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1دورية أكاديمية
المؤلفون: Picos-Cárdenas VJ, Leal-Ugarte E, Meza-Espinoza JP
المصدر: International Medical Case Reports Journal, Vol Volume 17, Pp 651-652 (2024)
مصطلحات موضوعية: aphallia, horseshoe kidney, ureterohydronephrosis, Medicine (General), R5-920
وصف الملف: electronic resource
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2دورية أكاديمية
المصدر: La Pediatria Medica e Chirurgica, Vol 45, Iss 2 (2023)
مصطلحات موضوعية: Primary obstructive megaureter, ureterohydronephrosis, endoscopic treatment, balloon dilation, endourology, Pediatrics, RJ1-570, Surgery, RD1-811
وصف الملف: electronic resource
العلاقة: https://pmc.btvb.org/pmc/article/view/327Test; https://doaj.org/toc/0391-5387Test; https://doaj.org/toc/2420-7748Test
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3دورية أكاديمية
المؤلفون: KH.M. MIRAKOV
المصدر: Паёми Сино, Vol 24, Iss 4, Pp 471-478 (2022)
مصطلحات موضوعية: ureter, urodynamics, obstruction, ureterohydronephrosis, megaureter., Public aspects of medicine, RA1-1270
وصف الملف: electronic resource
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4دورية أكاديمية
المؤلفون: Marcelo Puppo Bigarella, Roberto Iglesias Lopes, Guilherme Gentile, Carolina Brito Faustino, Lais da Cunha Gamba, Guilherme Baumgardt Barbosa Lima, Henry Augusto Hoffman Melo, Grace Carvajal Mulatti
المصدر: CVIR Endovascular, Vol 5, Iss 1, Pp 1-4 (2022)
مصطلحات موضوعية: Ruptured pseudoaneurysm, External iliac artery, Ureteral obstruction, Bilateral ureterohydronephrosis, Endovascular repair, Diseases of the circulatory (Cardiovascular) system, RC666-701
وصف الملف: electronic resource
العلاقة: https://doaj.org/toc/2520-8934Test
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5دورية أكاديمية
المؤلفون: Bowen Zhang, Mengzhu Fu, Di Zhang, Yipeng Jin, Gang Liu
المصدر: Frontiers in Veterinary Science, Vol 9 (2023)
مصطلحات موضوعية: retrocaval ureter, ureterohydronephrosis, ultrasonography, computed tomography, antegrade pyelography, Veterinary medicine, SF600-1100
وصف الملف: electronic resource
العلاقة: https://www.frontiersin.org/articles/10.3389/fvets.2022.1013230/fullTest; https://doaj.org/toc/2297-1769Test
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6دورية أكاديمية
المؤلفون: I. M. Kagantsov, O. L. Belonog, A. A. Sukhotskaya, T. S. Nikulina, A. A. Sherbakov, N. A. Petrova, O. A. Li, D. V. Petrov, Yu. V. Volkova, S. A. Amidkhonova, T. M. Pervunina, И. М. Каганцов, О. Л. Белоног, А. А. Сухоцкая, Т. С. Никулина, А. А. Щербаков, Н. А. Петрова, О. А. Ли, Д. В. Петров, Ю. В. Волкова, С. А. Амидхонова, Т. М. Первунина
المصدر: Meditsinskiy sovet = Medical Council; № 12 (2023); 240-246 ; Медицинский Совет; № 12 (2023); 240-246 ; 2658-5790 ; 2079-701X
مصطلحات موضوعية: подвздошная кишка, Syndrom Warkany, newborns, ureterohydronephrosis, diverticulum, ileum, Синдром Warkany, новорожденные, уретерогидронефроз, дивертикул
وصف الملف: application/pdf
العلاقة: https://www.med-sovet.pro/jour/article/view/7679/6813Test; Wisniewska M., Mazurek M. Trisomy 8 mosaicism syndrome. J Appl Genet. 2002;43(1):115-118. Available at: https://pubmed.ncbi.nlm.nih.gov/12084977Test/.; Aksit S., Turker M., Yapark I., Caglayan S., Coskun D., Kansoy S. A case of trisomy 8 mosaicism. Turkish Journal of Medical Sciences. 1998;(28):107-109. Available at: https://journals.tubitak.gov.tr/medical/vol28/iss1/23Test/.; Hale N.E., Keane J.F. Jr. Piecing together a picture of trisomy 8 mosaicism syndrome. J Am Osteopath Assoc. 2010;110(1):21-23. Available at: https://pubmed.ncbi.nlm.nih.gov/20093650Test.; Agrawal A., Agrawal R. Warkany syndrome: a rare case report. Case Rep Pediatr. 2011;2011:437101. https://doi.org/10.1155/2011/437101Test.; Udayakumar A.M., Al-Kindy A. Constitutional trisomy 8 mosaicism syndrome: case report and review. J Pediatr Genet. 