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Artykuły w czasopismach na temat "Gastrointestinal"

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Kurugöl, Zafer, i İlker Devrim. "Gastrointestinal Infections". Journal of Pediatric Infection 8, nr 2 (16.06.2014): 71–81. http://dx.doi.org/10.5152/ced.2013.1509.

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Santhanam, AN, RW Sillar i IC Roberts-Thomson. "Gastrointestinal: Gastrointestinal lipomas". Journal of Gastroenterology and Hepatology 21, nr 10 (październik 2006): 1628. http://dx.doi.org/10.1111/j.1440-1746.2006.04704.x.

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Naniwadekar, A., i A. Malhotra. "Gastrointestinal: Gastrointestinal histoplasmosis". Journal of Gastroenterology and Hepatology 23, nr 4 (kwiecień 2008): 668. http://dx.doi.org/10.1111/j.1440-1746.2008.05371.x.

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Patil, Divya Teja, Anil Kumar Sakalecha, Parameshwar Keerthi B.H i Yashas Ullas L. "Duodenal Gastrointestinal Stromal Tumor". JOURNAL OF CLINICAL AND BIOMEDICAL SCIENCES 9, nr 2 (15.06.2019): 53–55. http://dx.doi.org/10.58739/jcbs/v09i2.2.

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Gastrointestinal stromal tumors (GIST) are nonepithelial tumors arising from the interstitial cells of Cajal. They express KIT protein-CD117 on immunohistochemistry. GIST can arise anywhere in the GIT, including the mesentery, omentum, and ret-roperitoneum. In the duodenum, 2nd or 3rd part of duodenum is the most common site. Imatinib is the drug of choice and sur-gical resection is the main modality of treatment. Keywords: Gastrointestinal Stromal Tumor
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Daley, Tom D., i Jerrold E. Armstrong. "Oral Manifestations of Gastrointestinal Diseases". Canadian Journal of Gastroenterology 21, nr 4 (2007): 241–44. http://dx.doi.org/10.1155/2007/952673.

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The present paper offers a detailed review of the oral manifestations of various gastrointestional diseases or conditions, with suggestions on how they may be relevant to the practice of gastroenterology. The review includes Crohn’s disease, ulcerative colitis, Gardner syndrome, Peutz-Jeghers syndrome, malabsorption conditions related to hematopoiesis, gastrointestinal malignancy metastatic to the jaws, jaundice and gastric reflux diseases.
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&NA;. "Gastrointestinal". Current Opinion in Critical Care 1, nr 2 (kwiecień 1995): B27. http://dx.doi.org/10.1097/00075198-199504000-00015.

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LEWIS, ANNE MARIE. "Gastrointestinal". Nursing 29, nr 4 (kwiecień 1999): 52–54. http://dx.doi.org/10.1097/00152193-199904000-00017.

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&NA;. "GASTROINTESTINAL". Clinical Nuclear Medicine 24, nr 10 (październik 1999): 827. http://dx.doi.org/10.1097/00003072-199910000-00036.

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&NA;. "GASTROINTESTINAL". Clinical Nuclear Medicine 24, nr 12 (grudzień 1999): 1006. http://dx.doi.org/10.1097/00003072-199912000-00037.

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&NA;. "GASTROINTESTINAL". Clinical Nuclear Medicine 25, nr 1 (styczeń 2000): 83. http://dx.doi.org/10.1097/00003072-200001000-00035.

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Rozprawy doktorskie na temat "Gastrointestinal"

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White, J. S. "Models of intestinal barrier function and their application in the study of biliary obstruction". Thesis, Queen's University Belfast, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.368529.

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Vianna, Karina Costa Maia. "Tumor estomal gastrointestinal (GIST)". reponame:Repositório Institucional da UFPR, 2012. http://hdl.handle.net/1884/26630.

