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1 us on lymphangioleiomyomatosis and pulmonary Langerhans cell histiocytosis.
2 those of histiocytic human diseases, such as Langerhans cell histiocytosis.
3 ytic conditions, Erdheim-Chester disease and Langerhans cell histiocytosis.
4 lymphomas, neuroblastoma, some sarcomas, and Langerhans cell histiocytosis.
5 ues for the routine staging and diagnosis of Langerhans cell histiocytosis.
6 iterans organizing pneumonia), and pulmonary Langerhans' cell histiocytosis.
7 ng cancer and in Erdheim-Chester disease and Langerhans'-cell histiocytosis.
9 hough lymphangioleiomyomatosis and pulmonary Langerhans cell histiocytosis are perhaps more frequentl
10 In this study we have developed a model for Langerhans cell histiocytosis comprising a CD1a-positive
11 most common histiocytic disorders, including Langerhans cell histiocytosis, Erdheim-Chester disease,
17 ations have been observed in 57% of cases of Langerhans cell histiocytosis (LCH) and 54% of cases of
18 novel somatic ARAF mutation in a child with Langerhans cell histiocytosis (LCH) and demonstrate that
19 enesis of 2 of the most common histiocytoses-Langerhans cell histiocytosis (LCH) and Erdheim-Chester
21 have been observed in half of patients with Langerhans cell histiocytosis (LCH) and in 50% to 100% o
27 nase (ERK) signaling pathway is activated in Langerhans cell histiocytosis (LCH) histiocytes, but onl
45 ing data to date on a group of patients with Langerhans cell histiocytosis (LCH), which historically
50 gree of organ involvement at presentation of Langerhans' cell histiocytosis (LCH) with subsequent dis
53 mon in patients who received transplants for Langerhans cell histiocytosis relative to other indicati
54 9 patients with ECD and ECD overlapping with Langerhans cell histiocytosis (so-called mixed histiocyt
55 Erdheim-Chester disease (ECD) is a rare non-Langerhans cell histiocytosis that most commonly affects
56 n the cohort with Erdheim-Chester disease or Langerhans'-cell histiocytosis, the response rate was 43
57 with histopathologically confirmed pulmonary Langerhans'-cell histiocytosis to ascertain their vital
58 Erdheim-Chester disease (ECD) is a rare non-Langerhans cell histiocytosis, to whose pathogenesis neo
59 pendent of these risk factors, patients with Langerhans cell histiocytosis were at significantly incr
60 th survival after the diagnosis of pulmonary Langerhans'-cell histiocytosis were analyzed with the Co
61 d eruptive histiocytosis (GEH) is a rare non-Langerhans cell histiocytosis with a benign, self-healin
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