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Journals and Conferences
A case of cardiac failure with pulmonary hypertension in a neonate with laryngomalacia is described. The interest of clinical and echocardiographical follow up and transcutaneous blood gas measurements to monitor the course of any upper airway obstruction is emphasized.
A potentially useful method to monitor respiratory mechanics in artificially ventilated patients consists of analyzing the relationship between tracheal pressure (P), lung volume (V), and gas flow (V) by multiple linear regression (MLR) using a suitable model. Contrary to other methods, it does not require any particular flow waveform and, therefore, may be… (More)
Comparison of the QT interval and corrected QT interval values that were calculated by the methods of Bazett (QTc1) and Fridericia (QTc2) were made between dogs with or without cardiac diseases to determine the influence of the QT interval on canine heart failure. Upon comparison of the measured values on ECG between the cardiac disease and non-cardiac… (More)
OBJECTIVES To test the tolerability of long-term administration of benazepril in dogs with congestive heart failure (CHF). METHODS The study was a prospective, randomized, double-blinded, placebo-controlled clinical trial. A total of 162 dogs with New York Heart Association (NYHA) class II-IV heart failure caused by chronic valvular disease (CVD) or… (More)
The authors report the case of a 20 day-old neonate who presented with boutonneuse fever. According to their knowledge, this is the first reported case occurring in a neonate. In this child, the infection seemed to be unusually severe with rapid evolution and encephalic signs.
We describe a new case of postaxial acrofacial dysostosis (Miller) syndrome. This syndrome consists of mandibulofacial dysostosis, similar to that seen in Treacher Collins syndrome, and postaxial limb deficiency. The mode of inheritance remains uncertain.
The authors report on one case of 3-hydroxy-3-methylglutaryl-coenzyme A lyase (HMG-Co A lyase) deficiency in a 3 year-old girl, presenting as Reye's syndrome. Urinary organic profile suggested this inherited metabolic disease; decreased activity of HMG-Co A lyase was demonstrated in cultured fibroblasts. The metabolic etiologies of Reye's syndrome are… (More)