Academic literature on the topic 'Kidney and liver histopathology'
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Journal articles on the topic "Kidney and liver histopathology"
DeBowes, Linda J., Derek Mosier, Ellen Logan, Colin E. Harvey, Stephen Lowry, and Daniel C. Richardson. "Association of Periodontal Disease and Histologic Lesions in Multiple Organs from 45 Dogs." Journal of Veterinary Dentistry 13, no. 2 (June 1996): 57–60. http://dx.doi.org/10.1177/089875649601300201.
Full textWakawa, A. I., and S. B. Audu. "Histopathological alterations in gills, kidney and liver of Nile Tilapia (Oreochromis niloticus) fingerlings exposed to aqueous leaf extract of Desert Date (Balanites aegyptiaca)." Zoologist (The) 18, no. 1 (April 8, 2021): 67–73. http://dx.doi.org/10.4314/tzool.v18i1.12.
Full textSugihartini, Nining, and M. Alif Fajri. "Gambaran Histopatologi Organ Hati dan Ginjal Mencit Balb/c setelah Pemberian Krim Ekstrak Teh Hijau (Camellia sinensis L.)." JURNAL FARMASI DAN ILMU KEFARMASIAN INDONESIA 3, no. 1 (August 4, 2017): 32. http://dx.doi.org/10.20473/jfiki.v3i1.4092.
Full textSugihartini, Nining, and M. Alif Fajri. "Gambaran Histopatologi Organ Hati dan Ginjal Mencit Balb/c setelah Pemberian Krim Ekstrak Teh Hijau (Camellia sinensis L.)." JURNAL FARMASI DAN ILMU KEFARMASIAN INDONESIA 3, no. 1 (August 4, 2017): 32. http://dx.doi.org/10.20473/jfiki.v3i12016.32-38.
Full textAlwelaie, Manar A., Mohsen G. Al-Mutary, Nikhat J. Siddiqi, Maha M. Arafah, Abdullah S. Alhomida, and Haseeb A. Khan. "Time-Course Evaluation of Iminodipropionitrile-Induced Liver and Kidney Toxicities in Rats: A Biochemical, Molecular and Histopathological Study." Dose-Response 17, no. 2 (April 1, 2019): 155932581985223. http://dx.doi.org/10.1177/1559325819852233.
Full textCamargo, Marina M. P., and Cláudia B. R. Martinez. "Histopathology of gills, kidney and liver of a Neotropical fish caged in an urban stream." Neotropical Ichthyology 5, no. 3 (September 2007): 327–36. http://dx.doi.org/10.1590/s1679-62252007000300013.
Full textEl-Shenawy, Nahla S., Rasha A. Al-Eisa, Fawzia El-Salmy, and Omema Salah. "Prophylactic effect of vitamin E against hepatotoxicity, nephrotoxicity, haematological indices and histopathology induced by diazinon insecticide in mice." Current Zoology 55, no. 3 (June 1, 2009): 219–26. http://dx.doi.org/10.1093/czoolo/55.3.219.
Full textLutfiyah, Lailatul. "Sublethal Toxicity of Organophosphate Pesticides and its Effect on Hematology Parameter, Histopatology Hematopoietic Organ of Silver Rasbora (Rasbora argyrotaenia)." Journal of Aquaculture Science 5, no. 2 (October 26, 2020): 68. http://dx.doi.org/10.31093/joas.v5i2.94.
Full text& et al., Mustafa. "HISTOPATHOLOGYANDLEVELOF BIOACCUMULATION OFSOME HEAVY METALS IN FISH, CARASOBARBUSLUTEUS AND CYPRINUSCARPIOTISSUES CAUGHTFROM TIGRIS RIVER, BAGHDAD." IRAQI JOURNAL OF AGRICULTURAL SCIENCES 51, no. 2 (April 26, 2020): 698–704. http://dx.doi.org/10.36103/ijas.v51i2.997.
Full textDemetris, Anthony J., John G. Lunz III, Parmjeet Randhawa, Tong Wu, Michael Nalesnik, and Angus W. Thomson. "Monitoring of human liver and kidney allograft tolerance: a tissue/histopathology perspective." Transplant International 22, no. 1 (January 2009): 120–41. http://dx.doi.org/10.1111/j.1432-2277.2008.00765.x.
