and progression | Diagnostic imaging | Diagnosis | Index Medicus | masqueraders | dyskinetic and ataxic phenotypes | neurogenetic | spastic
Journal Article
Journal Article
Glia, ISSN 0894-1491, 04/2013, Volume 61, Issue 4, pp. 567 - 586
Journal Article