Academic literature on the topic 'Renal medullla'
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Journal articles on the topic "Renal medullla"
Ukey, Rahul Kisan, Reshma Baburao Shinde, Anil Shivshankar Rahule, Prafulla Nikam, and C. V. Diwan. "HISTOGENESIS OF HUMAN FETAL RENAL MEDULLA." International Journal of Anatomy and Research 6, no. 3.2 (August 10, 2018): 5544–49. http://dx.doi.org/10.16965/ijar.2018.277.
Full textGrossman, E. B., and S. C. Hebert. "Renal inner medullary choline dehydrogenase activity: characterization and modulation." American Journal of Physiology-Renal Physiology 256, no. 1 (January 1, 1989): F107—F112. http://dx.doi.org/10.1152/ajprenal.1989.256.1.f107.
Full textVeuthey, Tania, María Cecilia D'Anna, and Marta Elena Roque. "Role of the kidney in iron homeostasis: renal expression of Prohepcidin, Ferroportin, and DMT1 in anemic mice." American Journal of Physiology-Renal Physiology 295, no. 4 (October 2008): F1213—F1221. http://dx.doi.org/10.1152/ajprenal.90216.2008.
Full textKIM, SOO WAN, SAM HYEON CHO, BONG SUK OH, CHUNG HO YEUM, KI CHUL CHOI, KYU YOUN AHN, and JONGUN LEE. "Diminished Renal Expression of Aquaporin Water Channels in Rats with Experimental Bilateral Ureteral Obstruction." Journal of the American Society of Nephrology 12, no. 10 (October 2001): 2019–28. http://dx.doi.org/10.1681/asn.v12102019.
Full textJeon, Un Sil, Ki-Hwan Han, Soo-Hyun Park, Sang Do Lee, Mee Rie Sheen, Ju-Young Jung, Wan Young Kim, Jeff M. Sands, Jin Kim, and H. Moo Kwon. "Downregulation of renal TonEBP in hypokalemic rats." American Journal of Physiology-Renal Physiology 293, no. 1 (July 2007): F408—F415. http://dx.doi.org/10.1152/ajprenal.00502.2006.
Full textBurg, Maurice B., and Eugenia M. Peters. "Urea and methylamines have similar effects on aldose reductase activity." American Journal of Physiology-Renal Physiology 273, no. 6 (December 1, 1997): F1048—F1053. http://dx.doi.org/10.1152/ajprenal.1997.273.6.f1048.
Full textArmando, Ines, Miroslava Jezova, Augusto V. Juorio, José A. Terrón, Alicia Falcón-Neri, Cristina Semino-Mora, Hans Imboden, and Juan M. Saavedra. "Estrogen upregulates renal angiotensin II AT2receptors." American Journal of Physiology-Renal Physiology 283, no. 5 (November 1, 2002): F934—F943. http://dx.doi.org/10.1152/ajprenal.00145.2002.
Full textNakanishi, T., O. Uyama, and M. Sugita. "Osmotically regulated taurine content in rat renal inner medulla." American Journal of Physiology-Renal Physiology 261, no. 6 (December 1, 1991): F957—F962. http://dx.doi.org/10.1152/ajprenal.1991.261.6.f957.
Full textAldekeeva, A. S., Y. S. Kraynova, E. D. Rudenko, and N. Z. Klyueva. "MARcKS and nAP-22 proteins mRnA expression in renal cortex and renal medulla of rats with spontaneous hypertension." "Arterial’naya Gipertenziya" ("Arterial Hypertension") 24, no. 4 (September 26, 2018): 435–40. http://dx.doi.org/10.18705/1607-419x-2018-24-4-435-440.
Full textTanvetthayanont, Potsawat, Suppawiwat Ponglowhapan, Chutimon Thanaboonnipat, and Nan Choisunirachon. "Impact of gonadal status on ultrasonographic renal parenchymal dimensions in healthy cats." Journal of Feline Medicine and Surgery 22, no. 12 (March 20, 2020): 1148–54. http://dx.doi.org/10.1177/1098612x20910541.
Full textDissertations / Theses on the topic "Renal medullla"
Zhang, Wensheng. "Protein and oxygen transport across vasa recta in the renal medulla /." Thesis, Connect to Dissertations & Theses @ Tufts University, 2002.