Full textDissertations / Theses on the topic "Kidney and liver histopathology"
Tagliaferro, Aline Fernanda. "Avaliação da toxicidade aguda do inseticida endosulfan em alevinos de pacu (Piaractus mesopotamicus), com o emprego de biomarcadores histologicos." [s.n.], 2009. http://repositorio.unicamp.br/jspui/handle/REPOSIP/317910.
Full textDissertação (mestrado) - Universidade Estadual de Campinas, Instituto de Biologia
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Resumo: Dado o registro de endosulfan nas bacias do Pantanal Mato-Grossense, o risco para os organismos aquáticos que esse agrotóxico promove e a falta de informações sobre sua ação na ictiofauna dessa região, esta pesquisa objetivou verificar a sensibilidade do pacu, Piaractus mesopotamicus, ao endosulfan. Para a realização da intoxicação aguda (96h) em sistema estático, alevinos foram expostos às seguintes concentrações de endosulfan: 0; 0,71; 1,43; 2,14; 2,86; 3,57; 4,29 e 5µgL-1. Após 96h, os exemplares sobreviventes foram necropsiados e amostras de brânquia, fígado e rim foram colhidas para análise histopatológica, qualitativa e semi-quantitativa. A Concentração Letal Média (CL50) obtida foi de 5,66µgL-1 (24h) e 4,33µgL-1 (96h). Alterações branquiais e hepáticas foram perceptíveis à microscopia de luz (ML) e à microscopia eletrônica de transmissão (MET), já no rim somente alterações à MET foram detectadas. Nas brânquias, lamelas secundárias com hipertrofia do epitélio, telangectasia e destacamento epitelial foram as principais alterações. Já no fígado notaram-se degeneração hidrópica, inclusão nuclear, inclusão hialina e vacuolização citoplasmática, como as alterações mais frequentes. Entre as alterações à MET, de modo geral, as mais frequentes foram: alterações mitocondriais, presença de figura de mielina, alteração e/ou perda de microvilos e aumento do espaço intercelular. Embora, alguns exemplares apresentaram alterações celulares frequentes e severas, sugerindo sério dano induzido pelo endosulfan, a análise semi-quantitativa indicou grande variabilidade interindividual. Este último dado sugere fortemente, que a avaliação de biomarcadores histológicos de contaminação aquática deve ser acompanhada de avaliação semi-quantitativa das alterações induzidas associada à análise estatística, para uma fiel indicação do dano provocado à população de organismos-teste. Finalmente, o pacu mostrou-se um bom bioindicador de contaminação aquática por endosulfan o qual se mostrou extremamente tóxico para essa espécie. Assim, espera-se que esta pesquisa venha contribuir efetivamente para o estabelecimento de normas mais rigorosas, ou até mesmo a proibição, da utilização do endosulfan em território brasileiro à semelhança de outros países.
Abstract: The records of endosulfan in river basins of the Patanal wetlands in the state of Mato Grosso (Brazil), the risk to aquatic organisms and lack of information on the action of this pesticide on fish fauna in this region stimulated the present study, which aim was to determine the sensitivity of the pacu (Piaractus mesopotamicus) to endosulfan. For the acute intoxication test (96h) in a static system, fingerlings were exposed to the following concentrations of endosulfan: 0; 0.71; 1.43; 2.14; 2.86; 3.57; 4.29 and 5µgL-1. After 96h, the specimens were necropsied and samples were taken from the gill, liver and kidney for qualitative and semi-quantitative histopathological analysis. The Mean Lethal Concentration (LC50) was 5.66µgL-1 (24h) and 4.33µgL-1 (96h). Gill and liver alterations were visible through light microscopy and transmission electron microscopy (TEM); alterations in the kidney were only detected through TEM. The main alterations in the gills were secondary lamellae with epithelial hypertrophy, telangiectasis and epithelial lifting. The most frequent alterations in the liver were hydropic degeneration, hyaline inclusion and cytoplasmic vacuolization. The most frequent TEM findings were mitochondrial alterations, the presence of myelin figure, alterations in and/or loss of microvilli and increase in intercellular space. Although some specimens frequently exhibited severe cell alterations suggesting serious damage induced by endosulfan, the semi-quantitative analysis revealed considerable interindividual variability. This strongly suggests that the evaluation of histological biomarkers of aquatic contamination should be accompanied by a semi-quantitative assessment of alterations associated with statistical analysis in order to obtain a faithful indication of the damage caused to the population of test organisms. The pacu proved to be a good bioindicator of aquatic contamination by endosulfan, which proved to be extremely toxic to this species. It is hoped that the present study can effectively to contribute toward the establishment of stricter norms or even the banning of the use of endosulfan in Brazil, as has occurred in other countries.