2013;2(4):197-201. https://doi.org/10.3233/PGE-13069Test.; Puvabanditsin S., Gengel N., Botti C., Jacob M., Jalil M., Cabrera K., Mehta R. 8p 11 Microduplication Is Associated with Neonatal Stridor. Mol Syndromol. 2019;9(6):324-327. https//doi.org/10.1159/000494796.; Gibbons B., Tan S.Y., Barber J.C., Ng C.F., Knight L.A., Lam S., Ng I. Duplication of 8p with minimal phenotypic effect transmitted from a mother to her two daughters. J Med Genet. 1999;36(5):419-422. Available at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1734374Test/.; Mahjoubi F., Totian S., Kareeme S., Shafegatee Y. Trisomy 8p (p11.2-pter) due to maternal translocation t(8; 13)(p11;p12) in a child with dysmorphic features. Ind J Hum Genet. 2OO5;(11):111-113. Available at: http://www.bioline.org.br/pdf?hg05014Test.; Nusbaum C., Mikkelsen T.S., Zody M.C., Asakawa S., Taudien S., Garber M. et al. DNA sequence and analysis of human chromosome 8. Nature. 2006;19;439(7074):331-335. https//doi.org/10.1038/nature04406.; Yu S., Fiedler S., Stegner A., Graf W.D. Genomic profile of copy number variants on the short arm of human chromosome 8. Eur J Hum Genet. 2010;18(10):1114-1120. https//doi.org/10.1038/ejhg.2010.66.; Vander Pluym J.H., O'Sullivan J., Andrew G., Bolduc F.V. Genomic characterization of chromosome 8 pericentric trisomy. Clin Case Rep. 2015;3(7):570-577. https://doi.org/10.1002/ccr3.234Test.; Chen C.P., Chen M., Ko T.M., Ma G.C., Tsai F.J., Tsai M.S. et al. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 8. Taiwan J Obstet Gynecol. 2010;49(4):500-505. https//doi.org/10.1016/S1028-4559(10)60104-0.; Pierre R.V. Cytogenetic Studies in Peleukemia: Studies before and after Transition to Acute Leukemia in 17 Subjects. In: Bessis M., Brecher G. (eds.). Unclassifiable Leukemias. Springer, Berlin, Heidelberg; 1975, pp. 163-170. https://doi.org/10.1007/978-3-642-66126-6_27Test.; Ayraud N., Donzeau M., Raynaud S., Lambert J.C. Cytogenetic study of 88 cases of refractory anemia. Cancer Genet Cytogenet. 1983;8(3):243-248. https://doi.org/10.1016/0165-4608Test(83)90141-3.; Пименова М.А., Паровичникова Е.Н., Кохно А.В., Домрачева Е.В., Манакова Т.Е., Мальцева Ю.С. и др. Цитогенетическая характеристика гемопоэтических и стромальных клеток-предшественниц при миелодис-пластическом синдроме. Терапевтический архив. 2013;85(7):34-42. Режим доступа: https://elibrary.ru/item.asp?id=20191486Test.; Tefferi A., Vardiman J.W. Myelodysplastic syndromes. N Engl J Med. 2009;361(19):1872-1885. https://doi.org/10.1056/NEJMra0902908Test.; Saumell S., Sole F., Arenillas L., Montoro J., Valcarcel D., Pedro C. et al. Trisomy 8, a Cytogenetic Abnormality in Myelodysplastic Syndromes, Is Constitutional or Not? PLoS ONE. 2015;10(6):e0129375. https://doi.org/10.1371/journal.pone.0129375Test.; Saumell S., Florensa L., Luno E., Sanzo C., Canizo C., Hernandez J.M. et al. Prognostic value of trisomy 8 as a single anomaly and the influence of additional cytogenetic aberrations in primary myelodysplastic syndromes. Br J Haematol. 2012;159(3):311-321. https://doi.org/10.1111/bjh.12035Test.; Greenberg P.L., Tuechler H., Schanz J., Sanz G., Garcia-Manero G., Sole F. et al. Revised international prognostic scoring system (IPSS-R) for myelodysplastic syndromes. Blood. 2012;120(12):2454-2465. https://doi.org/10.1182/blood-2012-03-420489Test.; Hasle H., Clausen N., Pedersen B., Bendix-Hansen K. Myelodysplastic syndrome in a child with constitutional trisomy 8 mosaicism and normal phenotype. Cancer Genet Cytogenet. 1995;79(1):79-81. https://doi.org/10.1016/0165-4608Test(94)00099-w.; Ganmore I., Smooha G., Izraeli S. Constitutional aneuploidy and cancer pre-disposition. Hum Mol Genet. 2009;18(R1):R84-93. https://doi.org/10.1093/hmg/ddp084Test.; Ripperger T., Tauscher M., Praulich I., Pabst B., Teigler-Schlegel A., Yeoh A. et al. Constitutional trisomy 8p11.21-q11.21 mosaicism: a germline alteration predisposing to myeloid leukaemia. Br J Haematol. 