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1 s the major gene when PAH is associated with hereditary hemorrhagic telangiectasia.
2 n mice and its mutation in the human disease hereditary hemorrhagic telangiectasia.
3 nd endoglin (ENG), which are associated with hereditary hemorrhagic telangiectasia.
4 understanding of the human vascular disease, hereditary hemorrhagic telangiectasia.
5 use the autosomal dominant bleeding disorder hereditary hemorrhagic telangiectasia.
6 n mice and its mutation in the human disease hereditary hemorrhagic telangiectasia.
7 nd ALK1 lead to the human syndromes known as hereditary hemorrhagic telangiectasia 1 and 2, respectiv
8 opment and is involved in the development of hereditary hemorrhagic telangiectasia 2 (HHT2), a domina
9 liminary results of studies in patients with hereditary hemorrhagic telangiectasia (a genetic disorde
10 ve kindreds plus one individual patient with hereditary hemorrhagic telangiectasia and identified 10
11 ated with the BMP/TGF-beta pathways, such as hereditary hemorrhagic telangiectasia and juvenile polyp
12 contribute to the contrasting pathologies of hereditary hemorrhagic telangiectasia and pulmonary arte
14 hic, and imaging studies in 19 patients with hereditary hemorrhagic telangiectasia and symptomatic li
16 ng the vascular dilatation characteristic of hereditary hemorrhagic telangiectasia and the occlusion
17 The reasons for the variable phenotype in hereditary hemorrhagic telangiectasia are not understood
18 Pulmonary hypertension in association with hereditary hemorrhagic telangiectasia can involve mutati
19 type III receptor ENG (both associated with hereditary hemorrhagic telangiectasia), caveolin-1 (CAV1
20 store normal cardiac output in patients with hereditary hemorrhagic telangiectasia (HHT) and cardiac
21 d by deregulation of TGF-beta/BMP signaling: hereditary hemorrhagic telangiectasia (HHT) and cerebral
29 intestine, and brain, are characteristic of hereditary hemorrhagic telangiectasia (HHT), a disease c
30 two distinct genes, endoglin or ALK-1, cause hereditary hemorrhagic telangiectasia (HHT), an autosoma
31 netic and multifactorial diseases, including hereditary hemorrhagic telangiectasia (HHT), cancer, ath
35 g in human vascular disease, we investigated hereditary hemorrhagic telangiectasia (HHT), which is ca
36 ptoms of a genetic vascular dysplasia termed hereditary hemorrhagic telangiectasia (HHT), which is ch
42 y affecting quality of life in patients with hereditary hemorrhagic telangiectasia (HHT; also known a
43 tations in the human endoglin gene ENG cause hereditary hemorrhagic telangiectasia (HHT1), a disease
45 which is commonly present due to concurrent hereditary hemorrhagic telangiectasia: iron deficiency i
47 stive linkage of pulmonary hypertension with hereditary hemorrhagic telangiectasia on chromosome 12q1
49 mutations of the ALK1 gene in human type II hereditary hemorrhagic telangiectasia patients suggest t
50 tations in the human endoglin gene result in hereditary hemorrhagic telangiectasia type 1, a vascular
51 l-1 and ACVR1/ALK2, responsible for cases of hereditary hemorrhagic telangiectasia type 2 (HHT2) and
54 or implicated in the human vascular disorder hereditary hemorrhagic telangiectasia type 2 (HHT2).
55 l for the human autosomal dominant disorder, hereditary hemorrhagic telangiectasia type 2, in which d
56 -confirmed PAVMs (including 403 [90.5%] with hereditary hemorrhagic telangiectasia) were recruited to
57 activin-like kinase receptor 1 (ALK1) cause hereditary hemorrhagic telangiectasia, whereas bone morp
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