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Resumo: Introdução: Os tumores estromais gastrointestinais (GIST) são neoplasias raras que se originam das células intersticiais de Cajal .A última década foi de grande avanço com o esclarecimento dos mecanismos moleculares, seguido da terapia molecular, que propiciaram um grande aumento na sobrevida. Objetivo: Avaliar a experiência do Hospital de Clínicas de Curitiba no tratamento do GIST localizado e avançado, com análise das características clínicas e anatomo-patológicas e uso do imatinibe. Metodologia: Estudo retrospectivo de 32 pacientes com diagnóstico de GIST por imunohistoquímica, c-Kit positivo, no período de 2003 a 2008 Resultados: Os dados evidenciaram que a idade mediana foi de 66 anos, o tamanho mediano de 8,4 cm e as localizações mais frequentes foram estômago em 46,9% e intestino delgado em 40,9%. Considerado com alto risco de agressividade 37,5% dos pacientes. Do grupo total, 23 pacientes apresentavam doença localizada no diagnóstico, sendo que 39,1% recaíram, e 9 pacientes doença avançada. O seguimento mediano foi de 43,7 meses. A sobrevida global em 5 anos no grupo total foi de 56,2%, sendo que na doença localizada foi de 73,8% e na doença avançada foi de 37,5% (p=0,03). Não foi observado impacto dos fatores prognósticos na sobrevida. A utilização do imatinibe ocorreu em 16 pacientes, 43,8% por metástase inicial, 37,5% por recaída a distância, 12,5% por recaída local e 6,2% por margem cirúrgica comprometida. A sobrevida global com uso do imatinibe mediana foi de 53 meses e a sobrevida livre de primeira progressão de 32,9 meses. Ocorreu uma boa tolerabilidade ao imatinibe, com 2 pacientes com toxicidade grau 3 e apenas dois pacientes utilizaram o sunitinibe. Conclusão: A maioria dos tumores foram grandes, de localização gástrica e de alto risco de agressividade. A taxa de recaída na doença localizada foi alta. E a sobrevida global dos pacientes de doença localizada e que utilizaram o imatinibe foi considerada satisfatória.
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Thoree, Cheetranjan Vinay. "Characterisation of gastrointestinal microparticles". Thesis, King's College London (University of London), 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.555927.

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Intestinal Peyer's patches, through their specialized M cell-rich epithelium, can act as a portal of entry for bacteria, viruses, macromolecules and particles. Particles can be further classified as exogenous particles such as those derived from the diet in the form of food additives or endogenous particles which result from calcium and phosphate precipitation in the mid-distal intestinal lumen. Although exogenous dietary particles have been found to accumulate in "pigment cells" at the base of the human Peyer's patch, little is known about calcium phosphate particles. This thesis aimed (i) to investigate and compare the micro-anatomical site of exogenous and endogenous particles within the Peyer's patch, and (ii) to analyse the phenotype of cells involved in their uptake. Following an Introduction chapter (Chapter 1) and Methods chapter (Chapter 2), the focus of chapter 3 was to look for the presence of both calcium phosphate and exogenous particles in human intestinal Peyer's patches using the Von Kossa staining method and dark field microscopy, respectively. The elemental makeup of the endogenous particles was investigated by X-Ray Microanalysis (XRMA). This study revealed a sub-epithelial Peyer's patch dome-associated population of Von Kossapositive particle cells, the majority of which appeared to be calcium-rich, and more especially calcium- and phosphorus- rich. Exogenous particles associated with the usual basal pigment cells could similarly be found in the sub-epithelial dome cells and suggested that the exogenous particles made their way through the patch via intermediary cells. Following work concentrated on the phenotyping of cells responsible for the uptake of exogenous and endogenous particles (Chapters 4 and 5, respectively). Pigment cells of the Peyer's patch base were found to be macrophages, chiefly of a mature phenotype, and appeared metabolically and immunologically of low activation status. In contrast, calcium phosphate particles were found mainly in dendritic cells of the sub epithelial dome region of the Peyer's patch. The cell phenotype (CDIlc+, CDl lb+) was consistent with immune tolerance-inducing dendritic cells reported in the literature - the specific mechanism being induction of regulatory T cells. I have speculated on how the uptake of endogenous particles may influence such process.
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Ullah, Sana. "Factors governing gastrointestinal motility". Thesis, University of Hull, 2012. http://hydra.hull.ac.uk/resources/hull:7166.

