Electrophysiological features of inherited demyelinating neuropathies: A reappraisal in the era of molecular diagnosis.
about
Two novel connexin32 mutations cause early onset X-linked Charcot-Marie-Tooth diseaseMolecular regulators of nerve conduction - Lessons from inherited neuropathies and rodent genetic modelsCongenital hypomyelinating neuropathy with lethal conduction failure in mice carrying the Egr2 I268N mutation.Classification and diagnosis of the inherited neuropathies.The PMP22 gene and its related diseases.Proximal nerve magnetization transfer MRI relates to disability in Charcot-Marie-Tooth diseasesCharcot-Marie-Tooth disease subtypes and genetic testing strategiesDejerine-Sottas disease and hereditary demyelinating polyneuropathy of infancy.Immunological study of hereditary motor and sensory neuropathy type 1a (HMSN1a).Strategy for genetic testing in Charcot-Marie-disease.A locus-specific database for mutations in GDAP1 allows analysis of genotype-phenotype correlations in Charcot-Marie-Tooth diseases type 4A and 2K.Comparison between clinical disabilities and electrophysiological values in Charcot-Marie-Tooth 1A patients with PMP22 duplication.Clinical and electrophysiological aspects of Charcot-Marie-Tooth disease.Inherited peripheral neuropathies.Conduction block in PMP22 deficiency.Electrophysiological evaluation of chronic inflammatory demyelinating polyneuropathy and charcot-marie-tooth type 1: dispersion and correlation analysis.Inherited neuropathies: an update.An animal model for Charcot-Marie-Tooth disease type 4B1.Charcot-marie-tooth disease type 1X in women: Electrodiagnostic findings.Charcot-Marie-Tooth disease type 4C in Japan: report of a case.A novel mutation in the nerve-specific 5'UTR of the GJB1 gene causes X-linked Charcot-Marie-Tooth disease.Functional recovery of regenerating motor axons is delayed in mice heterozygously deficient for the myelin protein P(0) gene.Nerve conduction abnormalities in aging mice deficient for myelin-associated glycoprotein.Myelin abnormality in Charcot-Marie-Tooth type 4J recapitulates features of acquired demyelination.
P2860
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P2860
Electrophysiological features of inherited demyelinating neuropathies: A reappraisal in the era of molecular diagnosis.
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2000 nî lūn-bûn
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Electrophysiological features ...... he era of molecular diagnosis.
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Electrophysiological features ...... he era of molecular diagnosis.
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Electrophysiological features ...... he era of molecular diagnosis.
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label
Electrophysiological features ...... he era of molecular diagnosis.
@ast
Electrophysiological features ...... he era of molecular diagnosis.
@en
Electrophysiological features ...... he era of molecular diagnosis.
@nl
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Electrophysiological features ...... he era of molecular diagnosis.
@ast
Electrophysiological features ...... he era of molecular diagnosis.
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Electrophysiological features ...... he era of molecular diagnosis.
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P2860
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P1476
Electrophysiological features ...... the era of molecular diagnosis
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10.1002/1097-4598(200010)23:10<1472::AID-MUS3>3.0.CO;2-#
P50
P577
2000-10-01T00:00:00Z