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Journal of Investigational Allergology & Clinical Immunology
|
February 9, 2012
Molecular characterization of Bruton's tyrosine kinase deficiency in 12 Iranian patients with presumed X-linked agammaglobulinemia
S Nasseri, R Sorouri, Z Pourpak, et al.
Journal of Investigational Allergology & Clinical Immunology
|
February 15, 2011
A novel RAB27A mutation in a patient with Griscelli syndrome type 2
B S Shamsian, K Norbakhsh, N Rezaei, et al.
Zeitschrift Fur Gastroenterologie
|
December 6, 2011
NOD2 sequencing in Iranian children with Crohn's disease
F Motamed, M Najafi, M Taghvaei, et al.
International Journal of Hematology
|
March 7, 2008
Molecular diagnosis of X-linked chronic granulomatous disease in Iran
S Teimourian, Z Rezvani, M Badalzadeh, et al.
Journal of Investigational Allergology & Clinical Immunology
|
November 7, 2007
Analysis of class-switched memory B cells in patients with common variable immunodeficiency and its clinical implications
M Vodjgani, A Aghamohammadi, M Samadi, et al.
Journal of Investigational Allergology & Clinical Immunology
|
March 3, 2023
Analysis of Lymphocyte and Clinical Profile in Nonmonogenic Common Variable Immunodeficiency Patients With and Without Class Switch Recombination Defect
F Tofighi Zavareh, A Mirshafiey, R Yazdani, et al.
Journal of Investigational Allergology & Clinical Immunology
|
March 28, 2012
Severe primary antibody deficiency due to a novel mutation of mu heavy chain
I Mohammadzadeh, M Yeganeh, A Aghamohammadi, et al.
Journal of Investigational Allergology & Clinical Immunology
|
October 16, 2010
Ataxia-telangiectasia in a patient presenting with hyper-immunoglobulin M syndrome
A Aghamohammadi, K Imai, K Moazzami, et al.
Journal of Investigational Allergology & Clinical Immunology
|
November 23, 2013
Autoimmune phenotype in patients with common variable immunodeficiency
H Abolhassani, D Amirkashani, N Parvaneh, et al.
Allergologia Et Immunopathologia
|
July 28, 2019
Mendelian susceptibility to mycobacterial disease: Clinical and immunological findings of patients suspected for IL12Rβ1 deficiency
L Moradi, T Cheraghi, R Yazdani, et al.
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of 3
Search research articles
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Showing results (11-20 of 22) with videos related to
Sort By:
Page
of 3
Journal of Investigational Allergology & Clinical Immunology
|
February 9, 2012
Molecular characterization of Bruton's tyrosine kinase deficiency in 12 Iranian patients with presumed X-linked agammaglobulinemia
S Nasseri, R Sorouri, Z Pourpak, et al.
Journal of Investigational Allergology & Clinical Immunology
|
February 15, 2011
A novel RAB27A mutation in a patient with Griscelli syndrome type 2
B S Shamsian, K Norbakhsh, N Rezaei, et al.
Zeitschrift Fur Gastroenterologie
|
December 6, 2011
NOD2 sequencing in Iranian children with Crohn's disease
F Motamed, M Najafi, M Taghvaei, et al.
International Journal of Hematology
|
March 7, 2008
Molecular diagnosis of X-linked chronic granulomatous disease in Iran
S Teimourian, Z Rezvani, M Badalzadeh, et al.
Journal of Investigational Allergology & Clinical Immunology
|
November 7, 2007
Analysis of class-switched memory B cells in patients with common variable immunodeficiency and its clinical implications
M Vodjgani, A Aghamohammadi, M Samadi, et al.
Journal of Investigational Allergology & Clinical Immunology
|
March 3, 2023
Analysis of Lymphocyte and Clinical Profile in Nonmonogenic Common Variable Immunodeficiency Patients With and Without Class Switch Recombination Defect
F Tofighi Zavareh, A Mirshafiey, R Yazdani, et al.
Journal of Investigational Allergology & Clinical Immunology
|
March 28, 2012
Severe primary antibody deficiency due to a novel mutation of mu heavy chain
I Mohammadzadeh, M Yeganeh, A Aghamohammadi, et al.
Journal of Investigational Allergology & Clinical Immunology
|
October 16, 2010
Ataxia-telangiectasia in a patient presenting with hyper-immunoglobulin M syndrome
A Aghamohammadi, K Imai, K Moazzami, et al.
Journal of Investigational Allergology & Clinical Immunology
|
November 23, 2013
Autoimmune phenotype in patients with common variable immunodeficiency
H Abolhassani, D Amirkashani, N Parvaneh, et al.
Allergologia Et Immunopathologia
|
July 28, 2019
Mendelian susceptibility to mycobacterial disease: Clinical and immunological findings of patients suspected for IL12Rβ1 deficiency
L Moradi, T Cheraghi, R Yazdani, et al.
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of 3