Zahra Chavoshzadeh
10PUBLICATIONS
195CO-AUTHORS

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Publications (10)
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|Feb 02, 2026
Complete and partial forms of X-linked MCTS1 deficiency in patients with mycobacterial disease.Qinhua Zhou, Ivan Bagarić, Fabian Komma
|May 24, 2025
A novel variant in the STIM1 gene leading to combined immunodeficiency and congenital myopathy.Amirreza Taherkhani, Mahmood Gorjizad, Farzad Ahmadabadi
|Jan 08, 2025
Extended clinical phenotypes and treatment modalities in 32 JAGN1-deficient patients: a multicenter study by ESID and EBMT IEWP.Julia Fekadu-Siebald, Emilia Salzmann-Manrique, Jan Robert Heusel
|Aug 20, 2024
Two Unrelated Iranian Patients with Adenosine Deaminase 2 Deficiency: A Case Report and Review of Treatment.Parvaneh Karimzade, Aziz Eghbali, Mohammad Keramatipour
|Mar 21, 2023
Human PIK3R1 mutations disrupt lymphocyte differentiation to cause activated PI3Kδ syndrome 2.Tina Nguyen, Anthony Lau, Julia Bier
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Frequent Collaborators
4 joint publications
Mahnaz Jamee
4 joint publications
Hassan Abolhassani
3 joint publications
Nima Parvaneh
3 joint publications
Stuart G Tangye
3 joint publications
Jonathan Bohlen
3 joint publications
Jérémie Rosain
3 joint publications
Jean-Laurent Casanova
3 joint publications
Cindy S Ma
3 joint publications
Jacinta Bustamante
2 joint publications
Seyed Alireza Mahdaviani