Добірка наукової літератури з теми "Renal dysplasia"
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Статті в журналах з теми "Renal dysplasia"
Menon, Santosh, Nandita Kakkar, and B. D. Radotra. "Expression of Laminin and Fibronectin in Renal Dysplasia." Pediatric and Developmental Pathology 7, no. 6 (November 2004): 568–76. http://dx.doi.org/10.1007/s10024-003-5057-3.
Повний текст джерелаShimada, Kenji, Mototsugu Kanokogi, Shinji Okamoto, Masaak Arima, Yoshinori Mori, and Fumihiko Ikoma. "RENAL DYSPLASIA." Japanese Journal of Urology 76, no. 8 (1985): 1179–86. http://dx.doi.org/10.5980/jpnjurol1928.76.8_1179.
Повний текст джерелаShimada, Kenji, Mototsugu Kanokogi, Shinji Okamoto, Masaaki Arima, Yoshinori Mori, and Fumihiko Ikoma. "RENAL DYSPLASIA." Japanese Journal of Urology 76, no. 8 (1985): 1187–93. http://dx.doi.org/10.5980/jpnjurol1928.76.8_1187.
Повний текст джерелаChen, Rui-Yun, and Han Chang. "Renal Dysplasia." Archives of Pathology & Laboratory Medicine 139, no. 4 (April 1, 2015): 547–51. http://dx.doi.org/10.5858/arpa.2013-0660-rs.
Повний текст джерелаAresu, Luca, Renato Zanatta, Paola Pregel, Diego Caliari, Massimiliano Tursi, Federico Valenza, and Alberto Tarducci. "Bilateral juvenile renal dysplasia in a Norwegian Forest Cat." Journal of Feline Medicine and Surgery 11, no. 4 (April 2009): 326–29. http://dx.doi.org/10.1016/j.jfms.2008.08.004.
Повний текст джерелаSisalima, Paola, Mónica Cunalata, and Mónica Juma. "Renal multicystic dysplasia." Revista Médica del Hospital José Carrasco Arteaga 5, no. 1 (March 30, 2013): 94–98. http://dx.doi.org/10.14410/2013.5.1.94.98.
Повний текст джерелаMousa, Albeir Y., and Gurpreet Gill. "Renal fibromuscular dysplasia." Seminars in Vascular Surgery 26, no. 4 (December 2013): 213–18. http://dx.doi.org/10.1053/j.semvascsurg.2014.06.006.
Повний текст джерелаNemcek, AA, and CE Holmburg. "Reversible renal fibromuscular dysplasia." American Journal of Roentgenology 147, no. 4 (October 1986): 737–38. http://dx.doi.org/10.2214/ajr.147.4.737.
Повний текст джерелаSanders, R. C., A. R. Nussbaum, and K. Solez. "Renal dysplasia: sonographic findings." Radiology 167, no. 3 (June 1988): 623–26. http://dx.doi.org/10.1148/radiology.167.3.3283832.
Повний текст джерелаLima, Samara Rosolem, Leilane Aparecida Da Silva, Geovanny Bruno Gonçalves Dias, Letícya Lerner Lopes, Raquel Aparecida Sales Da Cruz, Luciana Sonne, Caroline Argenta Pescador, and Edson Moleta Colodel. "Displasia renal em cães: estudo retrospectivo (2008-2013)." Acta Scientiae Veterinariae 45 (June 27, 2017): 5. http://dx.doi.org/10.22456/1679-9216.85334.
Повний текст джерелаДисертації з теми "Renal dysplasia"
Cale, Catherine Mary. "Inflammatory mediators in normal and abnormal renal development." Thesis, University College London (University of London), 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.313993.
Повний текст джерелаThéolade, Anne. "Le syndrome Bor ou branchio-oto-rénal : gravité potentielle de l'atteinte rénale, à propos de trois observations." Université Louis Pasteur (Strasbourg) (1971-2008), 1990. http://www.theses.fr/1990STR1M061.
