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1 tinal stromal tumor (GIST) in the setting of nonhereditary and hereditary multiple tumor syndromes co
2 topic dermatitis, food allergies, urticaria, nonhereditary angioedema, systemic anaphylaxis, and alle
3 reditary cancer patients survive longer than nonhereditary cancer patients.
4 drenal tumors have also been associated with nonhereditary Carney's triad.
5 in most respects, are indistinguishable from nonhereditary cases.
6 protein A-1 (ApoA-1) amyloidosis occurs as a nonhereditary condition in atherosclerotic plaques, but
7 who experienced relapse was matched with two nonhereditary controls.
8 nts younger than age 50 years diagnosed with nonhereditary CRC were included.
9 broblast lines derived from individuals with nonhereditary CRC.
10 blastoma survivors (1,020 hereditary and 831 nonhereditary) diagnosed during 1914-2006.
11 y the same factors that influence therapy of nonhereditary disease.
12 malies (CLOVES) is a sporadically occurring, nonhereditary disorder characterized by asymmetric somat
13  from our database and matched (1:2) with 44 nonhereditary EOC controls (defined by no associated per
14 itive EOC patients have better outcomes than nonhereditary EOC patients.
15 her genes, and those whose disease is due to nonhereditary factors or chance.
16 CA diagnoses, predominantly of the wild-type nonhereditary form, which is now the most commonly diagn
17 cers had improved survival compared with the nonhereditary group (P=.004).
18  primary chemotherapy in comparison with the nonhereditary group, with a median time to recurrence of
19 s progressiva (FOP), another genetic HO, and nonhereditary HO mouse models.
20                                     Stellate nonhereditary idiopathic foveomacular retinoschisis (SNI
21                                     Stellate nonhereditary idiopathic foveomacular retinoschisis cont
22                                     Stellate nonhereditary idiopathic foveomacular retinoschisis with
23 t/beta-catenin pathway is a prerequisite for nonhereditary intestinal tumorigenesis, we asked whether
24 atic filariasis is the major global cause of nonhereditary lymphedema.
25                              Sporadic (i.e., nonhereditary) manifestations of several tumor types, in
26                              The epigenetic (nonhereditary) mechanism of hMLH1 promoter hypermethylat
27 tients (80 patients with hereditary, 25 with nonhereditary or unknown cerebellar ataxia).
28 tary (suspected or genetically confirmed) or nonhereditary or unknown type presenting with a total sc
29 stratified by disease subtype (hereditary vs nonhereditary or unknown) and site.
30 ereditary and 5.7% (95% CI, 2.4% to 11%) for nonhereditary patients.
31 cidence of a new cancer after hereditary and nonhereditary Rb and radiotherapy was calculated with ad
32 ; 95% CI, 16 to 21) exceeded the risk in 638 nonhereditary Rb patients (SIR, 1.2; 95% CI, 0.7 to 2.0)
33 erved number of cancers after hereditary and nonhereditary Rb to the expected number from the Connect
34  for hereditary RCC overlapped with those of nonhereditary RCC, and the prevalence of other associate
35 verlapping with the radiologic appearance of nonhereditary RCCs.
36 y tumors that occur at a younger age than do nonhereditary renal cancers.
37 mplications for understanding the origins of nonhereditary renal tumors.
38 itary retinoblastoma, and 5.0% (+/-3.0%) for nonhereditary retinoblastoma.
39 irus (cCMV) is the major cause of congenital nonhereditary sensorineural hearing loss in children.
40 MV) infection is a major cause of congenital nonhereditary sensorineural hearing loss.
41  follow-up through 2016, 33 hereditary and 7 nonhereditary survivors developed melanoma, and 26 hered
42  developed melanoma, and 26 hereditary and 9 nonhereditary survivors developed NMSC.
43 was 4.5% for melanoma and 3.7% for NMSC; for nonhereditary survivors, it was 0.7% and 1.5%, respectiv
44 at occurred earlier than that observed among nonhereditary survivors, likely reflecting genetic facto
45 ounger among hereditary survivors than among nonhereditary survivors.
46 how acquired mutation in several sporadic or nonhereditary tumors-parathyroid adenomas, gastrinomas,
47 ateral prophylactic mastectomy in women with nonhereditary, unilateral breast cancer requires a socia