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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
6 idate region for familial cerebral cavernous angioma and facilitate the search for the gene.
7  the terms cavernous malformation, cavernous angioma, and cavernoma.
8   Kaposiform hemangioendothelioma and tufted angioma are less common than IH but more often associate
9                           Cerebral cavernous angiomas are collections of closely clustered vessels wi
10 od-filled vascular channels of littoral cell angioma at histopathologic examination.
11                                      Retinal angiomas, cerebellar and spinal hemangioblastomas, solid
12 n and spinal-cord hemangioblastomas, retinal angiomas, clear-cell renal carcinoma, neuroendocrine tum
13                                 Three spider angiomas developed on the right foot/ankle about a week
14                                              Angioma formation at the injection sites did not appear
15 tions ranging from a short-lasting effect to angioma formation.
16 n containing the familial cerebral cavernous angioma gene.
17  responsible for familial cerebral cavernous angioma in a large Hispanic kindred was mapped to human
18                                Littoral cell angioma is a primary splenic neoplasm that most commonly
19 ed focal epicardial blood vessel density and angioma-like formation.
20 AV-VEGF- and AAV-LacZ-inoculated hearts, and angioma-like structure was not observed.
21                                 Furthermore, angioma-like structures associated with VEGF expression
22   phVEGF165-treated sites showed macroscopic angioma-like structures at the injection site while cont
23                  Familial cerebral cavernous angioma occurs as an autosomal dominant disorder, althou
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),
27      Vascular tumors ranged in severity from angiomas to hemangiosarcomas, some of which could be tra

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