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Nima Parvaneh

Showing results (91-100 of 161) with videos related to

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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.
Allergy, Asthma, and Clinical Immunology : Official Journal of the Canadian Society of Allergy and Clinical Immunology|February 22, 2023
Demographic, clinical, immunological, and molecular features of iranian national cohort of patients with defect in DCLRE1C geneSoodeh Ghadimi, Mahnaz Jamee, Hassan Abolhassani, et al.
Clinical Case Reports|July 12, 2016
DOCK8 deficiency in six Iranian patientsShiva Saghafi, Zahra Pourpak, Franziska Nussbaumer, et al.
Frontiers in Immunology|December 28, 2020
Griscelli Syndrome Type 2 Sine Albinism: Unraveling Differential RAB27A Effector EngagementYuta Ohishi, Sandra Ammann, Vahid Ziaee, et al.
Iranian Journal of Child Neurology|October 31, 2024
Exploring the Phenotypic Profile of Acute Flaccid Paralysis: Insights from a Third-Level Pediatric Emergency RoomSareh Hosseinpour, Roxana Pazouki, Mahmoud Reza Ashrafi, et al.
Orphanet Journal of Rare Diseases|January 7, 2022
Molecular and clinical characterization of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) in Iranian non-Jewish patients: report of two novel AIRE gene pathogenic variantsAria Setoodeh, Samareh Panjeh-Shahi, Fariba Bahmani, et al.
Annals of Clinical Microbiology and Antimicrobials|March 2, 2022
Effective anti-mycobacterial treatment for BCG disease in patients with Mendelian Susceptibility to Mycobacterial Disease (MSMD): a case seriesSeyed Alireza Mahdaviani, Mazdak Fallahi, Mahnaz Jamee, et al.
JAMA Dermatology|October 13, 2021
Homozygous MEFV Gene Variant and Pyrin-Associated Autoinflammation With Neutrophilic Dermatosis: A Family With a Novel Autosomal Recessive Mode of InheritanceHassan Vahidnezhad, Leila Youssefian, Amir Hossein Saeidian, et al.
Respirology (Carlton, Vic.)|January 7, 2010
Comparison of pulmonary diseases in common variable immunodeficiency and X-linked agammaglobulinaemiaAsghar Aghamohammadi, Abdolreza Allahverdi, Hassan Abolhassani, et al.
BMC Immunology|July 27, 2025
Complete Complement Factor I (CFI) deficiency: a systematic review of forty-nine patients including three novel casesErta Rajabi, Mahsa Choroom Kheirabadi, Nasrin Alipour Olyaei, et al.
Pageof 17

Showing results (91-100 of 161) with videos related to

Sort By:
Pageof 17
European Journal of Pediatrics|March 5, 2008
Novel BTK mutation presenting with vaccine-associated paralytic poliomyelitisSetareh Mamishi, Shohreh Shahmahmoudi, Hamideh Tabatabaie, et al.
Allergy, Asthma, and Clinical Immunology : Official Journal of the Canadian Society of Allergy and Clinical Immunology|February 22, 2023
Demographic, clinical, immunological, and molecular features of iranian national cohort of patients with defect in DCLRE1C geneSoodeh Ghadimi, Mahnaz Jamee, Hassan Abolhassani, et al.
Clinical Case Reports|July 12, 2016
DOCK8 deficiency in six Iranian patientsShiva Saghafi, Zahra Pourpak, Franziska Nussbaumer, et al.
Frontiers in Immunology|December 28, 2020
Griscelli Syndrome Type 2 Sine Albinism: Unraveling Differential RAB27A Effector EngagementYuta Ohishi, Sandra Ammann, Vahid Ziaee, et al.
Iranian Journal of Child Neurology|October 31, 2024
Exploring the Phenotypic Profile of Acute Flaccid Paralysis: Insights from a Third-Level Pediatric Emergency RoomSareh Hosseinpour, Roxana Pazouki, Mahmoud Reza Ashrafi, et al.
Orphanet Journal of Rare Diseases|January 7, 2022
Molecular and clinical characterization of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) in Iranian non-Jewish patients: report of two novel AIRE gene pathogenic variantsAria Setoodeh, Samareh Panjeh-Shahi, Fariba Bahmani, et al.
Annals of Clinical Microbiology and Antimicrobials|March 2, 2022
Effective anti-mycobacterial treatment for BCG disease in patients with Mendelian Susceptibility to Mycobacterial Disease (MSMD): a case seriesSeyed Alireza Mahdaviani, Mazdak Fallahi, Mahnaz Jamee, et al.
JAMA Dermatology|October 13, 2021
Homozygous MEFV Gene Variant and Pyrin-Associated Autoinflammation With Neutrophilic Dermatosis: A Family With a Novel Autosomal Recessive Mode of InheritanceHassan Vahidnezhad, Leila Youssefian, Amir Hossein Saeidian, et al.
Respirology (Carlton, Vic.)|January 7, 2010
Comparison of pulmonary diseases in common variable immunodeficiency and X-linked agammaglobulinaemiaAsghar Aghamohammadi, Abdolreza Allahverdi, Hassan Abolhassani, et al.
BMC Immunology|July 27, 2025
Complete Complement Factor I (CFI) deficiency: a systematic review of forty-nine patients including three novel casesErta Rajabi, Mahsa Choroom Kheirabadi, Nasrin Alipour Olyaei, et al.
Pageof 17