Treatment for Charcot-Marie-Tooth disease (Q24242777)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18254090%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

review article

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title

Treatment for Charcot-Marie-Tooth disease (English)

1 reference

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2 January 2020

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P Young

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2 January 2020

P De Jonghe

series ordinal

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2 January 2020

F Stögbauer

series ordinal

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2 January 2020

T Butterfass-Bahloul

series ordinal

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2 January 2020

publication date

23 January 2008

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Cochrane Database of Systematic Reviews

2 January 2020

published in

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2 January 2020

issue

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2 January 2020

page(s)

CD006052

1 reference

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Double-blind controlled trials of Cronassial in chronic neuromuscular diseases and ataxia.

2 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD006052.PUB2

Effective orthotic therapy for the painful cavus foot: a randomized controlled trial

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD006052.PUB2

Resistance training exercise and creatine in patients with Charcot-Marie-Tooth disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD006052.PUB2

Creatine monohydrate does not increase strength in patients with hereditary neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD006052.PUB2

Progressive resistance training in neuromuscular patients. Effects on force and surface EMG.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD006052.PUB2

Effects of exercise and creatine on myosin heavy chain isoform composition in patients with Charcot-Marie-Tooth disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD006052.PUB2

Brace modification improves aerobic performance in Charcot-Marie-Tooth disease: a single-subject design

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD006052.PUB2

Evaluation and management of upper extremity neuropathies in Charcot-Marie-Tooth disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD006052.PUB2

Resistance training effectiveness in patients with Charcot-Marie-Tooth disease: recommendations for exercise prescription

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD006052.PUB2

Microvascular decompression for trigeminal neuralgia in Charcot-Marie-Tooth disease

21 January 2018

1 reference

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Biochemical rationale and the cardiac response of patients with muscle disease to therapy with coenzyme Q10.

21 January 2018

1 reference

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A review of the progress towards developing health-related quality-of-life instruments for international clinical studies and outcomes research

21 January 2018

1 reference

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Hereditary demyelinating motor and sensory neuropathy

21 January 2018

1 reference

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Current Therapy for Charcot-Marie-Tooth Disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD006052.PUB2

Structure and localization of the gene encoding human peripheral myelin protein 2 (PMP2).

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD006052.PUB2

De novo mutation of the myelin P0 gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III)

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD006052.PUB2

Mutation of the Myelin Po Gene in Charcot-Marie-Tooth Neuropathy Type 1

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD006052.PUB2

Short form 36 (SF36) health survey questionnaire: normative data for adults of working age

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD006052.PUB2

Neurological dysfunction and axonal degeneration in Charcot-Marie-Tooth disease type 1A.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD006052.PUB2

Clinical features and molecular genetics of hereditary peripheral neuropathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD006052.PUB2

Gene dosage is a mechanism for Charcot-Marie-Tooth disease type 1A

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD006052.PUB2

Animal models for inherited peripheral neuropathies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD006052.PUB2

The effect of myelinating Schwann cells on axons.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD006052.PUB2

Role of immune cells in animal models for inherited neuropathies: facts and visions

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD006052.PUB2

Psychometric evaluation of a new sensory scale in immune-mediated polyneuropathies. Inflammatory Neuropathy Cause and Treatment (INCAT) Group

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD006052.PUB2

Ascorbic acid treatment corrects the phenotype of a mouse model of Charcot-Marie-Tooth disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD006052.PUB2

Therapeutic administration of progesterone antagonist in a model of Charcot-Marie-Tooth disease (CMT-1A).

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD006052.PUB2

Reliability and validity of the CMT neuropathy score as a measure of disability.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD006052.PUB2

Mutation of a putative protein degradation gene LITAF/SIMPLE in Charcot-Marie-Tooth disease 1C.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD006052.PUB2

Disease mechanisms in inherited neuropathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD006052.PUB2

Interobserver agreement for the assessment of handicap in stroke patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD006052.PUB2

MFN2 mutation distribution and genotype/phenotype correlation in Charcot-Marie-Tooth type 2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD006052.PUB2

The causes of Charcot-Marie-Tooth disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD006052.PUB2

Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD006052.PUB2

The peripheral myelin protein gene PMP-22 is contained within the Charcot-Marie-Tooth disease type 1A duplication

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD006052.PUB2

A multicenter, randomized, double-blind, placebo-controlled trial of long-term ascorbic acid treatment in Charcot-Marie-Tooth disease type 1A (CMT-TRIAAL): The study protocol [EudraCT no.: 2006-000032-27]

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD006052.PUB2

The periacetabular osteotomy. Minimum 2 year followup in more than 100 hips.

21 January 2018

1 reference

12 December 2020

Surface EMG of proximal leg muscles in neuromuscular patients and in healthy controls. Relations to force and fatigue

1 reference

12 December 2020

Triple arthrodesis: twenty-five and forty-four-year average follow-up of the same patients

1 reference

12 December 2020

Total neuropathy score: validation and reliability study

1 reference

12 December 2020

Correlation between weakness and axonal loss in patients with CMT1A

1 reference

12 December 2020

Animal models for inherited peripheral neuropathies: chances to find treatment strategies?

