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Year Number of Results
1978 1
1982 1
1983 1
1991 1
1994 2
1998 1
2001 1
2004 1
2005 3
2007 1
2008 2
2009 3
2010 3
2011 1
2012 5
2013 7
2014 9
2015 9
2016 7
2017 7
2018 7
2019 5
2020 11
2021 4
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90 results

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Page 1
Charcot-Marie-Tooth: From Molecules to Therapy.
Morena J, Gupta A, Hoyle JC. Morena J, et al. Int J Mol Sci. 2019 Jul 12;20(14):3419. doi: 10.3390/ijms20143419. Int J Mol Sci. 2019. PMID: 31336816 Free PMC article. Review.
Charcot-Marie-Tooth (CMT) is the most prevalent category of inherited neuropathy. The most common inheritance pattern is autosomal dominant, though there also are X-linked and autosomal recessive subtypes. ...
Charcot-Marie-Tooth (CMT) is the most prevalent category of inherited neuropathy. The most common inheritance pattern is autos …
Clinical practice guideline for the management of paediatric Charcot-Marie-Tooth disease.
Yiu EM, Bray P, Baets J, Baker SK, Barisic N, de Valle K, Estilow T, Farrar MA, Finkel RS, Haberlová J, Kennedy RA, Moroni I, Nicholson GA, Ramchandren S, Reilly MM, Rose K, Shy ME, Siskind CE, Yum SW, Menezes MP, Ryan MM, Burns J. Yiu EM, et al. J Neurol Neurosurg Psychiatry. 2022 May;93(5):530-538. doi: 10.1136/jnnp-2021-328483. Epub 2022 Feb 9. J Neurol Neurosurg Psychiatry. 2022. PMID: 35140138 Review.
BACKGROUND AND OBJECTIVES: Charcot-Marie-Tooth disease (CMT) is the most common inherited neuropathy and often presents during childhood. Guidelines for the optimal management of common problems experienced by individuals with CMT do not exist, for either children o …
BACKGROUND AND OBJECTIVES: Charcot-Marie-Tooth disease (CMT) is the most common inherited neuropathy and often presents during …
Treatment of Charcot-Marie-Tooth neuropathies.
Beloribi-Djefaflia S, Attarian S. Beloribi-Djefaflia S, et al. Rev Neurol (Paris). 2023 Jan-Feb;179(1-2):35-48. doi: 10.1016/j.neurol.2022.11.006. Epub 2022 Dec 30. Rev Neurol (Paris). 2023. PMID: 36588067 Review.
Charcot-Marie-Tooth Disease and Other Hereditary Neuropathies.
Klein CJ. Klein CJ. Continuum (Minneap Minn). 2020 Oct;26(5):1224-1256. doi: 10.1212/CON.0000000000000927. Continuum (Minneap Minn). 2020. PMID: 33003000 Review.
Gene-targeted therapies have begun entering the clinic. Currently, for most inherited neuropathy categories, specific symptomatic management and family counseling remain the mainstays of therapy....
Gene-targeted therapies have begun entering the clinic. Currently, for most inherited neuropathy categories, specific symptoma …
Epidemiologic Study of Charcot-Marie-Tooth Disease: A Systematic Review.
Barreto LC, Oliveira FS, Nunes PS, de França Costa IM, Garcez CA, Goes GM, Neves EL, de Souza Siqueira Quintans J, de Souza Araújo AA. Barreto LC, et al. Neuroepidemiology. 2016;46(3):157-65. doi: 10.1159/000443706. Epub 2016 Feb 6. Neuroepidemiology. 2016. PMID: 26849231 Free article. Review.
BACKGROUND: Charcot-Marie-Tooth disease (CMT) is the most common inherited neuropathy. CMT is classified into 2 main subgroups: CMT type 1 (CMT1; demyelinating form) and CMT type 2 (CMT2; axonal form). ...
BACKGROUND: Charcot-Marie-Tooth disease (CMT) is the most common inherited neuropathy. CMT is classified into 2 main subgroups …
Hereditary neuropathy.
Pisciotta C, Shy ME. Pisciotta C, et al. Handb Clin Neurol. 2023;195:609-617. doi: 10.1016/B978-0-323-98818-6.00009-1. Handb Clin Neurol. 2023. PMID: 37562889 Review.
Neuropathy.
Pisciotta C, Shy ME. Pisciotta C, et al. Handb Clin Neurol. 2018;148:653-665. doi: 10.1016/B978-0-444-64076-5.00042-9. Handb Clin Neurol. 2018. PMID: 29478606 Review.
Strategy for genetic analysis in hereditary neuropathy.
Masingue M, Fernández-Eulate G, Debs R, Tard C, Labeyrie C, Leonard-Louis S, Dhaenens CM, Masson MA, Latour P, Stojkovic T. Masingue M, et al. Rev Neurol (Paris). 2023 Jan-Feb;179(1-2):10-29. doi: 10.1016/j.neurol.2022.11.007. Epub 2022 Dec 22. Rev Neurol (Paris). 2023. PMID: 36566124 Review.
A practical approach to the genetic neuropathies.
Rossor AM, Evans MR, Reilly MM. Rossor AM, et al. Pract Neurol. 2015 Jun;15(3):187-98. doi: 10.1136/practneurol-2015-001095. Epub 2015 Apr 21. Pract Neurol. 2015. PMID: 25898997 Review.
This review provides a diagnostic approach to patients with suspected inherited neuropathy and an algorithm for genetic testing that includes recent advances in genetics such as next-generation sequencing. We also discuss important aspects of the long-term managemen …
This review provides a diagnostic approach to patients with suspected inherited neuropathy and an algorithm for genetic testin …
Genetic neuropathies presenting with CIDP-like features in childhood.
Fernandez-Garcia MA, Stettner GM, Kinali M, Clarke A, Fallon P, Knirsch U, Wraige E, Jungbluth H. Fernandez-Garcia MA, et al. Neuromuscul Disord. 2021 Feb;31(2):113-122. doi: 10.1016/j.nmd.2020.11.013. Epub 2020 Nov 30. Neuromuscul Disord. 2021. PMID: 33386210 Review.
A review of the few Paediatric cases reported in the literature showed similar delays in diagnosis and no significant changes to immunomodulatory treatment. Our findings emphasize the importance of considering an inherited neuropathy in children with a CIDP-like pre …
A review of the few Paediatric cases reported in the literature showed similar delays in diagnosis and no significant changes to immunomodul …
90 results