The DOI matches its Crossref record; 75 of the 75 references it cites were found in a registry or an index.
Diagnosis, natural history, and management of Charcot–Marie–Tooth disease
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
1 retracted
Rehabilitation interventions for foot drop in neuromuscular disease
Sackley, C. M., Disler, P. B., Turner‐Stokes, L. F., Wade, D. T., Brittle, N., & Hoppitt, T. (2009) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd003908.pub3 · Cited by 94
RetractedDNA duplication associated with Charcot-Marie-Tooth disease type 1A
Lupski, J. R., de Oca-Luna, R. M., Slaugenhaupt, S., Pentao, L., Guzzetta, V., Trask, B. J., Saucedo-Cardenas, O., Barker, D. F., Killian, J. M., Garcia, C. A., et al. (1991) · Cell · doi:10.1016/0092-8674(91)90613-4 · Cited by 1,333
Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a)
Raeymaekers, P., Timmerman, V, Nelis, E., De Jonghe, P., Hoogenduk, J. E., Baas, F., Barker, D. F., Martin, J. J., De Visser, M., Bolhuis, P. A., et al. (1991) · Neuromuscular Disorders · doi:10.1016/0960-8966(91)90055-w · Cited by 607
Epidemiology of peripheral neuropathy.
Martyn, C. N., & Hughes, R. A. (1997) · Journal of Neurology, Neurosurgery & Psychiatry · doi:10.1136/jnnp.62.4.310 · Cited by 597
Nelis, E., & Van Broeckhoven, C. (1996) · European Journal of Human Genetics · doi:10.1159/000472166 · Cited by 431
Neurological dysfunction and axonal degeneration in Charcot-Marie-Tooth disease type 1A
Krajewski, K. M. (2000) · Brain · doi:10.1093/brain/123.7.1516 · Cited by 414
MFN2 mutation distribution and genotype/phenotype correlation in Charcot-Marie-Tooth type 2
Verhoeven, K. (2006) · Brain · doi:10.1093/brain/awl126 · Cited by 409
Reliability and validity of the CMT neuropathy score as a measure of disability
Shy, M. E., Blake, J., Krajewski, K., Fuerst, D. R., Laura, M., Hahn, A. F., Li, J., Lewis, R. A., & Reilly, M. (2005) · Neurology · doi:10.1212/01.wnl.0000156517.00615.a3 · Cited by 357
Ascorbic acid treatment corrects the phenotype of a mouse model of Charcot-Marie-Tooth disease
Passage, E., Norreel, J. C., Noack-Fraissignes, P., Sanguedolce, V., Pizant, J., Thirion, X., Robaglia-Schlupp, A., Pellissier, J. F., & Fontés, M. (2004) · Nature Medicine · doi:10.1038/nm1023 · Cited by 349
Reliability and validity of the CMT neuropathy score as a measure of disability
Padua, L., Aprile, I., Caliandro, P., Pazzaglia, C., Commodari, I., & Tonali, P. (2006) · Neurology · doi:10.1212/01.wnl.0000216104.34658.82 · Cited by 324
Cited by
Mitochondrial optic neuropathies—Disease mechanisms and therapeutic strategies
Yu-Wai-Man, P., Griffiths, P. G., & Chinnery, P. F. (2011) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2010.11.002 · Cited by 633
Heat shock proteins: Cellular and molecular mechanisms in the central nervous system
Stetler, R. A., Gan, Y., Zhang, W., Liou, A. K., Gao, Y., Cao, G., & Chen, J. (2010) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2010.05.002 · Cited by 305
The epidemiology and risk factors of chronic polyneuropathy
Hanewinckel, R., van Oijen, M., Ikram, M. A., & van Doorn, P. A. (2016) · European Journal of Epidemiology · doi:10.1007/s10654-015-0094-6 · Cited by 293
Local translation of extranuclear lamin B promotes axon maintenance
Yoon, B. C., Jung, H., Dwivedy, A., O'Hare, C. M., Zivraj, K. H., & Holt, C. E. (2012) · Cell · doi:10.1016/j.cell.2011.11.064 · Cited by 263
Metadata
- Authors
- Pareyson, D., & Marchesi, C.
- Venue
- The Lancet Neurology
- Publisher
- Elsevier BV
- Published
- 2009-07
- Volume
- 8
- Issue
- 7
- Pages
- 654-667
- ISSN
- 1474-4422 (ISSN-L)
- OpenAlex
- W2159457567
- Cited by
- 621
- References
- 75
- FWCI
- 13.55
- Type
- journal article
- Language
- en
- Open access
- closed
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Diagnosis, natural history, and management of Charcot–Marie–Tooth disease. https://app.cochat.ai/papers/10.1016/s1474-4422(09)70110-3
- The paper
- Pareyson, D., & Marchesi, C. (2009). Diagnosis, natural history, and management of Charcot–Marie–Tooth disease. The Lancet Neurology. https://doi.org/10.1016/s1474-4422(09)70110-3
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.