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2 evealed BRAF p.Val600Glu in 95% of papillary craniopharyngiomas (36 of 39 tumors) and mutation of CTN
4 in patients with an underlying diagnosis of craniopharyngioma (9.28 [5.84-14.75] vs 1.61 [1.30-1.99]
5 of tumours resembling human adamantinomatous craniopharyngioma (ACP), derived from Sox2- cells in a p
7 tified age at diagnosis, sex, a diagnosis of craniopharyngioma, and untreated gonadotropin deficiency
10 or localized primary brain tumors, including craniopharyngioma, ependymoma, and juvenile pilocytic as
11 beta-catenin) in nearly all adamantinomatous craniopharyngiomas examined (11/12, 92%) and recurrent m
13 bal attention disorders were associated with craniopharyngioma (P < .0001), supratentorial tumors (P
16 igh concentration of proteins (colloid cyst, craniopharyngioma, Rathke's cleft cyst, ectopic posterio
17 Age at diagnosis, female sex, and above all, craniopharyngioma were significant independent risk fact
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