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Iranian Journal of Allergy, Asthma, and Immunology|September 16, 2019
Identification of a Novel C16orf57 Mutation in Iranian Patient with Clericuzio-type Poikiloderma with Neutropenia (CPN): A Case ReportFarhad Abolnezhadian, Sara Iranparast
Iranian Journal of Immunology : IJI|October 1, 2014
Autoimmune hemolytic anemia in a patient with probable ataxia telangiectasia: a case reportSoheila Alyasin, Maryam Khoshkhui, Farhad Abolnezhadian
Iranian Journal of Immunology : IJI|December 31, 2020
Identical Twins with a Mutation in the STK4 Gene Showing Clinical Manifestations of the Mutation at Different Ages: A Case ReportFarhad Abolnezhadian, Sara Iranparast, Fatemeh Ahmadpour
Iranian Journal of Allergy, Asthma, and Immunology|January 16, 2019
MHC Class II Deficiency with Normal CD4+ T Cell Counts: A Case ReportFarhad Abolnezhadian, Ali Saeedi-Boroujeni, Sara Iranparast
Iranian Journal of Immunology : IJI|September 29, 2015
A Case of Probable MHC Class II Deficiency with Disseminated BCGitisSoheyla Alyasin, Farhad Abolnezhadian, Maryam Khoshkhui
Iranian Journal of Allergy, Asthma, and Immunology|December 7, 2016
The Effect of Autologous Serum Therapy on Disease Severity in Patients with Chronic UrticariaFarhad Abolnezhadian, Soheila Alyasin, Reza Amin, et al.
Immunologic Research|June 25, 2020
A novel mutation in RFXANK gene and low B cell count in a patient with MHC class II deficiency: a case reportFarhad Abolnezhadian, Razieh Dehghani, Sajad Dehnavi, et al.
European Journal of Pediatrics|June 26, 2026
Comparison of complete blood count (CBC) parameters in patients with Sanjad-sakati syndrome and healthy controls in Abuzar Hospital, AhvazSetare Choromzade, Mojtaba Aghaei, Najmaldin Saki, et al.
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