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Cesare Faldini, Domenico Fenga, Ilaria Sanzarello, Matteo Nanni, Francesco Traina and Michele Attilio A. Rosa

talipes equinovarus in a non-selected population of 49314 deliveries in Norway. Ultrasound Obstet Gynecol 2007;30:838-44. 9. Radler C, Myers AK, Burghardt RD, et al. Maternal attitudes towards prenatal diagnosis of idiopathic clubfoot. Ultrasound Obstet Gynecol 2011;37:658-62. 10. Canto MJ, Cano S, Palau J, et al. Prenatal diagnosis of clubfoot in low-risk population: associated anomalies and long-term outcome. Prenat Diagn 2008;28:343-6. 11. Keret D, Ezra E, Lokiec F, et al. Efficacy of prenatal ultrasonography in confirmed club foot. J Bone Joint

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Iwona Strzelecka, Maciej Słodki, Andrzej Zieliński, Iwona Maroszyńska and Maria Respondek-Liberska

, Paladini D. Cardiac creening examination of the fetus: guidelines for performing the ‘basic’ and ‘extended basic’ cardiac scan. ISUOG Guidelines Ultrasound Obstet Gynecol 2006; 27: 107-113 6. Respondek-Liberska M.: Prenatal echocardiography and prenatal cardiology, Mak-Med, Gdańsk 1998 7. Gembruch U. Prenatal diagnosis of congenital heart disease. Prenat Diagn. 1997 Dec;17:1283-98 8. Respondek-Liberska M. Prenatal echocardiography in 1st,2nd and 3rd trimester in singelton pregnancy. Prenatal Cardiology 2012

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Sezin Yakut, Zafer Çetin, Mehmet Şimşek, İbrahim İnanç Mendilcioğlu, Havva Serap Toru, Sibel Berker Karaüzüm and Güven Lüleci

References 1. Dallaire L. Integration of prenatal diagnosis of genetic diseases into medical practice. Can Med Assoc J. 1976;115:713-4. 2. Stembalska A, Slezak R, Pesz K, Gil J, Sasiadek M. Prenatal diagnosis-principles of diagnostic procedures and genetic counseling. Folia Histochem Cytobiol. 2007;45 Suppl 1:S11-6. 3. Baena N, De Vigan C, Cariati E, Clementi M, Stoll C, Caballin MR, Guitart M; EUROSCAN Working Group. Prenatal detection of rare chromosomal autosomal abnormalities in Europe. Am J Med Genet A

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M. Vasilevska, E. Ivanovska, K. Kubelka Sabit, E. Sukarova-Angelovska and G. Dimeska

References 1. Warburton D. De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints. Am J Hum Genet. 1991; 49(5): 995-1013. 2. Gardner RJM, Sutherland GR. Chromosome Abnormalities and Genetic Counseling, 3rd ed. New York: Oxford University Press, 2004. 3. Shaffer LG, Slovak ML, Campbell LJ, Eds. ISCN (2009): an international system for human cytogenetic nomenclature. Basel: S. Karger, 2009. 4

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Małgorzata Sabatowska, Małgorzata Soroka and Maciej Słodki

References 1. Mc Ewing RL, Chaoui R.: Congenitally corrected transposition of great arteries: clues for prenatal diagnosis. Ulrasound Obstet Gynecol 2004, 23: 68-72 2. Respondek-Liberska M.: Kardiologia prenatalna dla położników i kardiologów dziecięcych. Czelej 2006 3. Szymkiewicz-Dangel J.: Kardiologia Płodu. Zasady diagnostyki i terapii. Poznań 2007, Ośrodek Wydawnictw Naukowych 4. Paladini D, Volpe P, Marasini M, Russo MG, Vassallo M, Gentile M & Calabro R.: Diagnosis, characterization and

