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1 ssels within the dermis, resembling a tufted angioma.
2 ation therapy is the development of sporadic angiomas.
3 erning, with no evidence of malformations or angiomas.
4 ents had multiple classic cerebral cavernous angiomas.
5 ite kindred with familial cerebral cavernous angioma and confirm the mapping to 7q11-22, including th
6  It lacks the "hemosiderin rim" of cavernous angioma and demonstrates increased susceptibility only o
7 idate region for familial cerebral cavernous angioma and facilitate the search for the gene.
8  the terms cavernous malformation, cavernous angioma, and cavernoma.
9   Kaposiform hemangioendothelioma and tufted angioma are less common than IH but more often associate
10                                    Cavernous angiomas are cerebral vascular malformations that are us
11                           Cerebral cavernous angiomas are collections of closely clustered vessels wi
12 od-filled vascular channels of littoral cell angioma at histopathologic examination.
13                                    Cavernous angiomas (CA) are common vascular anomalies causing brai
14                                      Retinal angiomas, cerebellar and spinal hemangioblastomas, solid
15 n and spinal-cord hemangioblastomas, retinal angiomas, clear-cell renal carcinoma, neuroendocrine tum
16                                 Three spider angiomas developed on the right foot/ankle about a week
17                                              Angioma formation at the injection sites did not appear
18 tions ranging from a short-lasting effect to angioma formation.
19 lso used the technique to distinguish cherry angiomas from normal human skin by comparing the molecul
20 n containing the familial cerebral cavernous angioma gene.
21  responsible for familial cerebral cavernous angioma in a large Hispanic kindred was mapped to human
22 aims to describe the behavior of a cavernous angioma in its natural history, documenting: a) its de n
23                                Littoral cell angioma is a primary splenic neoplasm that most commonly
24 ed focal epicardial blood vessel density and angioma-like formation.
25 AV-VEGF- and AAV-LacZ-inoculated hearts, and angioma-like structure was not observed.
26                                 Furthermore, angioma-like structures associated with VEGF expression
27   phVEGF165-treated sites showed macroscopic angioma-like structures at the injection site while cont
28                  Familial cerebral cavernous angioma occurs as an autosomal dominant disorder, althou
29 ith those of infantile hemangioma and tufted angioma of children, but features of the clinical presen
30 epatic metastasis, one patient had a hepatic angioma, one patient had an extraadrenal pheochromocytom
31 sociated with upper eyelid or leptomeningeal angiomas, seizures, prior hemispherectomy, or pulsed-dye
32 er vascular tumors include congenital tufted angiomas (TAs), kaposiform hemangioendotheliomas (KHEs),
33      Vascular tumors ranged in severity from angiomas to hemangiosarcomas, some of which could be tra
34 rient the etiological diagnosis of cavernous angioma versus other alternatives: de novo appearance, f
35                   Lower eyelid and choroidal angiomas were associated with glaucoma diagnosis, sugges
36                      However, leptomeningeal angiomas were not associated, possibly because these are