Mestrado
Histologia
Mestre em Biologia Celular e Estrutural
Kolber, Milton. "Emprego do Hamster sírio (Mesocricetus auratus) como modelo biológico para a indução de portador renal de leptospiras." Universidade de São Paulo, 2006. http://www.teses.usp.br/teses/disponiveis/10/10134/tde-27082007-100854/.
Full textThe use of hamsters (Mesocricetus auratus) as experimental model for the reproduction of leptospires kidney carrier condition was investigated on youngs males and females with 80 to 120 g of living weight. The animals were experimentally infected with pathogenic strain of serovar Pomona able of causing the death by leptospirosis between the fifth and the tenth post-infection day. On the second day post-infection the animals were treated with erythromycin estolate at the concentrations of 10, 20, 40 and 80 mg/ kg of living weight. At the 30th day of experimental infection the survivors were anesthetized with isoflurane and blood sample were collected for the determination of kidney and liver functions (Total proteins, Albumin, Urea, Creatinine, Alkaline Phosphatase, Alanine Aminotransferase, Aspartate Aminotransferase, Indirect Bilirubins, Direct Bilirubins and Total Bilirubins), and the of agglutinine title by the microscopic agglutination test (MAT). The animals were killed whit the reinforcement of the anesthesis, and necropsied for the collection of kidney and liver sample for histopathologic tests by staining of Hematoxylin-Eosina and Warthin-Starry, such as the isolation of leptospiras by cultivation into Fletcher´s medium. There were controls of the infecctious inoculum, antibiotic treatment and of the management system adopted. The number of DL 50 effectively applied in the infectious inoculum was 7,11. The antibiotic controls presented elevation of the alkaline phosphatase level and vacuolar degeneration of hepatocytes at the concentrations of 40 to 80 mg of antibiotic. The leptospire\'s kidney carriers were obtained in the animals treated with 40 or 80 mg of Erythromycin Estolate, regardless of the sex; these animals showed increase in creatinine\'s and total protein serum levels but of albumin, urea, alanine aminotransferase, aspartate aminotransferase, direct bilirubins, indirect bilirubins and total bilirubins were the same as found in animals not infected by leptospires and not treated with the antibiotic. The histological changes found in the animals induced as leptospires carrier were vacuolar degeneration in hepatocytes, blood in the portal tract, and glomerular congestion. The agglutinine titles for the homologous serovar, expressed on base 10 logarithm, were at least 1.19.
Paiva, Paula Pereira de 1984. "Avaliação da intoxicação aguda induzida por atrazina em espécie da ictiofauna do pantanal mato-grossense, pacu (Piaractus mesopotamicus), com o emprego de biomarcadores morfológicos." [s.n.], 2010. http://repositorio.unicamp.br/jspui/handle/REPOSIP/317909.