Find full textAdviser: Aurelie Edwards. Submitted to the Dept. of Chemical Engineering. Includes bibliographical references (leaves 210-219). Access restricted to members of the Tufts University community. Also available via the World Wide Web;
Ahrens, Nikolai. "Evidence for and characterization of cytoplasmic dynein and kinesin in renal medulla and cortex." Thesis, University of Oxford, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.386898.
Full textSanches, Osimar de Carvalho [UNESP]. "Histopatologia da série eritróide da medula óssea e do tecido renal de cães com insuficiência renal crônica." Universidade Estadual Paulista (UNESP), 2005. http://hdl.handle.net/11449/95897.
Full textUniversidade Estadual Paulista (UNESP)
A insuficiência renal crônica é a principal afecção renal dos cães e a anemia é a principal seqüela desta infecção. Os rins são os principais responsáveis pela produção do hormônio estimulador e regulador da eritropoiese - eritropoetina. O presente estudo teve por objetivos investigar e descrever as alterações histopatológicas dos rins e da linhagem eritróide na medula óssea de cães portadores de insuficiência renal crônica (IRC), identificando e quantificando as células precursoras das hemácias na medula óssea. Foram utilizados 15 animais controle e 15 animais portadores de insuficiência renal crônica. As amostras foram analisadas em microscopia ótica, tendo como auxílio à coloração de Giemsa, que foi utilizada para diferenciar os precursores eritróides. Os animais do grupo controle apesar de apresentarem alterações morfológicas nos rins, estas não foram suficientes para promover alterações nos parâmetros hematológicos, bem como na bioquímica sérica. Já nos animais do grupo com IRC as alterações morfológicas se caracterizaram por glomerulonefrite crônica, seguida da glomerulonefrite proliferativa mesangial, glomerulonefrite membranoproliferativa e da glomerulonefrite membranosa com 46,66%, 26,66%, 13,33% e 13,33% dos animais respectivamente. Vale ressaltar ainda que 73,33% dos animais exibiam nefrite intersticial crônica e 20% apresentavam nefrite intersticial focal. Dos quinze animais do grupo com IRC, 80% exibiam quadro de anemia, sendo 46,66% do tipo normocítica normocrômica, 20% macrocítica hipocrômica, 6,66% com anemia microcítica normocrômica e 6,66% do tipo macrocítica hipocrômica. As alterações morfológicas túbulo-intersticiais apresentaram maior correlação com as concentrações de uréia e creatinina e com a contagem dos precursores eritróides.
The chronic renal failure, the main renal afection of the dogs and the anemia is the main sequel of this afection. The kidneys are the main responsible for the production of the hormone stimulator and regulator of the erythropoiesis - erythropoietin. The present work had as objectives to investigate and to describe the histopathologics alterations of the kidneys and of the erythroid lineage in the bone marrow of dogs bearers of chronic renal failure (CRF), identifying and quantifying the precursory cells of the erythrocytes in the bone marrow. 15 control animals and 15 animals bearers of chronic renal failure were used. The samples were analyzed in optic microscopy, with the use of the Giemsa coloration, used to differentiate the erythroid precursors. The animals of the control group inspite of the morphologic alterations presented in the kidneys, were not enough to promote alterations in the hematological parameters, as well as in the serum biochemistry. In the animals of the group with CRF the morphologic alterations are characterized by chronic glomerulonephritis, following by proliferative mesangial glomerulonephritis, membranousproliferative glomerulonephritis and the membranous glomerulonephritis with 46,66%, 26,66%, 13,33% and 13,33% of the animals respectively. It is worth to stand out that 73,33% of the animals exhibited chronic interstitial nephritis and 20% presented focal interstitial nephritis. Of the 15 animals of the group with CRF, 80% exhibited anemia, being 46,66% of the type normocytic normochromic, 20% macrocytic hypochromic, 6,66% with anemia microcytic normochromic and 6,66% of the type macrocytic hypochromic. The morphologic tubulo-interstitial alterations presented larger correlation with the urea concentrations and creatinine and with the counting of the erythroid precursors.