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Introduction: The reasons for the rapid resolution of diabetes (DM) following bariatric surgery in a significant proportion of patients with morbid obesity remain unclear. This thesis investigates the putative role of changes in gastrointestinal (GI) motility and GI hormones as well as the possible significance of alterations in energy expenditure that occur as a consequence of weight loss. Methodology: My preliminary studies involved a systematic review of GI motility in obesity, and retrospective studies measuring GI motility with alternative methods including capsule endoscopy and hydrogen breath test. Subsequent to this I measured changes in GI motility in two very different patient cohorts; one following bariatric surgery for morbid obesity and the other a group of patients with proven gastroparesis treated with gastric neuromodulation (GNM). Parallel to the above I conducted studies of indirect calorimetry in these patients in an attempt to determine if changes in energy expenditure which occur as a consequence of weight loss were significant. Results: In our prospective study temporary GNM significantly improved gastric emptying and nutritional intake. There was conclusive evidence to causally relate alterations in GI motility and Glucagon like peptide -1 (GLP-1) with weight loss and resolution of DM following bariatric surgery. An interesting "spin off" result of my studies was validation of capsule endoscopy (CE) as a means of assessing GI motility. My results obtained from measure if indirect calorimetrty clearly show that standard equations tend to over estimate the energy requirements of this group. The implications of this are discussed. Conclusions: 1. Fast pouch emptying; an early and exaggerated GLP-1 response contributes in resolution of type 2 diabetes following RYGB. 2. GNM is an effective treatment for gastroparesis. 3. Capsule endoscopy may be used to assess GI motility. 4. Prediction equations over estimate energy requirements in morbidly obese patients.
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Silva, Vera Lisa Generosa da. "Estase gastrointestinal no coelho". Master's thesis, Universidade Técnica de Lisboa. Faculdade de Medicina Veterinária, 2012. http://hdl.handle.net/10400.5/4935.

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Dissertação de Mestrado Integrado em Medicina Veterinária
Actualmente, como o coelho é um animal de estimação frequente, é importante que o Médico Veterinário esteja bem informado sobre este paciente "exótico", para que assim o consiga acompanhar devidamente. Uma das urgências mais comum neste animal, é a estase gastrointestinal (GI), que é uma doença adquirida, em que ocorre uma diminuição ou interrupção da motilidade do tracto GI. É dos problemas mais desafiantes com que o veterinário poderá ser confrontado, sendo o seu tratamento complexo e a resposta terapêutica do paciente, lenta. Esta dissertação resultou de um estágio curricular, com a duração de seis meses, realizado no Centro Veterinário de Exóticos do Porto. São apresentados e discutidos dez casos clínicos de estase GI, em coelhos de estimação, presentes à consulta durante esse período. Os sinais mais frequentemente observados nestes animais, incluíram anorexia, diminuição/ausência na produção de fezes e dilatação abdominal. A principal causa da estase GI nestes pacientes deveu-se a uma dieta inadequada, no entanto, outras etiologias frequentes foram, ainda, o stress e a dor (muito vulgarmente causada por problemas dentários). De acordo com os casos clínicos observados, é de salientar a importância da precocidade na administração do tratamento adequado, para que assim se consiga restabelecer a motilidade GI, não descurando, no entanto, o diagnóstico da etiologia primária, que deve ser realizado simultaneamente.
ABSTRACT - Gastrointestinal stasis in rabbit - Nowadays, the rabbit is a fairly common pet, for this reason, it is important for the Veterinarian, to be updated on this “exotic” patient, in order to handle and treat it, accordingly. One of the most common emergencies in this species, is gastrointestinal stasis, an acquired disease, where reduced to inexistent GI tract motility occurs. It is one of the most challenging problems the veterinarian might be presented with, due to its complex treatment and slow recovery of the patient. This essay was the result of a six months training, on Centro Veterinário de Exóticos do Porto. Ten GI stasis clinical cases, on rabbit pets, are presented and discussed; all of them took place during the training. The most commonly observed signs included anorexia, reduced /no faeces output and abdominal enlargement. The main cause for GI stasis in these patients, was an inadequate diet, although, other frequent aetiologies were stress and pain (commonly caused by dental problems). According to the analyzed clinical cases, it is mandatory to emphasize the importance of early adequate treatment administration, so GI motility might be re-established. Nevertheless, diagnosing the primary aetiology must take place simultaneously.
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Шевченко, Володимир Порфирович, Владимир Порфирьевич Шевченко, Volodymyr Porfyrovych Shevchenko, Z. Jawad i O. Amazu. "Nsaid - related gastrointestinal bleeding". Thesis, Видавництво СумДУ, 2008. http://essuir.sumdu.edu.ua/handle/123456789/4899.

