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Abbreviation: FECH
Appearance Frequency: 158 time(s)
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Long Form No. Long Form Research Area Co-occurring Abbreviation PubMed/MEDLINE Info. (Year, Title)
1  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.
2  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.
3  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].
4  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.
5  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.
6  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.