Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Atqah, AbdulWahab"'
Autor:
Atqah AbdulWahab, Mona Allangawi, Merlin Thomas, Ilham Bettahi, Siveen K. Sivaraman, Jayakumar Jerobin, Prem Chandra, Abdul-Badi Abou-Samra, Manjunath Ramanjaneya
Publikováno v:
Translational Medicine Communications, Vol 5, Iss 1, Pp 1-7 (2020)
Abstract Background Cystic fibrosis (CF) lung disease is associated with chronic inflammation leading to progress in lung function. Adiponectin is a predominantly anti-inflammatory adipokine that may have a role in CF lung. This study aims to determi
Externí odkaz:
https://doaj.org/article/661f0f5dab99482485ba59b6a863942b
Publikováno v:
Multidisciplinary Respiratory Medicine, Vol 14, Iss 1, Pp 1-6 (2019)
Abstract Cystic fibrosis (CF) is a genetic disease caused by a defect of CF transmembrane conductance regulator (CFTR) gene. CF affects multiple systems, predominantly with respiratory involvement. In Qatar, researchers have been exploring various as
Externí odkaz:
https://doaj.org/article/80d08dc24f7f467dac47e5673978a31b
Publikováno v:
Children, Vol 9, Iss 2, p 252 (2022)
Allergic bronchopulmonary aspergillosis (ABPA) is an immune-mediated inflammatory airway disease that predominantly affects patients with cystic fibrosis (CF) and, less commonly, patients with asthma. ABPA can lead to irreversible lung injury and bro
Externí odkaz:
https://doaj.org/article/8e7143cd6eb448b8870b2dc5c6d0e7bc
Publikováno v:
Pathogens, Vol 10, Iss 10, p 1349 (2021)
Bloodstream Candida infections constitute a major threat for hospitalized patients in intensive care units and immunocompromised hosts. Certain serum cytokines play a decisive role in anti-microbial host defense. Cytokines may act as discriminatory b
Externí odkaz:
https://doaj.org/article/66796d07bce2485c8b5908dc7faaa699
Publikováno v:
BMC Research Notes, Vol 10, Iss 1, Pp 1-5 (2017)
Abstract Objectives Candida dubliniensis is an emerging yeast and demonstrated a high adherence property to cystic fibrosis respiratory tract. Therefore, it is important to determine the persistence of C. dubliniensis and to assess the possible relat
Externí odkaz:
https://doaj.org/article/3c909059908e4224b58b6ec5f34cb679
Autor:
Atqah AbdulWahab, Khalid Zahraldin, Mazen A Sid Ahmed, Sulieman Abu Jarir, Mohammed Muneer, Shehab F Mohamed, Jemal M Hamid, Abubaker A. I. Hassan, Emad Bashir Ibrahim
Publikováno v:
Lung India, Vol 34, Iss 6, Pp 527-531 (2017)
Introduction: Multidrug-resistant Pseudomonas aeruginosa (MDR-PA) is an important and growing issue in the care of patients with cystic fibrosis (CF), and a major cause of morbidity and mortality. Objective: The objective of the study was to describe
Externí odkaz:
https://doaj.org/article/24453cf96e714d949a1f677e01d4d424
Publikováno v:
Kompass Neumología. 4:105-110
La aspergilosis broncopulmonar alérgica (ABPA) es una enfermedad inflamatoria de las vías respiratorias, de origen inmunitario, que afecta principalmente a pacientes con fibrosis quística (FQ) y, con menor frecuencia, a pacientes con asma. La ABPA
Autor:
Basel Habra, Atqah AbdulWahab
Publikováno v:
Children, Vol 5, Iss 11, p 149 (2018)
Bird Fancier’s Lung (BFL) is a rare, nonatopic immunologic response to repeated or intense inhalation of avian (bird) proteins/antigens found in the feathers or droppings of many species of birds, which leads to an immune-mediated inflammatory reac
Externí odkaz:
https://doaj.org/article/55a42fff0128475698415fabbedc9b8c
Publikováno v:
Children, Vol 5, Iss 3, p 42 (2018)
Asthma is one of the most common chronic disorders among children. Zinc (Zn) is an essential dietary antioxidant and may have a special role in assisting the airways of asthmatic subjects. The primary objective of this study was to measure serum Zn l
Externí odkaz:
https://doaj.org/article/1edc1ae931144322ba07ebdb2f844665
Autor:
Muhammad Faiyaz‐Ul‐Haque, Mohammed Mubarak, Atqah AbdulWahab, Ammar C. AlRikabi, Abbas H. Alsaeed, Maram Al‐Otaiby, Zafar Nawaz, Syed H. E. Zaidi, Sulman Basit
Publikováno v:
Journal of cutaneous pathologyREFERENCES. 49(7)
Arterial tortuosity syndrome (ATS) is a rare autosomal recessive disease characterized by elongation and tortuosity of the large- and medium-sized arteries. ATS patients display features that are also found in Ehlers-Danlos syndrome (EDS) patients. A