Classification of the hereditary motor and sensory neuropathies
- PMID: 11073363
- DOI: 10.1097/00019052-200010000-00009
Classification of the hereditary motor and sensory neuropathies
Similar articles
-
[Hereditary motor-sensory neuropathies (Charcot-Marie-Tooth syndrome) and related neuropathies. Current classification and genotype-phenotype correlation].Nervenarzt. 1999 Dec;70(12):1052-61. doi: 10.1007/s001150050539. Nervenarzt. 1999. PMID: 10637810 Review. German.
-
Hereditary motor and sensory neuropathies or Charcot-Marie-Tooth diseases: an update.J Neurol Sci. 2014 Dec 15;347(1-2):14-22. doi: 10.1016/j.jns.2014.10.013. Epub 2014 Oct 16. J Neurol Sci. 2014. PMID: 25454638 Review.
-
The dominantly inherited motor and sensory neuropathies: clinical and molecular advances.Muscle Nerve. 2006 May;33(5):589-97. doi: 10.1002/mus.20477. Muscle Nerve. 2006. PMID: 16392117 Review.
-
[Genetics of neuropathies].Nervenarzt. 2013 Feb;84(2):157-65. doi: 10.1007/s00115-012-3640-4. Nervenarzt. 2013. PMID: 23325310 Review. German.
-
Linkage analysis of distal hereditary motor neuropathy type II (distal HMN II) in a single pedigree.J Neurol Sci. 1992 May;109(1):41-8. doi: 10.1016/0022-510x(92)90091-x. J Neurol Sci. 1992. PMID: 1517763
Cited by
-
Role of immune cells in animal models for inherited neuropathies: facts and visions.J Anat. 2002 Apr;200(4):405-14. doi: 10.1046/j.1469-7580.2002.00045.x. J Anat. 2002. PMID: 12090406 Free PMC article. Review.
-
Investigation of Mutations in Exon 14 of SH3TC2 Gene and Exon 7 of NDRG1 Gene in Iranian Charcot-Marie-Tooth Disease Type 4 (CMT4D) Patients.Iran J Child Neurol. 2020 Spring;14(2):93-100. Iran J Child Neurol. 2020. PMID: 32256628 Free PMC article.
-
Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse.Am J Hum Genet. 2002 Mar;70(3):726-36. doi: 10.1086/339274. Epub 2002 Jan 17. Am J Hum Genet. 2002. PMID: 11799477 Free PMC article.
-
Neurology and orthopaedics.J Neurol Neurosurg Psychiatry. 2007 Mar;78(3):224-32. doi: 10.1136/jnnp.2006.092072. J Neurol Neurosurg Psychiatry. 2007. PMID: 17308288 Free PMC article. Review.
-
Molecular genetics of autosomal-dominant demyelinating Charcot-Marie-Tooth disease.Neuromolecular Med. 2006;8(1-2):43-62. doi: 10.1385/nmm:8:1-2:43. Neuromolecular Med. 2006. PMID: 16775366 Review.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources