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Abbreviation: FECH
Appearance Frequency: 158 time(s)
Long forms: 6

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Long Form No. Long Form Research Area Co-occurring Abbreviation PubMed/MEDLINE Info. (Year, Title)
ferrochelatase
(140 times)
Biochemistry
(26 times)
EPP (65 times)
PpIX (38 times)
ALA (10 times)
1991 Assignment of the human ferrochelatase gene (FECH) and a locus for protoporphyria to chromosome 18q22.
ferrochelatase gene
(9 times)
Dermatology
(3 times)
EPP (7 times)
dPCR (1 time)
FEP (1 time)
1991 Assignment of the human ferrochelatase gene (FECH) and a locus for protoporphyria to chromosome 18q22.
18F-fluoroethylcholine
(4 times)
Diagnostic Imaging
(1 time)
SUV (2 times)
CT (1 time)
FDG (1 time)
2013 [Application of positron-emission tomography-magnetic resonance imaging fusion in biopsy and resection of gliomas].
Further Enabling Care at Home
(3 times)
Medicine
(1 time)
ED (1 time)
2018 Hospital postdischarge intervention trialled with family caregivers of older people in Western Australia: potential translation into practice.
ferrochelatase activity
(1 time)
Genetics, Medical
(1 time)
EPP (1 time)
PCR (1 time)
1995 Human ferrochelatase: a novel mutation in patients with erythropoietic protoporphyria and an isoform caused by alternative splicing.
ferrochelatase-encoding gene
(1 time)
Dermatology
(1 time)
EP (1 time)
EPP (1 time)
XLDPP (1 time)
2015 X-linked dominant protoporphyria: The first reported Japanese case.