Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Firouzeh Tabassomi"'
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 26, Iss 4, Pp 783-785 (2015)
Externí odkaz:
https://doaj.org/article/22e152b4c8024e6dbc1b39d3cf7ddde8
Publikováno v:
Pediatric Transplantation. 18:E69-E73
PH type 2 is caused by decreased activity of GRHPR enzyme that eventually leads to ESRD and systemic oxalosis. Here, we describe an Iranian pediatric patient with PH2 and early ESRD development who received recommended treatment by undergoing isolate
Molecular diagnosis of primary immunodeficiency diseases in a developing country: Iran as an example
Publikováno v:
Expert Review of Clinical Immunology. 10:385-396
Primary immunodeficiency diseases (PID) comprise a heterogeneous group of inherited diseases with a wide spectrum of clinical manifestations and laboratory abnormalities. Definite diagnosis of a PID is performed most reliably by detection of a gene m
Autor:
AmirHossein Latif, Reza Yazdani, Firouzeh Tabassomi, Nima Rezaei, Hassan Abolhassani, Asghar Aghamohammadi, Gholamreza Azizi
Publikováno v:
Expert review of clinical immunology. 11(11)
Selective immunoglobulin A deficiency (SIgAD) is the most common predominantly antibody deficiency, with a wide range of presentations from asymptomatic to severe manifestations. Although many studies have investigated different aspects of SIgAD, no
Autor:
Taher Cheraghi, Tahaamin Shokuhfar, Babak Torabi Sagvand, Mehran Ebrahimi, Mohammad Gharagozlou, Reza Amin, Saeid Bazregari, Babak Mirminachi, Lennart Hammarström, Nima Parvaneh, Najmoddin Kalantari, Sara Kashef, Asghar Aghamohammadi, Davood Razavinejad, Firouzeh Tabassomi, Alireza Khayatzadeh, Hassan Abolhassani, Shervin Shahinpour, Mohsen Ebrahimi, Mohamad Hosein Eslamian, Javad Ghaffari, Masoud Movahedi, Reza Faridhosseini, Nasrin Behniafard, Nima Rezaei, Abbas Khalili, Soheila Aleyasin, Mohammad Hassan Bemanian, Alireza Shafiei, Iraj Mohammadzadeh, Farahzad Jabbari-Azad, Roya Sherkat, AmirHossein Latif, Abbas Dabbaghzade
Publikováno v:
Expert review of clinical immunology. 10(10)
Common variable immune deficiency (CVID) is the most frequent form of symptomatic primary immunodeficiency disease, characterized by hypogammaglobulinemia, recurrent infections and increased predisposition to autoimmunity and malignancies. The aim of
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation. 27:791
Primary hyperoxaluria Type-1 (PH-1) is caused by a deficiency of alanine-glyoxylate aminotransferase manifesting as urolithiasis, nephrocalcinosis, and end-stage renal disease (ESRD). Among treatment options, best outcomes have been achieved by seque