Повний текст джерелаCRUNELLE, VALERIE, and DELTEIL FLORENCE PINTON. "La dysplasie multikystique renale de l'enfant : a propos de 56 observations." Lille 2, 1992. http://www.theses.fr/1992LIL2M264.
Повний текст джерелаAnsari, Ehsanollah. "Apport de l'imagerie médicale actuelle dans le diagnostic et traitement des dysplasies fibromusculaires de l'artère rénale." Montpellier 1, 1990. http://www.theses.fr/1990MON11130.
Повний текст джерелаJACOTEY, GILLES. "Etude d'un cas de syndrome de turner associe a une dysplasie renale multikystique sur un pseudo-rein en fer a cheval." Lyon 1, 1988. http://www.theses.fr/1988LYO1M428.
Повний текст джерелаMariani, Beatriz Marinho de Paula. "Padronização das técnicas de PNA e PCR em tempo real para detecção das mutações ativadoras no GNAS na síndrome de McCune-Albright." Universidade de São Paulo, 2012. http://www.teses.usp.br/teses/disponiveis/5/5135/tde-20122012-105425/.
Повний текст джерелаThe McCune-Albright Syndrome (MAS) is a genetic disease, with incidence estimated at 1/100.000 and 1/1000000 cases per year. MAS is clinically characterized by the triad: bone fibrous dysplasia (FD) café-au-lait skin spots and endocrine hyperfunction, such as: precocious puberty (PP), Cushing's syndrome, hyperthyroidism and acromegaly. The diagnosis of MAS is originally based on clinical characteristics associated with hormonal and imaging studies. However, atypical and partial forms often hamper the accurate diagnosis of the syndrome. For this study we selected 32 patients, 1male and 31 females, all being treated in Hospital das Clínicas, School of Medicine, University of São Paulo. As a positive result, we showed for the first time the use of Real Time PCR/genotyping for the detection of activating mutations of the stimulatory G protein, using blood leucocytes DNA. This technique was sensible and can bring fast results for the patient and the physician, making the diagnosis easier. Our study proposes the use of allelic discrimination by Taqman system, which can be used as a probe that allows the identification of specific genotypes. These techniques could help detect these mutations in peripheral blood when the affected tissue is not available.
Morcel, Karine. "Génétique du syndrome de Mayer-Rokitansky-Küster-Hauser : étude d'un gène candidat, le gène ITIH5." Rennes 1, 2009. http://www.theses.fr/2009REN1B127.
Повний текст джерелаThe Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is featured by a congenital utero-vaginal aplasia associated with other malformations. Familial cases were described. A different deletion was found in 4 independent patients within the four chromosomal loci affedted in DiGeorge syndrome (DGS) (22q11, 10p14, 8p23 and 4q34-ter). In 10p14-15, one gene, ITIH5, was affected by the deletion. It is a member of the ITI gene family, playing a role in extracellular matrix dynamics. In the mouse, Itih5 expresssion is strong and increases during embryonic development in the female genital tract. Moreover, the genital tracts seem to synthesize a specific isoform of the Itih5 protein. In conclusion, the loci involved in DGS deletion syndrome might as well be involved in the MRKH syndrome which would then be part of a wider and heterogeneous deletion syndrome. Furthermore our results show that ITIH5 haploinsufficiency could account for the MRKH syndrome
Ohta, Hiroshi. "Molecular pathobiology for renal tubular dysplasia in Japanese black cattle due to claudin-16 deficiency." Doctoral thesis, 2006. http://hdl.handle.net/2115/32739.
Повний текст джерелаGoel, Pranay. "Characterisation of pathophysiological function of NEDD4-2 in kidney." Thesis, 2016. http://hdl.handle.net/2440/109813.
Повний текст джерелаThesis (Ph.D.) (Research by Publication) -- University of Adelaide, School of Medicine, 2016.
Ondič, Ondrej. "Praktická aplikace imunohistochemických a molekulárně - genetických metod v diferenciální diagnostice lézí urogenitálního a gynekologického traktu." Doctoral thesis, 2018. http://www.nusl.cz/ntk/nusl-391332.
