Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Shaghayegh Tajik"'
Autor:
Monir Seyedmofidi, Narges Soleimanifar, Katayoon Bidad, Maryam Golara, Mohammad Reza Fazlollahi, Mohammad Hosein Niknam, Shaghayegh Tajik, Morteza Samadi
Publikováno v:
مجله دانشکده پزشکی اصفهان, Vol 36, Iss 504, Pp 1376-1381 (2019)
مقدمه: آسم، یک بیماری التهابی مزمن برگشتپذیر راههای هوایی میباشد که تأثیر سیتوکاینهای التهابی در تشدید بیماری آسم ثابت شده است و ه
Externí odkaz:
https://doaj.org/article/7fe4ac38124c416d8faf27664464966c
Autor:
Seyedeh Zalfa Modarresi, Nastaran Sabetkish, Mohsen Badalzadeh, Shaghayegh Tajik, Behnaz Esmaeili, Mohammad Reza Fazlollahi, Massoud Houshmand, Jaber Gharehdaghi, Shirin Niroomanesh, Fatemeh Rahimi Sherbaf, Zahra Alizadeh, Nazanin Khodayari Namini, Marzieh Maddah, Zahra Pourpak, Mostafa Moin
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 19, Iss 5 (2020)
This study aims to investigate the role of prenatal diagnosis (PND) in Iranian couples with a previous history of primary immunodeficiency disorders (PIDD) in their family. All referred couples with a family history of PIDD and a tendency for PND wer
Externí odkaz:
https://doaj.org/article/7417154740e44c9e95d0ec71b2447598
Autor:
Zahra Alizadeh, Parisa Dashti, Marzieh Mazinani, Maryam Nourizadeh, Leila Shakerian, Shaghayegh Tajik, Masoud Movahedi, Setareh Mamishi, Zahra Pourpak, Mohammad Reza Fazlollahi
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 19, Iss 3 (2020)
X-linked agammaglobulinemia (XLA) is a primary immunodeficiency caused by genetic defects in the Bruton tyrosine kinase (Btk) gene. XLA is characterized as an antibody deficiency by recurrent bacterial infections, the absence of peripheral B cells, a
Externí odkaz:
https://doaj.org/article/382b27b517b24a61bcf9f51aa21d0bd2
Autor:
Marzieh Maddah, Mohammad Reza Fazlollahi, Reza Shiari, Farhad Shahram, Setareh Mamishi, Delara Babaie, Maryam Monajemzadeh, Soheila Sotudeh, Amir Ali Hamidieh, Mohsen Badalzadeh, Shaghayegh Tajik, Leila Sedighipour, Zahra Pourpak
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 18, Iss 4 (2019)
Chronic granulomatous disease (CGD) is a rare genetic disorder of neutrophil activity, resulting in increased rate of recurrent infections with catalase–positive bacteria and fungi, as well as various autoimmune diseases such as sarcoidosis, rheuma
Externí odkaz:
https://doaj.org/article/a15f81fe1d2840ddab146a221b2044bb
Autor:
Shaghayegh Tajik, Mohsen Badalzadeh, Mohammad Reza Fazlollahi, Massoud Houshmand, Fariborz Zandieh, Shamim Khandan, Zahra Pourpak
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 15, Iss 5 (2016)
Chronic granulomatous disease (CGD) is a rare primary immunodeficiency disorder due to a genetic defect in one of the components of nicotinamide adenine dinucleotide phosphate (NADPH) oxidase complex. This complex is composed of membrane-bound gp91-p
Externí odkaz:
https://doaj.org/article/91bdf9a173374a0d82b0391f7c7e8fa3
Autor:
Mohsen Badalzadeh, Fatemeh Fattahi, Mohammad Reza Fazlollahi, Shaghayegh Tajik, Mohammad Hassan Bemanian, Fatemeh Behmanesh, Massoud Movahedi, Massoud Houshmand, Zahra Pourpak
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 11, Iss 4 (2012)
Chronic granulomatous disease (CGD), a rare inherited primary immunodeficiency disorder, is caused by mutation in any one of the genes encoding components of nicotinamide adenine dinucleotide phosphate (NADPH)-oxidase enzyme. NCF2 gene (encoding P67-
Externí odkaz:
https://doaj.org/article/36fa381275204b529a88e7db2b87af16
Autor:
Shaghayegh Tajik, Mohsen Badalzadeh, Massoud Houshmand, Zahra Alizadeh, Leila Moradi, Amir Ali Hamidieh, Alireza Shafiei, Javad Ahmadiani Heris, Seiamak Bahram, Anne Molitor, Raphael Carapito, Mostafa Moin, Mohammad Reza Fazlollahi, Zahra Pourpak
Publikováno v:
Scandinavian Journal of Immunology. 97
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5acb164ba89385856ed7578f4e307bf8
https://doi.org/10.1111/sji.13264
https://doi.org/10.1111/sji.13264
Autor:
Mohammad Vaezi, Maryam Souri, Seyed Amin Setarehdan, Amir Ali Hamidieh, Mohammad Reza Fazlollahi, Zahra Pourpak, Mohsen Badalzadeh, Shaghayegh Tajik, Seyed Alireza Mahdaviani, Kamran Alimoghaddam, Ardeshir Ghavamzadeh
Publikováno v:
Annals of Hematology. 101:869-880
Chronic granulomatous disease (CGD) is a life-threatening immunodeficiency condition. To date, hematopoietic stem cell transplantation (HSCT) is the only curative modality. We prospectively studied the outcomes of fifteen CGD patients undergoing HSCT
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98d65d7535b60ae94246e5bb86823344
https://doi.org/10.1007/s00277-022-04751-9
https://doi.org/10.1007/s00277-022-04751-9
Autor:
Mostafa Moin, Behnoosh Tayebi, Taher Nejadsattari, Shaghayegh Tajik, Zahra Pourpak, Gholam Ali Kardar, Maryam Sharif Shoushtari, Ahmad Majd, Mohsen Badalzadeh, Raheleh Shokouhi Shoormasti, Mohammad-Ali Assarehzadegan, Mohammad Reza Fazlollahi, Songwe Fanuel
Publikováno v:
Allergo Journal International. 29:233-239
Fraxinus excelsior (Ash) is a common tree and is important cause of winter–spring pollinosis in many temperate regions in the world. In this study, a high molecular weight allergen from ash pollen was identified. In all, 20 individuals allergic to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9eb72f4c1a91c10388ef94956dd2b086
https://doi.org/10.1007/s40629-020-00129-3
https://doi.org/10.1007/s40629-020-00129-3
Autor:
Shirin Niroomanesh, Behnaz Esmaeili, Marzieh Maddah, Mostafa Moin, Zahra Pourpak, Zahra Alizadeh, Seyedeh Zalfa Modarresi, Massoud Houshmand, Jaber Gharehdaghi, Fatemeh Rahimi Sherbaf, Mohammad Reza Fazlollahi, Nazanin Khodayari Namini, Mohsen Badalzadeh, Nastaran Sabetkish, Shaghayegh Tajik
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 19, Iss 5 (2020)
This study aims to investigate the role of prenatal diagnosis (PND) in Iranian couples with a previous history of primary immunodeficiency disorders (PIDD) in their family. All referred couples with a family history of PIDD and a tendency for PND wer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86e88d69a35b5de71fc6ed107587ccd1
https://ijaai.tums.ac.ir/index.php/ijaai/article/view/2541
https://ijaai.tums.ac.ir/index.php/ijaai/article/view/2541