Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Habib Zayeni"'
Nephrotic syndrome due to focal segmental glomerulosclerosis complicating scleroderma: a case report
Autor:
Mahsa Mehdipour Dalivand, Asghar Hadjiabbasi, Elham Ramezanzadeh, Seyed Mahmood Habibzadeh, Kimia Goudarzi, Reza Shahriarirad, Habib Zayeni
Publikováno v:
Journal of Medical Case Reports, Vol 18, Iss 1, Pp 1-6 (2024)
Abstract Background Systemic scleroderma (SSc) is an insidious autoimmune connective tissue disorder with multiorgan involvement. Renal involvement is one of the important causes of morbidity and mortality in scleroderma; however, nephrotic syndrome
Externí odkaz:
https://doaj.org/article/feec477498c547a7861bc85dc33370aa
Autor:
Fatemeh Nejatifar, Neda Mirbolouk, Irandokht Shenavar Masooleh, Ehsan Kazemnejad, Banafsheh Ghavidel-Parsa, Amir Mohammad Ghanbari, Habib Zayeni
Publikováno v:
Heliyon, Vol 9, Iss 10, Pp e20576- (2023)
Introduction: Systemic sclerosis is a chronic and progressive connective tissue disease with various manifestation. Inflammatory status is developed in early stages and is followed by major organs’ dysfunction. Disease severity is evaluated mostly
Externí odkaz:
https://doaj.org/article/84e9ca1dad8f41148c56c79500f731c1
Autor:
Banafsheh Ghavidel-Parsa, Mohammad-Javad Khosousi, Sepehr Tohidi, Ali Bidari, Saman Soltani, Habib Zayeni, Ali Montazeri
Publikováno v:
BMC Rheumatology, Vol 6, Iss 1, Pp 1-9 (2022)
Abstract Background The Invalidation Illness Inventory (3*I) is an instrument that assesses invalidation (including discounting and lack of understanding dimensions) experienced by patients with rheumatic disorders. This study aimed to translate and
Externí odkaz:
https://doaj.org/article/e827d1111f6f4d6385b45e7644d1840a
Autor:
Hassan Behboudi, Habib Zayeni, Asghar Haji-Abbasi, Zahra Moravvej, Ebrahim Azaripour, Yousef Alizadeh, Reza Soltani-Moghadam
Publikováno v:
Journal of Ophthalmic & Vision Research, Vol 17, Iss 1, Pp 135-139 (2022)
Abstract Purpose: To present a case of linear scleroderma known as “en coup de sabre” associated with Coats'- like response. Case Report: A 12-year-old boy presented with subacute painless vision loss in the ipsilateral side of the patient's en c
Externí odkaz:
https://doaj.org/article/27ab921067fa43fe8d116f67ed4647a2
Autor:
Fereshteh Beigmohammadi, Saeed Aslani, Hoda Kavosi, Ali Javinani, Shayan Mostafaei, Mehran Pournazari, Baharak Tasorian, Elham Farhadi, Asghar Hajiabbasi, Habib Zayeni, Alireza Khabbazi, Ahmadreza Jamshidi, Irandokht Shenavar Masooleh, Zahra Tamartash, Mahdi Vojdanian, Mahdi Mahmoudi
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 22, Iss 1 (2023)
Takayasu arteritis (TA) is a chronic inflammatory disorder characterized by vascular damage and fibrosis in the intima that commonly occurs in the aorta. In many damaged sites in TA patients, natural killer (NK) cells have been shown to be hyperactiv
Externí odkaz:
https://doaj.org/article/e698cb0505a84d508c26d6439ea4895f
Autor:
Irandokht Shenavar Masooleh, Habib Zayeni, Asghar Haji-Abbasi, Manouchehr Azarpira, Ali Hadian, Amir Hassankhani, Banafsheh Ghavidel Parsa
Publikováno v:
Indian Heart Journal, Vol 68, Iss 3, Pp 332-335 (2016)
Background: Cardiovascular disease is one of the extra-articular manifestations of rheumatoid arthritis (RA) that is the most common cause of death in these patients. So we decided to evaluate RA patients in terms of history, clinical examination, el
Externí odkaz:
https://doaj.org/article/cb0ad2b967c145a68c143404fd688030
Autor:
Habib Zayeni, Asghar Haji-Abbasi, Seyed Ali Alavi Foumani, Mehdi Tohidi, Irandokht Shenavar Masooleh, Banafsheh Ghavidel Parsa, Mehrdad Aghaei, Amir Hassankhani, Pooneh Ghavidel Parsa, Alireza Amir Maafi
Publikováno v:
Lung India, Vol 33, Iss 1, Pp 49-52 (2016)
Background: Interstitial lung disease (ILD) is a type of pulmonary manifestation in patients with rheumatoid arthritis (RA). Mostly RA-ILD has no symptoms and is only diagnosed by clinical examination, pulmonary function test (PFT), and high-resoluti
Externí odkaz:
https://doaj.org/article/e3cddd7cccc545c5bbd12312b3f83ffd
Autor:
Naser Aghdami, Abdorahman Rostamian, Sima Sedighi, Masoumeh Akhlaghi, Habib Zayeni, Farhad Gharibdost, Mehrdad Aghaei, Mahdieh Shojaa
Publikováno v:
فصلنامه دانشگاه علوم پزشکی جهرم, Vol 9, Iss 1, Pp 23-26 (2011)
Introduction:Scleroderma is a systemic disorder with unknown etiology most notably characterized by skin thickening and internal organ involvement. Endothelin-1 plays an important role in skin fibrosis. This study aimed to compare endothelin-1 level
Externí odkaz:
https://doaj.org/article/83fe844a339f49b0ac6a4e601709fa46
Autor:
Mardad Aghaei, Farhad Gharibdost, Habib Zayeni, Masoomeh Akhlaghi, Sima Sedighi, Abdalrahman Rostamian, naser Aghdami, Mahdeyeh Shojaa
Publikováno v:
فصلنامه دانشگاه علوم پزشکی جهرم, Vol 9, Iss 1, Pp 23-27 (2011)
Introduction: Scleroderma is a systemic disorder with unknown etiology most notably characterized by skin thickening and damage of organs. Endothelin-1(ET-1) plays a role in skin fibrosis. This study aimed to survey and compareET-1level in systematic
Externí odkaz:
https://doaj.org/article/7baf0ef008264f658c2a049df5bf3814
Autor:
Mehrdad Aghaei, Farhad Gharibdost, Habib Zayeni, Maryam Akhlaghi, Sima Sedighi, Abduo Rahman Rostamian, Naser Aghdami, Mahdieh Shojaa
Publikováno v:
Indian Dermatology Online Journal, Vol 3, Iss 1, Pp 14-16 (2012)
Introduction: Scleroderma is a systemic disorder with unknown etiology most notably characterized by skin thickening and organ damage. Endothelin-1 (ET-1) plays a role in skin fibrosis. The aim of this study was survey and comparison of ET-1 level in
Externí odkaz:
https://doaj.org/article/446377658c2d4366b7a8567715bcbdeb