Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Joseph G. Cal"'
Publikováno v:
Annals of Thoracic Medicine, Vol 16, Iss 2, Pp 178-187 (2021)
BACKGROUND: Information regarding acute exacerbation (AE) in patients with interstitial lung disease (ILD) is limited. OBJECTIVES: The objective of the study was to elucidate the clinical features and outcome of AE among ILD patients. METHODS: We ret
Externí odkaz:
https://doaj.org/article/a4787e678f464e6a9ed699c5cd86c589
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:
Esam H Alhamad, Joseph G Cal
Publikováno v:
Annals of Thoracic Medicine, Vol 15, Iss 4, Pp 238-243 (2020)
BACKGROUND: There is a paucity of information regarding prognostic factors associated with reduced survival in interstitial lung disease (ILD) patients without pulmonary hypertension (PH). AIMS: The aim of this study was to determine physiological an
Externí odkaz:
https://doaj.org/article/62538089abda4ef98176ef108d025269
Publikováno v:
Annals of Thoracic Medicine
Annals of Thoracic Medicine, Vol 16, Iss 2, Pp 178-187 (2021)
Annals of Thoracic Medicine, Vol 16, Iss 2, Pp 178-187 (2021)
BACKGROUND: Information regarding acute exacerbation (AE) in patients with interstitial lung disease (ILD) is limited. OBJECTIVES: The objective of the study was to elucidate the clinical features and outcome of AE among ILD patients. METHODS: We ret
Autor:
Esam H Alhamad, Joseph G Cal, Hussam F Alfaleh, Mostafa Q Alshamiri, Ahmad A AlBoukai, Suliman A AlHomida
Publikováno v:
Annals of Thoracic Medicine, Vol 8, Iss 2, Pp 78-85 (2013)
Context: Several international studies have described the epidemiology of pulmonary hypertension (PH). However, information about the incidence and prevalence of PH in Saudi Arabia is unknown. Aims: To report cases of PH and compare the demographic a
Externí odkaz:
https://doaj.org/article/fae5a7d0fb654c62b291033cf090ff6f
Autor:
Joseph G Cal, Esam H. Alhamad
Publikováno v:
Annals of Thoracic Medicine
Annals of Thoracic Medicine, Vol 15, Iss 4, Pp 238-243 (2020)
Annals of Thoracic Medicine, Vol 15, Iss 4, Pp 238-243 (2020)
BACKGROUND: There is a paucity of information regarding prognostic factors associated with reduced survival in interstitial lung disease (ILD) patients without pulmonary hypertension (PH). AIMS: The aim of this study was to determine physiological an
Clinical characteristics, comorbidities, and outcomes in patients with idiopathic pulmonary fibrosis
Autor:
Waleed M Aharbi, Ammar C. Al-Rikabi, Ahmad A. Al-Boukai, Joseph G Cal, Nuha N. Alrajhi, Esam H. Alhamad
Publikováno v:
Annals of Thoracic Medicine, Vol 15, Iss 4, Pp 208-214 (2020)
Annals of Thoracic Medicine
Annals of Thoracic Medicine
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
Predictors of Mortality in Patients with Interstitial Lung Disease-Associated Pulmonary Hypertension
Publikováno v:
Journal of Clinical Medicine
Journal of Clinical Medicine, Vol 9, Iss 3828, p 3828 (2020)
Volume 9
Issue 12
Journal of Clinical Medicine, Vol 9, Iss 3828, p 3828 (2020)
Volume 9
Issue 12
Background: Pulmonary hypertension (PH) is a well-established complication in interstitial lung disease (ILD) patients. The aim of this study is to investigate the physiological and hemodynamic parameters that predict mortality in patients with ILD-P
Autor:
Nuha N. Alrajhi, Mohammed A. Omair, Ammar C. Al-Rikabi, Joseph G Cal, Esam H. Alhamad, Ahmad A. Al-Boukai, Muthurajan P Paramasivam, Mohammed Alessa
Publikováno v:
Respiratory medicine. 174
Background Significant overlap may occur between idiopathic interstitial pneumonia (IIP) and connective tissue diseases (CTDs) that do not meet the established classification criteria for any known CTDs (i.e., occult CTD). Performing minor salivary g