Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 11 (of 11 Records) |
Query Trace: Aortic Coarctation[original query] |
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No evidence for angiotensin type 2 receptor gene polymorphism in intron 1 in patients with coarctation of the aorta and Ullrich-Turner syndrome. Pediatric cardiology 0 27 (5): 636-9. Struwe E, Krammer K, Dötsch J, Metzler M, Dörr H G, Cesnjevar R, Rascher W, Koch |
Thrombosis in children with cardiac pathology: analysis of acquired and inherited risk factors. Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2008 Jun 19 (4): 294-304. Alioglu Bulent, Avci Zekai, Tokel Kursat, Atac F Belgin, Ozbek Nam |
Impact of genomic polymorphism on arterial hypertension after aortic coarctation repair. International journal of cardiology 2011 Aug 151 (1): 63-8. Hager Alfred, Bildau Judith, Kreuder Joachim, Kaemmerer Harald, Hess Jo |
Exercise capacity after coarctation repair relates to the c.46A > G genomic polymorphism of the ss2-adrenoreceptor and the c.704T > C angiotensinogen polymorphism. European journal of preventive cardiology 2012 Apr 19 (2): 199-204. Hager Alfred, Bildau Judith, Kreuder Joachim, Schreiber Christian, Kaemmerer Harald, Hess Jo |
R25C mutation in the NKX2.5 gene in Italian patients affected with non-syndromic and syndromic congenital heart disease. Journal of cardiovascular medicine (Hagerstown, Md.) 2013 Aug 14 (8): 582-6. Beffagna Giorgia, Cecchetto Antonella, Dal Bianco Lucia, Lorenzon Alessandra, Angelini Annalisa, Padalino Massimo, Vida Vladimiro, Bhattacharya Shoumo, Stellin Giovanni, Rampazzo Alessandra, Daliento Lucia |
Low transcriptional activity haplotype of matrix metalloproteinase 1 is less frequent in bicuspid aortic valve patients. Gene 2013 Jul 524 (2): 304-8. Martín María, Pichel Irene A, Flórez Muñoz Juan P, Naves-Díaz Manuel, Palacín María, Cannata-Andía Jorge B, Morís César, Rodríguez Isab |
Rare GATA5 sequence variants identified in individuals with bicuspid aortic valve. Pediatric research 2014 Aug 76 (2): 211-6. Bonachea Elizabeth M, Chang Sheng-Wei, Zender Gloria, LaHaye Stephanie, Fitzgerald-Butt Sara, McBride Kim L, Garg Vi |
Variants in the NOTCH1 gene in patients with aortic coarctation. Congenital heart disease 0 9 (5): 391-6. Freylikhman Olga, Tatarinova Tatyana, Smolina Natalia, Zhuk Sergey, Klyushina Alexandra, Kiselev Artem, Moiseeva Olga, Sjoberg Gunnar, Malashicheva Anna, Kostareva An |
Phenotype in girls and women with Turner syndrome: Association between dysmorphic features, karyotype and cardio-aortic malformations. European journal of medical genetics 2018 1 61 (6): 301-306. Noordman Iris, Duijnhouwer Anthonie, Kapusta Livia, Kempers Marlies, Roeleveld Nel, Schokking Michiel, Smeets Dominique, Freriks Kim, Timmers Henri, van Alfen-van der Velden Janiël |
Association of NKX2-5, GATA4, and TBX5 polymorphisms with congenital heart disease in Egyptian children. Molecular genetics & genomic medicine 2019 Mar e612. Behiry Eman G, Al-Azzouny Mahmoud A, Sabry Dina, Behairy Ola G, Salem Nessrine |
Histologic and morphologic character of pediatric renal artery occlusive disease. Journal of vascular surgery 2020 (1): 161-171. Coleman Dawn M, Heider Amer, Gordon David, Ganesh Santhi K, Eliason Jonathan L, Stanley James |
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- Page last updated:Apr 22, 2024
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