1 reference

12 December 2020

Pathological findings in the x-linked form of Charcot-Marie-Tooth disease: a morphometric and ultrastructural analysis

1 reference

12 December 2020

Disease mechanisms and potential therapeutic strategies in Charcot-Marie-Tooth disease

1 reference

12 December 2020

Hereditary Motor and Sensory Neuropathy With Treatable Extrapyramidal Features

1 reference

12 December 2020

Autonomic vascular disorders in neuropathies and the methods for their pathogenetic therapy

1 reference

12 December 2020

Differential diagnosis of Charcot-Marie-Tooth disease and related neuropathies

1 reference

12 December 2020

[Treatment of patients with neuromuscular disease in a warm climate]

1 reference

12 December 2020

Exercise for people with peripheral neuropathy

1 reference

12 December 2020

Strength training and aerobic exercise training for muscle disease

1 reference

12 December 2020

Triple arthrodesis in the treatment of fixed cavovarus deformity in adolescent patients with Charcot-Marie-Tooth disease

1 reference

12 December 2020

NT-3 promotes nerve regeneration and sensory improvement in CMT1A mouse models and in patients

1 reference

12 December 2020

136th ENMC International Workshop: Charcot-Marie-Tooth disease type 1A (CMT1A)8-10 April 2005, Naarden, The Netherlands

1 reference

12 December 2020

DNA duplication associated with Charcot-Marie-Tooth disease type 1A

1 reference

12 December 2020

Low doses of TRH in amyotrophic lateral sclerosis and in other neurological diseases

1 reference

12 December 2020

[A comparative evaluation of the efficacy of physical treatment methods in Charcot-Marie-Tooth neural amyotrophy]

1 reference

12 December 2020

Long-term results of triple arthrodesis in Charcot-Marie-Tooth disease

1 reference

12 December 2020

[Treatment of patients with Charcot-Marie-Tooth neural amyotrophy]

1 reference

12 December 2020

[Physical therapy of hereditary neuropathies]

1 reference

12 December 2020

Dietary essential fatty acids, vitamin E, and Charcot-Marie-Tooth disease

1 reference

12 December 2020

[Pathogenesis and treatment of neural amyotrophy]

1 reference

12 December 2020

The Steroid Treatment of Hereditary Motor and Sensory Neuropathy

1 reference

12 December 2020

Prednisone-responsive hereditary motor and sensory neuropathy

1 reference

12 December 2020

Posterior tibial tendon transfer: a review of the literature and analysis of 74 procedures

1 reference

12 December 2020

The clinical features of hereditary motor and sensory neuropathy types I and II

1 reference

12 December 2020

Extensor pollicis longus opponensplasty

1 reference

12 December 2020

Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice

1 reference

12 December 2020

Treatment of the Upper Limb in Charcot–Marie–Tooth Disease

1 reference

12 December 2020

Two successful double-blind trials with coenzyme Q10 (vitamin Q10) on muscular dystrophies and neurogenic atrophies

1 reference

12 December 2020

Strength training in patients with myotonic dystrophy and hereditary motor and sensory neuropathy: A randomized clinical trial

1 reference

12 December 2020

Treatment of stable chronic demyelinating polyneuropathy with 3,4-diaminopyridine

1 reference

12 December 2020

Reduction of knee torques and leg-related functional abilities in hereditary motor and sensory neuropathy

1 reference

12 December 2020

Intermediate nerve conduction velocities define X-linked Charcot-Marie-Tooth neuropathy families

1 reference

12 December 2020

Treatment of equinocavovarus deformity in adults with the use of a hinged distraction++ apparatus

1 reference

12 December 2020

Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative study

1 reference

12 December 2020

Heterozygous peripheral myelin protein 22-deficient mice are affected by a progressive demyelinating tomaculous neuropathy

1 reference

12 December 2020

Quadriceps strength and timed motor performances in myotonic dystrophy, Charcot-Marie-Tooth disease, and healthy subjects

1 reference

12 December 2020

Growth hormone replacement in an adult with mild growth hormone deficiency and hereditary motor and sensory neuropathy: growth hormone restores independent mobility

1 reference

12 December 2020

10.1002/14651858.CD006052.PUB2

Identifiers

DOI

2 references

Consolidated OpenCitations Corpus – April 2017

4573148

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18254090%20AND%20SRC:MED&resulttype=core&format=json

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2 January 2020

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Fatcat

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24 November 2022

mapped directly with Wikidata item

4573148

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Consolidated OpenCitations Corpus – April 2017

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18254090%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

PubMed publication ID

18254090

2 references

Consolidated OpenCitations Corpus – April 2017

4573148

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18254090%20AND%20SRC:MED&resulttype=core&format=json