Sanches, Osimar de Carvalho. "Histopatologia da série eritróide da medula óssea e do tecido renal de cães com insuficiência renal crônica /." Botucatu : [s.n.], 2005. http://hdl.handle.net/11449/95897.
Full textResumo: A insuficiência renal crônica é a principal afecção renal dos cães e a anemia é a principal seqüela desta infecção. Os rins são os principais responsáveis pela produção do hormônio estimulador e regulador da eritropoiese - eritropoetina. O presente estudo teve por objetivos investigar e descrever as alterações histopatológicas dos rins e da linhagem eritróide na medula óssea de cães portadores de insuficiência renal crônica (IRC), identificando e quantificando as células precursoras das hemácias na medula óssea. Foram utilizados 15 animais controle e 15 animais portadores de insuficiência renal crônica. As amostras foram analisadas em microscopia ótica, tendo como auxílio à coloração de Giemsa, que foi utilizada para diferenciar os precursores eritróides. Os animais do grupo controle apesar de apresentarem alterações morfológicas nos rins, estas não foram suficientes para promover alterações nos parâmetros hematológicos, bem como na bioquímica sérica. Já nos animais do grupo com IRC as alterações morfológicas se caracterizaram por glomerulonefrite crônica, seguida da glomerulonefrite proliferativa mesangial, glomerulonefrite membranoproliferativa e da glomerulonefrite membranosa com 46,66%, 26,66%, 13,33% e 13,33% dos animais respectivamente. Vale ressaltar ainda que 73,33% dos animais exibiam nefrite intersticial crônica e 20% apresentavam nefrite intersticial focal. Dos quinze animais do grupo com IRC, 80% exibiam quadro de anemia, sendo 46,66% do tipo normocítica normocrômica, 20% macrocítica hipocrômica, 6,66% com anemia microcítica normocrômica e 6,66% do tipo macrocítica hipocrômica. As alterações morfológicas túbulo-intersticiais apresentaram maior correlação com as concentrações de uréia e creatinina e com a contagem dos precursores eritróides.
Abstract: The chronic renal failure, the main renal afection of the dogs and the anemia is the main sequel of this afection. The kidneys are the main responsible for the production of the hormone stimulator and regulator of the erythropoiesis - erythropoietin. The present work had as objectives to investigate and to describe the histopathologics alterations of the kidneys and of the erythroid lineage in the bone marrow of dogs bearers of chronic renal failure (CRF), identifying and quantifying the precursory cells of the erythrocytes in the bone marrow. 15 control animals and 15 animals bearers of chronic renal failure were used. The samples were analyzed in optic microscopy, with the use of the Giemsa coloration, used to differentiate the erythroid precursors. The animals of the control group inspite of the morphologic alterations presented in the kidneys, were not enough to promote alterations in the hematological parameters, as well as in the serum biochemistry. In the animals of the group with CRF the morphologic alterations are characterized by chronic glomerulonephritis, following by proliferative mesangial glomerulonephritis, membranousproliferative glomerulonephritis and the membranous glomerulonephritis with 46,66%, 26,66%, 13,33% and 13,33% of the animals respectively. It is worth to stand out that 73,33% of the animals exhibited chronic interstitial nephritis and 20% presented focal interstitial nephritis. Of the 15 animals of the group with CRF, 80% exhibited anemia, being 46,66% of the type normocytic normochromic, 20% macrocytic hypochromic, 6,66% with anemia microcytic normochromic and 6,66% of the type macrocytic hypochromic. The morphologic tubulo-interstitial alterations presented larger correlation with the urea concentrations and creatinine and with the counting of the erythroid precursors.
Mestre
Dempsey, Sara. "Diuretic and natriuretic activity of FAAH inhibition in the renal medulla: a proposed role of palmitoylethanolamide and its regulation by renal medullary interstitial cells." VCU Scholars Compass, 2019. https://scholarscompass.vcu.edu/etd/5776.
Full textAdun, Eseoghene. "Vasopressin Alters the Expression of Aquaporins, Urea Transporters, and ER Stress Genes in the Mouse Renal Medulla." Thesis, The University of Arizona, 2012. http://hdl.handle.net/10150/243731.
Full textCaldas, Heloisa Cristina. "Efeito das células derivadas da medula óssea no tratamento da insuficiência renal crônica experimental." Faculdade de Medicina de São José do Rio Preto, 2011. http://bdtd.famerp.br/handle/tede/104.