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Tekkis, Paris Procopiou. "Risk-adjustment in gastrointestinal surgery". Thesis, University of London, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.406906.

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Stevenson, Diane J. "P2X7, inflammation and gastrointestinal disease". Thesis, University of Nottingham, 2008. http://eprints.nottingham.ac.uk/28897/.

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The inflammatory bowel diseases, ulcerative colitis and Crohn's disease are characterised by spontaneously relapsing and remitting inflammation, associated with increased mucosal levels of the inflammatory cytokine, interleukin-1 (IL-1)β. IL-1β processing and release is mediated by ATP stimulation of the purine receptor, P2X7. P2X7 is a membrane ion channel highly expressed in immune cells. Signal transduction occurs via rapid cation exchange, plasma membrane depolarisation and increased intracellular calcium. Additionally, prolonged or repeated P2X7 stimulation leads to formation of a non-selective membrane pore permeable to small molecules, and ultimately to cell death. The aim of this project was to investigate the properties of the P2X7 receptor in mononuclear cells, to show that it is associated with IL-1β release in the colon, and that this release can be modified by P2X7 antagonists. Studies of ethidium bromide uptake, a functional assay, showed that P2X7 receptors are present on LPMCs and displayed properties similar to those of PBMCs and THP-1 cells. P2X7 receptor-stimulation released mature IL-1β from LPMCs in a dose-dependent manner that, in IBD patients, matched the severity of their inflammation, and could be markedly reduced by P2X7 antagonists. P2X7 stimulation also results in increased exposure of phosphatidylserine on the outer cell membrane (PS flip), often considered to be a marker of apoptotic cell death. P2X7-stimulated PS flip however is reversible and is not associated with cell death following brief stimulation times. Cell death caused by longer stimulation did not have features of apoptosis, was more evident in monocytes than lymphocytes, with LPMCs being less susceptible than PBMCs and THP-1 cells. These studies have shown that the P2X7 receptor is intimately involved in the release of IL-1β from human colonic mononuclear cells, that the release is greater in cells from IBD tissue and can be markedly inhibited by P2X7 antagonists.
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Khosla, Rajiv. "Gastrointestinal transit of dosage forms". Thesis, University of Nottingham, 1987. http://eprints.nottingham.ac.uk/12741/.

