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1 erleukin-1 receptor antagonist used to treat autoinflammatory disorders.
2 implicated in the pathogenesis of hereditary autoinflammatory disorders.
3 ts of systemic inflammation in patients with autoinflammatory disorders.
4 ction and predispose individuals to specific autoinflammatory disorders.
5 rial rash, such as urticarial vasculitis and autoinflammatory disorders.
6 que IFN signaling signature, unlike in other autoinflammatory disorders.
7 ich places these entities in the category of autoinflammatory disorders.
8 ng of caspase-1 inhibitors such as VX-765 in autoinflammatory disorders.
9 e have been recently linked to three chronic autoinflammatory disorders.
10 ar connection between two seemingly distinct autoinflammatory disorders.
11 disrupt nucleic acid metabolism can lead to autoinflammatory disorders.
12 infections, malignancies, or autoimmune and autoinflammatory disorders.
13 n and features prominently in autoimmune and autoinflammatory disorders, allergy, acute and chronic i
15 g the distinguishing features of the classic autoinflammatory disorders, and appreciating the treatme
17 s well as the pathogenesis of autoimmune and autoinflammatory disorders, and serves to link adaptive
19 immunological reclassification of SJIA as an autoinflammatory disorder as well as detailing the drama
21 ase 1 (ERAP1), Hap10, is associated with the autoinflammatory disorder Behcet's disease (BD) in epist
22 tor-associated periodic syndrome (TRAPS), an autoinflammatory disorder caused by missense mutations i
23 involvement is a defining characteristic of autoinflammatory disorders caused by abnormal IL-1 signa
24 Blau syndrome is a rare, autosomal-dominant, autoinflammatory disorder characterized by granulomatous
25 TRAPS, OMIM 142680) is an autosomal dominant autoinflammatory disorder characterized by prolonged att
26 al Mediterranean Fever (FMF) is an inherited autoinflammatory disorder characterized by unprovoked ep
27 the gene encoding NLRP3 are associated with autoinflammatory disorders characterized with excessive
28 the gene encoding pyrin are associated with autoinflammatory disorder Familial Mediterranean Fever (
29 ense mutations in the CIAS1 gene cause three autoinflammatory disorders: familial cold autoinflammato
31 cal clues and tips that can help to identify autoinflammatory disorders in patients presenting with c
32 sum, and acne (PAPA), a dominantly inherited autoinflammatory disorder mediated predominantly by gran
33 inflammatory syndrome (FCAS) and the related autoinflammatory disorders, Muckle-Wells syndrome and ne
34 LP3/CIAS1/cryopyrin gene are linked to three autoinflammatory disorders: Muckle-Wells syndrome, famil
36 ed, inflammation may result in autoimmune or autoinflammatory disorders, neurodegenerative disease, o
37 function are the most frequent cause of this autoinflammatory disorder of childhood and are also asso
40 t multifocal osteomyelitis (CRMO) is a human autoinflammatory disorder that primarily affects bone.
41 The cryopyrinopathies are a group of rare autoinflammatory disorders that are caused by mutations
42 s (PFSs) comprise a subset of the hereditary autoinflammatory disorders that are defined by recurrent
44 ells syndrome (MWS) are dominantly inherited autoinflammatory disorders that cause rashes, fever, art
45 urther underscored by their association with autoinflammatory disorders, wherein localized inflammati
46 l Mediterranean fever (FMF) is an archetypal autoinflammatory disorder, which is autosomal recessive
47 anean fever (FMF) is a recessively inherited autoinflammatory disorder with high carrier frequencies
48 thogenesis of pustular psoriasis, a model of autoinflammatory disorders with predominant cutaneous ma
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