A Search Service for Abbreviation / Long Form

■ Search Result - Abbreviation : PMP22

Search Conditions:
Search Keyword : PMP22
Search Method : Exact match.
Research Area:

Results:  
Abbreviation: PMP22
Appearance Frequency: 428 time(s)
Long forms: 6

Display Settings:
[Entries Per Page]
 per page
Page Control
Page: of
Long Form No. Long Form Research Area Co-occurring Abbreviation PubMed/MEDLINE Info. (Year, Title)
peripheral myelin protein 22
(423 times)
Neurology
(221 times)
HNPP (90 times)
CMT1A (77 times)
CMT (68 times)
1992 The peripheral myelin protein gene PMP-22 is contained within the Charcot-Marie-Tooth disease type 1A duplication.
myelinopathies-peripheral myelin protein 22
(1 time)
Physiology
(1 time)
CH (1 time)
CMT (1 time)
Cx32 (1 time)
1999 Charcot-marie-tooth disease and related neuropathies: molecular basis for distinction and diagnosis.
peripheral membrane protein 22
(1 time)
Neurology
(1 time)
CNS (1 time)
Cx32 (1 time)
MAG (1 time)
2000 Myelin basic protein gene dosage effects in the PNS.
PMP22 Del HNPP
(1 time)
Rare Diseases
(1 time)
CI (1 time)
CNV (1 time)
HNPP (1 time)
2018 Frequency of hereditary neuropathy with liability to pressure palsies (HNPP) due to 17p11.2 deletion in a Korean newborn population.
PMP22tg
(1 time)
Neurology
(1 time)
CMT1A (1 time)
DRG (1 time)
2001 PMP22 transgenic dorsal root ganglia cultures show myelin abnormalities similar to those of human CMT1A.
Point mutations in peripheral myelin gene 22
(1 time)
Genetics, Medical
(1 time)
CMT1 (1 time)
Cx32 (1 time)
HNPP (1 time)
2001 Mutational analysis and genotype/phenotype correlation in Turkish Charcot-Marie-Tooth Type 1 and HNPP patients.