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1 , which is implicated in the pathogenesis of familial Mediterranean fever.
2 e site of mutants causing Opitz syndrome and familial Mediterranean fever.
3 may be a component of the pathophysiology of familial Mediterranean fever.
4 M20 is affected by mutations associated with familial Mediterranean fever.
6 rin-associated periodic syndromes (CAPS) and familial Mediterranean fever, 2 archetypical monogenic a
7 for pericarditis, as well as a basic part of familial Mediterranean fever and Behcet's disease manage
8 F-receptor-associated periodic syndrome, and familial Mediterranean fever and cryopyrin-associated pe
9 of inflammation, such as those that underlie familial Mediterranean fever and other autoinflammatory
10 al, genetic and pathophysiologic findings of familial Mediterranean fever and several of the other sy
11 is, Crohn's disease, ankylosing spondylitis, familial Mediterranean fever, and Castleman's disease.
12 ted, inflammatory bowel disease, malignancy, familial Mediterranean Fever, and the rarer connective t
14 Y domain causes the autoinflammatory disease familial Mediterranean fever by assembling an ASC-depend
15 hich is known to cause recessively inherited familial Mediterranean fever, conferred BD risk in the T
17 L-1beta)-mediated autoinflammatory diseases: familial Mediterranean fever (FMF) and hyperimmunoglobul
19 h chronic periodontitis (CP) who experienced familial Mediterranean fever (FMF) and their response to
20 r-IgD and periodic fever syndrome (HIDS) and familial Mediterranean fever (FMF) are both characterize
35 tiology of recurrent attacks of serositis in familial Mediterranean fever (FMF) is not completely und
39 proven alternative therapy for patients with familial Mediterranean fever (FMF) that is resistant to
40 e of kidney transplantation in patients with familial Mediterranean fever (FMF) who reach end-stage r
41 mid contig spanning the candidate region for familial Mediterranean fever (FMF), a recessively inheri
42 ed genetic mapping data for the gene causing familial Mediterranean fever (FMF), a recessively inheri
43 n the C-terminal B30.2 domain of pyrin cause familial Mediterranean fever (FMF), the most common Mend
44 During the course of cloning the gene for familial Mediterranean fever (FMF), we identified a numb
52 d periodic syndrome on chromosome 12p13, the familial Mediterranean fever locus (MEFV) on chromosome
53 re, we demonstrate that PSTPIP1 requires the familial Mediterranean fever protein pyrin to assemble t
55 gene (MEFV) cause the inflammatory disorder familial Mediterranean fever, pyrin is believed to regul
60 e hereditary recurrent fevers, which include familial Mediterranean fever, the tumor necrosis factor
61 classic hereditary periodic fever syndromes (familial Mediterranean fever, TNF receptor-associated pe
62 ough this complication is well recognized in familial Mediterranean fever, tumor necrosis factor rece
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