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Year Number of Results
1990 1
1992 2
1994 1
1995 1
1997 1
1999 2
2001 1
2002 5
2003 1
2006 5
2007 2
2008 1
2009 1
2010 2
2011 2
2012 2
2013 3
2014 4
2015 3
2016 1
2018 1
2019 5
2020 2
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Page 1
Systematic review of exercise for Charcot-Marie-Tooth disease.
Sman AD, Hackett D, Fiatarone Singh M, Fornusek C, Menezes MP, Burns J. Sman AD, et al. J Peripher Nerv Syst. 2015 Dec;20(4):347-62. doi: 10.1111/jns.12116. J Peripher Nerv Syst. 2015. PMID: 26010435 Review.
Charcot-Marie-Tooth disease (CMT) is a slowly progressive hereditary degenerative disease and one of the most common neuromuscular disorders. ...Although the majority of the studies identified changes in one or more outcome measurements across e
Charcot-Marie-Tooth disease (CMT) is a slowly progressive hereditary degenerative disease and one of the
Axonal Charcot-Marie-Tooth Disease: from Common Pathogenic Mechanisms to Emerging Treatment Opportunities.
McCray BA, Scherer SS. McCray BA, et al. Neurotherapeutics. 2021 Oct;18(4):2269-2285. doi: 10.1007/s13311-021-01099-2. Epub 2021 Oct 4. Neurotherapeutics. 2021. PMID: 34606075 Free PMC article. Review.
Genetic neuropathies that primarily cause axonal degeneration, as opposed to demyelination, are most often classified as Charcot-Marie-Tooth disease type 2 (CMT2) and are the focus of this review. Gene identification efforts over the past three …
Genetic neuropathies that primarily cause axonal degeneration, as opposed to demyelination, are most often classified as Charcot-M
TRPV4-mediated channelopathies.
Verma P, Kumar A, Goswami C. Verma P, et al. Channels (Austin). 2010 Jul-Aug;4(4):319-28. doi: 10.4161/chan.4.4.12905. Epub 2010 Jul 6. Channels (Austin). 2010. PMID: 20676052 Review.
Transient receptor potential vanilloid sub type 4 (TRPV4) is a member of non-selective cation channel that is important for sensation of several physical and chemical stimuli and also involved in multiple physiological functions. Recently it gained immense medical a …
Transient receptor potential vanilloid sub type 4 (TRPV4) is a member of non-selective cation channel that is important for se …
Pain in Charcot-Marie-Tooth disease: an update.
Azevedo H, Pupe C, Pereira R, Nascimento OJM. Azevedo H, et al. Arq Neuropsiquiatr. 2018 Apr;76(4):273-276. doi: 10.1590/0004-282x20180021. Arq Neuropsiquiatr. 2018. PMID: 29742248 Free article. Review.
Charcot-Marie-Tooth (CMT) disease, the most common inherited peripheral neuropathy, has pain as one of its clinical features, yet it remains underdiagnosed and undertreated. This literature review assessed data related to pain from CMT to determine its
Charcot-Marie-Tooth (CMT) disease, the most common inherited peripheral neuropathy, has pain as one of its clini
Charcot Marie Tooth disease (CMT): historical perspectives and evolution.
Kazamel M, Boes CJ. Kazamel M, et al. J Neurol. 2015;262(4):801-5. doi: 10.1007/s00415-014-7490-9. Epub 2014 Sep 9. J Neurol. 2015. PMID: 25201224 Review.
Prior to Charcot and Marie's and Tooth's reports, patients with peroneal muscular atrophy had been described by Virchow, Eulenburg, Friedreich, Osler, and others. In February 1886, Charcot and Marie published their original description of five p …
Prior to Charcot and Marie's and Tooth's reports, patients with peroneal muscular atrophy had been described by Virchow …
Charcot-Marie-Tooth disease (CMT): distinctive phenotypic and genotypic features in CMT type 2.
Gemignani F, Marbini A. Gemignani F, et al. J Neurol Sci. 2001 Feb 15;184(1):1-9. doi: 10.1016/s0022-510x(00)00497-4. J Neurol Sci. 2001. PMID: 11231025 Review.
Charcot-Marie-Tooth disease (CMT), or hereditary motor and sensory neuropathy (HMSN), includes two main subtypes of CMT1/HMSN I (demyelinating), and CMT2/HMSN II (axonal). ...
Charcot-Marie-Tooth disease (CMT), or hereditary motor and sensory neuropathy (HMSN), includes two main subtypes
Molecular genetics and neuropathology of Charcot-Marie-Tooth disease type 1A.
Lupski JR, Garcia CA. Lupski JR, et al. Brain Pathol. 1992 Oct;2(4):337-49. doi: 10.1111/j.1750-3639.1992.tb00710.x. Brain Pathol. 1992. PMID: 1341967 Review.
Charcot-Marie-Tooth (CMT) syndrome describes a genetically and clinically heterogeneous group of polyneuropathies. ...For CMT1, three gene loci (on chromosomes 1, 17 and the X chromosome) have been mapped. The locus on chromosome 17, CMT type 1A (CMT1A
Charcot-Marie-Tooth (CMT) syndrome describes a genetically and clinically heterogeneous group of polyneuropathies. ...F
Charcot-Marie-Tooth disease: an overview of genotypes, phenotypes, and clinical management strategies.
El-Abassi R, England JD, Carter GT. El-Abassi R, et al. PM R. 2014 Apr;6(4):342-55. doi: 10.1016/j.pmrj.2013.08.611. Epub 2014 Jan 13. PM R. 2014. PMID: 24434692 Review.
Charcot-Marie-Tooth (CMT) disease, which encompasses several hereditary motor and sensory neuropathies, is one of the most common neuromuscular disorders. ...Characterized by electrodiagnostic studies into demyelinating (type 1) and axonal (t
Charcot-Marie-Tooth (CMT) disease, which encompasses several hereditary motor and sensory neuropathies, is one o
Inherited peripheral neuropathy.
Keller MP, Chance PF. Keller MP, et al. Semin Neurol. 1999;19(4):353-62. doi: 10.1055/s-2008-1040850. Semin Neurol. 1999. PMID: 10716658 Review.
Hereditary disorders of the peripheral nerves constitute a group of frequently encountered neurological diseases. Charcot-Marie-Tooth neuropathy type 1 (CMT1) is genetically heterogeneous and characterized by demyelination with moderately to severely r …
Hereditary disorders of the peripheral nerves constitute a group of frequently encountered neurological diseases. Charcot-Marie
Junctophilins emerge as novel therapeutic targets.
Jiang J, Tang M, Huang Z, Chen L. Jiang J, et al. J Cell Physiol. 2019 Aug;234(10):16933-16943. doi: 10.1002/jcp.28405. Epub 2019 Mar 1. J Cell Physiol. 2019. PMID: 30825194 Review.
Junctophilins (JPs) emerge to play key role in human pathophysiology. This family includes four subtypes (JP1-4), which are differentially detected in excitable cells. Previous work demonstrated the knockout of JPs that seriously damage physiological functions in skeletal …
Junctophilins (JPs) emerge to play key role in human pathophysiology. This family includes four subtypes (JP1-4), which are different …
50 results