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Abbreviation : CMT1
Long Form : Charcot-Marie-Tooth neuropathy type 1
No. Year Title Co-occurring Abbreviation
2020 A Rare Case of Charcot-Marie-Tooth Disease Type 1C With an Unusual Presentation. CMT1C, EMG/NCS, LITAF, SIMPLE
2005 Genetic evaluation of inherited motor/sensory neuropathy. CMT2, Cx32, DSD, HMSNIII, HNPP, NDRG1, PMP22
2001 Charcot-Marie-Tooth disease type I and related demyelinating neuropathies: Mutation analysis in a large cohort of Italian families. EGR2, MPZ, PMP22
2001 Molecular basis of hereditary neuropathies. CMT2, CMT2A, DSD, HMSNIII, HNPP, PMP22
2000 Inherited peripheral neuropathy. CMT1A, CMT2, CMT2A, DSD, EGR2, HMSNIII, HNPP, PMP22
1999 Inherited neuropathies: from gene to disease. CMT2, CMT2A, DSD, HMSNIII, HNPP, PMP22
1995 [Mutation of the myelin Po gene in hereditary motor and sensory neuropathy]. CMT1A, PMP22, Po
1994 Inherited neuropathies: Charcot-Marie-Tooth disease and related disorders. CMT2, CMT2A, HNPP, PMP22
1994 Molecular genetics of Charcot-Marie-Tooth disease and related neuropathies. CMT2A, HMSNIII, HNPP, Mb, PMP22
10  1993 New mutation of the myelin P0 gene in a pedigree of Charcot-Marie-Tooth neuropathy 1. Ig
11  1992 Analysis of the DNA duplication 17p11.2 in Charcot-Marie-Tooth neuropathy type 1 pedigrees: additional evidence for a third autosomal CMT1 locus. ---
12  1989 Heterogeneity evidence and linkage studies on Charcot-Marie-Tooth disease. ---
13  1988 Chromosome I linkage studies in Charcot-Marie-Tooth neuropathy type I. NGFB, REN