يعرض 1 - 10 نتائج من 71 نتيجة بحث عن '"ureterohydronephrosis"', وقت الاستعلام: 0.81s تنقيح النتائج
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    المصدر: Meditsinskiy sovet = Medical Council; № 12 (2023); 240-246 ; Медицинский Совет; № 12 (2023); 240-246 ; 2658-5790 ; 2079-701X

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    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

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    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

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