Full textDissertação (mestrado) - Universidade Estadual de Campinas, Instituto de Biologia
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Resumo: Atrazina é um herbicida muito usado em agricultura intensiva e encontrado com alta freqüência em recursos hídricos na região do Pantanal Mato-grossense. Assim, devido aos riscos que a atrazina pode trazer à ictiofauna da região, foi proposta deste trabalho determinar a CL50 da atrazina em alevinos de pacu (Piaractus mesopotamicus). A determinação da CL50 em 96 h em sistema estático, realizada em duplicata, foi conduzida em aquários de vidro com 8 peixes cada, de peso médio de 5,06±0,31g, avaliando-se as seguintes concentrações nominais de atrazina: 0; 13,2; 17,6; 22,0; 26,4; 30,8; 35,2; 39,6 mg L-1, realizando-se também análise comportamental e análise anatomopatológica. Experimento de intoxicação aguda foi realizado em duplicata, nas mesmas condições do anterior, com a concentração da CL50 obtida (28,58 mg L-1), sendo empregados 6 exemplares de peso médio 6,68±0,36g. Amostras hepáticas e mesonéfricas foram colhidas e processadas para análise de microscopia de luz (ML), realizando-se nestas amostras análise semi-quantitativa das alterações encontradas, e para análise de microscopia eletrônica de transmissão (MET). Quanto à avaliação comportamental, foram observados nos grupos tratados: o escurecimento da pigmentação da pele, várias alterações na intensidade do movimento, perda de equilíbrio e presença da ação de boquejamento. Na avaliação anatomopatológica, foram observadas nos grupos tratados: dilatação da região ventral, exoftalmia, protrusão labial, hiperemia no opérculo e em todas as nadadeiras, presença de ar e/ou água no estômago e ascite sanguinolenta. Quanto à análise histopatológica, o grupo controle apresentou a típica morfologia hepática e renal para a espécie. No grupo tratado, severas alterações histopatológicas foram observadas em ML, a mais significativa em fígado foi a presença de inclusões hialinas no citoplasma dos hepatócitos e em rim a degeneração do túbulo proximal. À MET demonstrou que a atrazina causou severas alterações de organelas membranosas, sugestivas de estresse oxidativo e peroxidação lipídica, sendo as alterações mais freqüentes no fígado: inclusão lipídica nuclear e citoplasmática, tumefação do retículo endoplasmático rugoso e de mitocôndrias, degeneração do canalículo biliar com redução na quantidade de microvilos, e em rim, no túbulo proximal (TP): vacúolos citoplasmáticos e aumento do espaço intercelular na porção basolateral, figuras de mielina, tumefação mitocondrial, e, raramente, degeneração do TP. Estas alterações são compatíveis com intoxicação química, demonstrando que estes órgãos são bons biomarcadores de contaminação aquática em peixes. E por fim, o valor da CL50 sugere que a atrazina é levemente tóxica para o pacu, porém pelos demais resultados observados se inferem que só analisar a mortalidade não é o suficiente para determinar o dano causado por agrotóxicos em peixes, assim, recomenda-se o emprego de vários biomarcadores, tais como: análises comportamentais, histopatológicas, bioquímicas, etc.
Abstract: Atrazine is a widely used herbicide in intensive agriculture and a frequent contaminant of waterways in the Pantanal region of Brazil. In view of the potential risks of atrazine to the ichthyofauna of this region, in this work we examined the LC50 of atrazine in pacu (Piaractus mesopotamicus) fingerlings. For this study, fish (5.06 ± 0.31g; mean±SD) were housed eight per glass aquarium and exposed to various concentrations of atrazine (0, 13.2, 17.6, 22.0, 26.4, 30.8, 35.2 and 39.6 mg L-1) for 96 h in static system and this experiment was performed in duplicate, after which the LC50 was determined. Changes in fish behavior and anatomopathological analysis were monitored throughout the experiment. The histopathological alterations caused by atrazine were examined in six fish (6.68 ± 0.36g; mean±SD) using the LC50 (28.58 mg L-1) calculated from the concentration-response curve obtained above. This experiment was done in 96h in static system and performed in duplicate. Liver and mesonephric samples were processed for light microscopy (LM), performing in these samples the semi-quantitative analysis of the changes found, and for transmission electron microscopy (TEM) analysis. Exposure to atrazine caused darkening of the skin, alterations in the intensity of movements, loss of balance and an increase in the frequency of gasping. Anatomopathological assessment revealed dilation of the ventral region, exophthalmia, lip protrusion, skin hyperemia in the opercular region and in all fins, the presence of air and/or water in the stomach, and bloody ascites after the herbicide exposition. The histopathological analysis revealed the typical hepatic and renal morphology for the specie, in control group. Several histopathological changes were observed in exposed fish, but the changes most significant were: in liver, the presence of hyaline inclusions in the cytoplasm of hepatocytes, and proximal tubule (PT) degeneration in the kidney. The ultrastructure showed that the atrazine caused several membrane alterations suggestive of oxidative stress and lipid peroxidation. The most frequent in liver, TEM findings, were: nuclear and cytoplasmic lipid inclusions, swollen rough endoplasmic reticulum and mitochondria, degeneration in the bile canaliculi with a loss in the number of microvilli, and for kidney: an increase in the intercellular space of the basolateral region, myelin figures, swollen mitochondria, and, rarely, degeneration of PT. These lesions are consistent with chemical intoxication and indicate that the liver and kidney are good biomarkers of aquatic contamination in pacu. And, finally, the LC50 value suggests that atrazine is not highly toxic to pacu, however, use of mortality index in acute toxicity as the sole marker in ecotoxicological assays is inadequate and should be completed with other biomarkers such as behavioral, histopathology, biochemistry analyses, etc.
