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European Journal of Pediatrics|March 5, 2008
Novel BTK mutation presenting with vaccine-associated paralytic poliomyelitisSetareh Mamishi, Shohreh Shahmahmoudi, Hamideh Tabatabaie, et al.Immunogenetics|November 15, 2007
The hyper-IgE syndrome is not caused by a microdeletion syndromeDietmar Pfeifer, Cristina Woellner, Astrid Petersen, et al.Scientific Reports|September 23, 2015
Tumour-promoting role of SOCS1 in colorectal cancer cellsWilliam S Tobelaim, Claudia Beaurivage, Audrey Champagne, et al.NPJ Genomic Medicine|September 29, 2025
Biallelic variants in BBOX1 cause L-Carnitine deficiency and elevated γ-butyrobetaineXiao Li, Mehdi Yeganeh, Graham Sinclair, et al.Scandinavian Journal of Infectious Diseases|September 30, 2006
The clinical and laboratory survey of Iranian patients with hyper-IgE syndromeMostafa Moin, Abolhassan Farhoudi, Masoud Movahedi, et al.Journal of Clinical Immunology|June 26, 2007
The clinical, immunohematological, and molecular study of Iranian patients with severe congenital neutropeniaNima Rezaei, Mostafa Moin, Zahra Pourpak, et al.Iranian Journal of Allergy, Asthma, and Immunology|June 17, 2008
Evaluation of humoral immune function in patients with bronchiectasisParviz Tabatabaie, Asghar Aghamohammadi, Setareh Mamishi, et al.Journal of Clinical Immunology|March 20, 2008
Analysis of RAB27A gene in griscelli syndrome type 2: novel mutations including a deletion hotspotSetareh Mamishi, Mohammad Hossein Modarressi, Babak Pourakbari, et al.International Archives of Allergy and Immunology|September 1, 2006
Clinical, immunological and molecular characteristics of 37 Iranian patients with X-linked agammaglobulinemiaAsghar Aghamohammadi, Maurilia Fiorini, Mostafa Moin, et al.International Archives of Allergy and Immunology|February 13, 2008
Toll-like receptor stimulation induces higher TNF-alpha secretion in peripheral blood mononuclear cells from patients with hyper IgE syndromeMehdi Yeganeh, Philipp Henneke, Nima Rezaei, et al.Pageof 4