Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Ali Atay"'
Publikováno v:
Haseki Tıp Bülteni, Vol 53, Iss 1, Pp 16-19 (2015)
Externí odkaz:
https://doaj.org/article/0b93f8f4f6be413c9e19d3d74ace6fc7
Autor:
Melody Walker, Helen Moore, Ali Ataya, Ann Pham, Paul A. Corris, Reinhard Laubenbacher, Andrew J. Bryant
Publikováno v:
Pulmonary Circulation, Vol 14, Iss 2, Pp n/a-n/a (2024)
Abstract Pulmonary hypertension (PH) is a severe medical condition with a number of treatment options, the majority of which are introduced without consideration of the underlying mechanisms driving it within an individual and thus a lack of tailored
Externí odkaz:
https://doaj.org/article/19747005a1a144959b14b8674e4095d4
Publikováno v:
Haseki Tıp Bülteni, Vol 53, Iss 1, Pp 16-19 (2015)
Autor:
Akash Mathavan, Akshay Mathavan, Renuka Reddy, Kirk Jones, Christina Eagan, Hassan Alnuaimat, Ali Ataya
Publikováno v:
Pulmonary Circulation, Vol 13, Iss 4, Pp n/a-n/a (2023)
Abstract Hereditary hemorrhagic telangiectasia (HHT) is a rare autosomal dominant hereditary disorder characterized by recurrent spontaneous epistaxis, mucocutaneous telangiectasias, and solid organ arteriovenous malformations (AVMs). Pulmonary hyper
Externí odkaz:
https://doaj.org/article/c3dff2a3748348b2aea223e03cb2e42d
Autor:
Niamh Boyle, Marissa O'Callaghan, Ali Ataya, Nishant Gupta, Michael P. Keane, David J. Murphy, Cormac McCarthy
Publikováno v:
Breathe, Vol 18, Iss 4 (2022)
The term “pulmonary renal syndrome” describes a clinical syndrome which is characterised by the presence of both diffuse alveolar haemorrhage and glomerulonephritis. It encompasses a group of diseases with distinctive clinical and radiological ma
Externí odkaz:
https://doaj.org/article/1270ae0cf46c4de78a0180b545177407
Autor:
Akash Mathavan, Akshay Mathavan, Cyrus Vahdatpour, Christina Eagan, Saminder Singh Kalra, Ali Ataya
Publikováno v:
Pulmonary Circulation, Vol 12, Iss 2, Pp n/a-n/a (2022)
Abstract Proteus syndrome is a rare progressive multisystem disorder characterized by asymmetric, disproportionate overgrowth of bone, skin, and other tissue types. Molecular pathogenesis has been identified as somatic activating mutations of the AKT
Externí odkaz:
https://doaj.org/article/7df646c09d92483888fa1a16cab0edf0
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
Autoantibodies to multiple cytokines have been identified and some, including antibodies against granulocyte-macrophage colony-stimulating factor (GM-CSF), have been associated with increased susceptibility to infection. High levels of GM-CSF autoant
Externí odkaz:
https://doaj.org/article/421e8c5a8d954e5abbc5404e63fbe51c
Autor:
Martin R. Zamora, Ali Ataya
Publikováno v:
Therapeutic Advances in Chronic Disease, Vol 12_suppl (2021)
Alpha-1 antitrypsin (AAT) augmentation is effective in slowing the progression of emphysema due to AAT deficiency (AATD) but cannot prevent eventual progression to end-stage lung disease and complete respiratory failure, which is the leading cause of
Externí odkaz:
https://doaj.org/article/1461c6b0ac384132859262cd5799ee90
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 10, Iss 11 (2021)
Abstract Pulmonary hypertension (PH) attributable to left heart disease (LHD) is believed to be the most common form of PH and is strongly associated with increased mortality and morbidity in this patient population. Specific therapies for PH‐LHD h
Externí odkaz:
https://doaj.org/article/7b64de33b8dc429aa6bf68394db0ee4c
Autor:
Mwelwa Chizinga, Saminder Singh Kalra, Ayoub Innabi, Mindaugas Rackauskas, Ali Ataya, Amir Emtiazjoo
Publikováno v:
Respiratory Medicine Case Reports, Vol 33, Iss , Pp 101409- (2021)
Background: Macrophage activating syndrome (MAS) is a form of hemophagocytic lymphohistiocytosis (HLH), a rare complication of autoimmune disease that is characterized by cytokine storm and multiorgan failure. Case summary: A 32-year-old male present
Externí odkaz:
https://doaj.org/article/15838a8f89034a39a3b6c3bead874e55