Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Nima Parvaneh

Showing results (41-50 of 161) with videos related to

Pageof 17
Sort By:
Journal of Human Immunity|May 22, 2026
TLR7 F507S gain-of-function mutation presenting with early-onset SLE and hypertriglyceridemia: Response to JAK inhibitionNima Parvaneh, Hossein Karami, Leila Shahbaznejad, et al.
Iranian Journal of Allergy, Asthma, and Immunology|July 13, 2022
The Efficacy of a New Protocol of Oral Immunotherapy to Wheat for Desensitization and Induction of ToleranceSamin Sharafian, Aliakbar Amirzargar, Mohammad Gharagozlou, et al.
Journal of Microbiology, Immunology, and Infection = Wei Mian Yu Gan Ran Za Zhi|April 29, 2011
Impact of delayed diagnosis in children with primary antibody deficienciesAsghar Aghamohammadi, Ahmad Bahrami, Setareh Mamishi, et al.
International Archives of Allergy and Immunology|June 4, 2008
Progression of selective IgA deficiency to common variable immunodeficiencyAsghar Aghamohammadi, Javad Mohammadi, Nima Parvaneh, et al.
Allergologia Et Immunopathologia|July 13, 2020
Serum sickness-like reactions in Iranian children: a registry-based study in a referral centerAzam Mohsenzadeh, Masoud Movahedi, Mohammad Saatchi, et al.
Ejhaem|July 18, 2022
Bacillus Calmette-Guérin (BCG)-associated hemophagocytic lymphohistiocytosis in the setting of IFN-γR1 deficiency: A diagnostic dilemmaAnahita Razaghian, Leila Parvaneh, Mona Delkhah, et al.
Journal of Laboratory Physicians|April 26, 2018
Complement deficiency in pediatric-onset systemic lupus erythematosusParisa Afzali, Anna Isaeian, Peyman Sadeghi, et al.
Journal of Clinical Immunology|July 9, 2020
Ocular Manifestations of Chronic Granulomatous Disease: First Report of Coats' Disease and Literature ReviewMahsima Shabani, Roxana Pazouki, Mahmoud Parvin, et al.
Iranian Journal of Allergy, Asthma, and Immunology|September 16, 2019
Associations of Behavioral Disorders with Asthma in Iranian ChildrenMohammad Tajdini, Mohammad Effatpanah, Majid Zaki-Dizaji, et al.
Pediatric Rheumatology Online Journal|September 5, 2022
TNFAIP3 mutation causing haploinsufficiency of A20 with a hemophagocytic lymphohistiocytosis phenotype: a report of two casesNahid Aslani, Kosar Asnaashari, Nima Parvaneh, et al.
Pageof 17

Showing results (41-50 of 161) with videos related to

Sort By:
Pageof 17
Journal of Human Immunity|May 22, 2026
TLR7 F507S gain-of-function mutation presenting with early-onset SLE and hypertriglyceridemia: Response to JAK inhibitionNima Parvaneh, Hossein Karami, Leila Shahbaznejad, et al.
Iranian Journal of Allergy, Asthma, and Immunology|July 13, 2022
The Efficacy of a New Protocol of Oral Immunotherapy to Wheat for Desensitization and Induction of ToleranceSamin Sharafian, Aliakbar Amirzargar, Mohammad Gharagozlou, et al.
Journal of Microbiology, Immunology, and Infection = Wei Mian Yu Gan Ran Za Zhi|April 29, 2011
Impact of delayed diagnosis in children with primary antibody deficienciesAsghar Aghamohammadi, Ahmad Bahrami, Setareh Mamishi, et al.
International Archives of Allergy and Immunology|June 4, 2008
Progression of selective IgA deficiency to common variable immunodeficiencyAsghar Aghamohammadi, Javad Mohammadi, Nima Parvaneh, et al.
Allergologia Et Immunopathologia|July 13, 2020
Serum sickness-like reactions in Iranian children: a registry-based study in a referral centerAzam Mohsenzadeh, Masoud Movahedi, Mohammad Saatchi, et al.
Ejhaem|July 18, 2022
Bacillus Calmette-Guérin (BCG)-associated hemophagocytic lymphohistiocytosis in the setting of IFN-γR1 deficiency: A diagnostic dilemmaAnahita Razaghian, Leila Parvaneh, Mona Delkhah, et al.
Journal of Laboratory Physicians|April 26, 2018
Complement deficiency in pediatric-onset systemic lupus erythematosusParisa Afzali, Anna Isaeian, Peyman Sadeghi, et al.
Journal of Clinical Immunology|July 9, 2020
Ocular Manifestations of Chronic Granulomatous Disease: First Report of Coats' Disease and Literature ReviewMahsima Shabani, Roxana Pazouki, Mahmoud Parvin, et al.
Iranian Journal of Allergy, Asthma, and Immunology|September 16, 2019
Associations of Behavioral Disorders with Asthma in Iranian ChildrenMohammad Tajdini, Mohammad Effatpanah, Majid Zaki-Dizaji, et al.
Pediatric Rheumatology Online Journal|September 5, 2022
TNFAIP3 mutation causing haploinsufficiency of A20 with a hemophagocytic lymphohistiocytosis phenotype: a report of two casesNahid Aslani, Kosar Asnaashari, Nima Parvaneh, et al.
Pageof 17