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1 1Glu mutant, linked to Crouzon syndrome with acanthosis nigricans.
2 istance, diabetes mellitus, dyslipidemia and acanthosis nigricans.
3 ore, lack of running water, insulin use, and acanthosis nigricans.
4 All patients have widespread, early-onset acanthosis nigricans.
5 the mild phenotype in Crouzon syndrome with Acanthosis Nigricans.
6 the genetic cause for Crouzon syndrome with Acanthosis Nigricans.
7 facial features, and atypical and extensive acanthosis nigricans.
9 of 268] vs 40.4% [19 of 47], P = .004), and acanthosis nigricans (AN) (36.9% [89 of 241] vs 20.0% [9
10 R2 Y394C mutation evidenced by cutis gyrata, acanthosis nigricans, and craniosynostosis and provides
11 ory diseases (such as atopic dermatitis), in acanthosis nigricans, as an extension of epidermal nevus
13 our individuals developed extensive areas of acanthosis nigricans beginning in early childhood, suffe
15 paraneoplastic syndromes such as xanthomas, acanthosis nigricans, carcinoid syndrome, unusual erythe
16 the furrowed skin disorder of cutis gyrata, acanthosis nigricans, craniosynostosis, craniofacial dys
17 try; secondary outcomes were the presence of acanthosis nigricans, dietary intake derived from 2 days
22 and accompanied by other features, including acanthosis nigricans, organomegaly, hyperandrogenism, an
23 (d = -1.64 [95% CI, -2.87 to -0.41] cm), and acanthosis nigricans prevalence (d = -3.55% [95% CI, -6.
24 ofacial malformations, Crouzon syndrome with acanthosis nigricans results in characteristic cutaneous
25 achondroplasia with developmental delay and acanthosis nigricans (SADDAN), are associated with gluta
26 achondroplasia with developmental delay and acanthosis nigricans" (SADDAN) because it differs signif
27 achondroplasia with developmental delay and acanthosis nigricans) syndrome and thanatophoric dysplas
28 35, those of Hispanic ethnicity, those with acanthosis nigricans, those who had tried and failed die
29 The prevalence of overweight, obesity, and acanthosis nigricans was further reduced in communities,