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Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology
|
December 21, 2007
Severe combined immunodeficiency: a cohort of 40 patients
Mehdi Yeganeh, Marzieh Heidarzade, Zahra Pourpak, et al.
Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology
|
May 19, 2007
Vaccine-associated paralytic poliomyelitis in a patient with MHC class II deficiency
Nima Parvaneh, Shohreh Shahmahmoudi, Hamideh Tabatabai, et al.
Journal of Tropical Pediatrics
|
September 9, 2008
Vitamin D insufficiency among children and adolescents living in Tehran, Iran
Ali Rabbani, Seyed-Moayed Alavian, Mohammad Esmaeil Motlagh, et al.
Acta Dermatovenerologica Croatica : ADC
|
July 14, 2010
Cutaneous granulomas in common variable immunodeficiency: case report and review of literature
Asghar Aghamohammadi, Hassan Abolhassani, Nima Rezaei, et al.
Pediatric Blood & Cancer
|
November 23, 2016
Visceral leishmaniasis in two patients with IL-12p40 and IL-12Rβ1 deficiencies
Nima Parvaneh, Vincent Barlogis, Abdolvahab Alborzi, et al.
Iranian Journal of Allergy, Asthma, and Immunology
|
September 11, 2008
Presence of Idiopathic Thrombocytopenic Purpura and autoimmune hemolytic anemia in the patients with common variable immunodeficiency
Asghar Ramyar, Asghar Aghamohammadi, Kasra Moazzami, et al.
Iranian Journal of Allergy, Asthma, and Immunology
|
February 16, 2007
Screening of the Bruton Tyrosine Kinase (BTK) Gene Mutations in 13 Iranian Patients with Presumed X-Linked Agammaglobulinemia
Asghar Aghamohammadi, Nima Parvaneh, Hirokazu Kanegana, et al.
Journal of Clinical Immunology
|
June 16, 2010
Characterization of 11 new cases of leukocyte adhesion deficiency type 1 with seven novel mutations in the ITGB2 gene
Nima Parvaneh, Setareh Mamishi, Amir Rezaei, et al.
Pediatric Rheumatology Online Journal
|
June 13, 2023
A case series of ten plus one deficiency of adenosine deaminase 2 (DADA2) patients in Iran
Kosar Asna Ashari, Nahid Aslani, Nima Parvaneh, et al.
Clinical Biochemistry
|
December 11, 2007
Novel mutations of NP in two patients with purine nucleoside phosphorylase deficiency
Nima Parvaneh, Shahram Teimourian, Gabriella Jacomelli, et al.
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Search research articles
Search
Showing results (81-90 of 161) with videos related to
Sort By:
Page
of 17
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology
|
December 21, 2007
Severe combined immunodeficiency: a cohort of 40 patients
Mehdi Yeganeh, Marzieh Heidarzade, Zahra Pourpak, et al.
Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology
|
May 19, 2007
Vaccine-associated paralytic poliomyelitis in a patient with MHC class II deficiency
Nima Parvaneh, Shohreh Shahmahmoudi, Hamideh Tabatabai, et al.
Journal of Tropical Pediatrics
|
September 9, 2008
Vitamin D insufficiency among children and adolescents living in Tehran, Iran
Ali Rabbani, Seyed-Moayed Alavian, Mohammad Esmaeil Motlagh, et al.
Acta Dermatovenerologica Croatica : ADC
|
July 14, 2010
Cutaneous granulomas in common variable immunodeficiency: case report and review of literature
Asghar Aghamohammadi, Hassan Abolhassani, Nima Rezaei, et al.
Pediatric Blood & Cancer
|
November 23, 2016
Visceral leishmaniasis in two patients with IL-12p40 and IL-12Rβ1 deficiencies
Nima Parvaneh, Vincent Barlogis, Abdolvahab Alborzi, et al.
Iranian Journal of Allergy, Asthma, and Immunology
|
September 11, 2008
Presence of Idiopathic Thrombocytopenic Purpura and autoimmune hemolytic anemia in the patients with common variable immunodeficiency
Asghar Ramyar, Asghar Aghamohammadi, Kasra Moazzami, et al.
Iranian Journal of Allergy, Asthma, and Immunology
|
February 16, 2007
Screening of the Bruton Tyrosine Kinase (BTK) Gene Mutations in 13 Iranian Patients with Presumed X-Linked Agammaglobulinemia
Asghar Aghamohammadi, Nima Parvaneh, Hirokazu Kanegana, et al.
Journal of Clinical Immunology
|
June 16, 2010
Characterization of 11 new cases of leukocyte adhesion deficiency type 1 with seven novel mutations in the ITGB2 gene
Nima Parvaneh, Setareh Mamishi, Amir Rezaei, et al.
Pediatric Rheumatology Online Journal
|
June 13, 2023
A case series of ten plus one deficiency of adenosine deaminase 2 (DADA2) patients in Iran
Kosar Asna Ashari, Nahid Aslani, Nima Parvaneh, et al.
Clinical Biochemistry
|
December 11, 2007
Novel mutations of NP in two patients with purine nucleoside phosphorylase deficiency
Nima Parvaneh, Shahram Teimourian, Gabriella Jacomelli, et al.
Page
of 17