References of "1995"
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See detailPlasma progesterone and IGF-I levels at puberty in Italian Simmental and Friesian heifers with various genetic merit.
Prandi, A.; Rossi, C.; Tondolo, A. et al

in Journal of Animal Science (1995), 73(Suppl 1), 222

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See detailFlow through porous media
Dassargues, Alain ULiege

Scientific conference (1995)

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See detailLa mesure générale anti-abus de droit étendue aux impôts indirects
Caprasse, Olivier ULiege; Bours, Jean-Pierre ULiege

in Fiscalité: un bilan des mesures anti-évasion fiscale (1995)

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See detailError estimates and indicators for adaptive analysis of bulk forming
Dyduch, M.; Cescotto, Serge ULiege; Habraken, Anne ULiege

in Owen, D. R. J.; Onate, E. (Eds.) Computational plasticity. Fundamentals and Applications (1995)

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See detailThe N- and C-termini of the tricarboxylate carrier are exposed to the cytoplasmic side of the inner mitochondrial membrane.
Capobianco, L.; Bisaccia, F.; Michel, A. et al

in FEBS Letters (1995), 357

Polyclonal antibodies were raised in rabbits against two synthetic peptides corresponding to the N- and C-terminal regions of the rat-liver mitochondrial tricarboxylate carrier. ELISA tests performed with ... [more ▼]

Polyclonal antibodies were raised in rabbits against two synthetic peptides corresponding to the N- and C-terminal regions of the rat-liver mitochondrial tricarboxylate carrier. ELISA tests performed with intact and permeabilized rat-liver mitoplasts showed that both anti-N-terminal and anti-C-terminal antibodies bind only to the cytoplasmic surface of the inner membrane, indicating that both termini of the membrane-bound tricarboxylate carrier are exposed to the mitochondrial intermembrane space. Furthermore, tryptic digestion of intact mitoplasts markedly decreased the binding of anti-N-terminal and anti-C-terminal antibodies to the tricarboxylate carrier. These results are consistent with an arrangement of the tricarboxylate carrier monomer into an even number of transmembrane segments, with the N- and C-termini protruding toward the cytosol. [less ▲]

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See detailCocina, cuisine y clase. Estudio de sociología comparada
Goody, Jack; Willson, Patricia ULiege

Book published by Editorial Gedisa (1995)

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See detailFundamentals of transformed skeletal muscle used for cardiac assistance. An overview
Radermacker, M. A.; Chachques, J. C.; Sluse, Francis ULiege et al

in Research in Surgery (1995), 7

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See detailNimesulide
Dupont, L.; Pirotte, Bernard ULiege; Masereel, B. et al

in Acta Crystallographica (1995), C51

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See detailGH receptor gene TaqI RFLP and milk traits in Italian Holstein-Friesian and Simmental cattle.
Falaki, Mohamed; Renaville, Robert ULiege; Sneyers, Myriam et al

in Journal of Animal Science (1995), 73(Suppl 1), 113

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See detailFeed restriction and IGFBP in bulls: effects of increasing starving period lengths.
Massart, Serge; Van Eenaeme, Christian ULiege; Renaville, Robert ULiege et al

in Journal of Animal Science (1995), 73(suppl 1), 225

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See detailGlucose inhibits human placental GH secretion, in vitro
Patel, N.; Alsat, E.; Igout, Ahmed ULiege et al

in Journal of Clinical Endocrinology and Metabolism (1995), 80(5), 1743-6

Human placenta specifically expresses the GH-V gene leading to the production of placental Growth Hormone (PGH). During pregnancy, PGH levels increase progressively in maternal blood, but its regulation ... [more ▼]

Human placenta specifically expresses the GH-V gene leading to the production of placental Growth Hormone (PGH). During pregnancy, PGH levels increase progressively in maternal blood, but its regulation remains unknown. In this study the effect of glucose on PGH secretion by human term placenta was tested, in vitro, by means of two different experimental models: organ culture of villous tissue and primary culture of isolated cytotrophoblasts. PGH was assayed in the culture medium by an immunoradiometric assay using a specific PGH monoclonal antibody. The presence of glucose (25 mmol/L) in the culture medium significantly inhibited (p < 0.001) the secretion of PGH by either placental villous explants or by cultured trophoblast cells. This inhibitory effect of glucose on PGH secretion was dose-dependent. More than 50% inhibition being observed with 5.5 mmol/L. In the same conditions, the daily production of hPL and hCG, were unmodified. Furthermore, the glucose-induced inhibition of PGH secretion was more effective when cultured trophoblast cells are differentiated into syncytiotrophoblast. This study demonstrates, for the first time, that among the gestational polypeptide hormones secreted by the human placenta, only PGH secretion is modulated by glucose, suggesting a key metabolic role for this hormone during pregnancy. [less ▲]

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See detailThe role of the Zairian Health Services in the Rwandan refugee crisis.
Porignon, Denis ULiege; Noterman, J. P.; Hennart, P. et al

in Disasters (1995), 19(4), 356-60

In July 1994, a stream of Rwandan refugees entered the southern part of North Kivu Region, Zaire. The public health consequences of this crisis for the host population and health services have not been ... [more ▼]

In July 1994, a stream of Rwandan refugees entered the southern part of North Kivu Region, Zaire. The public health consequences of this crisis for the host population and health services have not been analysed up to now. The lack of human and financial resources did not prevent Zairian health structures and personnel from taking care of the many refugees settled outside the camps, following their arrival. The public health consequences of the crisis for the local population should be considered an integral part of the disaster. [less ▲]

