Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Sanjeev Devgarha"'
Publikováno v:
Heart India, Vol 5, Iss 1, Pp 17-23 (2017)
Objective: The goal of this study is to evaluate and compare the midterm outcomes of bioprosthetic heart valve replacement in terms of survival, valve-related events, quality of life, and economic aspects of treatment in population age 45 years and a
Externí odkaz:
https://doaj.org/article/965ebdae50e942ea90ef098eef6ccc98
Publikováno v:
Egyptian Journal of Chest Disease and Tuberculosis, Vol 65, Iss 2, Pp 451-454 (2016)
Gastropulmonary fistulas are themselves a very rare clinical entity and very less has been written about them in literature. Most of the cases listed in literature till now show that most of the gastropleural fistulas have been reported after intrath
Externí odkaz:
https://doaj.org/article/bcb97e05399d4378b08e422afbce5683
Publikováno v:
Heart India, Vol 4, Iss 2, Pp 56-60 (2016)
Introduction: Postoperative course of cardiac surgery patients in presence of liver dysfunction is associated with a lot of complications like excessive bleeding, coagulopathy, hepatic decompensation, multiple organ failure, infections which account
Externí odkaz:
https://doaj.org/article/ce3085e3a07c40fdb62d39fc1c203955
Publikováno v:
Egyptian Journal of Chest Disease and Tuberculosis, Vol 65, Iss 3, Pp 707-709 (2016)
Thoracic outlet syndrome [TOS] caused by a tumor of the rib is rare and has been reported only 12 times in the literature over the past one and one-half centuries, with the majority of cases due to osteochondroma. We report a case of chondrosarcoma o
Externí odkaz:
https://doaj.org/article/0ef1cf2c138845f38b32295cd57d3099
Publikováno v:
Egyptian Journal of Chest Disease and Tuberculosis, Vol 63, Iss 2, Pp 523-527 (2014)
Aneurysms of the aortic root and ascending aorta are often due to degenerative disease of media but tuberculosis is an important but extremely rare cause of aortic root dilatation especially in tropical countries like India where tuberculosis is ende
Externí odkaz:
https://doaj.org/article/58010c7a2c1f4af0bdc008020e123779
Publikováno v:
Egyptian Journal of Chest Disease and Tuberculosis, Vol 64, Iss 1, Pp 81-83 (2015)
Spontaneous bronchoesophageal fistula in the adult is a rare clinical entity. Most bronchoesophageal fistulae are due to malignancy, prolonged endotracheal intubation or trauma. Granulomatous infections like tuberculosis, HIV and mediastinitis are ra
Externí odkaz:
https://doaj.org/article/09cff4cddd274e118de2320eeb3f4d3f
Publikováno v:
Egyptian Journal of Chest Disease and Tuberculosis, Vol 64, Iss 1, Pp 209-211 (2015)
Spontaneous bronchoesophageal fistula in adults is a rare clinical entity. Most bronchoesophageal fistulae are due to malignancy, prolonged endotracheal intubation or trauma. Granulomatous infections like tuberculosis, HIV and mediastinitis are rare
Externí odkaz:
https://doaj.org/article/cef6340665c84a79b186fbc95e768b85
Autor:
Amita Yadav, Rajendra Mohan Mathur, Sanjeev Devgarha, Viju Joseph Abraham, Anula Sisodia, Gaurav Goyal
Publikováno v:
Egyptian Journal of Chest Disease and Tuberculosis, Vol 63, Iss 1, Pp 273-275 (2014)
Pulmonary sequestration is a rare congenital bronchopulmonary foregut malformation in which a segment of lung parenchyma is not connected to the tracheobronchial tree. This abnormal segment receives blood supply from the systemic circulation. Varying
Externí odkaz:
https://doaj.org/article/790ae8f09a4b430c93400a70a9790b48
Publikováno v:
Egyptian Journal of Chest Disease and Tuberculosis, Vol 62, Iss 4, Pp 651-653 (2013)
Hydatid disease with pulmonary tuberculosis coexisting in a patient is an extremely rare occurrence. A patient presenting with nonspecific chest symptoms must be adequately investigated and hydatidosis must be ruled out. This case report presents the
Externí odkaz:
https://doaj.org/article/c24d383171464c4db42a58db23e9b289
Publikováno v:
IOSR Journal of Dental and Medical Sciences. 16:124-127
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dac9cc5968d0af012702282ec9d4506e
https://doi.org/10.9790/0853-160306124127
https://doi.org/10.9790/0853-160306124127