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N Parvaneh

Showing results (1-10 of 22) with videos related to

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Journal of Investigational Allergology & Clinical Immunology|October 16, 2010
Correlation between common variable immunodeficiency clinical phenotypes and parental consanguinity in children and adultsA Aghamohammadi, H Abolhassani, K Moazzami, et al.
Journal of Investigational Allergology & Clinical Immunology|April 29, 2014
Genetic defects in B-cell development and their clinical consequencesH Abolhassani, N Parvaneh, N Rezaei, et al.
Journal of Investigational Allergology & Clinical Immunology|February 5, 2010
Severe congenital neutropenia in 2 siblings of consanguineous parents. The role of HAX1 deficiencyS Mamishi, S A Esfahani, N Parvaneh, et al.
Journal of Investigational Allergology & Clinical Immunology|October 24, 2018
A Novel TTC7A Deficiency Presenting With Combined Immunodeficiency and Chronic Gastrointestinal ProblemsS Sharafian, H Alimadadi, M Shahrooei, et al.
Journal of Investigational Allergology & Clinical Immunology|April 25, 2019
UNC13D Deficiency Associated With Epileptic Seizures and Antibody Deficiency: The First Case from the Iranian National RegistryR Yazdani, P Amirifar, H Abolhassani, et al.
Allergologia Et Immunopathologia|October 1, 2018
Evaluation of interleukin-12 receptor β1 and interferon gamma receptor 1 deficiency in patients with disseminated BCG infectionB Pourakbari, R Hosseinpour Sadeghi, S Mahmoudi, et al.
European Annals of Allergy and Clinical Immunology|September 9, 2017
New therapeutic approach by sirolimus for enteropathy treatment in patients with LRBA deficiencyG Azizi, H Abolhassani, R Yazdani, et al.
Iranian Journal of Microbiology|October 16, 2012
Seroepidemiology of Varicella Zoster Virus among children, adolescents and medical students in a referral children medical center, Tehran, IranB Pourakbari, L Shahbaznezhad, N Parvaneh, et al.
Allergologia Et Immunopathologia|September 10, 2014
Impaired in-vitro responses to IL-12 and IFN-γ in Iranian patients with Mendelian susceptibility to mycobacterial diseaseN Parvaneh, B Pourakbari, N Rezaei, et al.
Clinical and Experimental Dermatology|September 15, 2009
A novel deletion mutation in the human hairless (HR) gene in an Iranian family with atrichia and papular lesionsK Balighi, V Lajevardi, F Moeineddin, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
Journal of Investigational Allergology & Clinical Immunology|October 16, 2010
Correlation between common variable immunodeficiency clinical phenotypes and parental consanguinity in children and adultsA Aghamohammadi, H Abolhassani, K Moazzami, et al.
Journal of Investigational Allergology & Clinical Immunology|April 29, 2014
Genetic defects in B-cell development and their clinical consequencesH Abolhassani, N Parvaneh, N Rezaei, et al.
Journal of Investigational Allergology & Clinical Immunology|February 5, 2010
Severe congenital neutropenia in 2 siblings of consanguineous parents. The role of HAX1 deficiencyS Mamishi, S A Esfahani, N Parvaneh, et al.
Journal of Investigational Allergology & Clinical Immunology|October 24, 2018
A Novel TTC7A Deficiency Presenting With Combined Immunodeficiency and Chronic Gastrointestinal ProblemsS Sharafian, H Alimadadi, M Shahrooei, et al.
Journal of Investigational Allergology & Clinical Immunology|April 25, 2019
UNC13D Deficiency Associated With Epileptic Seizures and Antibody Deficiency: The First Case from the Iranian National RegistryR Yazdani, P Amirifar, H Abolhassani, et al.
Allergologia Et Immunopathologia|October 1, 2018
Evaluation of interleukin-12 receptor β1 and interferon gamma receptor 1 deficiency in patients with disseminated BCG infectionB Pourakbari, R Hosseinpour Sadeghi, S Mahmoudi, et al.
European Annals of Allergy and Clinical Immunology|September 9, 2017
New therapeutic approach by sirolimus for enteropathy treatment in patients with LRBA deficiencyG Azizi, H Abolhassani, R Yazdani, et al.
Iranian Journal of Microbiology|October 16, 2012
Seroepidemiology of Varicella Zoster Virus among children, adolescents and medical students in a referral children medical center, Tehran, IranB Pourakbari, L Shahbaznezhad, N Parvaneh, et al.
Allergologia Et Immunopathologia|September 10, 2014
Impaired in-vitro responses to IL-12 and IFN-γ in Iranian patients with Mendelian susceptibility to mycobacterial diseaseN Parvaneh, B Pourakbari, N Rezaei, et al.
Clinical and Experimental Dermatology|September 15, 2009
A novel deletion mutation in the human hairless (HR) gene in an Iranian family with atrichia and papular lesionsK Balighi, V Lajevardi, F Moeineddin, et al.
Pageof 3