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This thesis describes the results from a series of studies designed to evaluate the gastrointestinal transit of oral dosage forms. The transit of placebo pellet and tablet formulations was monitored using the technique of gamma scintigraphy. The formulations were radiolabelled with either technetium-99m or indium-lil. Four parameters, two physiological and two pharmaceutical, were selected for investigation. All the studies were conducted in healthy male volunteers. The first study examined the influence of the supine position on the gastric emptying of pellets in fasted and fed subjects. There was no marked difference between the supine and control gastric emptying data. As would be expected, food had a significant effect on gastric emptying. The influence of the time of day of administration on the gastrointestinal transit of pellets was investigated in fasted subjects. Transit of the pellets was not affected by their time of administration. The effect of the putative bioadhesive, polycarbophil, on the gastrointestinal transit of a pellet formulation was studied in fasted subjects. The pellets emptied from the stomach, rapidly and in an exponential manner. A set of studies was conducted to evaluate the transit of tablets in fed and fasted subjects. Tablet size did not affect gastric emptying, although there was an increase in the variability of gastric emptying with increasing tablet size. Food had a marked effect on gastric emptying. The rate of emptying was related to the energy content of the meal. Tablet size did not appear to be a determinant of transit through the ileocaecal sphincter. The colon transit and dispersion of the tablets was examined. Neither the ingestion of food nor defecation appeared to alter the rate of transit through the colon.
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Daly, R. "Gastrointestinal bacteria : attachment and interactions". Thesis, Queen's University Belfast, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.398156.

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Książki na temat "Gastrointestinal"

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Mackie, Roderick I., Bryan A. White i Richard E. Isaacson, red. Gastrointestinal Microbiology. Boston, MA: Springer US, 1997. http://dx.doi.org/10.1007/978-1-4757-0322-1.

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Fischbach, Wolfgang, red. Gastrointestinal Lymphoma. Berlin, Heidelberg: Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/978-3-642-57054-4.

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Sung, Joseph J. Y., Ernst J. Kuipers i Alan N. Barkun, red. Gastrointestinal Bleeding. Oxford, UK: John Wiley & Sons, Ltd, 2011. http://dx.doi.org/10.1002/9781444398892.

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Tham, Tony C. K., John S. A. Collins i Roy M. Soetikno, red. Gastrointestinal Emergencies. Oxford, UK: Wiley-Blackwell, 2008. http://dx.doi.org/10.1002/9781444303292.

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Greeley, George H., red. Gastrointestinal Endocrinology. Totowa, NJ: Humana Press, 1999. http://dx.doi.org/10.1007/978-1-59259-695-9.

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Russo, Suzanne, Sarah Hoffe i Edward Kim, red. Gastrointestinal Malignancies. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-64900-9.

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Graham, Autumn, i David J. Carlberg, red. Gastrointestinal Emergencies. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-319-98343-1.

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Dobelbower, Ralph R., red. Gastrointestinal Cancer. Berlin, Heidelberg: Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-83657-2.

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Jonnalagadda, Sreenivasa S., red. Gastrointestinal Endoscopy. New York, NY: Springer New York, 2015. http://dx.doi.org/10.1007/978-1-4939-2032-7.

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Pawlik, Timothy M., Shishir K. Maithel i Nipun B. Merchant, red. Gastrointestinal Surgery. New York, NY: Springer New York, 2015. http://dx.doi.org/10.1007/978-1-4939-2223-9.

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Części książek na temat "Gastrointestinal"

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Holliman, John H., Daniel L. Feeback i Nancy K. Hall. "Gastrointestinal". W Oklahoma Notes, 112–27. New York, NY: Springer US, 1988. http://dx.doi.org/10.1007/978-1-4684-0322-0_10.

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Papadopoulos, John. "Gastrointestinal". W Pocket Guide to Critical Care Pharmacotherapy, 91–97. New York, NY: Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-1853-9_7.

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Fry, John. "Gastrointestinal". W The Beecham Manual for Family Practice, 239–43. Dordrecht: Springer Netherlands, 1985. http://dx.doi.org/10.1007/978-94-011-6361-3_19.

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Hustinx, Roland. "Gastrointestinal". W PET-CT and PET-MRI in Oncology, 135–59. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/174_2011_432.

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Wasson, Cassandra, Albert Kelly, David Ninan i Quy Tran. "Gastrointestinal". W Absolute Obstetric Anesthesia Review, 13. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-96980-0_6.

