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Treatment for Charcot-Marie-Tooth disease
scientific article (published 2006-04-19)
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title
Treatment for Charcot-Marie-Tooth disease
(English)
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author name string
P Young
series ordinal
1
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F Stögbauer
series ordinal
2
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T Butterfass-Bahloul
series ordinal
3
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P de Jonghe
series ordinal
4
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publication date
19 April 2006
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published in
Cochrane Database of Systematic Reviews
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cites work
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Intermediate nerve conduction velocities define X-linked Charcot-Marie-Tooth neuropathy families
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The effect of myelinating Schwann cells on axons.
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Mutation of the myelin P0 gene in Charcot-Marie-tooth neuropathy type 1.
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Structure and localization of the gene encoding human peripheral myelin protein 2 (PMP2).
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The causes of Charcot-Marie-Tooth disease
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Pathological findings in the x-linked form of Charcot-Marie-Tooth disease: a morphometric and ultrastructural analysis
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Clinical features and molecular genetics of hereditary peripheral neuropathies
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Current Therapy for Charcot-Marie-Tooth Disease.
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DNA duplication associated with Charcot-Marie-Tooth disease type 1A
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Disease mechanisms and potential therapeutic strategies in Charcot-Marie-Tooth disease
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Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice
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Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A
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Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy
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Ascorbic acid treatment corrects the phenotype of a mouse model of Charcot-Marie-Tooth disease
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Therapeutic administration of progesterone antagonist in a model of Charcot-Marie-Tooth disease (CMT-1A).
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Disease mechanisms in inherited neuropathies
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The clinical features of hereditary motor and sensory neuropathy types I and II
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Neurological dysfunction and axonal degeneration in Charcot-Marie-Tooth disease type 1A.
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Correlation between weakness and axonal loss in patients with CMT1A
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Hereditary demyelinating motor and sensory neuropathy
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Short form 36 (SF36) health survey questionnaire: normative data for adults of working age
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Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative study
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7 January 2021
based on heuristic
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Heterozygous peripheral myelin protein 22-deficient mice are affected by a progressive demyelinating tomaculous neuropathy
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A review of the progress towards developing health-related quality-of-life instruments for international clinical studies and outcomes research
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based on heuristic
inferred from DOI database lookup
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10.1002/14651858.CD006052
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