Full textChronic renal failure (CRF) is characterized by progressive and irreversible loss of renal function and its treatment generates significant public spending for maintenance and care of patients on dialysis. Stem cell (SC) therapy, in its potential for treatment of chronic diseases, may be a promising strategy for repairing the damage from or slowing the progression of CRF. There are questions about cell type, quantity of cells, method and ideal place for deployment of SC and the role it plays in the repair of renal parenchyma. Objective: 1) To evaluate the effect of infusion of bone marrow derived cells (BMDC) in the treatment of experimental CRF; 2) Evaluate the combined effect of SC and biomaterial (BM) in the progression of CRF and study the effect of this therapy in different stages of CRF; 3) Evaluate the development of techniques for isolation and cultivation of human umbilical cord blood (HUCB) mesenchymal cells. Methods: Article 1: We used the 5/6 mass reduction model to induce experimental CRF. Kidney function was measured at the beginning of the experiment and 60 and 120 days after the surgery; Article 2: Animals were subdivided as to the amount of renal parenchyma injured (5/6 or 2/3), the use of BM as a scaffold to cell implantation, and cell type used (mononuclear or mesenchymal cells). Renal function was evaluated on days 0, 45, and 90 after surgery. Histological and immunohistochemical analyses were done in all groups at the end of the study; Article 3: Ten samples of HUCB were used and two different procedures for cultivation of mesenchymal stem cells (MSC) were tested: without Ficoll-Paque density gradient, to obtain nucleated cells; with Ficoll-Paque density gradient, for obtaining mononuclear cells. Results: Article 1: CRF progression analysis showed that treatment with BMDC significantly reduced the rate of decline of creatinine clearance (Clcr) when compared with the control group; Article 2:Treated animals showed significantly lower increases in serum creatinine and 24 hour proteinuria, and higher increases in Clcr after 90 days when compared to control animals in both models of CRF; Article 3: The MSC in culture from the method without Ficoll-Paque density gradient maintained growth forming confluent cell foci. Conclusions: Article 1: Progression of CRF can be delayed by injection of BMDC in the renal parenchyma; Article 2: a) Use of SC combined with BM can be an alternative way to administer BMDC; b) Cell therapy seems to be most effective when administered in less severe stages of CRF; Article 3: Nucleated cells without using Ficoll-Paque density gradient showed more efficiency in the cultivation of MSC from HUCB when compared with the procedure employing Ficoll-Paque density gradient
A insuficiência renal crônica (IRC) é caracterizada pela perda progressiva e irreversível da função renal e seu tratamento gera um gasto público significativo para manutenção de pacientes em tratamento dialítico. A terapia com células-tronco (CT), pelo seu potencial de tratamento das doenças crônicas, pode ser uma estratégia promissora para reparar ou retardar a progressão da IRC. Existem dúvidas sobre o tipo celular, a quantidade de células, o método e local ideal para implantação das CT e o papel por elas desempenhado na reparação do parênquima renal. Objetivos: 1) avaliar o efeito da infusão de células derivadas da medula óssea (CDMO) no tratamento da IRC experimental; 2) avaliar o efeito combinado das CT e biomaterial (BM) na progressão da IRC e estudar o efeito dessa terapia em diferentes estágios da IRC; 3) Avaliar o desenvolvimento de técnicas de isolamento e cultivo de células mesenquimais do sangue de cordão umbilical humano (SCU). Métodos: artigo 1: usamos o modelo de redução de massa 5/6 para induzir a IRC experimental. Função renal foi medida no início do experimento e 60 e 120 dias depois da cirurgia; artigo 2: animais foram subdivididos conforme a quantidade de parênquima renal lesado (5/6 ou 2/3), o uso de BM como arcabouço para o implante celular e o tipo de células utilizado (célula mononuclear ou mesenquimal). A função renal foi avaliada nos dias 0, 45 e 90 após cirurgia. Análise histológica e imunohistoquimica foram realizadas em todos os grupos ao final do estudo; artigo 3: Foram utilizadas dez amostras de SCU e testados dois diferentes procedimentos para cultivo de células-tronco mesenquimal (CTM): sem gradiente de densidade Ficoll-Paque, para obtenção