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Author/Creator Lavin, Martin

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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Available online (eLD content is only available in our Reading Rooms) ↗

8. 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) ↗