Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Mahnaz Sadeghi-Shabestari"'
Autor:
Soodeh Ghadimi, Mahnaz Jamee, Hassan Abolhassani, Nima Parvaneh, Nima Rezaei, Samaneh Delavari, Mahnaz Sadeghi-Shabestari, Sedigheh Rafiei Tabatabaei, Alireza Fahimzad, Shahnaz Armin, Zahra Chavoshzadeh, Samin Sharafian
Publikováno v:
Allergy, Asthma & Clinical Immunology, Vol 19, Iss 1, Pp 1-12 (2023)
Abstract Background DCLRE1C gene mutation leads to Artemis deficiency, a severe form of combined immunodeficiency (SCID). Impaired DNA repair and block in early adaptive immunity maturation results in T-B-NK+ immunodeficiency associated with radiosen
Externí odkaz:
https://doaj.org/article/8bcc5ba26be5425d84e53b665099de5b
Autor:
Niusha Sharifinejad, Seyed Alireza Mahdaviani, Shahrzad Fallah, Nasrin Khakbazan Fard, Alireza Norouzi, Mahnaz Jamee, Mahnaz Sadeghi-Shabestari, Majid Marjani, Mehran Malekshoar, Parisa Farnia, Ali Akbar Velayati
Publikováno v:
Allergy, Asthma & Clinical Immunology, Vol 18, Iss 1, Pp 1-5 (2022)
Abstract Background Mendelian susceptibility to mycobacterial disease (MSMD) is an uncommon disorder with increased susceptibility to less virulent mycobacteria including bacillus Calmette-Guérin (BCG). Fibrosing mediastinitis (FM) is also a rare co
Externí odkaz:
https://doaj.org/article/d3ff727f21744df0a47fe73578fd5063
Autor:
Farzad Emsaeili, Amirhouman Sadrhaghighi, Mahnaz Sadeghi-Shabestari, Parastou Nastarin, Aliakbar Niknafs
Publikováno v:
Journal of Dental Research, Dental Clinics, Dental Prospects, Vol 16, Iss 1, Pp 18-23 (2022)
Background. The etiology of obstructive sleep apnea (OSA) syndrome in children significantly differs from adults. In previous studies, only some of the indices have been investigated using CBCT. This study compares all the measurable indices of airwa
Externí odkaz:
https://doaj.org/article/a8bf00b0a6224c44b36704edbc2cfc2d
Autor:
Tannaz Moeini Shad, Reza Yazdani, Parisa Amirifar, Samaneh Delavari, Marzieh Heidarzadeh Arani, Seyed Alireza Mahdaviani, Mahnaz Sadeghi-Shabestari, Asghar Aghamohammadi, Nima Rezaei, Hassan Abolhassani
Publikováno v:
Frontiers in Immunology, Vol 12 (2022)
Ataxia-telangiectasia (AT) is a rare autosomal recessive neurodegenerative multisystem disorder. A minority of AT patients can present late-onset atypical presentations due to unknown mechanisms. The demographic, clinical, immunological and genetic d
Externí odkaz:
https://doaj.org/article/bc09feba54124673bcf9b84e5d028108
Autor:
Daniel Elieh Ali Komi, Mahnaz Sadeghi-Shabestari, Dariush Shanebandi, Zohreh Babaloo, Alireza Razavi, Saeed Sadigh-Eteghad, Tohid Kazemi
Publikováno v:
Research in Molecular Medicine, Vol 7, Iss 4, Pp 17-24 (2019)
Background: In addition to cellular and molecular mechanisms involved in the pathogenesis of asthma, mounting evidences demonstrate that single nucleotide polymorphisms (SNPs) in asthma relevant genes have a role in conferring susceptibility to the d
Externí odkaz:
https://doaj.org/article/8e95069c828f4544be48e10a50f88b3c
Autor:
Ilghar Zeinaly, Naghmeh Vossoughi, Daniel Elieh Ali Komi, Tohid Kazemi, Zohreh Babaloo, Alireza Razavi, Mohammad Sajay-Asbaghi, Mahnaz Sadeghi-Shabestari
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 17, Iss 6 (2018)
Orosomucoid 1-like 3 (ORMDL3) gene, located on chromosome 17q21, is an asthma candidate gene that encodes ORMDL3. This molecule has been reported to play a role in airway remodeling and bronchial hyper-responsiveness. In this study, we aimed to inves
Externí odkaz:
https://doaj.org/article/e85c5f0be97c4f18bd75d6fc35d1491d
Autor:
Mandana Rafeey, Bozorgmehr Nasir, Zahra Jalali, Nazanin Hazhir Karzar, Mahnaz Sadeghi-shabestari
Publikováno v:
Journal of Research in Clinical Medicine, Vol 8, Iss 1, Pp 29-29 (2020)
Introduction: The studies have been equivocal about the association of Helicobacter pylori infection with chronic urticaria (CU) given some controversial evidence in recovery of urticaria following H. pylori eradication. Methods: In this clinical tri
Externí odkaz:
https://doaj.org/article/9342ce052798452aa71e1bdbba8ab653
Publikováno v:
Acta Medica Iranica, Vol 56, Iss 6 (2018)
Neutropenia is characterized by a decrease in circulating neutrophil counts and consequent infections. The present study was performed so as to describe the clinical and laboratory findings of patients with congenital neutropenia in northwestern Iran
Externí odkaz:
https://doaj.org/article/8501390a809b426f8ff0da48c3fdd51f
Autor:
Mandana Rafeey, Morteza Jabbarpour-Bonyadi, Behzad Aliyari, Mahnaz Sadeghi-Shabestari, Fakhrossadat Mortazavi
Publikováno v:
Journal of Analytical Research in Clinical Medicine, Vol 3, Iss 2, Pp 112-117 (2015)
Introduction: Patients with Henoch-Shonlein purpura (HSP) have higher rates of Mediterranean fever (MEFV) mutations comparing general population. To our knowledge, there is no report in this regard among Azeri Turkish children. In this study, we eval
Externí odkaz:
https://doaj.org/article/6106a5b71f5042f9886a1e3f2edf9251
Autor:
Nikou Fotouhi, Morteza Bonyadi, Zohreh Jahanafrooz, Nahid Ahmadian, Mahnaz Sadeghi-Shabestari, Saeid Aslanabadi, Robabeh Ghergherehchi, Milad Pormosavi, Mandana Rafeey
Publikováno v:
African Journal of Paediatric Surgery, Vol 11, Iss 3, Pp 233-237 (2014)
Background: Biliary atresia (BA) is a progressive inflammatory destructive process of the bile ducts. This study evaluated the relationship between single-nucleotide polymorphisms in the promoter region of tumour necrosis factor-alpha (TNF-α) gene a
Externí odkaz:
https://doaj.org/article/3b638f37daff4b4aa18f940e6e74d022