Mestrado
Histologia
Mestre em Biologia Celular e Estrutural
Chan, Ting-bun, and 陳霆斌. "Comparison of surgical outcomes between post-hepatectomy HCC patients with chronic kidney disease and normal kidney." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2012. http://hub.hku.hk/bib/B48333475.
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Medicine
Master
Master of Medical Sciences
Habib, Shahid, Khalid Khan, Chiu-Hsieh Hsu, Edward Meister, Abbas Rana, and Thomas Boyer. "Differential Simultaneous Liver and Kidney Transplant Benefit Based on Severity of Liver Damage at the Time of Transplantation." ELMER PRESS INC, 2017. http://hdl.handle.net/10150/625529.
Full textLeino, Abbie D. "Tacrolimus Intra-Subject Variability in Adherent Kidney and Liver Transplant Recipients." University of Cincinnati / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1530265041482671.
Full textO'Callaghan, John M. "Evidence based hypothermic preservation of the kidney and liver for transplantation." Thesis, University of Oxford, 2014. http://ora.ox.ac.uk/objects/uuid:2ec9083b-bdaf-4fa4-8975-f9e9624b4ccd.
Full textKalin, Cigdem. "Effects Of Acrylamide And Resveratrol On Rabbit Liver And Kidney Antioxidant Enzymes." Master's thesis, METU, 2010. http://etd.lib.metu.edu.tr/upload/3/12611315/index.pdf.
Full text1.40-fold) by combined effect of resveratrol and acrylamide in liver and kidney. Furthermore, alone resveratrol administration increased (~1.37 &ndash
fold) GPx activity in kidney. Although, glutathione reductase (GR) was found to be significantly increased (~1.30-fold) in two different dose of resveratrol treated rabbit liver, it was not changed in acrylamide and their combined treatments. Despite, glutathione (GSH) content was decreased around 1.6 fold as a result of acrylamide treatment in rabbit liver and kidney cytosols, GSH level was returned to normal levels by resveratrol tretment in rabbit liver and kidney. Furthermore, acrylamide treatment significantly increased the SDH activity in blood serum (1.68-fold) and in liver (1.27-fold) with respect to control. On the other hand, resveratrol treatment brought this activity nearly normal level in acrylamide treated rabbits.. Besides, sorbitol deydrogenase (SDH) was found to be decreased (3.13-fold) significantly in rabbit liver cytosol as a result of single dose of 100 mg/kg b.w. resveratrol treatment. Moreover, catalase activity and MDA level were not affected from either resveratrol or acrylamide and with their combination effect in investigated rabbit organs. An important liver damage marker enzyme other than ALT and AST, SDH was characterized in terms of substrate, cofactor and enzyme concentration in rabbits which have been not investigated before and found to be 200 mM, 141 µ
M and 0.5 µ
L, respectively in rabbit liver. Furthermore, the Km value was first calculated in liver of New Zealand rabbits as 55,5 mM. In addition to these, in vitro effects of resveratrol on GST activity was also studied throughout this study. Resveratrol was shown to be a noncompetitive inhibitor for liver cytosolic GST against substrate CDNB with Ki of 175 µ
M. On the other hand, resveratrol was shown to be a competitive inhibitor for liver cytosolic GST against substrate GSH with Ki of 55 µ
M. The results of the present study have demonstrated for the first time that resveratrol induced some of the antioxidant enzyme activities and as well nonenzymatic antioxidants in rabbit liver and kidney. The results of GPx, GR, SDH activities and GSH level have also suggested that resveratrol may have protective effects on acrylamide induced hepatoxicity and renal toxicity. Therefore, it may be a therapeutic approach for the oxidative stress-related diseases such as cancer. However, further in vivo studies are required to clarify the effect of resveratrol on both acrylamide-induced toxicity and bioavailability in the body.
