Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Mina Izadyar"'
Autor:
Ghamar Taj Khotaei, Sara Jam, SeyedAhmad SeyedAlinaghi, Fatemeh Motamed, Farideh Nejat, Mohammad Taghi Haghi Ashtiani, Mina Izadyar
Publikováno v:
Acta Medica Iranica, Vol 48, Iss 2, Pp 91-94 (2010)
Vancomycin is a a glycopeptide antibiotic with bacetiocidal effects on gram positive bacteria by interfering with cell wall synthesis. The necessity for monitoring of serum vancomycin concentrations (SVCs) has been recently noticed at many institutio
Externí odkaz:
https://doaj.org/article/56860360b9b14a9daf14e0cc2ace0c7f
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 8, Iss 4 (2009)
Idiopathic CD4+ Lymphocytopenia is a rare combined immunodeficiency disease, characterized by low CD4+ T-cell count and increased susceptibility to opportunistic infections, autoimmunity and malignancies after exclusion of secondary forms of CD4 lymp
Externí odkaz:
https://doaj.org/article/d9b4cfc04f11492facbe4247120e4df0
Autor:
Mina Izadyar, Jila Dastan, Tayebeh Sabokbar, Solmaz Shoraka, Azadeh Shojaei, Habib Nasiri, Saeed Reza Ghaffari
Publikováno v:
Journal of Family and Reproductive Health, Vol 1, Iss 2 (2007)
Objective: This study was designed to investigate RBC indices and HbA2 levels in parents of major beta-thalassemia patients to detect possible silent beta- thalassemia carriers and examine its potential impact on the premarital genetic counseling. Ma
Externí odkaz:
https://doaj.org/article/fe14f2873e204a3287457477ad2dd82f
Autor:
Nima Rezaei, Abolhassan Farhoudi, Zahra Pourpak, Asghar Aghamohammadi, Asghar Ramyar, Mostafa Moin, Mohammad Gharagozlou, Masoud Movahedi, Behzad Mohammadpour, Bahram MirSaeid Ghazi, Mina Izadyar, Maryam Mahmoudi
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 3, Iss 1 (2004)
Cyclic neutropenia is a rare immunodeficiency syndrome, characterized by regular periodic oscillations in the circulating neutrophil count from normal to neutropenic levels through 3 weeks period, and lasting for 3-6 days. In order to determine the c
Externí odkaz:
https://doaj.org/article/fef6777621714811895eab0f9a2cbbf0
Autor:
Abolhasan Farhoudi, Zahra Chavoshzadeh, Zahra Pourpak, Mina Izadyar, Mohammad Gharagozlou, Masoud Movahedi, Asghar Aghamohamadi, Bahram Mir saeid Ghazi, Mostafa Moin, Nima Rezaei
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 2, Iss 4 (2003)
Chediak - Higashi Syndrome (CHS) is a rare, primary Immunodeficiency disorder with an autosomal recessive (AR) inheritance and characterized by re¬current infection, partial occulocutaneous albinism and an accelerated phase. In this report we descri
Externí odkaz:
https://doaj.org/article/8a39277be2954f91aaaf9d69b8fdc6f9
Autor:
Zahra Pourpak, Mostafa Moin, Maryam Mahmoudi, Magda Grudzien, Marshall S. Horwitz, Roya Sherkat, Fatemeh Mahjoub, Asghar Aghamohammadi, Manuela Germeshausen, Mina Izadyar, Mehdi Yeganeh, Abolhassan Farhoudi, Zahra Chavoshzadeh, Christoph Klein, Asghar Ramyar, Nima Rezaei
Publikováno v:
Journal of Clinical Immunology. 27:525-533
Severe congenital neutropenia (SCN) is a rareE primary immunodeficiency disorder characterized by early onset recurrent infections in association with persistent severe agranulocytosis. To identify the clinical, immunohematological, and molecular cha
Autor:
John M. Old, Suthat Fucharoen, Navratnam Kotea, Marina Kleanthous, Pranee Winichagoon, Mohammad Esmaeil Akbari, Panayiotis A. Ioannou, Sheikh Raizuddin, Renu Saxena, Shaheen N. Khan, Ishwar C. Verma, Baldip Khan, Mina Izadyar
Publikováno v:
Hemoglobin. 31:439-452
We studied 325 thalassemia intermedia patients from Iran, India, Pakistan, Thailand, Mauritius and Cyprus to examine factors which influence the phenotype. The beta-thalassemia (thal) mutations were determined for 219 beta-thal/beta-thal and 106 beta
Autor:
Habib Tavassoli, Mohammad Sadegh Aramli, Mohammad Lamei Rashti, Fatemeh Mahjoub, Mehri Najafi Sani, Eesa Jahanzad, Fatemeh Farahmand, Mina Izadyar
Publikováno v:
Experimental and toxicologic pathology : official journal of the Gesellschaft fur Toxikologische Pathologie. 67(5-6)
Iron deposition in liver is a major finding in thalassemic patients and because of direct iron toxicity to liver it is associated with several consequences for example liver fibrosis. Liver biopsies from 63 patients were evaluated, 40 (63.5%) were ma
Autor:
Zahra Pourpak, Bahram Mirsaeid Ghazi, A. Farhoudi, Mohammad Gharagozlou, Nima Rezaei, Asghar Aghamohammadi, Mina Izadyar, Asghar Ramyar, Behzad Mohammadpour, Masoud Movahedi, Maryam Mahmoudi, Mostafa Moin
Publikováno v:
Journal of Pediatric Hematology/Oncology. 27:351-356
Inherited neutropenia is characterized by a decrease in the absolute number of circulating neutrophils and an increased susceptibility to infections. The current study was performed to determine the clinical and laboratory findings of Iranian patient
Autor:
Leili Koochakzadeh, F. Farahani, Maryam Eghbali, Sima Hosseinverdi, Asghar Ramyar, Asghar Aghamohammadi, Mohammad Saeid Rahiminejad, Mona Hedayat, A. Tofighi, Mina Izadyar, Nima Rezaei, Alireza Zare Bidoki
Publikováno v:
Allergologia et immunopathologia. 43(6)
Background X-linked lymphoproliferative disease (XLP) is an often fatal inherited immunodeficiency disorder characterised by fulminant infectious mononucleosis, acquired haemophagocytic lymphohistiocytosis, dysgammaglobulinaemia and malignant lymphom