Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Ammar C AlRikabi"'
Autor:
Waseem M Hajjar, Abdelazeem Eldawlatly, Sami A Alnassar, Iftikhar Ahmed, Alaa Alghamedi, Zahid Shakoor, Ammar C Alrikabi, Adnan W Hajjar, Abdulaziz Ejaz Ahmad
Publikováno v:
Saudi Journal of Anaesthesia, Vol 15, Iss 1, Pp 1-6 (2021)
Background and Aims: Mechanical ventilation (MV) with high tidal volume (Vt.) may induce or aggravate lung injury in critically ill patients. It might also cause an overwhelming systemic inflammation leading to acute lung injury (ALI), diffuse alveol
Externí odkaz:
https://doaj.org/article/c4a8fe64e19b44539cbb50a13d521d69
Autor:
Esam H Alhamad, Joseph G Cal, Nuha N Alrajhi, Muthurajan P Paramasivam, Waleed M Alharbi, Mohammed AlEssa, Mohammed A Omair, Ammar C AlRikabi, Ahmad A AlBoukai
Publikováno v:
Annals of Thoracic Medicine, Vol 16, Iss 2, Pp 156-164 (2021)
BACKGROUND: Diagnosing primary Sjogren's syndrome (pSS)-associated interstitial lung disease (ILD) is complex and can be very challenging. In addition, information about the prognostic factors is limited. AIMS: We aimed to determine the clinical char
Externí odkaz:
https://doaj.org/article/8b34b7e2b697481383d9c10545393159
Clinical characteristics, comorbidities, and outcomes in patients with idiopathic pulmonary fibrosis
Autor:
Esam H Alhamad, Joseph G Cal, Nuha N Alrajhi, Waleed M Aharbi, Ammar C AlRikabi, Ahmad A AlBoukai
Publikováno v:
Annals of Thoracic Medicine, Vol 15, Iss 4, Pp 208-214 (2020)
BACKGROUND: Idiopathic pulmonary fibrosis (IPF) is a common subtype of interstitial lung disease (ILD). Information about the associated comorbidities and predictors of survival among Saudi patients with IPF is limited. AIMS: The aim of the study was
Externí odkaz:
https://doaj.org/article/c64fcaa4347644cd84b296d03633be82
Autor:
Nuha Nasser Alrajhi, Muthurajan P Paramasivam, Ahmad Amer Alboukai, Ammar C Alrikabi, Esam Hamad Alhamad
Publikováno v:
Annals of Thoracic Medicine, Vol 14, Iss 2, Pp 161-163 (2019)
Diffuse idiopathic pulmonary neuroendocrine cell hyperplasia (DIPNEC) is an abnormal proliferation of pulmonary neuroendocrine cells that occur without underlying etiology. Here, we report a unique case of 55-year-old female with unusual presentation
Externí odkaz:
https://doaj.org/article/df6a76a32178474c9c0f72065bd7fdfe
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d04260a4f033b830fe74042e0e69587d
https://pubmed.ncbi.nlm.nih.gov/35302653
https://pubmed.ncbi.nlm.nih.gov/35302653