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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1965 1
1967 2
1968 4
1969 3
1970 5
1971 5
1972 3
1973 2
1974 6
1975 3
1977 1
1978 8
1979 1
1982 5
1983 2
1984 2
1985 2
1986 2
1987 4
1988 7
1989 13
1990 12
1991 13
1992 13
1993 23
1994 18
1995 22
1996 25
1997 19
1998 20
1999 50
2000 34
2001 35
2002 29
2003 37
2004 29
2005 22
2006 51
2007 25
2008 33
2009 29
2010 25
2011 44
2012 45
2013 61
2014 50
2015 48
2016 45
2017 33
2018 39
2019 55
2020 51
2021 51
2022 43
2023 44
2024 8

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1,151 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. ...Next generation sequencing (NGS) has expanded and simplified the …
Charcot-Marie-Tooth (CMT) is the most prevalent category of inherited neuropathy. The most common inheritance pattern is autosomal do …
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.
Patients' management is based on rehabilitation and occupational therapy, fatigue, and pain treatment with regular follow-up according to the severity of the disease. In the last three decades, much progress has been made to identify mutations involved in the different typ …
Patients' management is based on rehabilitation and occupational therapy, fatigue, and pain treatment with regular follow-up according to th …
Diagnosis, natural history, and management of Charcot-Marie-Tooth disease.
Pareyson D, Marchesi C. Pareyson D, et al. Lancet Neurol. 2009 Jul;8(7):654-67. doi: 10.1016/S1474-4422(09)70110-3. Lancet Neurol. 2009. PMID: 19539237 Review.
Charcot-Marie-Tooth disease is the most common inherited neuromuscular disorder. There have been substantial advances in elucidating the molecular bases of this genetically heterogeneous neuropathy and, in most cases, molecular diagnosis is now possible. ...At prese …
Charcot-Marie-Tooth disease is the most common inherited neuromuscular disorder. There have been substantial advances in elucidating …
Hereditary Spastic Paraplegia: An Update.
Meyyazhagan A, Orlacchio A. Meyyazhagan A, et al. Int J Mol Sci. 2022 Feb 1;23(3):1697. doi: 10.3390/ijms23031697. Int J Mol Sci. 2022. PMID: 35163618 Free PMC article. Review.
Hereditary spastic paraplegia (HSP) is a rare neurodegenerative disorder with the predominant clinical manifestation of spasticity in the lower extremities. ...
Hereditary spastic paraplegia (HSP) is a rare neurodegenerative disorder with the predominant clinical manifestation of spasticity in
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.
PURPOSE OF REVIEW: This article provides an overview of Charcot-Marie-Tooth disease (CMT) and other inherited neuropathies. These disorders encompass a broad spectrum with variable motor, sensory, autonomic, and other organ system involvement. ...Emerging the …
PURPOSE OF REVIEW: This article provides an overview of Charcot-Marie-Tooth disease (CMT) and other inherited neuropathies. These dis …
Hereditary spastic paraplegia.
Murala S, Nagarajan E, Bollu PC. Murala S, et al. Neurol Sci. 2021 Mar;42(3):883-894. doi: 10.1007/s10072-020-04981-7. Epub 2021 Jan 13. Neurol Sci. 2021. PMID: 33439395 Review.
Hereditary spastic paraplegias (HSPs) are a group of neurodegenerative disorders which involve the corticospinal tracts and present with distinct spasticity and weakness of the lower extremities. ...
Hereditary spastic paraplegias (HSPs) are a group of neurodegenerative disorders which involve the corticospinal tracts and present w
Neurological update: hereditary neuropathies.
Kramarz C, Rossor AM. Kramarz C, et al. J Neurol. 2022 Sep;269(9):5187-5191. doi: 10.1007/s00415-022-11164-1. Epub 2022 May 21. J Neurol. 2022. PMID: 35596796 Free PMC article. Review.
In this update, we review the recent discovery of autosomal recessive variants in sorbitol dehydrogenase as one of the commonest and potentially treatable causes of hereditary motor neuropathy and CMT2. We also report on recent therapeutic advances in here
In this update, we review the recent discovery of autosomal recessive variants in sorbitol dehydrogenase as one of the commonest and potenti …
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 …
The Current State of Charcot-Marie-Tooth Disease Treatment.
Okamoto Y, Takashima H. Okamoto Y, et al. Genes (Basel). 2023 Jul 1;14(7):1391. doi: 10.3390/genes14071391. Genes (Basel). 2023. PMID: 37510296 Free PMC article. Review.
Charcot-Marie-Tooth disease (CMT) and associated neuropathies are the most predominant genetically transmitted neuromuscular conditions; however, effective pharmacological treatments have not established. ...
Charcot-Marie-Tooth disease (CMT) and associated neuropathies are the most predominant genetically transmitted neuromuscular conditio …
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. ...
Charcot-Marie-Tooth disease (CMT) is a slowly progressive hereditary degenerative disease and one of the most common ne …
1,151 results