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Murthy, Sree Prathap Mohana. "Gastrointestinal". W Get Through MRCPsych: Preparation for the CASC, Second edition, 200–202. Wyd. 2. London: CRC Press, 2022. http://dx.doi.org/10.1201/9780429073007-52.

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Guo, Yan-Shi, i Courtney M. Townsend. "Gastrointestinal Hormones and Gastrointestinal Cancer Growth". W Gastrointestinal Endocrinology, 189–214. Totowa, NJ: Humana Press, 1999. http://dx.doi.org/10.1007/978-1-59259-695-9_8.

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Gilger, Mark A., i Hisham M. Nazer. "Gastrointestinal Bleeding". W Textbook of Clinical Pediatrics, 1937–49. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-02202-9_199.

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Halabi, Issam M. "Gastrointestinal Tumors". W Textbook of Clinical Pediatrics, 1951–53. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-02202-9_200.

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Andronikou, Savvas. "Gastrointestinal Tract". W See Right Through Me, 503–34. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-23893-2_21.

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Streszczenia konferencji na temat "Gastrointestinal"

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Raynaud, Gaetan, Camille Simon-Chane, Pierre Jacob i Aymeric Histace. "Active Contour Segmentation based on Histograms and Dictionary Learning for Videocapsule Image Analysis". W Special Session on GastroIntestinal Image Analysis. SCITEPRESS - Science and Technology Publications, 2019. http://dx.doi.org/10.5220/0007694706090615.

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Dijkstra, Willem, André Sobiecki, Jorge Bernal i Alexandru Telea. "Towards a Single Solution for Polyp Detection, Localization and Segmentation in Colonoscopy Images". W Special Session on GastroIntestinal Image Analysis. SCITEPRESS - Science and Technology Publications, 2019. http://dx.doi.org/10.5220/0007694906160625.

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Duran-Lopez, Lourdes, Francisco Luna-Perejon, Isabel Amaya-Rodriguez, Javier Civit-Masot, Anton Civit-Balcells, Saturnino Vicente-Diaz i Alejandro Linares-Barranco. "Polyp Detection in Gastrointestinal Images using Faster Regional Convolutional Neural Network". W Special Session on GastroIntestinal Image Analysis. SCITEPRESS - Science and Technology Publications, 2019. http://dx.doi.org/10.5220/0007698406260631.

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Guo, Yun, i Bogdan Matuszewski. "GIANA Polyp Segmentation with Fully Convolutional Dilation Neural Networks". W Special Session on GastroIntestinal Image Analysis. SCITEPRESS - Science and Technology Publications, 2019. http://dx.doi.org/10.5220/0007698806320641.

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Kumari, Divya, Teodora Bochnakova, Lisa Walker, Nami Azar, Sidhartha Tavri i Indravadan Patel. "Palliative Gastrointestinal Interventions". W 4th Annual Meeting of the American Society of Digestive Disease Interventions. Thieme Medical Publishers, 2017. http://dx.doi.org/10.1055/s-0038-1641653.

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Bochankova, Teodora, Lisa Walker, Divya Kumari, Mohammed Al-Natour i Indravadan Patel. "Provocative Gastrointestinal Hemorrhage". W 4th Annual Meeting of the American Society of Digestive Disease Interventions. Thieme Medical Publishers, 2017. http://dx.doi.org/10.1055/s-0038-1641654.

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Munir, A., J. D. Parekh, A. Wells i M. J. Sanley. "Gastrointestinal Angiodysplasia and Ambrisentan". W American Thoracic Society 2019 International Conference, May 17-22, 2019 - Dallas, TX. American Thoracic Society, 2019. http://dx.doi.org/10.1164/ajrccm-conference.2019.199.1_meetingabstracts.a1514.

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Jurkov, A. S., A. Arriagada i M. P. Mintchev. "Implantable functional gastrointestinal neurostimulation". W 2009 Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE, 2009. http://dx.doi.org/10.1109/iembs.2009.5332682.

