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heart faille

Dimitri Arangalage, Laurent Lepage, Dorothée Faille, Claire Cimadevilla, Marie-Pierre Dilly, Emmanuelle Papy, Martine Alhenc-Gelas, Walid Ghodbane, Patrick Nataf, Bernard Iung, Philippe Gabriel Steg, Alec Vahanian, Nadine Ajzenberg, David Messika-Zeitoun
OBJECTIVES: The use of heparin exposes patients to heparin-induced thrombocytopenia, which is a challenging issue for both diagnosis and patient management. We sought to describe the clinical presentation, management and outcome of a series of patients diagnosed with heparin-induced thrombocytopenia after heart valve surgery. METHODS: All consecutive patients diagnosed with heparin-induced thrombocytopenia during the postoperative period of heart valve surgery over a 6-year period were prospectively enrolled in a single-centre registry...
June 14, 2016: European Journal of Cardio-thoracic Surgery
Evelyn Opala Faille, Aniruddh Setya, Leonard Eisenfeld
AIM: To develop an appropriate apparatus for monitoring physiological signals and offering noninvasive automated mechanical stimulations for interrupting apneic events in neonates. RATIONALE: Vibrotactile stimulation (VTS) maybe an effective, safer alternative to nursing hand stimulation in treating neonatal apnea. We therefore developed a new diagnostic and therapeutic instrument. METHODS: The main components of the system are a computer running Windows XP using an AMD Athlon TM 64 processor, a neonatal physiological monitor (Model 511; CAS Medical Inc...
October 2013: Connecticut Medicine
A Pou Serradell, J Lloreta Trull, J Corominas Torres, P Guicheney
BACKGROUND: Desmin-related myopathy is a familial myopathy and cardiomyopathy. Three subgroups have been outlined, an autosomal dominant (AD) granulofilamentous type with cardiomyopathy, an AD cytoplasmic/spheroid inclusion body type and an autosomic recessive Mallory body-like inclusion type. Recently, in one family belonging to the first group it has been identified a mutation within a gene coding for a chaperone protein, alphabeta-crystallin (CRYAB gene). OBJECTIVE: To describe a Spanish family with a desmin-related myopathy, an AD granulofilamentous type with cardiomyopathy, with a molecular study that does not express any point mutation in the CRYAB gene...
May 2001: Neurología: Publicación Oficial de la Sociedad Española de Neurología
M Baledent, J Messerschmitt, J L Bens, J C Quiret, N Faille
No abstract text is available yet for this article.
February 8, 1972: La Semaine des Hôpitaux: Organe Fondé Par L'Association D'enseignement Médical des Hôpitaux de Paris
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