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1 ssels within the dermis, resembling a tufted angioma.
2 ents had multiple classic cerebral cavernous angiomas.
3 ation therapy is the development of sporadic angiomas.
4 ite kindred with familial cerebral cavernous angioma and confirm the mapping to 7q11-22, including th
5 It lacks the "hemosiderin rim" of cavernous angioma and demonstrates increased susceptibility only o
8 Kaposiform hemangioendothelioma and tufted angioma are less common than IH but more often associate
12 n and spinal-cord hemangioblastomas, retinal angiomas, clear-cell renal carcinoma, neuroendocrine tum
17 responsible for familial cerebral cavernous angioma in a large Hispanic kindred was mapped to human
22 phVEGF165-treated sites showed macroscopic angioma-like structures at the injection site while cont
24 ith those of infantile hemangioma and tufted angioma of children, but features of the clinical presen
25 epatic metastasis, one patient had a hepatic angioma, one patient had an extraadrenal pheochromocytom
26 er vascular tumors include congenital tufted angiomas (TAs), kaposiform hemangioendotheliomas (KHEs),
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