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1 1Glu mutant, linked to Crouzon syndrome with acanthosis nigricans.
2 istance, diabetes mellitus, dyslipidemia and acanthosis nigricans.
3 All patients have widespread, early-onset acanthosis nigricans.
4 the mild phenotype in Crouzon syndrome with Acanthosis Nigricans.
5 the genetic cause for Crouzon syndrome with Acanthosis Nigricans.
6 facial features, and atypical and extensive acanthosis nigricans.
8 of 268] vs 40.4% [19 of 47], P = .004), and acanthosis nigricans (AN) (36.9% [89 of 241] vs 20.0% [9
9 R2 Y394C mutation evidenced by cutis gyrata, acanthosis nigricans, and craniosynostosis and provides
10 ory diseases (such as atopic dermatitis), in acanthosis nigricans, as an extension of epidermal nevus
12 our individuals developed extensive areas of acanthosis nigricans beginning in early childhood, suffe
13 paraneoplastic syndromes such as xanthomas, acanthosis nigricans, carcinoid syndrome, unusual erythe
14 the furrowed skin disorder of cutis gyrata, acanthosis nigricans, craniosynostosis, craniofacial dys
19 and accompanied by other features, including acanthosis nigricans, organomegaly, hyperandrogenism, an
20 ofacial malformations, Crouzon syndrome with acanthosis nigricans results in characteristic cutaneous
21 achondroplasia with developmental delay and acanthosis nigricans (SADDAN), are associated with gluta
22 achondroplasia with developmental delay and acanthosis nigricans" (SADDAN) because it differs signif
23 achondroplasia with developmental delay and acanthosis nigricans) syndrome and thanatophoric dysplas
24 35, those of Hispanic ethnicity, those with acanthosis nigricans, those who had tried and failed die
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