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Nima Parvaneh

Showing results (31-40 of 161) with videos related to

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Iranian Journal of Child Neurology|February 16, 2026
Commentary on "Exploring the Phenotypic Profile of Acute Flaccid Paralysis: Insights from a Third-Level Pediatric Emergency Room"Sareh Hosseinpour, Mahmoud Reza Ashrafi, Morteza Heidari, et al.
Journal of Clinical Immunology|August 2, 2014
Inborn errors of metabolism underlying primary immunodeficienciesNima Parvaneh, Pierre Quartier, Parastoo Rostami, et al.
Journal De Mycologie Medicale|January 4, 2021
Invasive Rasamsonia argillacea infection in chronic granulomatous disease: Report of a new case and literature reviewHamid Eshaghi, Leila Moradi, Parvaneh Adimi, et al.
Iranian Journal of Child Neurology|July 13, 2017
Tumefactive Multiple Sclerosis Variants: Report of Two Cases of Schilder and Balo DiseasesMahmoud Reza Ashrafi, Ali Reza Tavasoli, Houman Alizadeh, et al.
Ejhaem|June 8, 2026
RASGRP1 Deficiency Manifesting as Severe Vasculopathy and Fatal Autoimmune Hemolytic AnemiaKosar Asna Ashari, Bahareh Yaghmaie, Neda Pak, et al.
The Brazilian Journal of Infectious Diseases : an Official Publication of the Brazilian Society of Infectious Diseases|October 22, 2010
A single center 14 years study of infectious complications leading to hospitalization of patients with primary antibody deficienciesSetareh Mamishi, Aiden Nasiri Eghbali, Nima Rezaei, et al.
European Journal of Dermatology : EJD|April 22, 2008
Treatment of pemphigus vulgaris with mycophenolate mofetil as a steroid-sparing agentNafiseh Esmaili, Cheyda Chams-Davatchi, Mahin Valikhani, et al.
Brain & Development|September 5, 2006
Progressive multifocal leukoencephalopathy in purine nucleoside phosphorylase deficiencyNima Parvaneh, Mahmoud-Reza Ashrafi, Mehdi Yeganeh, et al.
European Journal of Pediatrics|June 18, 2010
Novel UBR1 gene mutation in a patient with typical phenotype of Johanson-Blizzard syndromeGholam Hossein Fallahi, Mozhgan Sabbaghian, Manijeh Khalili, et al.
Orphanet Journal of Rare Diseases|August 5, 2018
Clinical presentation and outcome in infantile Sandhoff disease: a case series of 25 patients from Iranian neurometabolic bioregistry with five novel mutationsAli Reza Tavasoli, Nima Parvaneh, Mahmoud Reza Ashrafi, et al.
Pageof 17

Showing results (31-40 of 161) with videos related to

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Pageof 17
Iranian Journal of Child Neurology|February 16, 2026
Commentary on "Exploring the Phenotypic Profile of Acute Flaccid Paralysis: Insights from a Third-Level Pediatric Emergency Room"Sareh Hosseinpour, Mahmoud Reza Ashrafi, Morteza Heidari, et al.
Journal of Clinical Immunology|August 2, 2014
Inborn errors of metabolism underlying primary immunodeficienciesNima Parvaneh, Pierre Quartier, Parastoo Rostami, et al.
Journal De Mycologie Medicale|January 4, 2021
Invasive Rasamsonia argillacea infection in chronic granulomatous disease: Report of a new case and literature reviewHamid Eshaghi, Leila Moradi, Parvaneh Adimi, et al.
Iranian Journal of Child Neurology|July 13, 2017
Tumefactive Multiple Sclerosis Variants: Report of Two Cases of Schilder and Balo DiseasesMahmoud Reza Ashrafi, Ali Reza Tavasoli, Houman Alizadeh, et al.
Ejhaem|June 8, 2026
RASGRP1 Deficiency Manifesting as Severe Vasculopathy and Fatal Autoimmune Hemolytic AnemiaKosar Asna Ashari, Bahareh Yaghmaie, Neda Pak, et al.
The Brazilian Journal of Infectious Diseases : an Official Publication of the Brazilian Society of Infectious Diseases|October 22, 2010
A single center 14 years study of infectious complications leading to hospitalization of patients with primary antibody deficienciesSetareh Mamishi, Aiden Nasiri Eghbali, Nima Rezaei, et al.
European Journal of Dermatology : EJD|April 22, 2008
Treatment of pemphigus vulgaris with mycophenolate mofetil as a steroid-sparing agentNafiseh Esmaili, Cheyda Chams-Davatchi, Mahin Valikhani, et al.
Brain & Development|September 5, 2006
Progressive multifocal leukoencephalopathy in purine nucleoside phosphorylase deficiencyNima Parvaneh, Mahmoud-Reza Ashrafi, Mehdi Yeganeh, et al.
European Journal of Pediatrics|June 18, 2010
Novel UBR1 gene mutation in a patient with typical phenotype of Johanson-Blizzard syndromeGholam Hossein Fallahi, Mozhgan Sabbaghian, Manijeh Khalili, et al.
Orphanet Journal of Rare Diseases|August 5, 2018
Clinical presentation and outcome in infantile Sandhoff disease: a case series of 25 patients from Iranian neurometabolic bioregistry with five novel mutationsAli Reza Tavasoli, Nima Parvaneh, Mahmoud Reza Ashrafi, et al.
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