de células nucleadas; por gradiente de densidade Ficoll-Paque, para obtenção de células mononucleares. Resultados: artigo 1: Análises da progressão da IRC mostraram que o tratamento com CDMO reduziu significativamente a taxa de declínio do clearance ( Clcr) quando comparados com o grupo controle; artigo 2: animais tratados apresentaram aumentos significativamente menores de creatinina sérica, proteinúria e Clcr maiores após 90 dias, quando comparado aos animais controles em ambos os modelos de IRC; artigo 3: as CTM em cultura provenientes do método sem gradiente de densidade Ficoll- Paque mantiveram o crescimento formando focos confluentes de células. Conclusões: artigo 1: a progressão da IRC pode ser retardada pela injeção de CDMO no parênquima renal; artigo 2: a) utilização da CT combinada com o BM pode ser uma via alternativa para administrar a CTMO; b) terapia celular parece ser mais eficaz quando administrada em estágios menos graves da IRC; artigo 3: As células nucleadas sem uso do gradiente de densidade Ficoll-Paque mostraram mais eficiente para o cultivo de CTM do SCU quando comparado ao procedimento com gradiente de densidade Ficoll-Paque.
Alexandre, Cristianne da Silva. "As células linhagem negativa (Lin) de medula óssea atenuam a progressão da doença renal crônica." Universidade de São Paulo, 2008. http://www.teses.usp.br/teses/disponiveis/5/5148/tde-10032008-150329/.
Full textProgressive renal failure continues to be a challenge. The use of bone marrowderived stem cells (SCs) represents a means of meeting that challenge. We used lineage-negative (Lin-) SCs to test the hypothesis that Lin- cell infusion decreases renal injury. Syngeneic Fischer 344 rats were submitted to 5/6 nephrectomy and divided into 3 groups: Nx (untreated); NxSC1 (receiving 2 × 106 Lin- cells on postnephrectomy day 15); and NxSC3 (receiving 2 × 106 Lin- cells on postnephrectomy days 15, 30 and 45). Controls were unoperated/untreated. On postnephrectomy day 60, clearance studies, immunohistochemistry and immunoblotting were performed. Lin- cell infusion effectively reduced postnephrectomy proteinuria, glomerulosclerosis, anemia, renal infiltration of immune cells and monocyte chemoattractant protein-1 protein expression, as well as decreasing the interstitial area. Immunostaining for proliferating cell nuclear antigen showed that, in comparison with controls, Nx rats presented greater cell proliferation, whereas NxSC1 rats and NxSC3 rats presented less cell proliferation than did Nx rats. Protein expression of p21 and VEGF increased after nephrectomy and decreased after Lin- cell infusion. Protein expression of eNOS reduced after nephrectomy and increased after cell infusion. These data suggest that SC treatment ameliorates progressive end-stage renal disease.
Issaian, Tadeh. "Three-Dimentional Architecture of the Renal Inner Medulla of the Desert Rodent Dipodomys Merriami: Potential Impact on the Urinary Concentrating Mechanism." Thesis, The University of Arizona, 2010. http://hdl.handle.net/10150/156916.
Full textPiera, Ryan Elias. "Mensuração ultra-sonográfica da relação córtico-medular renal em cães." Universidade de São Paulo, 2005. http://www.teses.usp.br/teses/disponiveis/10/10132/tde-06082007-104522/.
Full textThrough the ultrasound, a insurance and exact diagnostic, we can establish renal corticomedullary correlation (RCM) evaluating the volume of the cortical and medullary adding a quantitative evaluation to the used method in the interpretations ultrasonographics, that still are of qualitative character (subjective) and depend on the ability, the equipment and the experience of the medical veterinarian who will be making the examination. We use 30 animals of different races, with ages between 1 and 9 years, males and females, with weights in the band of 9 up to 40 kg, proceeding from clinical particular veterinarians. All had passed for examinations clinical and physical, revealing healthy and without description of illness or renais problems, what it was confirmed through laboratoriais examinations. After the gaugings for ultrasound the measures had been placed in formulas, which had given to the volumes of cortex and medullary, following then for a more necessary corticomedullary correlation. The results had shown that the values of RCM independently go of 2,26 the 3,33 of the renal volume, sex, weight and age, being these variants of low significance with the corticomedullary correlation.
