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1 d by an autosomal dominant inheritance and a young onset.
2 ide linkage scan in Pima Indians indicated a young-onset (aged <45 years) type 2 diabetes susceptibil
3 rich variation in phenotypes among cases of young-onset amyotrophic lateral sclerosis, bulbar onset
6 utations and determine their contribution in young-onset and more typical later onset Parkinson's dis
7 of African ancestry are more likely to have young-onset and oestrogen receptor (ER) negative breast
9 neuron disease with TDP-43 type B pathology; young-onset behavioural variant frontotemporal dementia
11 se was inversely associated with the risk of young-onset breast cancer (odds ratio = 0.58, 95% confid
12 was not associated with an increased risk of young-onset breast cancer (odds ratio = 0.80, 95% confid
13 proven in 1990 by mapping predisposition to young-onset breast cancer in families to chromosome 17q2
14 us progestin HT or unopposed estrogen HT and young-onset breast cancer using data from the Two Sister
15 eria or prediction models; isolated sporadic young-onset cases can be prescreened by tumor testing, w
16 % of controls versus 15% of cases and 20% of young-onset cases, both highly significant differences.
17 ants were 13102 patients diagnosed as having young-onset colon adenocarcinoma aged 18 to 49 years and
23 se may be more important in the aetiology of young-onset dementia than previously believed, and is of
25 mutation (p.G1117E) in the PASK gene from a young-onset diabetes family, which modulates glucose-sti
26 majority (438/597 (73%)) with other types of young-onset diabetes had an HbA1c above the upper limit
28 ine diabetes exposure or parental history of young-onset diabetes increased a child's absolute risk o
29 ibility, a genome-wide association study for young-onset diabetes was conducted in an American-Indian
30 chanisms and is therefore valid for studying young-onset disease in which genotype does not influence
35 with an apparent autosomal recessive, novel, young-onset, generalised form of dystonia parkinsonism.
36 vealed a far higher proportion of cases with young onset (>50%), with a steady decline to the contemp
37 n 10 years (89.4% vs. 76.8%), especially for young-onset HCCs <50 years (79.4% vs. 40.6%), under slig
38 wing it is also present in two patients with young-onset Huntington's disease (26 and 40 years old at
39 runcating FANCG mutations were identified in young onset (<55 years) pancreatic cancer cases with no
40 of familial aggregation of lung cancer among young onset (<or=55 years of age) lung cancer cases.
41 of primary progressive aphasia (naPPA) is a young-onset neurodegenerative disorder characterised by
43 I has a clear impact on the investigation of young-onset or complex dementia while reducing the overa
47 ive early-onset or juvenile parkinsonism and young-onset Parkinson's disease and also had similaritie
48 ith a fairly pure parkinsonian syndrome (eg, young-onset Parkinson's disease; YOPD) are due to typica
50 T serially to study members of a family with young-onset parkinsonism who are compound heterozygous f
54 .76, 95% confidence interval: 1.43, 2.15) or young-onset prostatitis (adjusted OR = 1.55, 95% confide
55 istories of sexually transmitted infections, young-onset prostatitis, and frequency of ejaculation, w
57 first description of a pathologically proved young-onset tauopathy with apparent recessive inheritanc
58 mutation from unaffected family members and young-onset type 1 (T1D) and type 2 diabetes (T2D) and t
60 s of the young (MODY), and 463 patients with young-onset type 2 diabetes (nonobese, diagnosed <45 yea
61 /A variant in the 3'-UTR was associated with young-onset type 2 diabetes (odds ratio 2.09 per copy of
62 this variant, were nominally associated with young-onset type 2 diabetes (P = 0.01; odds ratio 3.39)
63 an age, 52.2 years), and 83 individuals with young-onset type 2 diabetes (YT2D), diagnosed at age 45
65 Furthermore, evidence is accumulating that young-onset type 2 diabetes has a more aggressive diseas
67 8M substitution identified in a patient with young-onset type 2 diabetes may be a rare nonfunctional
68 irm our hypothesis that families segregating young-onset type 2 diabetes represent a more powerful re
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