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■ Search Result - Abbreviation : CMT2

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Abbreviation: CMT2
Appearance Frequency: 98 time(s)
Long forms: 11

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Long Form No. Long Form Research Area Co-occurring Abbreviation PubMed/MEDLINE Info. (Year, Title)
Charcot-Marie-Tooth disease type 2
(47 times)
Neurology
(29 times)
dHMN (6 times)
MFN2 (5 times)
MPZ (4 times)
1997 Mutilating neuropathic ulcerations in a chromosome 3q13-q22 linked Charcot-Marie-Tooth disease type 2B family.
Charcot-Marie-Tooth type 2
(18 times)
Neurology
(11 times)
HSP (6 times)
Mfn2 (4 times)
ALS (3 times)
2006 MFN2 mutation distribution and genotype/phenotype correlation in Charcot-Marie-Tooth type 2.
CMT type 2
(17 times)
Neurology
(8 times)
CMT (15 times)
CMT1 (7 times)
PMP22 (4 times)
1993 Molecular analyses of unrelated Charcot-Marie-Tooth (CMT) disease patients suggest a high frequency of the CMTIA duplication.
Charcot-Marie-Tooth neuropathy type 2
(8 times)
Neurology
(4 times)
CMT1 (5 times)
HNPP (5 times)
PMP22 (5 times)
1994 Inherited neuropathies: Charcot-Marie-Tooth disease and related disorders.
chromomethylase2
(2 times)
Science
(1 time)
CMT3 (1 time)
DRM2 (1 time)
IDN2 (1 time)
2014 SNF2 chromatin remodeler-family proteins FRG1 and -2 are required for RNA-directed DNA methylation.
Charcot-Marie-Tooth disease with normal or near-normal MNCV, i.e. type 2
(1 time)
Neurology
(1 time)
MNCV (1 time)
1998 Charcot-Marie-Tooth disease--muscle biopsy findings in relation to neurophysiology.
Charcot-Marie-Tooth type 2 disease
(1 time)
Genetics, Medical
(1 time)
CMT (1 time)
2004 A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2L) maps to chromosome 12q24.
Charcot-Marie-Tooth type 2 family
(1 time)
Neurology
(1 time)
--- 2001 Further evidence that neurofilament light chain gene mutations can cause Charcot-Marie-Tooth disease type 2E.
CMT disease type 2
(1 time)
Neurology
(1 time)
CMT (1 time)
DRG (1 time)
JNK (1 time)
2010 The mood stabilizer valproic acid improves defective neurite formation caused by Charcot-Marie-Tooth disease-associated mutant Rab7 through the JNK signaling pathway.
10  CMT, and type 2
(1 time)
Neurology
(1 time)
CMT (1 time)
Cx32 (1 time)
DSS (1 time)
1995 [Genetics of peripheral neuropathies and hereditary ataxias].
11  conduction velocities and by onion bulb formation: type 2
(1 time)
Medicine
(1 time)
CMT (1 time)
CMT1A (1 time)
PMP22 (1 time)
1996 [Molecular basis of Charcot-Marie-Tooth neuropathy].