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■ Abbreviation / Long Form : CMT1 / CMT type 1

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Total Number of Papers: 12
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Abbreviation:   CMT1  (>> Co-occurring Abbreviation)
Long Form:   CMT type 1
 Abbreviation Variation
 Long Form Variation
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No. Year Title Co-occurring Abbreviation
2022 Stance and swing phase ankle phenotypes in youth with Charcot-Marie-Tooth type 1: An evaluation using comprehensive gait analysis techniques. CMT
2021 Gait parameters as tools for analyzing phenotypic alterations of a mouse model of Charcot-Marie-Tooth disease. CMT, TrJ
2018 Characterising the phenotype and mode of inheritance of patients with inherited peripheral neuropathies carrying MME mutations. CMT2, dHMN, FALS
2016 Epidemiologic Study of Charcot-Marie-Tooth Disease: A Systematic Review. CMT, CMT2
2008 Capillary electrophoresis for the detection of PMP22 gene duplication: study in Mexican patients. CMT, PMP22
2008 [Charcot-Marie-Tooth disease]. CMT, HMSN, NT-3, PMP22
2004 Sensory manifestations in Charcot-Marie-Tooth disease. CMT, CMT2
2002 Molecular analysis in Japanese patients with Charcot-Marie-Tooth disease: DGGE analysis for PMP22, MPZ, and Cx32/GJB1 mutations. CMT, CMT2, DGGE, EGR2, MPZ, PMP22
1997 Mutational analysis of the MPZ, PMP22 and Cx32 genes in patients of Spanish ancestry with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies. CMT, CMT2, Cx32, DS, HNPP, MPZ, PMP22
10  1993 Localization of a gene (CMT2A) for autosomal dominant Charcot-Marie-Tooth disease type 2 to chromosome 1p and evidence of genetic heterogeneity. CMT
11  1993 Molecular analyses of unrelated Charcot-Marie-Tooth (CMT) disease patients suggest a high frequency of the CMTIA duplication. CMT, CMT, CMT2
12  1993 Molecular basis of Charcot-Marie-Tooth disease type 1A: gene dosage as a novel mechanism for a common autosomal dominant condition. CMT, CMT1A, CMT2