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See detailRat embryo fibroblasts immortalization by bovine leukemia virus Tax protein
Willems, Luc ULiege; Heremans, H.; Burny, A. et al

in Methods in Cell Science : An Official Journal of the Society for in Vitro Biology (1995)

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See detailAnesthetic management of laparoscopy: new developments
Joris, Jean ULiege

in Miller, Ronald D (Ed.) Anesthesia (1995)

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See detailPneumothorax during laparoscopic fundoplication: diagnosis and treatment with positive end-expiratory pressure.
Joris, Jean ULiege; Chiche, Jean-Daniel; Lamy, Maurice ULiege

in Anesthesia and Analgesia (1995), 81(5), 993-1000

Pneumothorax can develop during laparoscopy, particularly during laparoscopic fundoplication, since the left parietal pleura is exposed and can be torn during dissection in the diaphragmatic hiatus. Such ... [more ▼]

Pneumothorax can develop during laparoscopy, particularly during laparoscopic fundoplication, since the left parietal pleura is exposed and can be torn during dissection in the diaphragmatic hiatus. Such an event will result in specific pathophysiologic changes, since CO2, under pressure in the abdominal cavity, will pass into the pleural space. The aim of this study was to document the pathophysiologic changes induced by pneumothorax, and to evaluate the benefit of positive end-expiratory pressure (PEEP) to treat pneumothorax. Forty-six ASA physical status I and II patients scheduled for laparoscopic fundoplication were monitored extensively; heart rate, mean arterial pressure, end-tidal CO2 (PETCO2), oxygen saturation of hemoglobin (Spo2), minute ventilation, tidal volume, dynamic total lung thorax compliance, and airway pressures were recorded. In 25 patients, oxygen uptake, CO2 elimination and arterial blood gases were also measured. Pneumothorax was diagnosed in seven patients. It resulted in the following pathophysiologic changes: decrease in total lung thorax compliance, increase in airway pressures, and increase in CO2 absorption. Consequently, PACO2 and PETCO2 also increased. Spo2, however, remained normal. The use of PEEP largely corrected these respiratory changes. None of these pneumothoraces required drainage. These data suggest that pneumothorax is common during laparoscopic fundoplication. Early diagnosis is possible by simultaneous monitoring of PETCO2, total lung thorax compliance, and airway pressures. Finally, treatment with PEEP provides an alternative to chest tube placement when pneumothorax is secondary to passage of peritoneal CO2 into the interpleural space. [less ▲]

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See detailPain after laparoscopic cholecystectomy: characteristics and effect of intraperitoneal bupivacaine.
Joris, Jean ULiege; Thiry, E.; Paris, P. et al

in Anesthesia and Analgesia (1995), 81(2), 379-84

Although pain after laparoscopic cholecystectomy is less intense than after open cholecystectomy, some patients still experience considerable discomfort. Furthermore, the characteristics of ... [more ▼]

Although pain after laparoscopic cholecystectomy is less intense than after open cholecystectomy, some patients still experience considerable discomfort. Furthermore, the characteristics of postlaparoscopy pain differ considerably from those seen after laparotomy. Therefore, we investigated the time course of different pain components after laparoscopic cholecystectomy and the effects of intraperitoneal bupivacaine on these different components. Forty ASA physical status grade I-II patients were randomly assigned to receive either 80 mL of bupivacaine 0.125% with epinephrine 1/200,000 (n = 20) or the same volume of saline (n = 20) instilled under the right hemidiaphragm at the end of surgery. Intensity of total pain, visceral pain, parietal pain, and shoulder pain was assessed 1, 2, 4, 6, 8, 24, and 48 h after surgery. Analgesic consumption was also recorded. Patient data were similar in the two groups. In the saline group, visceral pain was significantly more intense than parietal pain at each time point; visceral and parietal pain were greater than shoulder pain during the first 8 h postoperatively. Intraperitoneal bupivacaine did not significantly affect any of the different components of postoperative pain. Analgesic consumption was similar in the two groups. This study demonstrates that visceral pain accounts for most of the pain experienced after laparoscopic cholecystectomy. Intraperitoneal bupivacaine is not effective for treating any type of pain after laparoscopic cholecystectomy. [less ▲]

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See detailProduction et élimination du gaz carbonique
Chiche, Jean-Daniel; Lamy, Maurice ULiege

in Scherpereel, Philippe; Lamy, Maurice (Eds.) Physiologie en anesthésiologie (1995)

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See detailInhaled nitric oxide for hemodynamic support after postpneumectomy ARDS
Chiche, Jean-Daniel; Canivet, Jean-Luc ULiege; Damas, Pierre ULiege et al

in Intensive Care Medicine (1995), 21(8), 675-678

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See detailOpioids in intensive care
Lamy, Maurice ULiege; Joris, Jean ULiege; Damas, Pierre ULiege et al

in Lawin, P.; Von Loewenich, V.; Schuster, H.-P. (Eds.) et al Intensivmedizin notfallmedizin anästhesiologie (1995)

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See detailHypnosis as adjunct therapy in conscious sedation for plastic surgery
Faymonville, Marie ULiege; Fissette, Jean ULiege; Mambourg, P.-H. et al

in Regional Anesthesia (1995), 20(2), 145-151

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