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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.
5 t of MCUL, as part of the variant hereditary leiomyomatosis and renal cancer (HLRCC) syndrome, and ha
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
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
21 syndrome, cell differentiation in hereditary leiomyomatosis, and autoimmunity in Goodpasture syndrome
24 Alport syndrome (AS) and associated diffuse leiomyomatosis (DL), a syndrome of disseminated smooth-m
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
31 as endometriosis and rarer entities such as leiomyomatosis peritonealis disseminata and gliomatosis
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
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