Повний текст джерелаКниги з теми "Renal dysplasia"
Schreuder, Michiel F. Renal dysplasia. Edited by Adrian Woolf. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0347.
Повний текст джерелаSchreuder, Michiel F. Renal hypoplasia. Edited by Adrian Woolf. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0348.
Повний текст джерелаHerrington, William G., Aron Chakera, and Christopher A. O’Callaghan. Renal vascular disease. Edited by Patrick Davey and David Sprigings. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199568741.003.0171.
Повний текст джерелаVester, Udo, and Stefanie Weber. Townes–Brocks syndrome. Edited by Adrian Woolf. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0359.
Повний текст джерелаSchreuder, Michiel F. Congenital solitary functioning kidney. Edited by Adrian Woolf. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0351.
Повний текст джерелаGoodyer, Paul. Kidney/ear syndromes. Edited by Giuseppe Remuzzi. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0170.
Повний текст джерелаThomas, David F. M. Vesicoureteric reflux. Edited by David F. M. Thomas. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199659579.003.0115.
Повний текст джерелаSchreuder, Michiel F. Posterior urethral valves. Edited by Adrian Woolf. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0354.
Повний текст джерелаSchreuder, Michiel F. Renal agenesis. Edited by Adrian Woolf. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0346.
Повний текст джерелаLambert, Heather. Primary vesicoureteric reflux and reflux nephropathy. Edited by Adrian Woolf. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199592548.003.0355_update_001.
Повний текст джерелаЧастини книг з теми "Renal dysplasia"
Goodyer, Paul. "Renal Dysplasia/Hypoplasia." In Pediatric Nephrology, 107–20. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-76341-3_5.
Повний текст джерелаGoodyer, Paul, and Indra R. Gupta. "Renal Dysplasia/Hypoplasia." In Pediatric Nephrology, 115–34. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-43596-0_4.
Повний текст джерелаCaliò, Anna, Diego Segala, and Guido Martignoni. "Multicystic Renal Dysplasia." In Encyclopedia of Pathology, 1–2. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-319-28845-1_4854-1.
Повний текст джерелаGoodyer, Paul, and Indra Gupta. "Renal Dysplasia/Hypoplasia." In Pediatric Nephrology, 1–23. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-27843-3_4-1.
Повний текст джерелаTaleb, Mohammed, and Christopher J. Cooper. "Fibromuscular Dysplasia: Renal." In Endovascular Interventions, 401–5. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-7312-1_35.
Повний текст джерелаCaliò, Anna, Diego Segala, and Guido Martignoni. "Multicystic Renal Dysplasia." In Encyclopedia of Pathology, 217–18. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-41894-6_4854.
Повний текст джерелаGreco, Barbara Ann. "Renal Vascular Fibromuscular Dysplasia." In Renal Vascular Disease, 23–37. London: Springer London, 2014. http://dx.doi.org/10.1007/978-1-4471-2810-6_2.
Повний текст джерелаBacharach, J. Michael. "Renal Artery Stenosis: Fibromuscular Dysplasia." In Atlas of Clinical Vascular Medicine, 12–13. Oxford, UK: Blackwell Publishing Ltd., 2013. http://dx.doi.org/10.1002/9781118618189.ch6.
Повний текст джерелаChalmers, David. "Congenital Upper Tract Anomalies: Duplication, Cystic Renal Dysplasia, Multicystic Dysplastic Kidney." In Practical Pediatric Urology, 247–61. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-54020-3_10.
Повний текст джерелаMyers, David A., and Jordan M. Symons. "Nephronophthisis and Renal–Hepatic–Pancreatic Dysplasia of Ivemark." In Fibrocystic Diseases of the Liver, 201–20. Totowa, NJ: Humana Press, 2010. http://dx.doi.org/10.1007/978-1-60327-524-8_9.
