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1 fected by mutations associated with familial Mediterranean fever.
2 s implicated in the pathogenesis of familial Mediterranean fever.
3 mutants causing Opitz syndrome and familial Mediterranean fever.
4 component of the pathophysiology of familial Mediterranean fever.
6 iated periodic syndromes (CAPS) and familial Mediterranean fever, 2 archetypical monogenic autoinflam
8 r-associated periodic syndrome, and familial Mediterranean fever and cryopyrin-associated periodic sy
9 mation, such as those that underlie familial Mediterranean fever and other autoinflammatory diseases,
10 ic and pathophysiologic findings of familial Mediterranean fever and several of the other systemic au
12 ammatory bowel disease, malignancy, familial Mediterranean Fever, and the rarer connective tissue dis
14 causes the autoinflammatory disease familial Mediterranean fever by assembling an ASC-dependent infla
15 nown to cause recessively inherited familial Mediterranean fever, conferred BD risk in the Turkish po
17 mediated autoinflammatory diseases: familial Mediterranean fever (FMF) and hyperimmunoglobulinemia D
19 periodontitis (CP) who experienced familial Mediterranean fever (FMF) and their response to non-surg
20 periodic fever syndrome (HIDS) and familial Mediterranean fever (FMF) are both characterized by atta
35 f recurrent attacks of serositis in familial Mediterranean fever (FMF) is not completely understood.
39 ternative therapy for patients with familial Mediterranean fever (FMF) that is resistant to or intole
40 ey transplantation in patients with familial Mediterranean fever (FMF) who reach end-stage renal dise
41 g spanning the candidate region for familial Mediterranean fever (FMF), a recessively inherited disor
42 c mapping data for the gene causing familial Mediterranean fever (FMF), a recessively inherited disor
43 erminal B30.2 domain of pyrin cause familial Mediterranean fever (FMF), the most common Mendelian aut
44 the course of cloning the gene for familial Mediterranean fever (FMF), we identified a number of tra
54 c syndrome on chromosome 12p13, the familial Mediterranean fever locus (MEFV) on chromosome 16p13, th
55 oinflammatory disease caused by mutations of Mediterranean fever (MEFV) encoding pyrin and characteri
56 racts with PYRIN, the protein encoded by the Mediterranean Fever (MEFV) gene whose mutations cause Fa
57 monstrate that PSTPIP1 requires the familial Mediterranean fever protein pyrin to assemble the ASC py
59 FV) cause the inflammatory disorder familial Mediterranean fever, pyrin is believed to regulate IL-1b
64 ary recurrent fevers, which include familial Mediterranean fever, the tumor necrosis factor receptor-
65 ereditary periodic fever syndromes (familial Mediterranean fever, TNF receptor-associated periodic sy
66 complication is well recognized in familial Mediterranean fever, tumor necrosis factor receptor-asso
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