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Brunner, M., D. Soll, K. Adler, A. Sasse, V. Ellenrieder i K. Alexander. "Brain metastases in upper gastrointestinal cancers - an underestimated complication in gastrointestinal oncology". W Viszeralmedizin 2021 Gemeinsame Jahrestagung Deutsche Gesellschaft für Gastroenterologie, Verdauungs- und Stoffwechselkrankheiten (DGVS), Sektion Endoskopie der DGVS, Deutsche Gesellschaft für Allgemein und Viszeralchirurgie (DGAV). Georg Thieme Verlag KG, 2021. http://dx.doi.org/10.1055/s-0041-1733484.

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Brunner, M., D. Soll, K. Adler, A. Sasse, V. Ellenrieder i K. Alexander. "Brain metastases in upper gastrointestinal cancers - an underestimated complication in gastrointestinal oncology". W Viszeralmedizin 2021 Gemeinsame Jahrestagung Deutsche Gesellschaft für Gastroenterologie, Verdauungs- und Stoffwechselkrankheiten (DGVS), Sektion Endoskopie der DGVS, Deutsche Gesellschaft für Allgemein und Viszeralchirurgie (DGAV). Georg Thieme Verlag KG, 2021. http://dx.doi.org/10.1055/s-0041-1733484.

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Raporty organizacyjne na temat "Gastrointestinal"

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Touch Surgery. Upper Gastrointestinal Anatomy. Touch Surgery Publications, grudzień 2018. http://dx.doi.org/10.18556/touchsurgery/2016.s0155.

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Stern, Robert M. Motion Adaptation Syndrome: Gastrointestinal Aspects. Fort Belvoir, VA: Defense Technical Information Center, listopad 2001. http://dx.doi.org/10.21236/ada390627.

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Gill, Steven R. Genomics of the Human Gastrointestinal Microbiome. Fort Belvoir, VA: Defense Technical Information Center, grudzień 2004. http://dx.doi.org/10.21236/ada432197.

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DeSesso, John M., i Richard D. Mavis. Identification of Critical Biological Parameters Affecting Gastrointestinal Absorption. Fort Belvoir, VA: Defense Technical Information Center, styczeń 1990. http://dx.doi.org/10.21236/ada236507.

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Tovani Palone, Marcos Roberto, i Vivian Patricia Saldias Vargas. Las fisuras labiopalatinas frente al equilibrio de la microbiota gastrointestinal. Buenos Aires: siicsalud.com, październik 2014. http://dx.doi.org/10.21840/siic/144114.

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Rondinone, Cristina. Nuevo papel del tracto gastrointestinal en el desarrollo de enfermedades metabólicas. Sociedad Española de Bioquímica y Biología Molecular (SEBBM), lipiec 2012. http://dx.doi.org/10.18567/sebbmdiv_anc.2012.07.1.

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Anderson, George M. Biomarkers for Autism and for Gastrointestinal and Sleep Problems in Autism. Fort Belvoir, VA: Defense Technical Information Center, październik 2012. http://dx.doi.org/10.21236/ada570226.

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Anderson, George M. Biomarkers for Autism and for Gastrointestinal and Sleep Problems in Autism. Fort Belvoir, VA: Defense Technical Information Center, październik 2013. http://dx.doi.org/10.21236/ada592834.

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Anderson, George M. Biomarkers for Autism And For Gastrointestinal And Sleep Problems In Autism. Fort Belvoir, VA: Defense Technical Information Center, październik 2011. http://dx.doi.org/10.21236/ada555058.

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fan, xin, he han, zhiyu sun, liwen zhang, gong chen, Said Abdulrahman Salim Mzee, hanqing yang i jixiang chen. Prognostic Value of Bleeding in Gastrointestinal Stromal Tumors: A meta analysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, czerwiec 2021. http://dx.doi.org/10.37766/inplasy2021.6.0027.

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