Gotowa bibliografia na temat „Esophageal substitue”
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Artykuły w czasopismach na temat "Esophageal substitue"
Marzaro, Maurizio, Mattia Algeri, Luigi Tomao, Stefano Tedesco, Tamara Caldaro, Valerio Balassone, Anna Chiara Contini i in. "Successful muscle regeneration by a homologous microperforated scaffold seeded with autologous mesenchymal stromal cells in a porcine esophageal substitution model". Therapeutic Advances in Gastroenterology 13 (styczeń 2020): 175628482092322. http://dx.doi.org/10.1177/1756284820923220.
Pełny tekst źródłaCatry, Jonathan, Minh Luong-Nguyen, Lousineh Arakelian, Tigran Poghosyan, Patrick Bruneval, Thomas Domet, Laurent Michaud i in. "Circumferential Esophageal Replacement by a Tissue-engineered Substitute Using Mesenchymal Stem Cells". Cell Transplantation 26, nr 12 (grudzień 2017): 1831–39. http://dx.doi.org/10.1177/0963689717741498.
Pełny tekst źródłaKędzierska, Zofia, Klaudia Dadas, Urszula Żurek, Ignacy Tołwiński, Aleksandra Świercz, Dominika Małachowska, Hubert Ciecierski-Koźlarek, Klaudia Antkowiak i Kateryna Shved. "Long-gap esophageal atresia: management, most frequent complications, and expert recommendations – review of literature". Journal of Education, Health and Sport 45, nr 1 (24.08.2023): 310–26. http://dx.doi.org/10.12775/jehs.2023.45.01.022.
Pełny tekst źródłaSato, Yu, Tatsuo Kanda, Shin-ichi Kosugi, Takashi Ishikawa, Tetsuya Tada i Toshifumi Wakai. "Pyloroantrectomy and Pedunculated Short Gastric-Tube Interposition in Esophageal Carcinoma Patients Associated With Early Gastric Adenocarcinoma". International Surgery 104, nr 3-4 (1.03.2020): 143–48. http://dx.doi.org/10.9738/intsurg-d-16-00011.1.
Pełny tekst źródłaMishra, Haris Chandra, Jyotiranjan Mohapatra, Sashibhusan Dash i Sanghamitra Dash. "Surgical management of upper cervical esophagus stricture caused by ingestion of corrosive substances – a single-center experience". European Journal of Clinical and Experimental Medicine 22, nr 1 (30.03.2024): 88–93. http://dx.doi.org/10.15584/ejcem.2024.1.16.
Pełny tekst źródłaFürst, H., T. P. Hüttl, F. Löhe i F. W. Schildberg. "German experience with colon interposition grafting as an esophageal substitute*". Diseases of the Esophagus 14, nr 2 (kwiecień 2001): 131–34. http://dx.doi.org/10.1046/j.1442-2050.2001.00170.x.
Pełny tekst źródłaMoreno-Osset, Eduardo, Manuel Tomas-Ridocci, Francisco Paris, Francisco Mora, Angel Garcia-Zarza, Ramon Molina, Juan Pastor i Adolfo Benages. "Motor Activity of Esophageal Substitute (Stomach, Jejunal, and Colon Segments)". Annals of Thoracic Surgery 41, nr 5 (maj 1986): 515–19. http://dx.doi.org/10.1016/s0003-4975(10)63031-7.
Pełny tekst źródłaGutschow, Christian A., Jean-Marie Collard, Renato Romagnoli, Jean-Marie Michel, Mauro Salizzoni i Arnulf H. Hölscher. "Bile exposure of the denervated stomach as an esophageal substitute". Annals of Thoracic Surgery 71, nr 6 (czerwiec 2001): 1786–91. http://dx.doi.org/10.1016/s0003-4975(01)02535-8.
Pełny tekst źródłaSchilling, M. K., Ch Maurer i M. W. Buechler. "Fundus rotation gastroplasty as esophageal substitute: Microcirculatory and clinical results". Gastroenterology 108, nr 4 (kwiecień 1995): A1245. http://dx.doi.org/10.1016/0016-5085(95)29274-8.
Pełny tekst źródłaReynolds, Marleta. "Motor activity of esophageal substitute (stomach, jejunal and colon segments)". Journal of Pediatric Surgery 22, nr 1 (styczeń 1987): 89. http://dx.doi.org/10.1016/s0022-3468(87)80049-0.
