Zobrazeno 1 - 10
of 1 666
pro vyhledávání: '"Pulmonary artery stenosis"'
Publikováno v:
Radiology Case Reports, Vol 19, Iss 11, Pp 5370-5375 (2024)
Endovascular stenting of the pulmonary artery treats arterial stenosis from pulmonary hypertension, congenital heart defects, or post-transplant stricture. Patients with malignant extrinsic pulmonary arterial compression, secondary to large mediastin
Externí odkaz:
https://doaj.org/article/69f4697fa9b84a22a63d999d4afd3795
Autor:
I. E. Kotlyar, A. E. Filchkova, N. V. Enenkov, A. S. Sidashova, D. O. Kondratyev, N. V. Dobrynina, K. I. Vasyushkina, T. A. Gorokhova
Publikováno v:
Рациональная фармакотерапия в кардиологии, Vol 20, Iss 4, Pp 485-492 (2024)
The article presents a clinical case of development of mural infective endocarditis (IE) with formation of vegetations in the region of the upper third of the interventricular septum in patient A., 51 years old, with uncorrected tetralogy of Fallot.
Externí odkaz:
https://doaj.org/article/39b35a403ed34ee29bdb5806497670c0
Autor:
Fahad M. Alshair, Amal S. Alsulami, Mohammad S. Shihata, Osman O. Alradi, Ragab S. Debis, Abdullah H. Baghaffar, Mazin A. Fatani
Publikováno v:
Journal of Cardiothoracic Surgery, Vol 19, Iss 1, Pp 1-9 (2024)
Abstract Background Arterial tortuosity syndrome is a rare Autosomal recessive disease that leads to a loss of function of the connective tissues of the body, this happens due to a mutation in the solute carrier family 2 member 10 (SLC2A10) gene. ATS
Externí odkaz:
https://doaj.org/article/8f1e39a419dc4a8c87a8a7aa400768f6
Autor:
R. Thomas Collins, Verena Gravenhorst, Gilles Faury, Joanna Kwiatkowska, Christian E. H. Schmelzer, Heike Schneider, Anna Waldoch, Rainer Pankau
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 13, Iss 19 (2024)
Williams–Beuren syndrome (WBS) is a congenital multisystem disorder affecting the cardiovascular, central nervous, and musculoskeletal systems. Cardiovascular abnormalities, which consist principally of vascular stenoses, occur in approximately 80%
Externí odkaz:
https://doaj.org/article/fb5bcb486ea247438f2528773024e5b7
Publikováno v:
International Journal of Cardiology Congenital Heart Disease, Vol 17, Iss , Pp 100531- (2024)
Externí odkaz:
https://doaj.org/article/61c0c1a0a98047c99c2a2e888e736bcf
Autor:
Takatoyo Kiko, Ryotaro Asano, Tomohiko Ishibashi, Hiroyuki Endo, Naruhiro Nishi, Hiroya Hayashi, Jin Ueda, Tatsuo Aoki, Akihiro Tsuji, Yoshikazu Nakaoka, Takeshi Ogo
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 13, Iss 15 (2024)
Background Ring finger protein 213 (RNF213) p.Arg4810Lys is a susceptibility gene for moyamoya disease, peripheral pulmonary artery stenosis (PPS), and other vascular diseases and thrombosis. We investigated the prevalence and clinical characteristic
Externí odkaz:
https://doaj.org/article/624953063d94400bacb8b8bd9a19a1ec
Publikováno v:
Неонатологія, хірургія та перинатальна медицина, Vol 14, Iss 2(52) (2024)
The widespread introduction of molecular genetic research methods into health care practice has made it possible to diagnose rare microdeletion syndromes in patients with multiple congenital malformations.. Aim of the study is to present the results
Externí odkaz:
https://doaj.org/article/51267e3f775d4036a1fe775ad0618fd6
Publikováno v:
BMC Pediatrics, Vol 23, Iss 1, Pp 1-5 (2023)
Abstract Background Elastin-driven genetic diseases are a group of complex diseases driven by elastin protein insufficiency and dominant-negative production of aberrant protein, including supravalvular aortic stenosis (SVAS) and autosomal dominant cu
Externí odkaz:
https://doaj.org/article/504d29542d134860ac817ae042723a2f
Autor:
Mengdi Zhang, Li Chen, Chao Bu, Hanxi Zhang, Jing Luo, Jing Wang, Qihua Sun, Qingyu Liu, Zhonghua Sun, Yu Li
Publikováno v:
Diagnostics, Vol 14, Iss 16, p 1762 (2024)
Pulmonary artery stenosis represents a group of disorders involving main, branch or peripheral pulmonary arteries with pain, dyspnea, hemoptysis or even no symptoms. Early diagnosis and timely intervention are crucial for reducing mortality, but time
Externí odkaz:
https://doaj.org/article/bdb7d1ad49de483da1da9a419105020a
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 11, Iss 8, p 232 (2024)
Objective: In this paper, we share our single-center experience of successful multidisciplinary management of patients with Alagille syndrome. In addition, we aim to highlight the need for an Alagille program for effectively managing these patients,
Externí odkaz:
https://doaj.org/article/8196d37d887a447bb7778e11df0e4723