Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Rakhmanov, Yeltay"'
Autor:
Jumadilova, Dinara1 (AUTHOR), Rakhmanov, Yeltay1 (AUTHOR), Khissamutdinov, Nail2 (AUTHOR), Zhankorazova, Aizhan1 (AUTHOR), Toktarbay, Bauyrzhan1 (AUTHOR), Khamitova, Zaukiya1 (AUTHOR), Zholshybek, Nurmakhan1 (AUTHOR), Bekbossynova, Makhabbat2 (AUTHOR), Dautov, Tairkhan3 (AUTHOR), Gaipov, Abduzhappar1 (AUTHOR), Tonti, Giovanni4 (AUTHOR), Salustri, Alessandro1 (AUTHOR) alessandro.salustri@nu.edu.kz
Publikováno v:
Scientific Reports. 11/9/2024, p1-11. 11p.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
The EuroBiotech Journal, Vol 2, Iss s1, Pp 1-4 (2018)
Cardiovascular disorders include various conditions characterized by morphological and functional defects of the heart and vascular system. Molecular biology techniques (in particular DNA sequencing) have recently offered new insights into the etiolo
Externí odkaz:
https://doaj.org/article/0c1af4a2032c4e4f8e2e1483a26c1d3b
Autor:
Rakhmanov Yeltay, Maltese Paolo Enrico, Fanelli Francesca, Beccari Tommaso, Dundar Munis, Bertelli Matteo
Publikováno v:
The EuroBiotech Journal, Vol 2, Iss s1, Pp 51-54 (2018)
Ventricular septal defects (VSDs) are the commonest heart malformations and may affect the membranous or the muscular septum. Clinical presentation depends on the amount of interventricular flow, which is determined by the size of the defect and the
Externí odkaz:
https://doaj.org/article/0126ab150e854230858db78f5d306798
Publikováno v:
The EuroBiotech Journal, Vol 2, Iss s1, Pp 74-77 (2018)
Large-caliber vessels are those with a diameter of 10 mm or more. Most aneurysms remain asymptomatic until they expand or rupture. Aortic aneurysms are of special interest for physicians and scientists because of their prevalence. Aortic aneurysms an
Externí odkaz:
https://doaj.org/article/27ea6535df33481b8220bea77cd27807
Autor:
Paolacci Stefano, Rakhmanov Yeltay, Maltese Paolo Enrico, Fanelli Francesca, Mattassi Raul Ettore, Amato Bruno, Bertelli Matteo
Publikováno v:
The EuroBiotech Journal, Vol 2, Iss s1, Pp 26-31 (2018)
Vascular anomalies (VAs) have phenotypic variability within the same entity, overlapping clinical features between different conditions, allelic and locus heterogeneity and the same disorder can be inherited in different ways. Most VAs are sporadic (
Externí odkaz:
https://doaj.org/article/16cd2c95b19f4237bd0589c3effd5fda
Autor:
Rakhmanov Yeltay, Maltese Paolo Enrico, Bruson Alice, Beccari Tommaso, Dundar Munis, Bertelli Matteo
Publikováno v:
The EuroBiotech Journal, Vol 2, Iss s1, Pp 67-70 (2018)
Bicuspid aortic valve (BAV) is a congenital defect in which the aortic valve has two rather than three leaflets. In many patients valve function may be normal but valve decompensation may occur due to other associated congenital abnormalities and sec
Externí odkaz:
https://doaj.org/article/3c46e29924f4401ba28d3b5712624ade
Autor:
Rakhmanov Yeltay, Maltese Paolo Enrico, Paolacci Stefano, Marinelli Carla, Castori Marco, Beccari Tommaso, Dundar Munis, Bertelli Matteo
Publikováno v:
The EuroBiotech Journal, Vol 2, Iss s1, Pp 38-41 (2018)
Marfan-like disorders are inherited conditions with features resembling Marfan syndrome but without a pathogenic variant in FBN1, and/or without a clinical diagnosis of Marfan syndrome according to the Revised Ghent criteria, and/or with a pathogenic
Externí odkaz:
https://doaj.org/article/49167326be094d72b009460908376610
Autor:
Paolacci Stefano, Rakhmanov Yeltay, Maltese Paolo Enrico, Zulian Alessandra, Michelini Sandro, Bertelli Matteo
Publikováno v:
The EuroBiotech Journal, Vol 2, Iss s1, Pp 5-9 (2018)
Lymphatic malformations (LMs) show phenotypic variability, as well as clinical and genetic heterogeneity. Inheritance is autosomal dominant, recessive or X-linked and major genes involved in predisposition for LMs are continuously being discovered. T
Externí odkaz:
https://doaj.org/article/5b010121aea747a9aecf1914c9bafa42