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Nima Parvaneh

Showing results (111-120 of 161) with videos related to

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Expert Review of Clinical Immunology|February 25, 2016
Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene DefectsHassan Abolhassani, Massimiliano Vitali, Vassilios Lougaris, et al.
Acta Medica Iranica|November 27, 2016
LPS-Responsive Beige-Like Anchor Gene Mutation Associated With Possible Bronchiolitis Obliterans Organizing Pneumonia Associated With Hypogammaglobulinemia and Normal IgM Phenotype and Low Number of B CellsSima Shokri, Mohammad Nabavi, Tatjana Hirschmugl, et al.
Gut and Liver|February 12, 2014
Evaluation of antibody response to polysaccharide vaccine and switched memory B cells in pediatric patients with inflammatory bowel diseaseGholamhossein Fallahi, Asghar Aghamohammadi, Ahmad Khodadad, et al.
Emerging Infectious Diseases|October 19, 2019
Vaccine-Derived Poliovirus Infection among Patients with Primary Immunodeficiency and Effect of Patient Screening on Disease Outcomes, IranMohammadreza Shaghaghi, Shohreh Shahmahmoodi, Ali Nili, et al.
Iranian Journal of Pediatrics|October 12, 2012
Assessment of pubertal development in Iranian girlsAli Rabbani, Mohammad-Esmaeil Motlagh, Kazem Mohammad, et al.
Immunology Letters|October 8, 2019
Genetic mutations and immunological features of severe combined immunodeficiency patients in IranZahra Shahbazi, Reza Yazdani, Sepideh Shahkarami, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|August 31, 2025
Neonatal diabetes mellitus is a significant feature of COXPD-24 caused by recessive NARS2 variantsRussell Donis, Matthew N Wakeling, Nicola Jeffery, et al.
Blood Cells, Molecules & Diseases|January 25, 2023
Hematologically important mutations: Leukocyte adhesion deficiency (second update)Dirk Roos, Karin van Leeuwen, Manisha Madkaikar, et al.
Journal of Clinical Immunology|August 16, 2023
Clinical, Immunological, and Genetic Findings in Iranian Patients with MHC-II Deficiency: Confirmation of c.162delG RFXANK Founder Mutation in the Iranian PopulationMohadese Sadat Mousavi Khorshidi, Yoann Seeleuthner, Zahra Chavoshzadeh, et al.
Blood Cells, Molecules & Diseases|December 3, 2011
Hematologically important mutations: leukocyte adhesion deficiency (first update)Edith van de Vijver, Anne Maddalena, Özden Sanal, et al.
Pageof 17

Showing results (111-120 of 161) with videos related to

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Pageof 17
Expert Review of Clinical Immunology|February 25, 2016
Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene DefectsHassan Abolhassani, Massimiliano Vitali, Vassilios Lougaris, et al.
Acta Medica Iranica|November 27, 2016
LPS-Responsive Beige-Like Anchor Gene Mutation Associated With Possible Bronchiolitis Obliterans Organizing Pneumonia Associated With Hypogammaglobulinemia and Normal IgM Phenotype and Low Number of B CellsSima Shokri, Mohammad Nabavi, Tatjana Hirschmugl, et al.
Gut and Liver|February 12, 2014
Evaluation of antibody response to polysaccharide vaccine and switched memory B cells in pediatric patients with inflammatory bowel diseaseGholamhossein Fallahi, Asghar Aghamohammadi, Ahmad Khodadad, et al.
Emerging Infectious Diseases|October 19, 2019
Vaccine-Derived Poliovirus Infection among Patients with Primary Immunodeficiency and Effect of Patient Screening on Disease Outcomes, IranMohammadreza Shaghaghi, Shohreh Shahmahmoodi, Ali Nili, et al.
Iranian Journal of Pediatrics|October 12, 2012
Assessment of pubertal development in Iranian girlsAli Rabbani, Mohammad-Esmaeil Motlagh, Kazem Mohammad, et al.
Immunology Letters|October 8, 2019
Genetic mutations and immunological features of severe combined immunodeficiency patients in IranZahra Shahbazi, Reza Yazdani, Sepideh Shahkarami, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|August 31, 2025
Neonatal diabetes mellitus is a significant feature of COXPD-24 caused by recessive NARS2 variantsRussell Donis, Matthew N Wakeling, Nicola Jeffery, et al.
Blood Cells, Molecules & Diseases|January 25, 2023
Hematologically important mutations: Leukocyte adhesion deficiency (second update)Dirk Roos, Karin van Leeuwen, Manisha Madkaikar, et al.
Journal of Clinical Immunology|August 16, 2023
Clinical, Immunological, and Genetic Findings in Iranian Patients with MHC-II Deficiency: Confirmation of c.162delG RFXANK Founder Mutation in the Iranian PopulationMohadese Sadat Mousavi Khorshidi, Yoann Seeleuthner, Zahra Chavoshzadeh, et al.
Blood Cells, Molecules & Diseases|December 3, 2011
Hematologically important mutations: leukocyte adhesion deficiency (first update)Edith van de Vijver, Anne Maddalena, Özden Sanal, et al.
Pageof 17