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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 immunodeficiencies
Nima 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 review
Hamid 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 Diseases
Mahmoud Reza Ashrafi, Ali Reza Tavasoli, Houman Alizadeh, et al.
Ejhaem
|
June 8, 2026
RASGRP1 Deficiency Manifesting as Severe Vasculopathy and Fatal Autoimmune Hemolytic Anemia
Kosar 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 deficiencies
Setareh 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 agent
Nafiseh Esmaili, Cheyda Chams-Davatchi, Mahin Valikhani, et al.
Brain & Development
|
September 5, 2006
Progressive multifocal leukoencephalopathy in purine nucleoside phosphorylase deficiency
Nima 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 syndrome
Gholam 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 mutations
Ali Reza Tavasoli, Nima Parvaneh, Mahmoud Reza Ashrafi, et al.
Page
of 17
Search research articles
Search
Showing results (31-40 of 161) with videos related to
Sort By:
Page
of 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 immunodeficiencies
Nima 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 review
Hamid 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 Diseases
Mahmoud Reza Ashrafi, Ali Reza Tavasoli, Houman Alizadeh, et al.
Ejhaem
|
June 8, 2026
RASGRP1 Deficiency Manifesting as Severe Vasculopathy and Fatal Autoimmune Hemolytic Anemia
Kosar 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 deficiencies
Setareh 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 agent
Nafiseh Esmaili, Cheyda Chams-Davatchi, Mahin Valikhani, et al.
Brain & Development
|
September 5, 2006
Progressive multifocal leukoencephalopathy in purine nucleoside phosphorylase deficiency
Nima 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 syndrome
Gholam 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 mutations
Ali Reza Tavasoli, Nima Parvaneh, Mahmoud Reza Ashrafi, et al.
Page
of 17