Herlenius, Gustaf. "Renal function after transplantation of the liver and intestine /." Gothenburg : Transplant Institute, Sahlghrenska University Hospital, Institute of Clinical Sciences at Sahlgrenska Academy, University of Gothenburg, 2010. http://hdl.handle.net/2077/21523.
Full textMaathuis, M. H. J. "Organ preservation and viability in kidney and liver transplantation experimental and clinical studies /." [S.l. : [Groningen : s.n.] ; University Library Groningen] [Host], 2008. http://irs.ub.rug.nl/ppn/.
Full textBooks on the topic "Kidney and liver histopathology"
1925-, Conn Harold O., ed. Histopathology of the liver. New York: Oxford University Press, 1993.
Find full textErlichman, Martin. Combined liver-kidney transplantation. Rockville, Md: U.S. Dept. of Health and Human Services, Public Health Service, Agency for Health Care Policy and Research, Office of Health Technology Assessment, 1995.
Find full textErlichman, Martin. Combined liver-kidney transplantation. Rockville, Md: U.S. Dept. of Health and Human Services, Public Health Service, Agency for Health Care Policy and Research, Office of Health Technology Assessment, 1995.
Find full textErlichman, Martin. Combined liver-kidney transplantation. Rockville, Md: U.S. Dept. of Health and Human Services, Public Health Service, Agency for Health Care Policy and Research, Office of Health Technology Assessment, 1995.
Find full textChung, Whan Kook. Liver diseases: An atlas of histopathology. Amsterdam: Elsevier, 1993.
Find full textBurt, Alastair D. MacSween's pathology of the liver. 6th ed. Edinburgh: Churchill Livingstone, 2012.
Find full textM, Petrovic Lydia, ed. Biopsy interpretation of the liver. 2nd ed. Philadelphia: Wolters Kluwer/Lippincott Williams & Wilkins Health, 2009.
Find full textParsons, Richard Bramwell. Cysteine metabolism in the brain, liver and kidney. Birmingham: University of Birmingham, 1998.
Find full textBook chapters on the topic "Kidney and liver histopathology"
Kelly, Paul J., Derek C. Allen, R. Iain Cameron, and Maurice B. Loughrey. "Liver." In Histopathology Specimens, 111–24. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-57360-1_10.
Full textAllen, Derek C., R. Iain Cameron, and Maurice B. Loughrey. "Liver." In Histopathology Specimens, 99–110. London: Springer London, 2012. http://dx.doi.org/10.1007/978-0-85729-673-3_10.
Full textMarley, N. J. E., and D. R. Davies. "Kidney." In Reporting Histopathology Sections, 169–86. Boston, MA: Springer US, 1997. http://dx.doi.org/10.1007/978-1-4899-7132-6_10.
Full textAllen, Derek C. "Liver Carcinoma." In Histopathology Reporting, 95–105. London: Springer London, 2013. http://dx.doi.org/10.1007/978-1-4471-5263-7_10.
Full textKelly, Paul J. "Liver Carcinoma." In Histopathology Reporting, 131–43. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-27828-1_11.
Full textAllen, Derek C. "Liver Carcinoma." In Histopathology Reporting, 85–94. London: Springer London, 2000. http://dx.doi.org/10.1007/978-1-4471-3671-2_10.
Full textDavies, S. E., and C. S. Foster. "Liver." In Reporting Histopathology Sections, 67–82. Boston, MA: Springer US, 1997. http://dx.doi.org/10.1007/978-1-4899-7132-6_4.
Full textGeller, Stephen A. "Liver: Tissue Handling and Evaluation." In Histopathology, 303–21. New York, NY: Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-1050-2_18.
Full textO’Rourke, Declan M., and Derek C. Allen. "Kidney, Renal Pelvis, and Ureter." In Histopathology Specimens, 301–19. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-57360-1_29.
Full textO’Rourke, Declan M., and Derek C. Allen. "Kidney, Renal Pelvis, and Ureter." In Histopathology Specimens, 279–93. London: Springer London, 2012. http://dx.doi.org/10.1007/978-0-85729-673-3_29.
