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Works matching AU Shadman, Behrouz

Results: 2

1

Identification of a compound heterozygous missense mutation in LAMA2 gene from a patient with merosin‐deficient congenital muscular dystrophy type 1A.

Published in:

Journal of Clinical Laboratory Analysis, 2021, v. 35, n. 11, p. 1, doi. 10.1002/jcla.23930

By:

Khorrami, Afshin;
Goleij, Pouya;
Karamad, Vahidreza;
Taheri, Elham;
Shadman, Behrouz;
Emami, Parisa;
Jahangirzadeh, Gholamreza;
Hajazimian, Saba;
Isazadeh, Alireza;
Baradaran, Behzad;
Heidari, Mansour

Publication type:

Article

2

Resistance mechanisms to immune checkpoints blockade by monoclonal antibody drugs in cancer immunotherapy: Focus on myeloma.

Published in:

Journal of Cellular Physiology, 2021, v. 236, n. 2, p. 791, doi. 10.1002/jcp.29905

By:

Isazadeh, Alireza;
Hajazimian, Saba;
Garshasbi, Hamid;
Shadman, Behrouz;
Baghbanzadeh, Amir;
Chavoshi, Reza;
Taefehshokr, Sina;
Farhoudi Sefidan Jadid, Mahdieh;
Hajiasgharzadeh, Khalil;
Baradaran, Behzad

Publication type:

Article