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1 in 38 unrelated individuals, 21 of whom were hypercalcemic.
2 ung or disseminated, but no other cases were hypercalcemic.
3 rescence from microneedles distinguished low hypercalcemic (1.7 mM) from high hypercalcemic (2.3 mM)
4 guished low hypercalcemic (1.7 mM) from high hypercalcemic (2.3 mM) ionized calcium levels as determi
5 was 1.68 +/- 0.1 mg/dl, 21% of patients were hypercalcemic, 63.2% had elevated parathyroid hormone (P
6 ormone 1,25D(3), but with significantly less hypercalcemic activity.
7 at allow the neurons to compensate for their hypercalcemic, activity-deprived state.
8 s available, 4 of 17 patients (24%) remained hypercalcemic after extensive reexploration.
9          Surprisingly, however, the hallmark hypercalcemic and hypophosphatemic responses were marked
10 p < 0.02) whereas men were more likely to be hypercalcemic (chi(2) = 7.38, p < 0.01).
11                                 The fetus is hypercalcemic compared to the mother and here we show th
12 OH)(2)D is often dysregulated with potential hypercalcemic complications.
13 ns, but not mice, was also mimicked by fetal hypercalcemic conditions, demonstrating that the physiol
14 proved our understanding of hypocalcemic and hypercalcemic conditions.
15                       Severe hypercalcemia ("hypercalcemic crisis") should be managed aggressively wi
16 ied in affected members of families with the hypercalcemic disorders, familial hypocalciuric hypercal
17 and cause human autosomal dominant hypo- and hypercalcemic disorders.
18 re associated with inherited human hypo- and hypercalcemic disorders.
19 , but its clinical utility is limited by its hypercalcemic effect.
20              These data demonstrate that the hypercalcemic effects of PTHrP are enhanced by TNF and t
21 n with MDA-MB-231 breast cancer cells, while hypercalcemic environments did not affect interaction.
22                                              Hypercalcemic episodes (>10.2 mg/dl) occurred more frequ
23 r of the syndrome, tumors also produce other hypercalcemic factors, such as tumor necrosis factor (TN
24 ntly elevated stanniocalcin (Stc1a), an anti-hypercalcemic hormone, in sox10 mutants.
25 esions were detected using x-rays in all the hypercalcemic mice examined.
26                                           In hypercalcemic mice, the absence of the CaSR in TAL preve
27                              Only 3200 (31%) hypercalcemic patients had PTH levels measured, 2914 (28
28                         We evaluated whether hypercalcemic patients underwent measurement of parathyr
29 en proposed to be a precursor of the classic hypercalcemic primary hyperparathyroidism (HPT).
30 rane of initial IMCD from low-protein fed or hypercalcemic rats; (2) active urea reabsorption in the
31 ntitumor activities of vitamin D without the hypercalcemic side effects.
32 e products: prevention of bone resorption in hypercalcemic states and a regulatory role in bone forma
33  A quarter of OBS patients showed persistent hypercalcemic symptoms, compared with only 7.7% in the C
34 calcium level and lower chance of persistent hypercalcemic symptoms, without any appreciable harm to
35 nificant changes in the understanding of the hypercalcemic syndromes associated with malignancy and w
36  serum levels of PTHrP while the patient was hypercalcemic that became undetectable when serum calciu
37 1,25-(OH)2D3 was needed in GKO mice, causing hypercalcemic toxicity.
38 n MCF10DCIS xenograft tumors without causing hypercalcemic toxicity.
39           Small cell carcinoma of the ovary, hypercalcemic type (SCCOHT) is a rare and aggressive for
40           Small cell carcinoma of the ovary, hypercalcemic type (SCCOHT) is a rare, aggressive cancer
41           Small cell carcinoma of the ovary, hypercalcemic type (SCCOHT) is a rare, highly aggressive
42         Small cell carcinoma of the ovary of hypercalcemic type (SCCOHT) is an extremely rare, aggres
43           Small cell carcinoma of the ovary, hypercalcemic type (SCCOHT) is the most common undiffere
44 bunits in small cell carcinoma of the ovary, hypercalcemic type (SCCOHT)(2-5), SMARCA4-deficient thor
45           Small cell carcinoma of the ovary, hypercalcemic type (SCCOHT), is a rare, deadly form of o
46  underlie small cell carcinoma of the ovary, hypercalcemic type (SCCOHT).
47 t is important to differentiate those of the hypercalcemic type from those of the pulmonary type.
48 nd other electrolytes did not differ between hypercalcemic WT and Ksp-Casr mice.