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1  of the kidney, atherosclerosis, and uterine leiomyomatosis.
2 ow or absent in tumors from individuals with leiomyomatosis.
3 n lymphoblastoid cells from individuals with leiomyomatosis.
4 d uterus, with the latter resembling uterine leiomyomatosis and prostatic hypertrophy.
5 t of MCUL, as part of the variant hereditary leiomyomatosis and renal cancer (HLRCC) syndrome, and ha
6 ry papillary renal carcinoma, and hereditary leiomyomatosis and renal carcinoma.
7                                   Hereditary leiomyomatosis and renal cell cancer (HLRCC) is an autos
8                                   Hereditary leiomyomatosis and renal cell cancer (HLRCC) is an inher
9 and uterine leiomyomata (MCL) and hereditary leiomyomatosis and renal cell cancer (HLRCC), and recent
10 ted individuals to a rare cancer, hereditary leiomyomatosis and renal cell cancer (HLRCC), characteri
11 e leiomyomatosis (MCUL1), and the hereditary leiomyomatosis and renal cell cancer (HLRCC), implicated
12 reditary cancer syndrome known as hereditary leiomyomatosis and renal cell cancer (HLRCC).
13 rate hydratase (FH) predispose to hereditary leiomyomatosis and renal cell cancer in affected individ
14  date, HIF-1alpha accumulation in hereditary leiomyomatosis and renal cell cancer tumors is thought t
15 l carcinoma (PRCC2, also known as hereditary leiomyomatosis and renal cell cancer), NRF2 activation i
16 iant of hereditary kidney cancer (hereditary leiomyomatosis and renal cell cancer).
17 and uterine leiomyomas as well as hereditary leiomyomatosis and renal cell cancer.
18 al cancer predisposition syndrome hereditary leiomyomatosis and renal cell cancer.
19 e enzyme fumarate hydratase cause hereditary leiomyomatosis and renal cell cancer.
20 tations of FH are responsible for hereditary leiomyomatosis and renal-cell cancer (HLRCC).
21 syndrome, cell differentiation in hereditary leiomyomatosis, and autoimmunity in Goodpasture syndrome
22                                              Leiomyomatosis-associated mutations are predicted to res
23                                   Esophageal leiomyomatosis can be suggested in a pediatric patient w
24  Alport syndrome (AS) and associated diffuse leiomyomatosis (DL), a syndrome of disseminated smooth-m
25                      Disseminated peritoneal leiomyomatosis (DPL, leiomyomatosis peritonealis dissemi
26 ic archives revealed six cases of esophageal leiomyomatosis in a 22-year period.
27 eptibility to multiple cutaneous and uterine leiomyomatosis (MCUL).
28 yndromes, the multiple cutaneous and uterine leiomyomatosis (MCUL1), and the hereditary leiomyomatosi
29  atresia (n = 26), corrosive injury (n = 8), leiomyomatosis (n = 5), and refractory gastroesophageal
30                                              Leiomyomatosis peritonealis disseminata (LPD) is a rare
31  as endometriosis and rarer entities such as leiomyomatosis peritonealis disseminata and gliomatosis
32                      The imaging findings of leiomyomatosis peritonealis disseminata were correlated
33 d female who was subsequently diagnosed with leiomyomatosis peritonealis disseminata with a few of th
34 aging findings were found to be specific for leiomyomatosis peritonealis disseminata with a malignant
35 Disseminated peritoneal leiomyomatosis (DPL, leiomyomatosis peritonealis disseminata) is a rare condi
36 ng (MRI) and was subsequently diagnosed with leiomyomatosis peritonealis disseminata.
37                                   Hereditary leiomyomatosis renal cell carcinoma, a hereditary form o

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