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1 milliliter (range, 31 to 2335) in those with X-linked hypophosphatemia.
2 ated in those with oncogenic osteomalacia or X-linked hypophosphatemia, an immunometric assay was dev
3 opeptidases on the X chromosome (Phex) cause X-linked hypophosphatemia, characterized by rickets, ost
4 mutation homologous to that in patients with X-linked hypophosphatemia, have a 2-fold greater urinary
5 nant mutation of the normal gene Pex causing X-linked hypophosphatemia in the mouse.
6                                              X-linked hypophosphatemia is the most prevalent inherite
7 age, 43.0+/-13.3 years) and 21 patients with X-linked hypophosphatemia (mean age, 34.9+/-17.2 years)
8  in 2018 for use in children and adults with X-linked hypophosphatemia (or XLH).
9 ated in those with oncogenic osteomalacia or X-linked hypophosphatemia, suggesting that this growth f
10 xpress FGF-23 messenger RNA, and to those in X-linked hypophosphatemia, which is caused by inactivati
11 ophosphatemia and impaired mineralization in X-linked hypophosphatemia (XLH) and its mouse homologue,
12                                Patients with X-linked hypophosphatemia (XLH) and the hyp-mouse, a mod
13 hereditary hypophosphatemic rickets, such as X-linked hypophosphatemia (XLH) and tumor-induced osteom
14         Inactivating mutations of Phex cause X-linked hypophosphatemia (XLH) by increasing levels of
15 ed in mineral balance that are implicated in X-linked hypophosphatemia (XLH) in humans, its murine ho
16                                              X-linked hypophosphatemia (XLH) is a skeletal disease ca
17                                              X-linked hypophosphatemia (XLH) is an X-linked dominant
18                                              X-linked hypophosphatemia (XLH) is the most common herit
19                                              X-linked hypophosphatemia (XLH) is the most frequent for
20                                              X-linked hypophosphatemia (XLH) leads to growth retardat
21                                              X-linked hypophosphatemia (XLH), a disorder characterize
22                      Mutations in PHEX cause X-linked hypophosphatemia (XLH), a form of hypophosphate
23           Mutations in the PHEX gene lead to X-linked hypophosphatemia (XLH), a form of inherited ric
24 sgenic mice as experimental models for human X-linked hypophosphatemia (XLH)-related degenerative ost