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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 with the autoinflammatory disorder familial Mediterranean fever.
5 component of the pathophysiology of familial Mediterranean fever.
6 ases, including gouty arthritis and familial Mediterranean fever.
7 agent in diseases such as gout and familial Mediterranean fever.
9 iated periodic syndromes (CAPS) and familial Mediterranean fever, 2 archetypical monogenic autoinflam
10 ical features and pathogenesis with familial Mediterranean fever, although it is a clinically distinc
11 issense mutation predicted to cause familial Mediterranean fever, an autoinflammatory disorder highly
12 arditis, as well as a basic part of familial Mediterranean fever and Behcet's disease management.
13 r-associated periodic syndrome, and familial Mediterranean fever and cryopyrin-associated periodic sy
14 polysaccharide shock and alleviates familial Mediterranean fever and experimental autoimmune encephal
15 mation, such as those that underlie familial Mediterranean fever and other autoinflammatory diseases,
16 ic and pathophysiologic findings of familial Mediterranean fever and several of the other systemic au
18 ammatory bowel disease, malignancy, familial Mediterranean Fever, and the rarer connective tissue dis
19 positive evolutionary selection of familial Mediterranean fever-associated genetic variants might be
21 causes the autoinflammatory disease familial Mediterranean fever by assembling an ASC-dependent infla
22 nown to cause recessively inherited familial Mediterranean fever, conferred BD risk in the Turkish po
23 of the most common AIDs, including familial Mediterranean fever, cryopyrin-associated periodic syndr
25 mediated autoinflammatory diseases: familial Mediterranean fever (FMF) and hyperimmunoglobulinemia D
26 autoinflammatory disorders, such as familial Mediterranean fever (FMF) and Pyrin-associated autoinfla
28 periodontitis (CP) who experienced familial Mediterranean fever (FMF) and their response to non-surg
29 periodic fever syndrome (HIDS) and familial Mediterranean fever (FMF) are both characterized by atta
45 f recurrent attacks of serositis in familial Mediterranean fever (FMF) is not completely understood.
48 le for the autoinflammatory disease Familial Mediterranean Fever (FMF) map to exon 10 encoding the B3
50 ternative therapy for patients with familial Mediterranean fever (FMF) that is resistant to or intole
51 ey transplantation in patients with familial Mediterranean fever (FMF) who reach end-stage renal dise
52 g spanning the candidate region for familial Mediterranean fever (FMF), a recessively inherited disor
53 c mapping data for the gene causing familial Mediterranean fever (FMF), a recessively inherited disor
56 erminal B30.2 domain of pyrin cause familial Mediterranean fever (FMF), the most common Mendelian aut
57 the course of cloning the gene for familial Mediterranean fever (FMF), we identified a number of tra
58 tcome of transplant recipients with familial Mediterranean fever (FMF)-associated AA amyloidosis.
59 tcome of transplant recipients with familial Mediterranean fever (FMF)-associated AA amyloidosis.
64 ariants in MEFV (Mendelian gene for Familial Mediterranean Fever [FMF]) were found in 6 MGBB particip
71 c syndrome on chromosome 12p13, the familial Mediterranean fever locus (MEFV) on chromosome 16p13, th
72 oinflammatory disease caused by mutations of Mediterranean fever (MEFV) encoding pyrin and characteri
73 racts with PYRIN, the protein encoded by the Mediterranean Fever (MEFV) gene whose mutations cause Fa
75 tic analysis of responsible gene of familial Mediterranean fever, MEFV showed E148Q heterozygous muta
76 monstrate that PSTPIP1 requires the familial Mediterranean fever protein pyrin to assemble the ASC py
78 FV) cause the inflammatory disorder familial Mediterranean fever, pyrin is believed to regulate IL-1b
83 icine more broadly, with studies of familial Mediterranean fever, the most common autoinflammatory di
84 ary recurrent fevers, which include familial Mediterranean fever, the tumor necrosis factor receptor-
85 ereditary periodic fever syndromes (familial Mediterranean fever, TNF receptor-associated periodic sy
86 complication is well recognized in familial Mediterranean fever, tumor necrosis factor receptor-asso