2011;155(2):209-217. https://doi.org/10.1111/j.1365-2141.2011.08817.xTest.; Maserati E., Aprili F., Vinante F., Locatelli F., Amendola G., Zatterale A. et al. Trisomy 8 in myelodysplasia and acute leukemia is constitutional in 15-20% of cases. Genes Chromosomes Cancer. 2002;33(1):93-97. https://doi.org/10.1002/gcc.1214Test.; Klein J., Graham Jr. J.M., Platt L.D., Schreck R. Trisomy 8 mosaicism in chorionic villus sampling: case report and counselling issues. Prenat Diagn. 1994;14(6):451-454. https://doi.org/10.1002/pd.1970140606Test.; Schneider M., Klein-Vogler U., Tomiuk J., Schliephacke M., Leipoldt M., Enders H. Pitfall: amniocentesis fails to detect mosaic trisomy 8 in a male newborn. Prenat Diagn. 1994;14(7):651-652. https://doi.org/10.1002/pd.1970140728Test.; Yan Haelst M.M., Van Opstal D., Lindhout D., Los F.J. Management of prenatally detected trisomy 8 mosaicism. Prenat Diagn. 2001;21(12):1075-1078. https://doi.org/10.1002/pd.215Test.; Cassina M., Calo A., Salviati L., Alghisi A., Montaldi A., Clementi M. Prenatal detection of trisomy 8 mosaicism: Pregnancy outcome and follow up of a series of 17 consecutive cases. Eur J Obstet Gynecol Reprod Biol. 2018;221:23-27. https://doi.org/10.1016/j.ejogrb.2017.12.012Test.; Thomsen S.H., Lund I.C.B., Fagerberg C., Bache I., Becher N., Vogel I. Trisomy 8 mosaicism in the placenta: A Danish cohort study of 37 cases and a literature review. Prenat Diagn. 2021;41(4):409-421. https://doi.org/10.1002/pd.5875Test.; https://www.med-sovet.pro/jour/article/view/7679Test
الإتاحة: https://doi.org/10.21518/ms2023-205Test
https://doi.org/10.1155/2011/437101Test
https://doi.org/10.3233/PGE-13069Test
https://doi.org/10.1159/000494796Test
https://doi.org/10.1038/nature04406Test
https://doi.org/10.1038/ejhg.2010.66Test
https://doi.org/10.1002/ccr3.234Test
https://doi.org/10.1016/S1028-4559Test(10)60104-0
https://doi.org/10.1007/978-3-642-66126-6_27Test
https://doi.org/10.1016/0165-4608Test(83)90141-3 -
7دورية أكاديمية
المؤلفون: Viorel Dragos Radu, Ingrid-Andrada Vasilache, Radu-Cristian Costache, Ioana-Sadiye Scripcariu, Dragos Nemescu, Alexandru Carauleanu, Valentin Nechifor, Veaceslav Groza, Pavel Onofrei, Lucian Boiculese, Demetra Socolov
المصدر: Medicina; Volume 58; Issue 5; Pages: 619
مصطلحات موضوعية: double-J stent, ureterohydronephrosis, urolithiasis, pyelonephritis, urosepsis, pregnancy
وصف الملف: application/pdf
العلاقة: Obstetrics and Gynecology; https://dx.doi.org/10.3390/medicina58050619Test
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8دورية أكاديمية
المؤلفون: V. Svekatun, V. Dmitryakov
المصدر: Pedagogy and Psychology of Sport, Vol 6, Iss 2, Pp 113-121 (2020)
مصطلحات موضوعية: heterochrony, ureterohydronephrosis, stenting, ureter, children, urodynamics, Special aspects of education, LC8-6691, Sports, GV557-1198.995, Psychology, BF1-990
وصف الملف: electronic resource
العلاقة: https://apcz.umk.pl/czasopisma/index.php/PPS/article/view/30357Test; https://doaj.org/toc/2450-6605Test
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9دورية أكاديمية
المؤلفون: Charikleia Demiri, Vassilis Lambropoulos, Vasileios Mouravas, Chrysostomos Kepertis, Dimitrios Godosis, Maria Tsopozidi, Ioannis Spyridakis
المصدر: The Pan African Medical Journal, Vol 36, Iss 260 (2020)
مصطلحات موضوعية: ureterohydronephrosis, paediatric surgery, endoscopic treatment, Medicine
وصف الملف: electronic resource
العلاقة: https://www.panafrican-med-journal.com/content/article/36/260/pdf/260.pdfTest; https://doaj.org/toc/1937-8688Test
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10دورية أكاديمية
المؤلفون: Svekatun, V., Dmitryakov, V.
المصدر: Pedagogy and Psychology of Sport; Vol. 6 No. 2 (2020); 113-121 ; Pedagogy and Psychology of Sport; Tom 6 Nr 2 (2020); 113-121 ; 2450-6605
مصطلحات موضوعية: heterochrony, ureterohydronephrosis, stenting, ureter, children, urodynamics
وصف الملف: application/pdf