Full textConference papers on the topic "Kidney and liver histopathology"
Araújo, Ikaro Campos, Leizer Schnitman, Angelo Amancio Duarte, and Washington LC Santos. "Automated Detection of Segmental Glomerulosclerosis in Kidney Histopathology." In Congresso Brasileiro de Inteligência Computacional. ABRICOM, 2018. http://dx.doi.org/10.21528/cbic2017-10.
Full textEfremova, Dina B., Dmitry A. Konovalov, Thanongchai Siriapisith, Worapan Kusakunniran, and Peter Haddawy. "Automatic segmentation of kidney and liver tumors in CT images." In 2019 Kidney Tumor Segmentation Challenge: KiTS19. University of Minnesota Libraries Publishing, 2019. http://dx.doi.org/10.24926/548719.038.
Full textRoy, Mousumi, Fusheng Wang, George Teodoro, Miriam B. Vos, Alton Brad Farris, and Jun Kong. "Segmentation of Overlapped Steatosis in Whole-Slide Liver Histopathology Microscopy Images." In 2018 40th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC). IEEE, 2018. http://dx.doi.org/10.1109/embc.2018.8512289.
Full textAalamifar, Fereshteh, Hassan Rivaz, Juan J. Cerrolaza, James Jago, Nabile Safdar, Emad M. Boctor, and Marius G. Linguraru. "Classification of kidney and liver tissue using ultrasound backscatter data." In SPIE Medical Imaging, edited by Johan G. Bosch and Neb Duric. SPIE, 2015. http://dx.doi.org/10.1117/12.2082300.
Full textLi, Fengyi, Yang Nan, Xiaoshuai Hou, Chunmei Xie, Jiaping Wang, ChuanFeng Lv, and GuoTong Xie. "Correlation-Guided Network for Fine-Grained Classification of Glomerular lesions in Kidney Histopathology Images." In 2020 42nd Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC) in conjunction with the 43rd Annual Conference of the Canadian Medical and Biological Engineering Society. IEEE, 2020. http://dx.doi.org/10.1109/embc44109.2020.9176234.
Full textAssis, G., and C. Cruz. "Zinc content in liver and kidney of piglets slaughtered in Portugal." In Safe Pork 2015: Epidemiology and control of hazards in pork production chain. Iowa State University, Digital Press, 2015. http://dx.doi.org/10.31274/safepork-180809-307.
Full text"Protective Effect of Turmeric on Liver and Kidney in Chicken Aflatoxicosis." In International Conference on Chemical, Environmental and Biological Sciences. International Institute of Chemical, Biological & Environmental Engineering, 2015. http://dx.doi.org/10.15242/iicbe.c0315125.
Full textWirtzfeld, L. A., E. S. L. Berndl, and M. C. Kolios. "Ultrasonic characterization of extra-cellular matrix in decellularized murine kidney and liver." In 2015 IEEE International Ultrasonics Symposium (IUS). IEEE, 2015. http://dx.doi.org/10.1109/ultsym.2015.0170.
Full textRazman, Nur Raihan, Wan Mahani Hafizah Wan Mahmud, and Nurul Aimi Shaharuddin. "Filtering technique in ultrasound for kidney, liver and pancreas image using Matlab." In 2015 IEEE Student Conference on Research and Development (SCOReD). IEEE, 2015. http://dx.doi.org/10.1109/scored.2015.7449365.
Full textNasution, Ali Napiah, and Sri Lestari R. Nasution. "Histopathology of Rat Kidney Organ Due to Ethanol Extract of Phaleria Macrocarpa Treatment Induced by Isoniazid." In International Conference on Health Informatics, Medical, Biological Engineering, and Pharmaceutical. SCITEPRESS - Science and Technology Publications, 2020. http://dx.doi.org/10.5220/0010296202430247.
Full textReports on the topic "Kidney and liver histopathology"
Norton, William N. Acute Exposure of Medaka to Carcinogens: An Ultrastructural, Cytochemical and Morphometric Analysis of Liver and Kidney. Fort Belvoir, VA: Defense Technical Information Center, February 1991. http://dx.doi.org/10.21236/ada242950.
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