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1 Osler's On Chorea uniquely captures the transition perio
2 n: Hodges and Smith, 1849), Bucknill (1882), Osler and Boller and Forbes reveal the changing attitude
3 in most instances, Osler and Charcot agreed, Osler used data from the new fields of genetics and bact
7 classic dermatological manifestations of IE (Osler nodes, Janeway lesions, purpura, and conjunctival
10 duced excessive daytime sleepiness; the mean Osler change was +7.9 minutes (SEM 2.9), when compared w
11 tations (1894), and in this pithy monograph, Osler offered a particularly useful evaluation of Charco
12 Hereditary haemorrhagic telangiectasia, or Osler-Rendu-Weber (ORW) syndrome, is an autosomal domina
13 editary hemorrhagic telangiectasia, or Rendu-Osler-Weber disease, is an autosomal dominant disorder c
14 y hemorrhagic telangiectasia (HHT), or Rendu-Osler-Weber disease, is an autosomal dominant disorder o
15 ry hemorrhagic telangiectasia (HHT, or Rendu-Osler-Weber syndrome), clinical evaluations and genetic
17 l-time clinical professorships, an idea that Osler opposed but that eventually became the prevailing
20 this sesquicentennial of his birth, William Osler continues to serve as a model of excellence for th
22 inciples and Practice of Medicine by William Osler while on a summer vacation at Lake Liberty, New Yo
23 and not an art." The thoughts of Sir William Osler in 1892 reflect the view of medicine over the past
28 uding 39 (8.0%) with purpura, 13 (2.7%) with Osler nodes, 8 (1.6%) with Janeway lesions, and 3 (0.6%)
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