Pełny tekst źródłaRozprawy doktorskie na temat "Esophageal substitue"
Lesieur, Romane. "Ingénierie tissulaire de l'oesophage". Electronic Thesis or Diss., Bordeaux, 2024. http://www.theses.fr/2024BORD0020.
Pełny tekst źródłaUpon removal of a portion of the esophagus, the restoration of the digestive continuity involves the surgical creation of an intrathoracic esophagogastric anastomosis. However, postoperative complications such as lung impairments, fistulas, strictures, graft necrosis, and gastroesophageal reflux are reported. The enhancement of surgical procedures for esophageal replacement has made promising progress by the development of a substitute through tissue engineering that utilizes a decellularized biological esophageal matrix (DEM). The primary objective of this study was to optimize the design of porcine DEM and characterize its biological and mechanical properties. The secondary objective was to cellularize DEM using readily available immune-privileged human mesenchymal stromal cells derived from Wharton's jelly (hMSCs-WJ).Esophageal decellularization was performed according to a protocol based on the dynamic perfusion of chemical and enzymatic solutions through the organ lumen. Histological analysis and residual DNA quantification of the DEM were conducted to determine the efficiency of the decellularization protocol. The ultrastructure of the DEM was analyzed using immunohistochemical (IHC) labeling, and the composition of the extracellular matrix (ECM) protein content was described by mass spectrometry. In-vitro cytotoxicity tests of DEM were conducted following ISO 10993-5 standards. The evaluation of suture retention strength, tensile strength, and bursting pressure of DEM aimed to describe the mechanical behavior of the substitute for clinical use.hMSCs-WJ used for DEM cellularization were extracted from human umbilical cords, and their flow cytometry profiling confirmed the purity of the cell population. The immune response of hMSCs-WJ was quantified after co-culture with peripheral blood mononuclear cells (PBMCs). PBMCs phenotyping assessed the expression of immune markers in contact with hMSCs-WJ, while enzyme-linked immunosorbent assay (ELISA) quantified cytokine release. The proposed DEM cellularization strategy involved the development of cell sheets from hMSCs-WJ. The validation of the cell sheet production protocol involved the characterization of the cellular phenotype by IHC analysis, and the mechanical study of the sheets measured their resistance to perforation.The absence of cellular content and residual DNA quantification in DEM confirmed the efficacy of decellularization according to current validation criteria. The ultrastructure and biological components of the ECM were preserved, and proteomic analysis highlighted protein complexity. Decellularization treatment did not induce DEM toxicity, and the mechanical behavior of DEM was suitable for its use as an esophageal substitute.Culturing hMSCs-WJ as cell sheets promoted the cellularization of the DEM. Once seeded, the sheets retained their cellular phenotype and immune-privileged characteristics. In-vitro tissue remodeling was visible, along with the formation of a new ECM produced by hMSCs-WJ.Characterization of the obtained DEM offered biological complexity and favorable mechanical behavior for its use as an esophageal substitute. DEM was cellularizable with hMSCs-WJ cell sheets, potentially promoting tissue integration and remodeling
Części książek na temat "Esophageal substitue"
Yoshida, M., i M. Iwatsuka. "Separated and Pedicled Wide Gastric Tube as an Esophageal Substitute". W Diseases of the Esophagus, 451–54. Berlin, Heidelberg: Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-86432-2_101.
Pełny tekst źródłaKudo, T., S. Abo i T. Itabashi. "Prognosis of Esophageal Substitute in Tissue Viability and Anastomotic Leakage". W Diseases of the Esophagus, 522–25. Berlin, Heidelberg: Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-86432-2_119.
Pełny tekst źródłaAndo, N., Y. Ikehata, T. Ohmori i O. Abe. "Prospective Studies on Postoperative Nutritional Status in Patients with Esophageal Carcinoma as Evaluated from Various Substitutes for Reconstruction: Gastric Tube Versus Colon Interposition". W Diseases of the Esophagus, 674–78. Berlin, Heidelberg: Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-86432-2_149.
Pełny tekst źródła"Use of the stomach as an esophageal substitute". W Operative Thoracic Surgery, 369–82. CRC Press, 2006. http://dx.doi.org/10.1201/b13418-41.
Pełny tekst źródłaOlszewski, Jurek, i Kalina Owczarek. "Jakość mowy zastępczej u chorych po usunięciu krtani bez protezy głosowej i z wszczepioną protezą głosową typu Provox II". W Problemy badawcze i diagnostyczne w logopedii. Wydawnictwo Uniwersytetu Łódzkiego, 2016. http://dx.doi.org/10.18778/8088-476-2.09.
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