Повний текст джерелаТези доповідей конференцій з теми "Renal dysplasia"
Dalrymple, RA, H. Maxwell, and C. Gardiner. "G460(P) Clinical phenotype of children and young people with renal dysplasia in scotland." In Royal College of Paediatrics and Child Health, Abstracts of the Annual Conference, 24–26 May 2017, ICC, Birmingham. BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health, 2017. http://dx.doi.org/10.1136/archdischild-2017-313087.453.
Повний текст джерелаOliveira, Jefferson Borges de, Caroline Berthier Zanin, Gustavo Carreira Henriques, Maiévi Liston, Rafael Glória Zatta, Rodrigo de Faria Martins, and Tatiana Pizzolotto Bruch. "Pallister-Hall Syndrome - case report." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.575.
Повний текст джерелаBergholt, Mads Sylvest, Wei Zheng, Khek Yu Ho, Khay Guan Yeoh, Ming Teh, Jimmy Bok Yan So, and Zhiwei Huang. "Real-time depth-resolved Raman endoscopy forin vivodiagnosis of dysplasia in Barrett's esophagus." In SPIE BiOS, edited by Israel Gannot. SPIE, 2013. http://dx.doi.org/10.1117/12.2003995.
Повний текст джерелаBaria, Enrico, Flavio Giordano, Anna M. Buccoliero, Riccardo Cicchi, and Francesco S. Pavone. "Fast and label-free optical detection of dysplastic and tumour brain tissues." In Optical Biopsy XVIII: Toward Real-Time Spectroscopic Imaging and Diagnosis, edited by Robert R. Alfano, Stavros G. Demos, and Angela B. Seddon. SPIE, 2020. http://dx.doi.org/10.1117/12.2546019.
Повний текст джерелаSteelman, Zachary A., Derek Ho, Yang Zhao, Haoran Zhang, Evan Jelly, Ge Song, Wesley Y. Kendall, et al. "Progress in angle-resolved low-coherence interferometry for real-time detection of epithelial dysplasia (Conference Presentation)." In Biomedical Applications of Light Scattering X, edited by Adam Wax and Vadim Backman. SPIE, 2020. http://dx.doi.org/10.1117/12.2545173.
Повний текст джерелаMichopoulos, S., G. Axiaris, P. Baxevanis, M. Stoupaki, V. Gagari, A. Karlaftis, E. Zampeli, D. Theodorou, M. Sotiropoulou, and K. Petraki. "REAL LIFE DATA FOR DYSPLASTIC BARRETT'S ESOPHAGUS MANAGEMENT AND FOLLOW-UP." In ESGE Days 2019. Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-1681896.
Повний текст джерелаKeyte, Georgina, Muhammad Iqbak, YKS Viswanath, and Anjan Dhar. "PTU-053 Dysplasia diagnosis at barrett’s surveillance – seattle protocol dominant strategy in real world non-expert centres." In British Society of Gastroenterology Annual Meeting, 17–20 June 2019, Abstracts. BMJ Publishing Group Ltd and British Society of Gastroenterology, 2019. http://dx.doi.org/10.1136/gutjnl-2019-bsgabstracts.266.
Повний текст джерелаAxiaris, G., A. Ioannou, E. Papathanasiou, M. Tzakri, G. Leonidakis, E. Zampeli, P. Baxevanis, and S. Michopoulos. "DYSPLASTIC BARRETT’S OESOPHAGUS (DBO): REAL WORLD DATA REGARDING LONG TERM FOLLOW-UP." In ESGE Days 2022. Georg Thieme Verlag KG, 2022. http://dx.doi.org/10.1055/s-0042-1745103.
Повний текст джерелаAbraham, Christine, John Rodriguez, Jenni Buckley, Shane Burch, and Mohammad Diab. "An Evaluation of the Accuracy of Computer Assisted Surgery in Preoperatively Three Dimensionally Planned Periacetabular Osteotomies." In ASME 2009 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2009. http://dx.doi.org/10.1115/sbc2009-206222.
Повний текст джерела