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1 g wet and dry weights and decreased specific lung compliance.
2 s including airway obstruction and increased lung compliance.
3 eration on computed tomography, and impacted lung compliance.
4 e activity, cytokine contents, and decreased lung compliance.
5 ation and lung histology) and improvement in lung compliance.
6 lar apoptosis and a decrease in quasi-static lung compliance.
7 eased the respiratory compliance by reducing lung compliance.
8 iratory distress syndrome was related to low lung compliance.
9 m inducing perivascular cuffs and decreasing lung compliance.
10 also protected from LPS-induced decrease in lung compliance.
11 nd airway resistance as well as decreases in lung compliance.
12 t alveolar edema, are sufficient to decrease lung compliance.
13 ll tolerated with minimal effects on dynamic lung compliance.
14 , diffuse pulmonary infiltrates, and altered lung compliance.
15 id not change gas exchange, hemodynamics, or lung compliance.
16 hese responses likely contribute to impaired lung compliance.
17 and exhibited normal oxygenation and dynamic lung compliance.
18 e shifted upward and to the left) and higher lung compliance (0.21 vs 00.9 L/cm H(2) O; P < .05) comp
19 irway pressure (20, 30, and 40 cm H2O), test lung compliance (10, 30, and 50 mL/cm H2O), endotracheal
20 +/- 35 vs. 267 +/- 98; p = .15), and static lung compliance (30.9 +/- 13.5 vs. 38.5 +/- 11.7; p = .2
21 g of face mask, manikin head, training lung (lung compliance, 50 mL/cm H2O; airway resistance, 5 cm H
22 f survival and quality of life influenced by lung compliance, albeit while accelerating disease progr
24 group (406+/-63 vs 148+/-33 mm Hg, P=0.01); lung compliance and airway resistance did not differ sig
27 injury, with preserved gas exchange, better lung compliance and histology scores, and decreased lung
29 ry in WT mice was characterized by decreased lung compliance and increased protein and cytokine conce
30 and a decrease in PaO2, a decrease in static lung compliance and inhibition of surfactant function.
32 certain phospholipids had similar activity (lung compliance and lung pressure-volume behavior) to ra
35 opterin was associated with better preserved lung compliance and PaO2/FIO2 ratio, which were associat
36 gous mice (Hhip(+/-)), we observed increased lung compliance and spontaneous emphysema in Hhip(+/-) m
40 ved lung function (specifically quasi-static lung compliance and tissue elastance) and reduced mucus
43 monary function (lung resistance and dynamic lung compliance), and inflammatory cell infiltration.
50 reduced morbidity and viral burden, improved lung compliance, and increased CD8(+) T cell numbers in
52 ses mortality, promotes lung injury, reduces lung compliance, and increases degradation of lung elast
53 -expiratory pressure, the decrease in static lung compliance, and the extent of infiltrates on the ch
54 monary function, including Pao2/Fio2, static lung compliance, and time to meeting weaning criteria.
57 a series of different airway resistances and lung compliances as would be seen in different types of
58 rious combinations of airway resistances and lung compliances, auto-PEEP can be generated to substant
59 e most predictive of lung volume: a) dynamic lung compliance; b) the slope of phase 3; c) the slope o
60 predictive of lung volume change: a) dynamic lung compliance; b) the slope of phase III; c) the slope
62 ctant, a lipoprotein complex which increases lung compliance by reducing alveolar surface tension.
64 g pressure (DP(TP))-the quotient of V(T) and lung compliance (C(L)), in response to intra-abdominal h
65 cessfully extubated had significantly better lung compliance (Cdyn: 0.59 +/- 0.91 versus 0.39 +/- 0.1
66 e dismutase (SOD) treatment on gas exchange, lung compliance (CL), and pulmonary vascular resistance
67 ed substantial and significant impairment in lung compliance compared with control littermates receiv
69 erial pulmonary function tests, blood gases, lung compliance, computed tomography (CT) imaging, and q
71 Airway opening pressure (P-Flex), static lung compliance (Crs), and trapped gas volume (TGV) were
74 cture is destroyed, which leads to decreased lung compliance, disrupted gas exchange, and ultimately
78 90% O2 resulted in the restoration of normal lung compliance, elastance, and pressure-volume loops (t
79 (6) CFU) rapidly lost weight, had diminished lung compliance, experienced lung hemorrhage, and respon
80 coil pressure at total lung capacity, static lung compliance, expiratory flow rates, and lung volumes
82 and is characterized by a virtual absence of lung compliance, highly disorganized lamellar bodies, an
83 O-exposed mice with ML335 or BL1249 improved lung compliance, histological lung injury scores, bronch
86 tation lung, and significantly reduced total lung compliance in late gestation embryos that lack lymp
88 lthough prone positioning improved posterior lung compliance in the early acute respiratory distress
91 o tidal volume (VD/VT) decreased, and static lung compliance increased with PEEP at LIP +1 cm H2O (p
92 l volume to DeltaPes (an estimate of dynamic lung compliance) increased (P < 0.05); finally, ventilat
93 a), lung pathology, pulmonary edema, reduced lung compliance, increased basal airway resistance, and
94 ncluded decreased pulmonary gas exchange and lung compliance, increased pulmonary edema, and extensiv
95 ncluded decreased pulmonary gas exchange and lung compliance, increased pulmonary edema, and inflamma
96 me, respiratory rate, minute volume, dynamic lung compliance, inspiratory resistance, and blood gases
97 here was no difference in lung resistance or lung compliance measured by body plethysmography between
98 tion, but they demonstrated neither abnormal lung compliance nor increased respiratory rate and displ
99 and absence of plasma inhibitors, but whole lung compliance of the SP-A(-/-,D/A) animals was not dif
105 creased capillary permeability, and improved lung compliance, particularly at 12-hr storage times.
106 IIai dramatically protected gas exchange and lung compliance, prevented lung edema and pulmonary hype
107 capacity was associated with a reduction in lung compliance (r(2) = 0.43; p = 0.03) and isotime esop
109 most dramatically characterized by decreased lung compliance that was associated with an intense mono
110 ulmonary function (total lung volume, static lung compliance, tissue damping, and tissue elastance).
111 ic responses (airway hyperresponsiveness and lung compliance) to Mp infection were more severely affe
112 13 to increase lung size, alveolar size, and lung compliance, to stimulate pulmonary inflammation, hy
113 ctant proteins SpC, SpB, and SpA, decline of lung compliance, transient fibrosis, and eventually emph
114 eduction in movement, and a fall in specific lung compliance unseen in conventional mouse asthma mode
116 asurements included physiological variables (lung compliance, vascular resistance, oxygenation capaci
117 ility to modify lipid properties and restore lung compliance was investigated with circular dichroism
121 Pulmonary inflammation and quasi-static lung compliance were largely unaffected by neutralizatio
122 e, pulmonary vascular resistance, and static lung compliance were measured at baseline and after mode
124 r bundle and the lung parenchyma, decreasing lung compliance without impacting central venous pressur