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Neil D. Avent, A Webb, TE Madgett, T Miran, K Sillence, N Kaushik and M Kiernan

be carried out. Available at [http://www.nhs.uk/Conditions/ Abortion/ Pages/When-should-it-be-done.aspx] Accessed on January 8 2012. 7. Bischoff FZ, Sinacori MK, Dang DD, et al. Cell-free fetal DNA and intact fetal cells in maternal blood circulation: implications for first and second trimester non-invasive prenatal diagnosis. Hum Reprod Update. 2001; 8(6): 493-500. 8. Chitty LS, van der Schoot CE, Hahn S, Avent ND. SAFE-The special non-invasive advances in fetal and neonatal evaluation network: aims and achievements. Prenat Diagn

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Iwona Gawron, Magdalena Borówka, Jacek Kołcz and Janusz H. Skalski

, Quereshi S, Rosenthal E, Sherland G, Simpson J, Rollings S, Tulloh R: Outcome of staged reconstructive surgery for hypoplastic left heart syndrome following antenatal diagnosis. Arch Dis Child 2001, 85:474-477 11. Levey A, Glickstein JS, Kleinman CS, Lavasseur SM, Chen J, Gersony WM, Williams IA: The impact of Prenatal Diagnosis of Complex Congenital Heart Disease on Neonatal Outcomes. Pediatr Cardiol 2010, 31:587-597 12. Viemann PM, Partsch CJ, et al: Congenital adrenal hypoplasia: clinical spectrum, experience with hormonal diagnosis

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Maria Respondek-Liberska, Łukasz Sokołowski, Maciej Słodki, Katarzyna Zych-Krekora, Iwona Strzelecka, Michał Krekora, Iwona Maroszyńska, Jadwiga Moll and Jacek Moll

Patients With Heterotaxy Syndrome. Ann Thorac Surg. 2015 Jun; 99(6) 6. Laux D, Fermont L, Bajolle F, Boudjemline Y, Stirnemann J, Bonnet D. Prenatal diagnosis of isolated total anomalous pulmonary venous connection: a series of 10 cases. Ultrasound Obstet Gynecol. 2013 Mar;41(3):291-7. 7. Law KM, Leung KY, Tang MH, Chau AK. Prenatal two- and three-dimensional sonographic diagnosis of total anomalous pulmonary venous connection. Ultrasound Obstet Gynecol. 2007 Oct;30(5) 8. Allan LD, Sharland GK. The echocardiographic diagnosis of totally anomalous

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A Guzel, M Yilmaz, O Demirhan, A Pazarbasi, S Kocaturk-Sel, M Erkoc, N Inandiklioglu, F Ozgunen and C Sariturk

configurations on chromosome 21 predispose to non-disjunction in both maternal meiosis I and meiosis II. Nat Genet. 1996; 14(4): 400-405. Grimshaw GM, Szczepura A, Hulten M. Evaluation of molecular tests for prenatal diagnosis of chromosome abnormalities. Health Technol Assess. 2003; 7(10): 1-77. Leung WC, Lau ET, Lao TT, Tang MH. Rapid aneuploidy screening (FISH or QF-PCR): the changing scene in prenatal diagnosis? Expert Rev Mol Diagn. 2004; 4(3): 333-337. Ogilvie CM. Prenatal diagnosis for

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Lech Dudarewicz, Anna Krzymińska, Wanda Hawuła, Magdalena Kozłowska, Urszula Laskowska, Agnieszka Gach, Maciej Borowiec, Wojciech Młynarski, Wojciech Ałaszewski and Lucjusz Jakubowski

References 1. Multiplex ligation-dependent probe amplification (MLPA) and prenatal diagnosis. Willis AS, van den Veyver I, Eng CM. Prenat Diagn. 2012 Apr;32(4):315-20 2. Subtelomeric MLPA: is it really useful in prenatal diagnosis? Mademont-Soler I, Morales C, Bruguera J, Madrigal I, Clusellas N, Margarit E, Sánchez A, Soler A: Prenat Diagn. 2010 Dec;30(12-13):1165-9. doi: 10.1002/pd.2635 3. Prenatal study of common submicroscopic „genomic disorders“ using MLPA with subtelomeric/microdeletion syndrome probe