Books on the topic "Renal medullla"
Mandal, Anil K. Renal Papilla and Hypertension. Springer London, Limited, 2012.
Find full textMandal, Anil K. The Renal Papilla and Hypertension. Springer, 2012.
Find full textHo, Kwok M. Kidney and acid–base physiology in anaesthetic practice. Edited by Jonathan G. Hardman. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199642045.003.0005.
Full textBook chapters on the topic "Renal medullla"
Pallone, Thomas L., and Aurélie Edwards. "Transport Processes in the Microcirculation of the Renal Medulla." In Membrane Transport and Renal Physiology, 211–31. New York, NY: Springer New York, 2002. http://dx.doi.org/10.1007/978-1-4684-9252-1_12.
Full textThomas, S. Randall. "Lactate Accumulation in Kidney Inner Medulla: A Vasa Recta Model." In Membrane Transport and Renal Physiology, 273–91. New York, NY: Springer New York, 2002. http://dx.doi.org/10.1007/978-1-4684-9252-1_14.
Full textEpstein, F. H., M. Brezis, and S. Rosen. "Role of the Medulla in Acute Renal Failure." In Current Concepts in Critical Care, 91–102. London: Springer London, 1990. http://dx.doi.org/10.1007/978-1-4471-1750-6_9.
Full textAngielski, S., T. Pawełozyk, D. Bizon, G. Piec, L. Wojnowski, and J. Stępiński. "DIFFERENCES IN ADENYLATE METABOLISM IN RENAL CORTEX AND MEDULLA." In Molecular Nephrology, edited by Walter G. Guder and Zoran Kovačević, 311–18. Berlin, Boston: De Gruyter, 1987. http://dx.doi.org/10.1515/9783110884746-048.
Full textKu, Min-Chi, María A. Fernández-Seara, Frank Kober, and Thoralf Niendorf. "Noninvasive Renal Perfusion Measurement Using Arterial Spin Labeling (ASL) MRI: Basic Concept." In Methods in Molecular Biology, 229–39. New York, NY: Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-0978-1_13.
Full textNakanishi, Takeshi, Yoshihiro Takamitsu, and Minoru Sugita. "Role of Taurine in the Kidney: Osmoregulatory Taurine Accumulation in Renal Medulla." In Advances in Experimental Medicine and Biology, 139–48. Boston, MA: Springer US, 1994. http://dx.doi.org/10.1007/978-1-4899-1471-2_15.
Full textPedersen, Michael, Pietro Irrera, Walter Dastrù, Frank G. Zöllner, Kevin M. Bennett, Scott C. Beeman, G. Larry Bretthorst, Joel R. Garbow, and Dario Livio Longo. "Dynamic Contrast Enhancement (DCE) MRI–Derived Renal Perfusion and Filtration: Basic Concepts." In Methods in Molecular Biology, 205–27. New York, NY: Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-0978-1_12.
Full textFox, Michelle Roper, Henry Kelly, and Sachin Patil. "Medulla: A Cyberinfrastructure-Enabled Framework for Research, Teaching, and Learning with Virtual Worlds." In Online Worlds: Convergence of the Real and the Virtual, 87–100. London: Springer London, 2009. http://dx.doi.org/10.1007/978-1-84882-825-4_7.
Full textRiazy, Leili, Bastien Milani, João S. Periquito, Kathleen Cantow, Thoralf Niendorf, Menno Pruijm, Erdmann Seeliger, and Andreas Pohlmann. "Subsegmentation of the Kidney in Experimental MR Images Using Morphology-Based Regions-of-Interest or Multiple-Layer Concentric Objects." In Methods in Molecular Biology, 549–64. New York, NY: Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-0978-1_33.
Full textMartirosian, P., C. Schraml, N. F. Schwenzer, G. Steidle, C. Rossi, A. Boss, V. Kumar, et al. "Fiber Architecture Mapping of the Renal Medulla Using Respiratory Triggered Diffusion Tensor Imaging at 3 Tesla." In IFMBE Proceedings, 346–49. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-03879-2_98.
