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Page 1
Case Report of a Novel NFkB Mutation in a Lymphoproliferative Disorder Patient.
Danandeh K, Jabbari P, Rayzan E, Zoghi S, Shahkarami S, Heredia RJ, Krolo A, Shamsian BS, Boztug K, Rezaei N. Danandeh K, et al. Among authors: shamsian bs. Endocr Metab Immune Disord Drug Targets. 2022;22(10):1040-1046. doi: 10.2174/1871530322666220407091356. Endocr Metab Immune Disord Drug Targets. 2022. PMID: 35392793
A novel RAB27A mutation in a patient with Griscelli syndrome type 2.
Shamsian BS, Norbakhsh K, Rezaei N, Safari A, Gharib A, Pourpak Z, Alavi S, Parvaneh N, Arzanian MT. Shamsian BS, et al. J Investig Allergol Clin Immunol. 2010;20(7):612-5. J Investig Allergol Clin Immunol. 2010. PMID: 21314004 Free article.
DRESS Syndrome Presents as Leukoencephalopathy.
Tonekaboni SH, Jafari N, Chavoshzadeh Z, Shamsian BS, Rezaei N. Tonekaboni SH, et al. Among authors: shamsian bs. Turk J Pediatr. 2015 Sep-Oct;57(5):541-4. Turk J Pediatr. 2015. PMID: 27411428
45 results