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1 gative first-degree relatives who were never autoantibody positive.
2 wly diagnosed IDDM patients tested were IA-2 autoantibody positive.
3 ually diminished in alpha-cells of NOD mice, autoantibody-positive (AA(+)) and overtly type 1 diabeti
5 time in situ, that in pancreas sections from autoantibody-positive (Ab+) donors, insulin area and bet
6 e predictive power of autoantibodies because autoantibody-positive (AbP) children have heterogeneous
8 (HLA) alleles for anti-citrullinated-protein-autoantibody-positive (ACPA(+)) rheumatoid arthritis (RA
9 e polymorphisms (SNPs) were genotyped in 556 autoantibody-positive African Americans with RA and 791
13 be useful in predicting disease severity in autoantibody-positive and autoantibody-negative patients
14 ucleatum) were significantly associated with autoantibody-positive and high-risk status (P < 0.05).
15 ears, associations that were evident both in autoantibody-positive and in autoantibody-negative disea
17 n of CD8 T cells in pancreata from T1D, T2D, autoantibody-positive, and healthy control subjects.
18 in children with newly diagnosed T1D and in autoantibody-positive at-risk children with impaired glu
19 atives followed to diabetes were ICA512/IA-2 autoantibody-positive but anti-phogrin autoantibody-nega
21 ntribute to type 1 diabetes (T1D) risk among autoantibody-positive children in The Environmental Dete
22 tetramer staining in 6 patients and 10 islet autoantibody-positive children showed large diversity wi
24 gnificantly higher in pretransplantation GAD autoantibody-positive daclizumab-treated recipients comp
26 hat T1D is more similar genetically to other autoantibody-positive diseases, significantly most simil
27 levels of interleukin-4 (IL-4) in anti-islet autoantibody-positive first-degree relatives of patients
28 complement factor H-related (CFHR) genes and autoantibody-positive form of hemolytic uremic syndrome
29 ons were higher in high-risk (P = 0.011) and autoantibody positive group (P = 0.010) than in the auto
30 alysis suggested that the gut microbiomes of autoantibody-positive individuals and seronegative FDRs
31 beta-cells in pancreatic sections from GAD65 autoantibody-positive individuals who have not yet progr
32 ide association study meta-analysis of 5,539 autoantibody-positive individuals with rheumatoid arthri
34 ed whether immunoglobulin G from aquaporin-4-autoantibody-positive neuromyelitis optica patients has
35 antibodies on 2 consecutive visits and still autoantibody positive or having diabetes at last follow-
36 h focal accumulation in the muscle fibers of autoantibody-positive patients compared with a homogeneo
38 estive evidence of a stronger association in autoantibody-positive patients with RA (OR 0.55, 95% con
39 king is associated not only with the risk of autoantibody-positive RA but also with the risk of autoa
41 of 33 [42%]; 3.8+/-4.5 at 10 microg/ml) and autoantibody-positive relatives at increased risk for ID
42 l insulin delays onset of type 1 diabetes in autoantibody-positive relatives of patients with type 1
46 ritis in an independent replication of 3,929 autoantibody-positive rheumatoid arthritis cases and 5,8
47 toantibodies in 88 dual (ICA512 and phogrin) autoantibody-positive sera could be completely blocked b
51 valence and type of lung abnormalities among autoantibody-positive subjects were similar to those amo
53 e consistent with inflammation are common in autoantibody-positive subjects without inflammatory arth
54 lls in early stages of T1D (i.e., in healthy autoantibody-positive subjects) and in more advanced pha
56 iagnosed patients ages 1-18 years with islet autoantibody-positive type 1 diabetes (n = 970) and cont
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