Full textConference papers on the topic "Renal medullla"
Tulum, Gokalp, N. Tugrul Artug, Onur Osman, Vural Taner Yilmaz, Tuncer Ergin, Ferhat Cuce, Ozgur Dandin, et al. "Fully Automated Segmentation of Renal, Cortex and Medulla." In 2018 Medical Technologies National Congress (TIPTEKNO). IEEE, 2018. http://dx.doi.org/10.1109/tiptekno.2018.8596993.
Full textROSAR, M. E. "A MATHEMATICAL MODEL OF THE INNER AND OUTER RENAL MEDULLA." In Proceedings of the International Conference. WORLD SCIENTIFIC, 2001. http://dx.doi.org/10.1142/9789812810885_0008.
Full textYilmaz, Vural Taner, Gokalp Tulum, Tuncer Ergin, Ferhat Cuce, Ozgur Dandin, Huseyin Kocak, Abdullah Kisaoglu, et al. "Calculation of Renal, Cortex and Medulla Volumes using Semi Automated Method." In 2018 Medical Technologies National Congress (TIPTEKNO). IEEE, 2018. http://dx.doi.org/10.1109/tiptekno.2018.8596888.
Full textCai, Qing, Ping Geng, Hong Li, Haoran Sun, and Yan Kang. "Semi-automatic segmentation of renal cortex and medulla based on dynamic magnetic resonance images." In 2010 3rd International Conference on Biomedical Engineering and Informatics (BMEI). IEEE, 2010. http://dx.doi.org/10.1109/bmei.2010.5639998.
Full textTang, Yucheng, Riqiang Gao, Ho Hin Lee, Zhoubing Xu, Brent V. Savoie, Shunxing Bao, Yuankai Huo, et al. "Renal cortex, medulla and pelvicaliceal system segmentation on arterial phase CT images with random patch-based networks." In Image Processing, edited by Bennett A. Landman and Ivana Išgum. SPIE, 2021. http://dx.doi.org/10.1117/12.2581101.
Full textSohrabi, Salman, Seyyed Mahdi Nemati Mehr, and Pedram Falsafi. "A Novel Approach for Compensating the Significance of Tubule’s Architecture in Urine Concentrating Mechanism of Renal Medulla." In ASME 2013 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/imece2013-63747.
Full textPereira, Paula Beatriz, Joice Rodrigues Dos Santos, and Victória Regina Dos Santos. "TRANSPLANTE DE MEDULA ÓSSEA PARA PACIENTES COM ANEMIA FALCIFORME." In II Congresso Brasileiro de Hematologia Clínico-laboratorial On-line. Revista Multidisciplinar em Saúde, 2022. http://dx.doi.org/10.51161/hematoclil/26.
Full textBardin, T., K. M. Tran, Q. D. Nguyen, N. H. Le, P. Richette, P. Le Van, J. M. Correas, and M. Resche-Rigon. "OP0357 Hyperechoic deposits in the renal medulla are associated with severe gout and decreased egfr: a transversal study in 503 vietnamese patients." In Annual European Congress of Rheumatology, EULAR 2018, Amsterdam, 13–16 June 2018. BMJ Publishing Group Ltd and European League Against Rheumatism, 2018. http://dx.doi.org/10.1136/annrheumdis-2018-eular.5027.
Full textRahman, Md Habibur, Shailee Mitra, Hasib Ahmed Prince, and Enamul Hasan Rozin. "Numerical Modelling of Tumor Ablation Process by Localized Heating with Four Armed Electric Probe and a Comparative Study Between Human Liver and Renal Medulla Tissue." In 2019 5th International Conference on Advances in Electrical Engineering (ICAEE). IEEE, 2019. http://dx.doi.org/10.1109/icaee48663.2019.8975546.
Full textSouza, Karolayne Silva, DIEGO CANUTO BISPO DA SILVA, and MILENA ROBERTA FREIRE DA SILVA. "ASPECTOS FISIOPATÓLOGICOS DO MIELOMA MÚLTIPLO: UMA REVISÃO BIBLIOGRÁFICA." In II Congresso Brasileiro de Imunologia On-line. Revista Multidisciplinar em Saúde, 2022. http://dx.doi.org/10.51161/ii-conbrai/6116.
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