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Author/Creator Amirifar, Parisa

3. Clinical, immunological and genetic findings in patients with UNC13D deficiency (FHL3): A systematic review. Issue 1 (24th August 2020)

Authors:
Amirifar, Parisa; Ranjouri, Mohammad Reza; Abolhassani, Hassan; Moeini Shad, Tannaz; Almasi‐Hashiani, Amir; Azizi, Gholamreza; Moamer, Soraya; Aghamohammadi, Asghar; Yazdani, Reza
Editors:
Genuneit, Jon
Journal:
Pediatric allergy and immunology
Issue:
Volume 32:Issue 1(2021)
Page Start:
186
Record Type:
Journal Article
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4. Cutaneous Granulomatosis and Class Switching Defect as a Presenting Sign in Ataxia-Telangiectasia: First Case from the National Iranian Registry and Review of the Literature. (17th August 2020)

Authors:
Amirifar, Parisa; Yazdani, Reza; Moeini Shad, Tannaz; Ghanadan, Alireza; Abolhassani, Hassan; Lavin, Martin; Sotoudeh, Soheila; Aghamohammadi, Asghar
Journal:
Immunological investigations
Issue:
Volume 49:Number 6(2020)
Page Start:
597
Record Type:
Journal Article
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5. Effect of Class Switch Recombination Defect on the Phenotype of Ataxia-Telangiectasia Patients. (17th February 2021)

Authors:
Amirifar, Parisa; Mozdarani, Hossein; Yazdani, Reza; Kiaei, Fatemeh; Moeini Shad, Tannaz; Shahkarami, Sepideh; Abolhassani, Hassan; Delavari, Samaneh; Sohani, Mahsa; Rezaei, Arezou; Hassanpour, Gholamreza; Akrami, Seyed Mohammad; Aghamohammadi, Asghar
Journal:
Immunological investigations
Issue:
Volume 50:Number 2/3(2021)
Page Start:
201
Record Type:
Journal Article
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6. Known and potential molecules associated with altered B cell development leading to predominantly antibody deficiencies. Issue 8 (24th July 2021)

Authors:
Amirifar, Parisa; Yazdani, Reza; Azizi, Gholamreza; Ranjouri, Mohammad Reza; Durandy, Anne; Plebani, Alessandro; Lougaris, Vassilios; Hammarstrom, Lennart; Aghamohammadi, Asghar; Abolhassani, Hassan
Editors:
Candotti, Fabio
Journal:
Pediatric allergy and immunology
Issue:
Volume 32:Issue 8(2021)
Page Start:
1601
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

7. The spectrum of ATM gene mutations in Iranian patients with ataxia‐telangiectasia. Issue 6 (2nd March 2021)

Authors:
Amirifar, Parisa; Ranjouri, Mohammad Reza; Pashangzadeh, Salar; Lavin, Martin; Yazdani, Reza; Moeini Shad, Tannaz; Mehrmohamadi, Mahya; Salami, Fereshte; Delavari, Samaneh; Moamer, Soraya; Aghamohammadi, Asghar; Akrami, Seyed Mohammad; Abolhassani, Hassan
Journal:
Pediatric allergy and immunology
Issue:
Volume 32:Issue 6(2021)
Page Start:
1316
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